Exact Mass: 228.0818

Exact Mass Matches: 228.0818

Found 376 metabolites which its exact mass value is equals to given mass value 228.0818, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

5,6-Dihydro-5-hydroxy-6-methyl-2H-pyran-2-one

2H-Pyran-2-one, 4-methoxy-6-(2-phenylethenyl)-, (E)- (9CI)

C14H12O3 (228.0786)


5,6-Dehydrokawain is an aromatic ether and a member of 2-pyranones. Desmethoxyyangonin is a natural product found in Alpinia blepharocalyx, Alpinia rafflesiana, and other organisms with data available. See also: Piper methysticum root (part of). 5,6-Dihydro-5-hydroxy-6-methyl-2H-pyran-2-one is found in beverages. 5,6-Dihydro-5-hydroxy-6-methyl-2H-pyran-2-one is found in kava (Piper methysticum). FDA advises against use of kava in food due to potential risk of severe liver damag Found in kava (Piper methysticum). FDA advises against use of kava in food due to potential risk of severe liver damage Desmethoxyyangonin is one of the six major kavalactones found in the Piper methysticum (kava) plant; reversible inhibitor of MAO-B. Desmethoxyyangonin is one of the six major kavalactones found in the Piper methysticum (kava) plant; reversible inhibitor of MAO-B.

   

Resveratrol

(E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol(E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol

C14H12O3 (228.0786)


Resveratrol is a stilbenol that is stilbene in which the phenyl groups are substituted at positions 3, 5, and 4 by hydroxy groups. It has a role as a phytoalexin, an antioxidant, a glioma-associated oncogene inhibitor and a geroprotector. It is a stilbenol, a polyphenol and a member of resorcinols. Resveratrol (3,5,4-trihydroxystilbene) is a polyphenolic phytoalexin. It is a stilbenoid, a derivate of stilbene, and is produced in plants with the help of the enzyme stilbene synthase. It exists as cis-(Z) and trans-(E) isomers. The trans- form can undergo isomerisation to the cis- form when heated or exposed to ultraviolet irradiation. In a 2004 issue of Science, Dr. Sinclair of Harvard University said resveratrol is not an easy molecule to protect from oxidation. It has been claimed that it is readily degraded by exposure to light, heat, and oxygen. However, studies find that Trans-resveratrol undergoes negligible oxidation in normal atmosphere at room temperature. Resveratrol is a plant polyphenol found in high concentrations in red grapes that has been proposed as a treatment for hyperlipidemia and to prevent fatty liver, diabetes, atherosclerosis and aging. Resveratrol use has not been associated with serum enzyme elevations or with clinically apparent liver injury. Resveratrol is a natural product found in Vitis rotundifolia, Vitis amurensis, and other organisms with data available. Resveratrol is a phytoalexin derived from grapes and other food products with antioxidant and potential chemopreventive activities. Resveratrol induces phase II drug-metabolizing enzymes (anti-initiation activity); mediates anti-inflammatory effects and inhibits cyclooxygenase and hydroperoxidase functions (anti-promotion activity); and induces promyelocytic leukemia cell differentiation (anti-progression activity), thereby exhibiting activities in three major steps of carcinogenesis. This agent may inhibit TNF-induced activation of NF-kappaB in a dose- and time-dependent manner. (NCI05) Resveratrol is a metabolite found in or produced by Saccharomyces cerevisiae. A stilbene and non-flavonoid polyphenol produced by various plants including grapes and blueberries. It has anti-oxidant, anti-inflammatory, cardioprotective, anti-mutagenic, and anti-carcinogenic properties. It also inhibits platelet aggregation and the activity of several DNA HELICASES in vitro. Resveratrol is a polyphenolic phytoalexin. It is also classified as a stilbenoid, a derivate of stilbene, and is produced in plants with the help of the enzyme stilbene synthase. The levels of resveratrol found in food vary greatly. Red wine contains between 0.2 and 5.8 mg/L depending on the grape variety, while white wine has much less. The reason for this difference is that red wine is fermented with grape skins, allowing the wine to absorb the resveratrol, whereas white wine is fermented after the skin has been removed. Resveratrol is also sold as a nutritional supplement. A number of beneficial health effects, such as anti-cancer, antiviral, neuroprotective, anti-aging, anti-inflammatory, and life-prolonging effects have been reported for resveratrol. The fact that resveratrol is found in the skin of red grapes and as a constituent of red wine may explain the "French paradox". This paradox is based on the observation that the incidence of coronary heart disease is relatively low in southern France despite high dietary intake of saturated fats. Resveratrol is thought to achieve these cardioprotective effects by a number of different routes: (1) inhibition of vascular cell adhesion molecule expression; (2) inhibition of vascular smooth muscle cell proliferation; (3) stimulation of endothelial nitric oxide synthase (eNOS) activity; (4) inhibition of platelet aggregation; and (5) inhibition of LDL peroxidation (PMID: 17875315, 14676260, 9678525). Resveratrol is a biomarker for the consumption of grapes and raisins. A stilbenol that is stilbene in which the phenyl groups are substituted at positions 3, 5, and 4 by hydroxy groups. COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9638; ORIGINAL_PRECURSOR_SCAN_NO 9635 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9646; ORIGINAL_PRECURSOR_SCAN_NO 9641 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9607; ORIGINAL_PRECURSOR_SCAN_NO 9606 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9642; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4383; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4396; ORIGINAL_PRECURSOR_SCAN_NO 4394 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4376 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9641; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4375; ORIGINAL_PRECURSOR_SCAN_NO 4373 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9614; ORIGINAL_PRECURSOR_SCAN_NO 9611 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4398; ORIGINAL_PRECURSOR_SCAN_NO 4397 IPB_RECORD: 1781; CONFIDENCE confident structure IPB_RECORD: 321; CONFIDENCE confident structure Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   
   

Deoxyuridine

1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione

C9H12N2O5 (228.0746)


Deoxyuridine, also known as dU, belongs to the class of organic compounds known as pyrimidine 2-deoxyribonucleosides. Pyrimidine 2-deoxyribonucleosides are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2. It is similar in chemical structure to uridine, but without the 2-hydroxyl group. Deoxyuridine exists in all living organisms, ranging from bacteria to humans. Within humans, deoxyuridine participates in a number of enzymatic reactions. In particular, deoxyuridine can be biosynthesized from deoxycytidine through its interaction with the enzyme cytidine deaminase. In addition, deoxyuridine can be converted into uracil and deoxyribose 1-phosphate through its interaction with the enzyme thymidine phosphorylase. Deoxyuridine is considered to be an antimetabolite that is converted into deoxyuridine triphosphate during DNA synthesis. Laboratory suppression of deoxyuridine is used to diagnose megaloblastic anemia due to vitamin B12 and folate deficiencies. In humans, deoxyuridine is involved in the metabolic disorder called UMP synthase deficiency (orotic aciduria). Outside of the human body, deoxyuridine has been detected, but not quantified in, several different foods, such as lichee, highbush blueberries, agaves, macadamia nut (M. tetraphylla), and red bell peppers. This could make deoxyuridine a potential biomarker for the consumption of these foods. 2-Deoxyuridine is a naturally occurring nucleoside. It is similar in chemical structure to uridine, but without the 2-hydroxyl group. It is considered to be an antimetabolite that is converted to deoxyuridine triphosphate during DNA synthesis. Laboratory suppression of deoxyuridine is used to diagnose megaloblastic anemia due to vitamin B12 and folate deficiencies. [HMDB]. Deoxyuridine is found in many foods, some of which are garden tomato (variety), hickory nut, banana, and hazelnut. Deoxyuridine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=951-78-0 (retrieved 2024-07-01) (CAS RN: 951-78-0). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.

   

Trioxsalen

6-Hydroxy-beta,2,7-trimethyl-5-benzofuranacrylic acid, delta-lactone

C14H12O3 (228.0786)


Trioxsalen, also known as trimethylpsoralen or trisoralen, is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one. Trioxsalen is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Trioxsalen can be found in wild celery, which makes trioxsalen a potential biomarker for the consumption of this food product. Trioxsalen can be found primarily in blood and urine. Trioxsalen (trimethylpsoralen, Trioxysalen or Trisoralen) is a furanocoumarin and a psoralen derivative. It is obtained from several plants, mainly Psoralea corylifolia. Like other psoralens it causes photosensitization of the skin. It is administered either topically or orally in conjunction with UV-A (the least damaging form of ultraviolet light) for phototherapy treatment of vitiligo and hand eczema. After photoactivation it creates interstrand cross-links in DNA, which can cause programmed cell death unless repaired by cellular mechanisms. In research it can be conjugated to dyes for confocal microscopy and used to visualize sites of DNA damage. The compound is also being explored for development of antisense oligonucleotides that can be cross-linked specifically to a mutant mRNA sequence without affecting normal transcripts differing at even a single base pair . Trioxsalen ispharmacologically inactive but when exposed to ultraviolet radiation or sunlight it is converted to its active metabolite to produce a beneficial reaction affecting the diseased tissue (DrugBank). Trioxsalen, also known as trimethylpsoralen, trioxysalen or trisoralen, belongs to the group of drugs called psoralens. It is also known as a furanocoumarin (PMID: 3196695). Trioxsalen is a pigmenting photosensitizing agent used to treat vitiligo, a condition characterized by loss of skin color (PMID: 4828534, 4441118). It is administered in conjunction with ultraviolet light A (UVA) to increase the skins sensitivity to sunlight. Trioxsalen functions through inducing interstrand crosslinks in DNA. It has been reported that use of trioxsalen increases the chance of skin cancer and cataracts. Trioxsalen is only found in individuals that have used or taken this drug. D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use D - Dermatologicals > D05 - Antipsoriatics > D05A - Antipsoriatics for topical use > D05AD - Psoralens for topical use D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins C78284 - Agent Affecting Integumentary System > C29708 - Anti-psoriatic Agent D003879 - Dermatologic Agents Trioxsalen (Trisoralen), a psoralen derivative, is a photochemical DNA crosslinker. Trioxsalen only works after photoactivation with near ultraviolet light. Trioxsalen is a photosensitizer that can be used for the research of vitiligo and hand eczema. Trioxsalen is used for visualization of genomic interstrand cross-links localized by laser photoactivation Trimethylpsoralen. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=3902-71-4 (retrieved 2024-09-04) (CAS RN: 3902-71-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

oxybenzone

2-Hydroxy-4-methoxybenzophenone

C14H12O3 (228.0786)


D020011 - Protective Agents > D011837 - Radiation-Protective Agents > D013473 - Sunscreening Agents C1892 - Chemopreventive Agent > C851 - Sunscreen D003879 - Dermatologic Agents D003358 - Cosmetics Same as: D05309 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4375; ORIGINAL_PRECURSOR_SCAN_NO 4373 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4383; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4376 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4396; ORIGINAL_PRECURSOR_SCAN_NO 4394 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4398; ORIGINAL_PRECURSOR_SCAN_NO 4397 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9607; ORIGINAL_PRECURSOR_SCAN_NO 9606 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9642; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9614; ORIGINAL_PRECURSOR_SCAN_NO 9611 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9638; ORIGINAL_PRECURSOR_SCAN_NO 9635 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9643; ORIGINAL_PRECURSOR_SCAN_NO 9641 CONFIDENCE standard compound; INTERNAL_ID 754; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9646; ORIGINAL_PRECURSOR_SCAN_NO 9641 CONFIDENCE standard compound; INTERNAL_ID 2758 CONFIDENCE standard compound; INTERNAL_ID 8629 CONFIDENCE standard compound; INTERNAL_ID 8143 CONFIDENCE standard compound; EAWAG_UCHEM_ID 230

   

Xanthyletin

8,8-dimethyl-2H,8H-pyrano[3,2-g]chromen-2-one

C14H12O3 (228.0786)


Xanthyletin is a member of the class of compounds known as linear pyranocoumarins. Linear pyranocoumarins are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety. Xanthyletin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Xanthyletin can be found in lemon, lime, mandarin orange (clementine, tangerine), and sweet orange, which makes xanthyletin a potential biomarker for the consumption of these food products.

   

Benzyl 4-hydroxybenzoate

Benzyl parahydroxybenzoic acid

C14H12O3 (228.0786)


CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9646; ORIGINAL_PRECURSOR_SCAN_NO 9641 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9607; ORIGINAL_PRECURSOR_SCAN_NO 9606 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9641; ORIGINAL_PRECURSOR_SCAN_NO 9638 DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; CONFIDENCE standard compound; INTERNAL_ID 780; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9646; ORIGINAL_PRECURSOR_SCAN_NO 9641 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4398; ORIGINAL_PRECURSOR_SCAN_NO 4397 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4338; ORIGINAL_PRECURSOR_SCAN_NO 4336 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4375; ORIGINAL_PRECURSOR_SCAN_NO 4373 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4383; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9614; ORIGINAL_PRECURSOR_SCAN_NO 9611 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9638; ORIGINAL_PRECURSOR_SCAN_NO 9635 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9642; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 780; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4357; ORIGINAL_PRECURSOR_SCAN_NO 4355 D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens Same as: D07518

   

3,4-Dihydro-8,9-dihydroxy-1(2H)-anthracenone

3,4-Dihydro-8,9-dihydroxy-1(2H)-anthracenone

C14H12O3 (228.0786)


   

4,4,6-Trimethylangelicin

4,4,6-Trimethylangelicin

C14H12O3 (228.0786)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins

   

(1R,10aS)-1,4,10,10a-Tetrahydrophenazine-1-carboxylate

(1R,10aS)-1,4,10,10a-tetrahydrophenazine-1-carboxylic acid

C13H12N2O2 (228.0899)


   

(1R)-1,4,5,10-Tetrahydrophenazine-1-carboxylate

(1R)-1,4,5,10-tetrahydrophenazine-1-carboxylic acid

C13H12N2O2 (228.0899)


   

4-(Pyridine-4-carbonyl)pyridin-1-ium-3-carboxamide

4-(Pyridine-4-carbonyl)pyridin-1-ium-3-carboxamide

C12H10N3O2+ (228.0773)


   

Glyphosate-isopropylammonium

Glyphosate-isopropylammonium

C6H17N2O5P (228.0875)


D000890 - Anti-Infective Agents > D000935 - Antifungal Agents D004791 - Enzyme Inhibitors > D014475 - Uncoupling Agents D010575 - Pesticides > D006540 - Herbicides D016573 - Agrochemicals

   

(Z)-Resveratrol

InChI=1/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1-

C14H12O3 (228.0786)


Cis-resveratrol is the cis-stereoisomer of resveratrol. (Z)-resveratrol is a natural product found in Vitis rupestris, Vaccinium macrocarpon, and other organisms with data available. A stilbene and non-flavonoid polyphenol produced by various plants including grapes and blueberries. It has anti-oxidant, anti-inflammatory, cardioprotective, anti-mutagenic, and anti-carcinogenic properties. It also inhibits platelet aggregation and the activity of several DNA HELICASES in vitro. Phytoalexin from hypocotyls of germinating peanuts (Arachis hypogaea). (Z)-Resveratrol is found in peanut, nuts, and common grape. (Z)-Resveratrol is found in common grape. Phytoalexin from hypocotyls of germinating peanuts (Arachis hypogaea). D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors D020011 - Protective Agents > D000975 - Antioxidants The cis-stereoisomer of resveratrol. D004791 - Enzyme Inhibitors cis-Resveratrol exhibits signifcant antiviral activity. cis-Resveratrol inhibits enteroviruses with IC50s of 12.2 μM and 37.6 μM for coxsackievirus B3 (CVB3) and enterovirus 71 (EV71), respectively[1].

   

Seselin

2H-1-Benzopyran-6-acrylic acid, 5-hydroxy-2,2-dimethyl-, .delta.-lactone

C14H12O3 (228.0786)


Seselin is a member of coumarins. It has a role as a metabolite. Seselin is a natural product found in Haplophyllum cappadocicum, Haplophyllum dshungaricum, and other organisms with data available. Constituent of Carum roxburghianum (Bishops weed). Seselin is found in many foods, some of which are sweet orange, herbs and spices, anise, and wild celery. Seselin is found in anise. Seselin is a constituent of Carum roxburghianum (Bishops weed) A natural product found in Citropsis articulata.

   

Oxybenzone

4-Methoxy-2-hydroxybenzophenone butyric acid

C14H12O3 (228.0786)


Oxybenzone is an organic compound used in sunscreens. It is a derivative of benzophenone. It forms colorless crystals that are readily soluble in most organic solvents. It is used as an ingredient in sunscreen and other cosmetics because it absorbs UV-A ultraviolet rays. D020011 - Protective Agents > D011837 - Radiation-Protective Agents > D013473 - Sunscreening Agents C1892 - Chemopreventive Agent > C851 - Sunscreen D003879 - Dermatologic Agents D003358 - Cosmetics Same as: D05309

   

Benzyl salicylate

Benzoic acid, 2-hydroxy-, phenylmethyl ester

C14H12O3 (228.0786)


Benzyl salicylate is found in cloves. Benzyl salicylate is isolated from essential oils e.g. Dianthus caryophyllus, Populus, Primula species Fixative in perfumes and flavourings Benzyl salicylate is a salicylic acid benzyl ester, a chemical compound most frequently used in cosmetics. It appears as an almost colourless liquid and is rather faint or odorless in nature Isolated from essential oils e.g. Dianthus caryophyllus, Populus, Primula subspecies Fixative in perfumes and flavourings D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates Benzyl salicylate?is a salicylic acid benzyl ester. It can be used as a fragrance additive or UV light absorber. Benzyl salicylate?is a salicylic acid benzyl ester. It can be used as a fragrance additive or UV light absorber.

   

Decitabine

4-amino-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3,5-triazin-2-one

C8H12N4O4 (228.0859)


Decitabine is indicated for treatment of patients with myelodysplastic syndrome (MDS). It is a chemical analogue of cytidine, a nucleoside present in DNA and RNA. Cells in the presence of Decitabine incorporate it into DNA during replication and RNA during transcription. The incorporation of Decitabine into DNA or RNA inhibits methyltransferase thereby causing demethylation in that sequence. This adversely affects the way that cell regulatory proteins are able to bind to the DNA/RNA substrate. L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BC - Pyrimidine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C471 - Enzyme Inhibitor > C2083 - DNA Methyltransferase Inhibitor C274 - Antineoplastic Agent > C132686 - Demethylating Agent D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Decitabine (NSC 127716) is an orally active deoxycytidine analogue antimetabolite and a DNA methyltransferase inhibitor. Decitabine incorporates into DNA in place of cytosine can covalently trap DNA methyltransferase to DNA causing irreversible inhibition of the enzyme. Decitabine induces cell G2/M arrest and cell apoptosis. Decitabine has potent anticancer activity[1][2].

   

Pemirolast

9-methyl-3-(2H-1,2,3,4-tetrazol-5-yl)-4H-pyrido[1,2-a]pyrimidin-4-one

C10H8N6O (228.076)


Pemirolast potassium is a slightly yellow powder that is soluble in water. It is a mast cell stabilizer that acts as an antiallergic agent. As an ophthalmic aqueous sterile solution, pemirolast is used for the prevention of itching of the eyes caused by allergies such as hay fever, and allergic conjunctivitis. Pemirolast is potentially useful for prophylaxis of pulmonary hypersensitivity reactions to drugs such as paclitaxel. C78273 - Agent Affecting Respiratory System > C29712 - Anti-asthmatic Agent > C29714 - Mast Cell Stabilizer D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists

   

2,4-Difurfurylfuran

2,4-bis(furan-2-ylmethyl)furan

C14H12O3 (228.0786)


2,4-Difurfurylfuran is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]")

   

o-Tolyl salicylate

Benzoic acid, 2-hydroxy-, 2-methylphenyl ester

C14H12O3 (228.0786)


o-Tolyl salicylate is a flavouring ingredient. Flavouring ingredient

   

3-[4-(1-Imidazolylmethyl)phenyl]-2-propenoic acid

3-{4-[(1H-imidazol-1-yl)methyl]phenyl}prop-2-enoic acid

C13H12N2O2 (228.0899)


   

1-((2S,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

1-((2S,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

C9H12N2O5 (228.0746)


   

1-[(2R,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-2-oxolanyl]-2-pyrimidinone

1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one

C9H12N2O5 (228.0746)


   

1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-

1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-

C14H12O3 (228.0786)


Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   

Antigastrin

2-phenyl-2-(pyridin-2-yl)ethanethioamide

C13H12N2S (228.0721)


   

Benzilic acid

alpha,alpha-Diphenyl-alpha-hydroxyacetic acid

C14H12O3 (228.0786)


   

Dioxolane-THYMINE

1-[2-(hydroxymethyl)-1,3-dioxolan-4-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

C9H12N2O5 (228.0746)


   

1,3,5-Triazin-2(1H)-one, 4-amino-1-(2-deoxy-beta-D-erythro-pentofuranosyl)-

4-amino-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydro-1,3,5-triazin-2-one

C8H12N4O4 (228.0859)


   

trihydroxystilbene

4-(2-phenylethenyl)benzene-1,2,3-triol

C14H12O3 (228.0786)


   

Resveratrol

3,4,5-Trihydroxystilbene

C14H12O3 (228.0786)


COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D000975 - Antioxidants CONFIDENCE standard compound; EAWAG_UCHEM_ID 3241 C26170 - Protective Agent > C275 - Antioxidant D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   

Aaptamine

11,12-dimethoxy-2,6-diazatricyclo[7.3.1.05,13]trideca-1,3,5(13),7,9,11-hexaene

C13H12N2O2 (228.0899)


Aaptamine is a natural product found in Aaptos, Aaptos aaptos, and other organisms with data available.

   

Isoangenomalin

Isoangenomalin

C14H12O3 (228.0786)


   

2,4,7-Trihydroxy-9,10-dihydrophenanthrene

2,4,7-Trihydroxy-9,10-dihydrophenanthrene

C14H12O3 (228.0786)


   
   

Triptispinocoumarin

Triptispinocoumarin

C14H12O3 (228.0786)


   

2-isopropyl-7H-furo[3,2-g]chromen-7-one

2-isopropyl-7H-furo[3,2-g]chromen-7-one

C14H12O3 (228.0786)


   
   

3,4,5-Trimethoxystilbene

3,4,5-Trimethoxystilbene

C14H12O3 (228.0786)


   
   

3,7-dihydroxy-1,9-dimethyldibenzofuran

3,7-dihydroxy-1,9-dimethyldibenzofuran

C14H12O3 (228.0786)


   
   

4-hydroxy-3-(4-hydroxybenzyl)benzaldehyde

4-hydroxy-3-(4-hydroxybenzyl)benzaldehyde

C14H12O3 (228.0786)


   
   

7-Acetyl-4-methyl-1-azulenecarboxylic acid

7-Acetyl-4-methyl-1-azulenecarboxylic acid

C14H12O3 (228.0786)


   

Desmethoxyyangonin

Desmethoxyyangonin

C14H12O3 (228.0786)


Desmethoxyyangonin is one of the six major kavalactones found in the Piper methysticum (kava) plant; reversible inhibitor of MAO-B. Desmethoxyyangonin is one of the six major kavalactones found in the Piper methysticum (kava) plant; reversible inhibitor of MAO-B.

   

3,5,4-trihydroxystilbene

3,5,4-trihydroxystilbene

C14H12O3 (228.0786)


   

1,1-Diphenyl-2-thiourea

1,1-Diphenyl-2-thiourea

C13H12N2S (228.0721)


   

(3-Chloro-adamantan-1-yl)-acetic acid

(3-Chloro-adamantan-1-yl)-acetic acid

C12H17ClO2 (228.0917)


   

4-Methoxy-N-pyridin-3-yl-benzamide

4-Methoxy-N-pyridin-3-yl-benzamide

C13H12N2O2 (228.0899)


   

Maybridge3_001125

Maybridge3_001125

C13H12N2O2 (228.0899)


   

1-((2R,3R,5S)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

1-((2R,3R,5S)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

C9H12N2O5 (228.0746)


   

3-[4-(1-imidazolylmethyl)phenyl]-2-propenoic acid

3-[4-(1-imidazolylmethyl)phenyl]-2-propenoic acid

C13H12N2O2 (228.0899)


   

Aspernigrin A

Aspernigrin A

C13H12N2O2 (228.0899)


A member of the class of 4-pyridones that is 4-pyridone in which the hydrogens at positions 3 and 6 have been replaced by aminocarbonyl and benzyl groups, respectively. It has been isolated from the Cynodon dactylon-associated endophytic fungus Cladosporium herbarum IFB-E002 and from a sponge-derived Aspergillus niger.

   

Demethylfrutescin|Desmethylfrutescin

Demethylfrutescin|Desmethylfrutescin

C14H12O3 (228.0786)


   

2-methoxy-6-<2-(phenyl)ethenyl>pyran-4-one|2-Methoxy-6-trans-styryl-pyran-4-on|2-methoxy-6-trans-styryl-pyran-4-one

2-methoxy-6-<2-(phenyl)ethenyl>pyran-4-one|2-Methoxy-6-trans-styryl-pyran-4-on|2-methoxy-6-trans-styryl-pyran-4-one

C14H12O3 (228.0786)


   

DTXSID60853756

DTXSID60853756

C14H12O3 (228.0786)


   

CHEMBL474974

CHEMBL474974

C14H12O3 (228.0786)


   

Phenyl 4-methoxybenzoate

Phenyl 4-methoxybenzoate

C14H12O3 (228.0786)


   

Umbelliferone-(3-methyl-buta-1t.3-dien-1-yl)-ether|Umbelliferone-<3-methyl-buta-1t.3-dien-1-yl>-ether

Umbelliferone-(3-methyl-buta-1t.3-dien-1-yl)-ether|Umbelliferone-<3-methyl-buta-1t.3-dien-1-yl>-ether

C14H12O3 (228.0786)


   

Phosphonooxyaceton-diaethylacetal|phosphoric acid mono-(2,2-diethoxy-propyl ester)|Phosphorsaeure-mono-(2,2-diaethoxy-propylester)

Phosphonooxyaceton-diaethylacetal|phosphoric acid mono-(2,2-diethoxy-propyl ester)|Phosphorsaeure-mono-(2,2-diaethoxy-propylester)

C7H17O6P (228.0763)


   

Isotriptospinocoumarin

Isotriptospinocoumarin

C14H12O3 (228.0786)


   

Norlapachol

Norlapachol

C14H12O3 (228.0786)


   

3-O-desmethylfrutescin

3-O-desmethylfrutescin

C14H12O3 (228.0786)


   

9-oxoplatyphyllide

9-oxoplatyphyllide

C14H12O3 (228.0786)


   

(2E)-4-methoxy-2-(nitrosomethylidene)-6-phenyl-1H-pyridine

(2E)-4-methoxy-2-(nitrosomethylidene)-6-phenyl-1H-pyridine

C13H12N2O2 (228.0899)


   

Benzyl 3-hydroxybenzoate

Benzyl 3-hydroxybenzoate

C14H12O3 (228.0786)


   
   

ACMC-20n4i6

ACMC-20n4i6

C14H12O3 (228.0786)


   

4-[2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

4-[2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

C14H12O3 (228.0786)


   

2-Methoxyphenyl benzoate

2-Methoxyphenyl benzoate

C14H12O3 (228.0786)


   

DTXSID20823738

DTXSID20823738

C14H12O3 (228.0786)


   

DTXSID30792461

DTXSID30792461

C14H12O3 (228.0786)


   

2,5-Difurfurylfuran

2,5-Difurfurylfuran

C14H12O3 (228.0786)


   

2-(4-Methoxyphenyl)benzoic acid

2-(4-Methoxyphenyl)benzoic acid

C14H12O3 (228.0786)


   
   
   
   

2-E-<2-oxo-cyclopent-3-ene-1-ylidene>ethyl benzoate|Benzoyl-5-(2-Hydroxyethylidene)-2-cyclopenten-1-one

2-E-<2-oxo-cyclopent-3-ene-1-ylidene>ethyl benzoate|Benzoyl-5-(2-Hydroxyethylidene)-2-cyclopenten-1-one

C14H12O3 (228.0786)


   

Harmine N-oxide

Harmine N-oxide

C13H12N2O2 (228.0899)


   

Methyl 2-phenoxybenzoate

Methyl 2-phenoxybenzoate

C14H12O3 (228.0786)


   

NSC309132;4-Deoxyuridine

NSC309132;4-Deoxyuridine

C9H12N2O5 (228.0746)


   

Benzyl salicylate

Benzoic acid, 2-hydroxy-, phenylmethyl ester

C14H12O3 (228.0786)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4375; ORIGINAL_PRECURSOR_SCAN_NO 4373 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4383; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4376 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4396; ORIGINAL_PRECURSOR_SCAN_NO 4394 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4398; ORIGINAL_PRECURSOR_SCAN_NO 4397 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9607; ORIGINAL_PRECURSOR_SCAN_NO 9606 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9642; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9614; ORIGINAL_PRECURSOR_SCAN_NO 9611 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9638; ORIGINAL_PRECURSOR_SCAN_NO 9635 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9641; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 962; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9646; ORIGINAL_PRECURSOR_SCAN_NO 9641 Benzyl salicylate?is a salicylic acid benzyl ester. It can be used as a fragrance additive or UV light absorber. Benzyl salicylate?is a salicylic acid benzyl ester. It can be used as a fragrance additive or UV light absorber.

   

9,10-dihydrophenanthrene-2,4,7-triol

2,4,7-Trihydroxy-9,10-dihydrophenanthrene

C14H12O3 (228.0786)


2,4,7-Trihydroxy-9,10-dihydrophenanthrene is a natural product found in Dendrobium moniliforme and Pholidota chinensis with data available.

   

Angenomalin

(8S)-8-(prop-1-en-2-yl)-8,9-dihydro-2H-furo[2,3-h][1]benzopyran-2-one

C14H12O3 (228.0786)


(+)-angenomalin is a furanocoumarin that is 8,9-dihydro-2H-furo[2,3-h][1]benzopyran-2-one carrying a prop-1-en-2-yl substituent at position 8. It has a role as a plant metabolite. It is a furanocoumarin and an olefinic compound. Angenomalin is a natural product found in Angelica anomala, Prangos pabularia, and Angelica sachalinensis with data available. A furanocoumarin that is 8,9-dihydro-2H-furo[2,3-h][1]benzopyran-2-one carrying a prop-1-en-2-yl substituent at position 8.

   

Benzophenone-3

Benzophenone-3

C14H12O3 (228.0786)


CONFIDENCE Reference Standard (Level 1)

   

Resveratrol

trans-resveratrol

C14H12O3 (228.0786)


Resveratrol, also known as 3,4,5-trihydroxystilbene or trans-resveratrol, is a member of the class of compounds known as stilbenes. Stilbenes are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. Thus, resveratrol is considered to be an aromatic polyketide lipid molecule. Resveratrol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Resveratrol is a bitter tasting compound and can be found in a number of food items such as broccoli, yellow wax bean, bilberry, and turnip, which makes resveratrol a potential biomarker for the consumption of these food products. Resveratrol can be found primarily in urine, as well as throughout most human tissues. Resveratrol exists in all eukaryotes, ranging from yeast to humans. Resveratrol (3,5,4′-trihydroxy-trans-stilbene) is a stilbenoid, a type of natural phenol, and a phytoalexin produced by several plants in response to injury or, when the plant is under attack by pathogens such as bacteria or fungi. Sources of resveratrol in food include the skin of grapes, blueberries, raspberries, mulberries . Resveratrol suppresses NF-kappaB (NF-kappaB) activation in HSV infected cells. Reports have indicated that HSV activates NF-kappaB during productive infection and this may be an essential aspect of its replication scheme [PMID: 9705914] (DrugBank). relative retention time with respect to 9-anthracene Carboxylic Acid is 0.738 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.740 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.730 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.733 Acquisition and generation of the data is financially supported by the Max-Planck-Society COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS IPB_RECORD: 2101; CONFIDENCE confident structure IPB_RECORD: 2901; CONFIDENCE confident structure Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   

Ozagrel

3-[4-(1H-imidazol-1-ylmethyl)phenyl]-2E-propenoic acid

C13H12N2O2 (228.0899)


D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists C78275 - Agent Affecting Blood or Body Fluid > C1327 - Antiplatelet Agent D006401 - Hematologic Agents > D005343 - Fibrinolytic Agents D050299 - Fibrin Modulating Agents D002317 - Cardiovascular Agents D004791 - Enzyme Inhibitors C471 - Enzyme Inhibitor

   

Deoxyuridine

2-deoxyuridine

C9H12N2O5 (228.0746)


2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.

   

4-methoxy-6-[(E)-2-phenylethenyl]pyran-2-one

NCGC00091904-06!4-methoxy-6-[(E)-2-phenylethenyl]pyran-2-one

C14H12O3 (228.0786)


   

2,2-dimethylpyrano[3,2-g]chromen-8-one

NCGC00095444-05!2,2-dimethylpyrano[3,2-g]chromen-8-one

C14H12O3 (228.0786)


   

8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one

NCGC00385940-01!8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one

C14H12O3 (228.0786)


   

6-benzyl-4-oxo-1H-pyridine-3-carboxamide

NCGC00380293-01!6-benzyl-4-oxo-1H-pyridine-3-carboxamide

C13H12N2O2 (228.0899)


   

5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

NCGC00017352-31!5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

C14H12O3 (228.0786)


   

2-Deoxyuridine

2-Deoxyuridine

C9H12N2O5 (228.0746)


   

3-Deoxyuridine

3-Deoxyuridine

C9H12N2O5 (228.0746)


   

2-deoxyuridine

2-deoxyuridine

C9H12N2O5 (228.0746)


A pyrimidine 2-deoxyribonucleoside having uracil as the nucleobase. D009676 - Noxae > D000963 - Antimetabolites COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.

   

trans-resveratrol

trans-resveratrol

C14H12O3 (228.0786)


A resveratrol in which the double bond has E configuration.

   

Xanthyletine

Xanthyletine

C14H12O3 (228.0786)


   

Xanthyletin

Xanthyletin

C14H12O3 (228.0786)


   

3,4,5-Trihydroxystilbene

3,4,5-Trihydroxystilbene

C14H12O3 (228.0786)


Annotation level-1

   

cis-resveratrol

5[(1Z)-2-(4-hydroxyphenyl)ethenyl]-1,3-benzenediol

C14H12O3 (228.0786)


Annotation level-1 cis-Resveratrol exhibits signifcant antiviral activity. cis-Resveratrol inhibits enteroviruses with IC50s of 12.2 μM and 37.6 μM for coxsackievirus B3 (CVB3) and enterovirus 71 (EV71), respectively[1].

   
   

4-methoxy-6-[(E)-2-phenylethenyl]pyran-2-one [IIN-based: Match]

NCGC00091904-06!4-methoxy-6-[(E)-2-phenylethenyl]pyran-2-one [IIN-based: Match]

C14H12O3 (228.0786)


   

4-methoxy-6-[(E)-2-phenylethenyl]pyran-2-one [IIN-based on: CCMSLIB00000845942]

NCGC00091904-06!4-methoxy-6-[(E)-2-phenylethenyl]pyran-2-one [IIN-based on: CCMSLIB00000845942]

C14H12O3 (228.0786)


   
   

p-Tolyl salicylate

Benzoic acid,2-hydroxy-, 4-methylphenyl ester

C14H12O3 (228.0786)


CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4379 D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4375; ORIGINAL_PRECURSOR_SCAN_NO 4373 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4383; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4376 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4396; ORIGINAL_PRECURSOR_SCAN_NO 4394 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4398; ORIGINAL_PRECURSOR_SCAN_NO 4397 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9607; ORIGINAL_PRECURSOR_SCAN_NO 9606 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9642; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9614; ORIGINAL_PRECURSOR_SCAN_NO 9611 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9638; ORIGINAL_PRECURSOR_SCAN_NO 9635 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9641; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 1261; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9646; ORIGINAL_PRECURSOR_SCAN_NO 9641

   

Desmethoxyyangonin_major

Desmethoxyyangonin_major

C14H12O3 (228.0786)


   

Resveratrol_major

Resveratrol_major

C14H12O3 (228.0786)


   

Resveratrol_minor

Resveratrol_minor

C14H12O3 (228.0786)


   

Deoxyuridine_major

Deoxyuridine_major

C9H12N2O5 (228.0746)


   

Agmatine sulfate

Agmatine sulfate

C5H16N4O4S (228.0892)


Agmatine sulfate exerts modulatory action at multiple molecular targets, such as neurotransmitter systems, ion channels and nitric oxide synthesis. It is an endogenous agonist at imidazoline receptor and a NO synthase inhibitor.

   

4-Hydroxy-4-biphenylacetic acid

4-Hydroxy-4-biphenylacetic acid

C14H12O3 (228.0786)


   

Decitabine

Decitabine

C8H12N4O4 (228.0859)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BC - Pyrimidine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C471 - Enzyme Inhibitor > C2083 - DNA Methyltransferase Inhibitor C274 - Antineoplastic Agent > C132686 - Demethylating Agent D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Decitabine (NSC 127716) is an orally active deoxycytidine analogue antimetabolite and a DNA methyltransferase inhibitor. Decitabine incorporates into DNA in place of cytosine can covalently trap DNA methyltransferase to DNA causing irreversible inhibition of the enzyme. Decitabine induces cell G2/M arrest and cell apoptosis. Decitabine has potent anticancer activity[1][2].

   

pemirolast

9-methyl-3-(2H-1,2,3,4-tetrazol-5-yl)-4H-pyrido[1,2-a]pyrimidin-4-one

C10H8N6O (228.076)


C78273 - Agent Affecting Respiratory System > C29712 - Anti-asthmatic Agent > C29714 - Mast Cell Stabilizer D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists

   

2,4-Difurfurylfuran

2,4-bis(furan-2-ylmethyl)furan

C14H12O3 (228.0786)


   

FEMA 3734

Benzoic acid, 2-hydroxy-, 2-methylphenyl ester

C14H12O3 (228.0786)


   

Zebularine

Zebularine

C9H12N2O5 (228.0746)


C471 - Enzyme Inhibitor > C2083 - DNA Methyltransferase Inhibitor C274 - Antineoplastic Agent > C132686 - Demethylating Agent Zebularine (NSC309132; 4-Deoxyuridine) is a DNA methyltransferase inhibitor. Zebularine also inhibits cytidine deaminase with a Ki of 0.95 μM.

   

trans-Resveratrol-d4

trans-Resveratrol-d4

C14H12O3 (228.0786)


   

2-METHOXY-BENZOIC ACID PHENYL ESTER

2-METHOXY-BENZOIC ACID PHENYL ESTER

C14H12O3 (228.0786)


   

M-TOLYL-PHOSPHONIC ACID DIETHYL ESTER

M-TOLYL-PHOSPHONIC ACID DIETHYL ESTER

C11H17O3P (228.0915)


   

3-(4-METHOXY-1-NAPHTHYL)ACRYLIC ACID

3-(4-METHOXY-1-NAPHTHYL)ACRYLIC ACID

C14H12O3 (228.0786)


   

Phosphorous acid,diethyl phenylmethyl ester

Phosphorous acid,diethyl phenylmethyl ester

C11H17O3P (228.0915)


   

2-((tert-Butoxycarbonyl)amino)oxazole-5-carboxylic acid

2-((tert-Butoxycarbonyl)amino)oxazole-5-carboxylic acid

C9H12N2O5 (228.0746)


   

2-(Phenoxymethyl)benzoic acid

2-(Phenoxymethyl)benzoic acid

C14H12O3 (228.0786)


   

2-methoxy-biphenyl-3-carboxylic acid

2-methoxy-biphenyl-3-carboxylic acid

C14H12O3 (228.0786)


   

4-dimethylamino-1-naphthyl isothiocyanate

4-dimethylamino-1-naphthyl isothiocyanate

C13H12N2S (228.0721)


   

5-fluoro AMT (hydrochloride)

5-fluoro AMT (hydrochloride)

C11H14ClFN2 (228.0829)


   

methyl 3-phenoxybenzoate

methyl 3-phenoxybenzoate

C14H12O3 (228.0786)


   

4-(butylsulfanylmethyl)-5-methylfuran-2-carboxylic acid

4-(butylsulfanylmethyl)-5-methylfuran-2-carboxylic acid

C11H16O3S (228.082)


   

5-methoxy-2-phenyl-benzoic acid

5-methoxy-2-phenyl-benzoic acid

C14H12O3 (228.0786)


   

Ethanolate, titanium salt (4:1)

Ethanolate, titanium salt (4:1)

C8H20O4Ti (228.0841)


   

2-methoxy-3-phenylbenzoic acid

2-methoxy-3-phenylbenzoic acid

C14H12O3 (228.0786)


   

2-(2-phenylphenoxy)acetate

2-(2-phenylphenoxy)acetate

C14H12O3 (228.0786)


   

2-(Benzyloxy)benzoic acid

2-(Benzyloxy)benzoic acid

C14H12O3 (228.0786)


   

2-(1,2,3,6-tetrahydropyridin-4-yl)-5-(trifluoromethyl)pyridine

2-(1,2,3,6-tetrahydropyridin-4-yl)-5-(trifluoromethyl)pyridine

C11H11F3N2 (228.0874)


   

2-(HYDROXY-PHENYL-METHYL)-BENZOIC ACID

2-(HYDROXY-PHENYL-METHYL)-BENZOIC ACID

C14H12O3 (228.0786)


   

1-(2-CHLORO-4-FLUORO-BENZYL)-PIPERAZINE

1-(2-CHLORO-4-FLUORO-BENZYL)-PIPERAZINE

C11H14ClFN2 (228.0829)


   

2-Amino-5-methyl-4-(4-methylphenyl)thiophene-3-carbonitrile

2-Amino-5-methyl-4-(4-methylphenyl)thiophene-3-carbonitrile

C13H12N2S (228.0721)


   

3-naphthalen-1-yl-3-oxo-propionic acid methyl ester

3-naphthalen-1-yl-3-oxo-propionic acid methyl ester

C14H12O3 (228.0786)


   

(S)-4,5-ISOPROPYLIDENEHEXANONITRILE

(S)-4,5-ISOPROPYLIDENEHEXANONITRILE

C13H12N2O2 (228.0899)


   

6-(2-AMINO-PHENYL)-NICOTINIC ACID METHYL ESTER

6-(2-AMINO-PHENYL)-NICOTINIC ACID METHYL ESTER

C13H12N2O2 (228.0899)


   

3-Phenoxybenzhydrazide

3-Phenoxybenzhydrazide

C13H12N2O2 (228.0899)


   

PIPERAZIN-1-YL(PYRAZIN-2-YL)METHANONE HYDROCHLORIDE

PIPERAZIN-1-YL(PYRAZIN-2-YL)METHANONE HYDROCHLORIDE

C9H13ClN4O (228.0778)


   

2-Phenoxybenzhydrazide

2-Phenoxybenzhydrazide

C13H12N2O2 (228.0899)


   

Methyl 4-hydroxy-7-vinyl-2-naphthoate

Methyl 4-hydroxy-7-vinyl-2-naphthoate

C14H12O3 (228.0786)


   

2-(HYDROXYMETHYL)-[1,1-BIPHENYL]-2-CARBOXYLIC ACID

2-(HYDROXYMETHYL)-[1,1-BIPHENYL]-2-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

Benzenepropanoic acid, a,b-dicyano-, ethyl ester

Benzenepropanoic acid, a,b-dicyano-, ethyl ester

C13H12N2O2 (228.0899)


   

2-(4-methoxyphenoxy)benzaldehyde

2-(4-methoxyphenoxy)benzaldehyde

C14H12O3 (228.0786)


   

bis(dimethylamino)phenylchlorosilane

bis(dimethylamino)phenylchlorosilane

C10H17ClN2Si (228.0849)


   

2H-1-Benzopyran-2-one,3-acetyl-8-(2-propen-1-yl)-

2H-1-Benzopyran-2-one,3-acetyl-8-(2-propen-1-yl)-

C14H12O3 (228.0786)


   

BENZENESULFONIC ACID NEOPENTYL ESTER

BENZENESULFONIC ACID NEOPENTYL ESTER

C11H16O3S (228.082)


   

5-amino-2-phenyl-3H-triazolo[4,5-d]pyrimidin-7-one

3-amino-8-phenyl-2,4,7,8,9-pentazabicyclo[4.3.0]nona-1,3,6-trien-5-one

C10H8N6O (228.076)


   

N-(2-Methoxyphenyl)isonicotinamide

N-(2-Methoxyphenyl)isonicotinamide

C13H12N2O2 (228.0899)


   

3-Pyridinecarboxamide,N-(2-methoxyphenyl)-

3-Pyridinecarboxamide,N-(2-methoxyphenyl)-

C13H12N2O2 (228.0899)


   

N-(2-METHOXYPHENYL)PICOLINAMIDE

N-(2-METHOXYPHENYL)PICOLINAMIDE

C13H12N2O2 (228.0899)


   

4-oxo-8-propan-2-yloxy-1H-quinoline-3-carbonitrile

4-oxo-8-propan-2-yloxy-1H-quinoline-3-carbonitrile

C13H12N2O2 (228.0899)


   

METHYL 4-HYDROXY-[1,1-BIPHENYL]-2-CARBOXYLATE

METHYL 4-HYDROXY-[1,1-BIPHENYL]-2-CARBOXYLATE

C14H12O3 (228.0786)


   

METHYL 2-HYDROXY-[1,1-BIPHENYL]-4-CARBOXYLATE

METHYL 2-HYDROXY-[1,1-BIPHENYL]-4-CARBOXYLATE

C14H12O3 (228.0786)


   

METHYL 2-HYDROXY-[1,1-BIPHENYL]-3-CARBOXYLATE

METHYL 2-HYDROXY-[1,1-BIPHENYL]-3-CARBOXYLATE

C14H12O3 (228.0786)


   

2-Methoxy-[1,1-biphenyl]-4-carboxylic acid

2-Methoxy-[1,1-biphenyl]-4-carboxylic acid

C14H12O3 (228.0786)


   

methyl 3-(6-aminopyridin-3-yl)benzoate

methyl 3-(6-aminopyridin-3-yl)benzoate

C13H12N2O2 (228.0899)


   

Benzyl 6-aminonicotinate

Benzyl 6-aminonicotinate

C13H12N2O2 (228.0899)


   

(4-Allylmorpholin-2-yl)methanamine dihydrochloride

(4-Allylmorpholin-2-yl)methanamine dihydrochloride

C8H18Cl2N2O (228.0796)


   

3-Amino-2-(phenylamino)benzoic acid

3-Amino-2-(phenylamino)benzoic acid

C13H12N2O2 (228.0899)


   

ethyl-4-phenyl pyrimidine-5-carboxylate

ethyl-4-phenyl pyrimidine-5-carboxylate

C13H12N2O2 (228.0899)


   

4-Methoxy-2-biphenylcarboxylic acid

4-Methoxy-2-biphenylcarboxylic acid

C14H12O3 (228.0786)


   

Thiocarbanilide

Thiocarbanilide

C13H12N2S (228.0721)


   

4-(aminomethyl)piperidineinformamidine dihydrochloride

4-(aminomethyl)piperidineinformamidine dihydrochloride

C7H18Cl2N4 (228.0908)


   

2-PHENYL-2-PIPERIDIN-1-YL-ETHYLAMINE

2-PHENYL-2-PIPERIDIN-1-YL-ETHYLAMINE

C13H12N2O2 (228.0899)


   

4-NAPHTHALEN-1-YL-4-OXO-BUTYRIC ACID

4-NAPHTHALEN-1-YL-4-OXO-BUTYRIC ACID

C14H12O3 (228.0786)


   

METHYL1-AMINO-1-CYCLOPENTANECARBOXYLATE

METHYL1-AMINO-1-CYCLOPENTANECARBOXYLATE

C14H12O3 (228.0786)


   

(2-BUTOXY-5-CHLOROPHENYL)BORONIC ACID

(2-BUTOXY-5-CHLOROPHENYL)BORONIC ACID

C10H14BClO3 (228.0724)


   

4-Butoxy-3-chlorophenylboronic acid

4-Butoxy-3-chlorophenylboronic acid

C10H14BClO3 (228.0724)


   

2,5-BIS(TRIMETHYLSILYL)THIOPHENE

2,5-BIS(TRIMETHYLSILYL)THIOPHENE

C10H20SSi2 (228.0824)


   

Benzaldehyde, 3-(ethenyloxy)-4-(4-methyl-1H-imidazol-1-yl)

Benzaldehyde, 3-(ethenyloxy)-4-(4-methyl-1H-imidazol-1-yl)

C13H12N2O2 (228.0899)


   

2-(2-methoxyphenyl)benzoic acid

2-(2-methoxyphenyl)benzoic acid

C14H12O3 (228.0786)


   

2-hydroxy-3-phenylmethoxybenzaldehyde

2-hydroxy-3-phenylmethoxybenzaldehyde

C14H12O3 (228.0786)


   

5-Methoxy-N-phenylnicotinamide

5-Methoxy-N-phenylnicotinamide

C13H12N2O2 (228.0899)


   

5-Chloro-2-cyclohexylamino-3-fluoropyridine

5-Chloro-2-cyclohexylamino-3-fluoropyridine

C11H14ClFN2 (228.0829)


   

N-benzyl-4-nitroaniline

N-benzyl-4-nitroaniline

C13H12N2O2 (228.0899)


   

3-METHYL-4-NITRO-BIPHENYL-2-YLAMINE

3-METHYL-4-NITRO-BIPHENYL-2-YLAMINE

C13H12N2O2 (228.0899)


   

1-(3-AZETIDINYL)-4-PIPERIDINOLDIHYDROCHLORIDE

1-(3-AZETIDINYL)-4-PIPERIDINOLDIHYDROCHLORIDE

C8H18Cl2N2O (228.0796)


   

2,5-DIMETHOXY-4-(METHYLTHIO)BENZENEETHANOL

2,5-DIMETHOXY-4-(METHYLTHIO)BENZENEETHANOL

C11H16O3S (228.082)


   

3-(phenoxymethyl)benzoic acid

3-(phenoxymethyl)benzoic acid

C14H12O3 (228.0786)


   

Methyl 5-methyl-2-(pyrimidin-2-yl)benzoate

Methyl 5-methyl-2-(pyrimidin-2-yl)benzoate

C13H12N2O2 (228.0899)


   

3-Benzyloxy-4-hydroxybenzaldehyde

3-Benzyloxy-4-hydroxybenzaldehyde

C14H12O3 (228.0786)


   

Chloro(dimethyl)(3-phenoxypropyl)silane

Chloro(dimethyl)(3-phenoxypropyl)silane

C11H17ClOSi (228.0737)


   

1-hydroxy-2-phenyl-6,7-dihydro-5H-benzimidazol-4-one

1-hydroxy-2-phenyl-1,5,6,7-tetrahydro-4H-benzimidazol-4-one

C13H12N2O2 (228.0899)


   

1-(β-D-2-DEOXYRIBOFURANOSYL)-3-NITROPYRROLE

1-(β-D-2-DEOXYRIBOFURANOSYL)-3-NITROPYRROLE

C9H12N2O5 (228.0746)


   

4-PYRIMIDIN-5-YL-BENZOIC ACID ETHYL ESTER

4-PYRIMIDIN-5-YL-BENZOIC ACID ETHYL ESTER

C13H12N2O2 (228.0899)


   

4-thiophen-2-yl-2,3-dihydro-1H-1,5-benzodiazepine

4-thiophen-2-yl-2,3-dihydro-1H-1,5-benzodiazepine

C13H12N2S (228.0721)


   

(4-Biphenylyloxy)acetic acid

(4-Biphenylyloxy)acetic acid

C14H12O3 (228.0786)


   

4-Benzyloxybenzoic acid

4-(Benzyloxy)benzoic acid

C14H12O3 (228.0786)


   

3-(2-Methoxyphenoxy)benzaldehyde

3-(2-Methoxyphenoxy)benzaldehyde

C14H12O3 (228.0786)


   

1-methylpiperazin-2-one trifluoroacetate

1-methylpiperazin-2-one trifluoroacetate

C7H11F3N2O3 (228.0722)


   

(3-CHLORO-5-ISOBUTOXYPHENYL)BORONIC ACID

(3-CHLORO-5-ISOBUTOXYPHENYL)BORONIC ACID

C10H14BClO3 (228.0724)


   

H-D-Phe(4-NO2)-OH.H2O

H-D-Phe(4-NO2)-OH.H2O

C9H12N2O5 (228.0746)


   

3-Butoxy-2-chlorophenylboronic acid

3-Butoxy-2-chlorophenylboronic acid

C10H14BClO3 (228.0724)


   

Benzyl phenyl carbonate

Benzyl phenyl carbonate

C14H12O3 (228.0786)


   

4-Methoxy-4-biphenylcarboxylic acid

4-Methoxy-4-biphenylcarboxylic acid

C14H12O3 (228.0786)


   

Diethyl benzylphosphonate

Diethyl benzylphosphonate

C11H17O3P (228.0915)


   

4-biphenylglyoxal hydrate

4-biphenylglyoxal hydrate

C14H12O3 (228.0786)


   

3-(4-methoxyphenoxy)benzaldehyde

3-(4-methoxyphenoxy)benzaldehyde

C14H12O3 (228.0786)


   

(1r)-1-methylpropyl-4-methylbenzenesulfonate

(1r)-1-methylpropyl-4-methylbenzenesulfonate

C11H16O3S (228.082)


   

PHENOL, 4-AMINO-, 1-(4-AMINOBENZOATE)

PHENOL, 4-AMINO-, 1-(4-AMINOBENZOATE)

C13H12N2O2 (228.0899)


   

methyl 4-(3-hydroxyphenyl)benzoate

methyl 4-(3-hydroxyphenyl)benzoate

C14H12O3 (228.0786)


   

2-(4-FLUORO-PHENYL)-2H-BENZOTRIAZOL-5-YLAMINE

2-(4-FLUORO-PHENYL)-2H-BENZOTRIAZOL-5-YLAMINE

C12H9FN4 (228.0811)


   

5-(Benzyloxy)-2-hydroxybenzaldehyde

5-(Benzyloxy)-2-hydroxybenzaldehyde

C14H12O3 (228.0786)


   

CARBAMIC ACID, 2-PYRIDINYL-, PHENYLMETHYL ESTER

CARBAMIC ACID, 2-PYRIDINYL-, PHENYLMETHYL ESTER

C13H12N2O2 (228.0899)


   

Butyl 4-methylbenzenesulfonate

Butyl 4-methylbenzenesulfonate

C11H16O3S (228.082)


   

1-ethyl-2-methyl-5-(trifluoromethyl)-1H-benzimidazole

1-ethyl-2-methyl-5-(trifluoromethyl)-1H-benzimidazole

C11H11F3N2 (228.0874)


   

2-(2-methoxyphenoxy)benzaldehyde

2-(2-methoxyphenoxy)benzaldehyde

C14H12O3 (228.0786)


   

3-METHOXY-[1,1-BIPHENYL]-2-CARBOXYLIC ACID

3-METHOXY-[1,1-BIPHENYL]-2-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

4-Nitro-L-phenylalanine monohydrate

4-Nitro-L-phenylalanine monohydrate

C9H12N2O5 (228.0746)


   

4-(Phenoxymethyl)benzoic acid

4-(Phenoxymethyl)benzoic acid

C14H12O3 (228.0786)


   

3'-Deoxyuridine

1-[(2R,3R,5S)-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione

C9H12N2O5 (228.0746)


3'-Deoxyuridine is a potential anticancer and antiviral agent. 3'-deoxyuridine inhibits bovine diarrhoea virus (BVDV) production.

   

Trimethoxy(4-methoxyphenyl)silane

Trimethoxy(4-methoxyphenyl)silane

C10H16O4Si (228.0818)


   

Phenol,4-[2-(4-methoxyphenyl)diazenyl]-

Phenol,4-[2-(4-methoxyphenyl)diazenyl]-

C13H12N2O2 (228.0899)


   

Thiourea,N-[1,1-biphenyl]-4-yl-

Thiourea,N-[1,1-biphenyl]-4-yl-

C13H12N2S (228.0721)


   

3-(HYDROXYMETHYL)-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

3-(HYDROXYMETHYL)-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

1-phenyl-5,6-dihydro-4H-cyclopenta[c]pyrazole-3-carboxylic acid

1-phenyl-5,6-dihydro-4H-cyclopenta[c]pyrazole-3-carboxylic acid

C13H12N2O2 (228.0899)


   

2-Benzyloxy-5-hydroxy-benzaldehyde

2-Benzyloxy-5-hydroxy-benzaldehyde

C14H12O3 (228.0786)


   

1-piperidin-4-ylazetidin-3-ol

1-piperidin-4-ylazetidin-3-ol

C8H18Cl2N2O (228.0796)


   

METHYL 4-HYDROXY-[1,1-BIPHENYL]-3-CARBOXYLATE

METHYL 4-HYDROXY-[1,1-BIPHENYL]-3-CARBOXYLATE

C14H12O3 (228.0786)


   

N-Benzyl-2-nitroaniline

N-Benzyl-2-nitroaniline

C13H12N2O2 (228.0899)


   

Benzilic acid

Benzilic acid

C14H12O3 (228.0786)


   

4-(HYDROXYMETHYL)-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

4-(HYDROXYMETHYL)-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

2-Naphthalenebutanoicacid, g-oxo-

2-Naphthalenebutanoicacid, g-oxo-

C14H12O3 (228.0786)


   

3-Hydroxy-5-methylphenyl benzoate

3-Hydroxy-5-methylphenyl benzoate

C14H12O3 (228.0786)


   

5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

C14H12O3 (228.0786)


   

Benzoic acid,4-(4-methylphenoxy)-

Benzoic acid,4-(4-methylphenoxy)-

C14H12O3 (228.0786)


   

2-HYDROXYMETHYL-BIPHENYL-3-CARBOXYLIC ACID

2-HYDROXYMETHYL-BIPHENYL-3-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

3-(2-methyl-1H-indol-3-yl)pyrrolidine-2,5-dione

3-(2-methyl-1H-indol-3-yl)pyrrolidine-2,5-dione

C13H12N2O2 (228.0899)


   

DEHYDROEPIANDROSTERONEACETATE

DEHYDROEPIANDROSTERONEACETATE

C14H12O3 (228.0786)


   

3-methoxy-biphenyl-4-carboxylic acid

3-methoxy-biphenyl-4-carboxylic acid

C14H12O3 (228.0786)


   

2-methoxy-biphenyl-4-carboxylic acid

2-methoxy-biphenyl-4-carboxylic acid

C14H12O3 (228.0786)


   

2-Methyl-2-propanyl 4-methylbenzenesulfonate

2-Methyl-2-propanyl 4-methylbenzenesulfonate

C11H16O3S (228.082)


   

4-Methoxy-3-biphenylcarboxylic acid

4-Methoxy-3-biphenylcarboxylic acid

C14H12O3 (228.0786)


   

4-[(Pyridin-4-ylmethyl)-amino]-benzoic acid

4-[(Pyridin-4-ylmethyl)-amino]-benzoic acid

C13H12N2O2 (228.0899)


   

3-AMINO-4-PHENYLAMINO-BENZOIC ACID

3-AMINO-4-PHENYLAMINO-BENZOIC ACID

C13H12N2O2 (228.0899)


   

CHEMPACIFIC 39976

CHEMPACIFIC 39976

C13H12N2O2 (228.0899)


   

(4,5-DIPHENYL-4H-[1,2,4]TRIAZOL-3-YLSULFANYL)-ACETICACID

(4,5-DIPHENYL-4H-[1,2,4]TRIAZOL-3-YLSULFANYL)-ACETICACID

C8H12N4O4 (228.0859)


   

(4-Phenoxyphenyl)acetic acid

(4-Phenoxyphenyl)acetic acid

C14H12O3 (228.0786)


   

4-(3-methylphenoxy)benzoic acid

4-(3-methylphenoxy)benzoic acid

C14H12O3 (228.0786)


   

4-(HYDROXYMETHYL)-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

4-(HYDROXYMETHYL)-[1,1-BIPHENYL]-3-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

3-(HYDROXYMETHYL)-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

3-(HYDROXYMETHYL)-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

methyl 3-(3-aminophenyl)pyridine-4-carboxylate

methyl 3-(3-aminophenyl)pyridine-4-carboxylate

C13H12N2O2 (228.0899)


   

(S)-(+)-1-METHYLPROPYL 4-METHYLBENZENESULFONATE

(S)-(+)-1-METHYLPROPYL 4-METHYLBENZENESULFONATE

C11H16O3S (228.082)


   

3-methoxy-biphenyl-3-carboxylic acid

3-methoxy-biphenyl-3-carboxylic acid

C14H12O3 (228.0786)


   

2-(3-methoxyphenoxy)benzaldehyde

2-(3-methoxyphenoxy)benzaldehyde

C14H12O3 (228.0786)


   

2-(4-methylphenoxy)pyridine-3-carboxamide

2-(4-methylphenoxy)pyridine-3-carboxamide

C13H12N2O2 (228.0899)


   

2-Phenoxyphenylacetic acid

2-Phenoxyphenylacetic acid

C14H12O3 (228.0786)


   

4-Phenoxybenzhydrazide

4-Phenoxybenzhydrazide

C13H12N2O2 (228.0899)


   

1,8-Octane diisothiocyanate

1,8-Octane diisothiocyanate

C10H16N2S2 (228.0755)


   

3-Naphthalen-2-yl-3-oxo-propionic acid methylester

3-Naphthalen-2-yl-3-oxo-propionic acid methylester

C14H12O3 (228.0786)


   

Phenol,3-methoxy-, 1-benzoate

Phenol,3-methoxy-, 1-benzoate

C14H12O3 (228.0786)


   

Acetamide,2-phenoxy-N-3-pyridinyl-

Acetamide,2-phenoxy-N-3-pyridinyl-

C13H12N2O2 (228.0899)


   

4-(3-Pyrrolidinyl)morpholine dihydrochloride

4-(3-Pyrrolidinyl)morpholine dihydrochloride

C8H18Cl2N2O (228.0796)


   

(3-Butoxy-5-chlorophenyl)boronic acid

(3-Butoxy-5-chlorophenyl)boronic acid

C10H14BClO3 (228.0724)


   

(5-BUTOXY-2-CHLOROPHENYL)BORONIC ACID

(5-BUTOXY-2-CHLOROPHENYL)BORONIC ACID

C10H14BClO3 (228.0724)


   

(2-CHLORO-5-ISOBUTOXYPHENYL)BORONIC ACID

(2-CHLORO-5-ISOBUTOXYPHENYL)BORONIC ACID

C10H14BClO3 (228.0724)


   

(3-Butoxy-4-chlorophenyl)boronic acid

(3-Butoxy-4-chlorophenyl)boronic acid

C10H14BClO3 (228.0724)


   

(4-CHLORO-3-ISOBUTOXYPHENYL)BORONIC ACID

(4-CHLORO-3-ISOBUTOXYPHENYL)BORONIC ACID

C10H14BClO3 (228.0724)


   

(4-CHLORO-2-ISOBUTOXYPHENYL)BORONIC ACID

(4-CHLORO-2-ISOBUTOXYPHENYL)BORONIC ACID

C10H14BClO3 (228.0724)


   

(2-Butoxy-4-chlorophenyl)boronic acid

(2-Butoxy-4-chlorophenyl)boronic acid

C10H14BClO3 (228.0724)


   

4-[6-(TRIFLUOROMETHYL)PYRID-2-YL]-1,2,3,6-TETRAHYDROPYRIDINE

4-[6-(TRIFLUOROMETHYL)PYRID-2-YL]-1,2,3,6-TETRAHYDROPYRIDINE

C11H11F3N2 (228.0874)


   

4-(4-Methoxyphenoxy)benzaldehyde

4-(4-Methoxyphenoxy)benzaldehyde

C14H12O3 (228.0786)


   

METHYL 3-HYDROXY-[1,1-BIPHENYL]-4-CARBOXYLATE

METHYL 3-HYDROXY-[1,1-BIPHENYL]-4-CARBOXYLATE

C14H12O3 (228.0786)


   

3-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

3-METHOXY-[1,1-BIPHENYL]-4-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

4-(4-OXO-PIPERIDINE-1-CARBONYL)-BENZONITRILE

4-(4-OXO-PIPERIDINE-1-CARBONYL)-BENZONITRILE

C13H12N2O2 (228.0899)


   

3-phenoxyphenylacetic acid

3-phenoxyphenylacetic acid

C14H12O3 (228.0786)


   

Trimethyl(4-vinylbenzyl)phosphonium chloride

Trimethyl(4-vinylbenzyl)phosphonium chloride

C12H18P.Cl (228.0835)


   

4-hYDROXY-4-METHYL-BIPHENYL-3-CARBOXYLIC ACID

4-hYDROXY-4-METHYL-BIPHENYL-3-CARBOXYLIC ACID

C14H12O3 (228.0786)


   

ETHYL 1-(CYANOMETHYL)-1H-INDOLE-2-CARBOXYLATE

ETHYL 1-(CYANOMETHYL)-1H-INDOLE-2-CARBOXYLATE

C13H12N2O2 (228.0899)


   

1-beta-D-Ribofuranosyl-4(1H)-pyrimidinone

1-beta-D-Ribofuranosyl-4(1H)-pyrimidinone

C9H12N2O5 (228.0746)


   

1-Benzyl-2-(trifluoromethyl)-4,5-dihydro-1H-imidazole

1-Benzyl-2-(trifluoromethyl)-4,5-dihydro-1H-imidazole

C11H11F3N2 (228.0874)


   

isobutyl p-toluenesulfonate

isobutyl p-toluenesulfonate

C11H16O3S (228.082)


   

2-(benzylamino)nicotinic acid

2-(benzylamino)nicotinic acid

C13H12N2O2 (228.0899)


   

3-Hydroxy-4-benzyloxy benzaldehyde

3-Hydroxy-4-benzyloxy benzaldehyde

C14H12O3 (228.0786)


   

3-(Benzyloxy)benzoic acid

3-(Benzyloxy)benzoic acid

C14H12O3 (228.0786)


   

Methyl 4-hydroxy-4-biphenylcarboxylate

Methyl 4-hydroxy-4-biphenylcarboxylate

C14H12O3 (228.0786)


   

P-TOLYL-PHOSPHONIC ACID DIETHYL ESTER

P-TOLYL-PHOSPHONIC ACID DIETHYL ESTER

C11H17O3P (228.0915)


   

1-(2-CHLORO-6-FLUOROBENZYL)PIPERAZINE

1-(2-CHLORO-6-FLUOROBENZYL)PIPERAZINE

C11H14ClFN2 (228.0829)


   

3-(4-methylphenoxy)benzoic acid

3-(4-methylphenoxy)benzoic acid

C14H12O3 (228.0786)


   

[1,1-Biphenyl]-4-aceticacid, a-hydroxy-

[1,1-Biphenyl]-4-aceticacid, a-hydroxy-

C14H12O3 (228.0786)


   

Benzyl 2,4-Dihydroxyphenyl Ketone

Benzyl 2,4-Dihydroxyphenyl Ketone

C14H12O3 (228.0786)


   

[1,1-Biphenyl]-3-carboxylicacid, 2-hydroxy-, methyl ester

[1,1-Biphenyl]-3-carboxylicacid, 2-hydroxy-, methyl ester

C14H12O3 (228.0786)


   

2-Chloro-1,4-di-n-propoxybenzene

2-Chloro-1,4-di-n-propoxybenzene

C12H17ClO2 (228.0917)


   

2-[4-(hydroxymethyl)phenyl]benzoic acid

2-[4-(hydroxymethyl)phenyl]benzoic acid

C14H12O3 (228.0786)


   

N-(4-Aminophenyl)-2-hydroxybenzamide

N-(4-Aminophenyl)-2-hydroxybenzamide

C13H12N2O2 (228.0899)


   

5-Deoxyuridine

5-Deoxyuridine

C9H12N2O5 (228.0746)


   

2-Phenyl-2-(2-pyridyl)thioacetamide

2-Phenyl-2-(2-pyridyl)thioacetamide

C13H12N2S (228.0721)


   

6-Benzyl-4-oxo-1,4-dihydropyridine-3-carboxamide

6-Benzyl-4-oxo-1,4-dihydropyridine-3-carboxamide

C13H12N2O2 (228.0899)


   

(E)-4-methoxy-2-phenylpyridine-6-carbaldehyde oxime

(E)-4-methoxy-2-phenylpyridine-6-carbaldehyde oxime

C13H12N2O2 (228.0899)


   

Fenpentadiol

Fenpentadiol

C12H17ClO2 (228.0917)


C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent

   

10-Methyl-3-phenothiazinamine

10-Methyl-3-phenothiazinamine

C13H12N2S (228.0721)


   

2-(3,5-dimethyl-1H-pyrrol-2-yl)-1,3-benzothiazole

2-(3,5-dimethyl-1H-pyrrol-2-yl)-1,3-benzothiazole

C13H12N2S (228.0721)


   

2-methoxy-N-(2-pyridinyl)benzamide

2-methoxy-N-(2-pyridinyl)benzamide

C13H12N2O2 (228.0899)


   

2-(Pyridin-4-ylmethylamino)benzoic acid

2-(Pyridin-4-ylmethylamino)benzoic acid

C13H12N2O2 (228.0899)


   

N-[(E)-(4-methylphenyl)methylideneamino]furan-2-carboxamide

N-[(E)-(4-methylphenyl)methylideneamino]furan-2-carboxamide

C13H12N2O2 (228.0899)


   

N-(3-pyridinylmethyl)-1,3-benzodioxol-5-amine

N-(3-pyridinylmethyl)-1,3-benzodioxol-5-amine

C13H12N2O2 (228.0899)


   

(E)-1-(3-furyl)-3-(4-methoxyphenyl)-2-propen-1-one

(E)-1-(3-furyl)-3-(4-methoxyphenyl)-2-propen-1-one

C14H12O3 (228.0786)


   

N-Phenylbenzenecarbothiohydrazide

N-Phenylbenzenecarbothiohydrazide

C13H12N2S (228.0721)


   

Benzylparaben

Benzyl parahydroxybenzoate

C14H12O3 (228.0786)


D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens Same as: D07518

   

AIDS-224739

2H-Pyran-2-one, 4-methoxy-6-(2-phenylethenyl)-, (E)- (9CI)

C14H12O3 (228.0786)


Desmethoxyyangonin is one of the six major kavalactones found in the Piper methysticum (kava) plant; reversible inhibitor of MAO-B. Desmethoxyyangonin is one of the six major kavalactones found in the Piper methysticum (kava) plant; reversible inhibitor of MAO-B.

   

Tocris-1418

5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

C14H12O3 (228.0786)


D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors D020011 - Protective Agents > D000975 - Antioxidants D004791 - Enzyme Inhibitors cis-Resveratrol exhibits signifcant antiviral activity. cis-Resveratrol inhibits enteroviruses with IC50s of 12.2 μM and 37.6 μM for coxsackievirus B3 (CVB3) and enterovirus 71 (EV71), respectively[1].

   

AI3-00517

InChI=1\C14H12O3\c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11\h1-9,15H,10H

C14H12O3 (228.0786)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates Benzyl salicylate?is a salicylic acid benzyl ester. It can be used as a fragrance additive or UV light absorber. Benzyl salicylate?is a salicylic acid benzyl ester. It can be used as a fragrance additive or UV light absorber.

   

AIDS-113822

1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1-H-pyrimidine-2,4-dione

C9H12N2O5 (228.0746)


D009676 - Noxae > D000963 - Antimetabolites COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.

   

trioxsalen

5-Benzofuranacrylic acid, 6-hydroxy-.beta.,2,7-trimethyl-, .delta.-lactone

C14H12O3 (228.0786)


D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use D - Dermatologicals > D05 - Antipsoriatics > D05A - Antipsoriatics for topical use > D05AD - Psoralens for topical use D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins C78284 - Agent Affecting Integumentary System > C29708 - Anti-psoriatic Agent D003879 - Dermatologic Agents Trioxsalen (Trisoralen), a psoralen derivative, is a photochemical DNA crosslinker. Trioxsalen only works after photoactivation with near ultraviolet light. Trioxsalen is a photosensitizer that can be used for the research of vitiligo and hand eczema. Trioxsalen is used for visualization of genomic interstrand cross-links localized by laser photoactivation[1][2][3].

   

SRT-501

InChI=1\C14H12O3\c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11\h1-9,15-17H\b2-1

C14H12O3 (228.0786)


COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   

methyl (2S)-3-(1H-indol-3-yl)-2-isocyanopropanoate

methyl (2S)-3-(1H-indol-3-yl)-2-isocyanopropanoate

C13H12N2O2 (228.0899)


   

trihydroxystilbene

trihydroxystilbene

C14H12O3 (228.0786)


   

2(1H)-Pyrimidinone, 1-beta-D-ribofuranosyl-

2(1H)-Pyrimidinone, 1-beta-D-ribofuranosyl-

C9H12N2O5 (228.0746)


   

Benzoic acid 3-hydroxybenzyl ester

Benzoic acid 3-hydroxybenzyl ester

C14H12O3 (228.0786)


   

N-(5-methyl-3-isoxazolyl)-3-phenylacrylamide

N-(5-methyl-3-isoxazolyl)-3-phenylacrylamide

C13H12N2O2 (228.0899)


   

3-Cyano-5,5-dimethoxycarbonyl-N-methylisoxazolidine

3-Cyano-5,5-dimethoxycarbonyl-N-methylisoxazolidine

C9H12N2O5 (228.0746)


   

6-Methyl-2-(methylthio)-4-pyrimidinol, TMS derivative

6-Methyl-2-(methylthio)-4-pyrimidinol, TMS derivative

C9H16N2OSSi (228.0753)


   

3-Benzylamino-2-cyanomethyl-2-buten-4-olide

3-Benzylamino-2-cyanomethyl-2-buten-4-olide

C13H12N2O2 (228.0899)


   

trioxsalen

trioxsalen

C14H12O3 (228.0786)


D - Dermatologicals > D05 - Antipsoriatics > D05B - Antipsoriatics for systemic use > D05BA - Psoralens for systemic use D - Dermatologicals > D05 - Antipsoriatics > D05A - Antipsoriatics for topical use > D05AD - Psoralens for topical use D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins C78284 - Agent Affecting Integumentary System > C29708 - Anti-psoriatic Agent D003879 - Dermatologic Agents Trioxsalen (Trisoralen), a psoralen derivative, is a photochemical DNA crosslinker. Trioxsalen only works after photoactivation with near ultraviolet light. Trioxsalen is a photosensitizer that can be used for the research of vitiligo and hand eczema. Trioxsalen is used for visualization of genomic interstrand cross-links localized by laser photoactivation[1][2][3].

   

(1R,10aS)-1,4,10,10a-tetrahydrophenazine-1-carboxylic acid

(1R,10aS)-1,4,10,10a-tetrahydrophenazine-1-carboxylic acid

C13H12N2O2 (228.0899)


A member of the class of phenazines that is 1,4,10,10a-tetrahydrophenazine substituted at position 1 by a carboxy group (the 1R,10aS-diastereomer).

   

(1R)-1,4,5,10-tetrahydrophenazine-1-carboxylic acid

(1R)-1,4,5,10-tetrahydrophenazine-1-carboxylic acid

C13H12N2O2 (228.0899)


   

o-Tolyl salicylate

Benzoic acid,2-hydroxy-, 2-methylphenyl ester

C14H12O3 (228.0786)


   

4-amino-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3,5-triazin-2-one

4-amino-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3,5-triazin-2-one

C8H12N4O4 (228.0859)


D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors

   

caerulomycin K

caerulomycin K

C13H12N2O2 (228.0899)


A pyridine alkaloid that is 2-phenylpyridine substituted by a methoxy group at position 4 and a (E)-(hydroxyimino)methyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.

   

Cyclo(Asn-Asn)

Cyclo(Asn-Asn)

C8H12N4O4 (228.0859)


   

Deoxypseudouridine

Deoxypseudouridine

C9H12N2O5 (228.0746)


Deoxypseudouridine is a nucleoside analog.

   

6-benzyl-4-oxo-1h-pyridine-3-carboximidic acid

6-benzyl-4-oxo-1h-pyridine-3-carboximidic acid

C13H12N2O2 (228.0899)


   

(8s)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

(8s)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

C14H12O3 (228.0786)


   

4-hydroxy-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one

4-hydroxy-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one

C9H12N2O5 (228.0746)


   

2-hydroxy-3-(2-methylprop-1-en-1-yl)naphthalene-1,4-dione

2-hydroxy-3-(2-methylprop-1-en-1-yl)naphthalene-1,4-dione

C14H12O3 (228.0786)


   

2,12-dimethoxy-7,11-diazatricyclo[6.4.1.0⁴,¹³]trideca-1,3,5,8(13),9,11-hexaene

2,12-dimethoxy-7,11-diazatricyclo[6.4.1.0⁴,¹³]trideca-1,3,5,8(13),9,11-hexaene

C13H12N2O2 (228.0899)


   

10-methyl-4-methylidene-2h,3h-pyrano[3,2-c]chromen-5-one

10-methyl-4-methylidene-2h,3h-pyrano[3,2-c]chromen-5-one

C14H12O3 (228.0786)


   

4,10-dimethyl-2h-pyrano[3,2-c]chromen-5-one

4,10-dimethyl-2h-pyrano[3,2-c]chromen-5-one

C14H12O3 (228.0786)


   

4-hydroxy-1-[(2s,5s)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one

4-hydroxy-1-[(2s,5s)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one

C9H12N2O5 (228.0746)


   

methyl 5-[(1e)-2-phenylethenyl]furan-2-carboxylate

methyl 5-[(1e)-2-phenylethenyl]furan-2-carboxylate

C14H12O3 (228.0786)


   

2-benzyl-6-methoxycyclohexa-2,5-diene-1,4-dione

2-benzyl-6-methoxycyclohexa-2,5-diene-1,4-dione

C14H12O3 (228.0786)


   

4-[(1e)-2-(3-hydroxyphenyl)ethenyl]benzene-1,2-diol

4-[(1e)-2-(3-hydroxyphenyl)ethenyl]benzene-1,2-diol

C14H12O3 (228.0786)


   

2,4,4'-trihydroxystilbene

NA

C14H12O3 (228.0786)


{"Ingredient_id": "HBIN004215","Ingredient_name": "2,4,4'-trihydroxystilbene","Alias": "NA","Ingredient_formula": "C14H12O3","Ingredient_Smile": "C1=CC(=CC=C1C=CC2=C(C=C(C=C2)O)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "21833","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

(2-hydroxyphenyl)methyl benzoate

benzoic acid (2-hydroxyphenyl)methyl ester; benzoic acid (2-hydroxybenzyl) ester

C14H12O3 (228.0786)


{"Ingredient_id": "HBIN005823","Ingredient_name": "(2-hydroxyphenyl)methyl benzoate","Alias": "benzoic acid (2-hydroxyphenyl)methyl ester; benzoic acid (2-hydroxybenzyl) ester","Ingredient_formula": "C14H12O3","Ingredient_Smile": "C1=CC=C(C=C1)C(=O)OCC2=CC=CC=C2O","Ingredient_weight": "228.24 g/mol","OB_score": "79.02599998","CAS_id": "NA","SymMap_id": "SMIT11908","TCMID_id": "NA","TCMSP_id": "MOL010945","TCM_ID_id": "NA","PubChem_id": "12731045","DrugBank_id": "NA"}

   

3,13-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-5,11-diol

3,13-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-5,11-diol

C14H12O3 (228.0786)


   

(2r)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

(2r)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

C14H12O3 (228.0786)


   

7-[(3-methylbuta-1,3-dien-1-yl)oxy]chromen-2-one

7-[(3-methylbuta-1,3-dien-1-yl)oxy]chromen-2-one

C14H12O3 (228.0786)


   

1-methyl-4-(methylsulfanyl)-9h-pyrido[3,4-b]indole

1-methyl-4-(methylsulfanyl)-9h-pyrido[3,4-b]indole

C13H12N2S (228.0721)


   

7-{[(1e)-3-methylbuta-1,3-dien-1-yl]oxy}chromen-2-one

7-{[(1e)-3-methylbuta-1,3-dien-1-yl]oxy}chromen-2-one

C14H12O3 (228.0786)


   

methyl 2-methoxy-6-(penta-2,4-diyn-1-yl)benzoate

methyl 2-methoxy-6-(penta-2,4-diyn-1-yl)benzoate

C14H12O3 (228.0786)


   

n-[(4-methoxy-6-phenylpyridin-2-yl)methylidene]hydroxylamine

n-[(4-methoxy-6-phenylpyridin-2-yl)methylidene]hydroxylamine

C13H12N2O2 (228.0899)


   

1-[(1s)-1-hydroxyethyl]-9h-pyrido[3,4-b]indol-3-ol

1-[(1s)-1-hydroxyethyl]-9h-pyrido[3,4-b]indol-3-ol

C13H12N2O2 (228.0899)


   

2-methoxy-6-[(1e)-2-phenylethenyl]pyran-4-one

2-methoxy-6-[(1e)-2-phenylethenyl]pyran-4-one

C14H12O3 (228.0786)


   

3-hydroxy-2-methyl-[1,1'-biphenyl]-4-carboxylic acid

3-hydroxy-2-methyl-[1,1'-biphenyl]-4-carboxylic acid

C14H12O3 (228.0786)


   

(1r)-1-[5-(1h-indol-3-yl)-1,3-oxazol-2-yl]ethanol

(1r)-1-[5-(1h-indol-3-yl)-1,3-oxazol-2-yl]ethanol

C13H12N2O2 (228.0899)


   

(1r,11r)-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-triene-3,9-dione

(1r,11r)-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-triene-3,9-dione

C14H12O3 (228.0786)


   

2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6-diol

2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6-diol

C14H12O3 (228.0786)


   

4-benzyl-6-hydroxypyridine-3-carboximidic acid

4-benzyl-6-hydroxypyridine-3-carboximidic acid

C13H12N2O2 (228.0899)


   

(2s)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

(2s)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

C14H12O3 (228.0786)


   

8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

C14H12O3 (228.0786)


   

1-methyl-3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid

1-methyl-3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid

C13H12N2O2 (228.0899)


   

2-isopropylfuro[3,2-g]chromen-7-one

2-isopropylfuro[3,2-g]chromen-7-one

C14H12O3 (228.0786)


   

2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-7-one

C14H12O3 (228.0786)


   

11-methoxy-2-methyl-2,6-diazatricyclo[7.3.1.0⁵,¹³]trideca-1(12),3,5(13),6,8,10-hexaen-12-ol

11-methoxy-2-methyl-2,6-diazatricyclo[7.3.1.0⁵,¹³]trideca-1(12),3,5(13),6,8,10-hexaen-12-ol

C13H12N2O2 (228.0899)


   

(8r)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

(8r)-8-(prop-1-en-2-yl)-8h,9h-furo[2,3-h]chromen-2-one

C14H12O3 (228.0786)


   

2,12-dimethoxy-7,11-diazatricyclo[6.4.1.0⁴,¹³]trideca-1(12),2,4,6,8(13),9-hexaene

2,12-dimethoxy-7,11-diazatricyclo[6.4.1.0⁴,¹³]trideca-1(12),2,4,6,8(13),9-hexaene

C13H12N2O2 (228.0899)


   

4,8-dimethoxy-9h-pyrido[3,4-b]indole

4,8-dimethoxy-9h-pyrido[3,4-b]indole

C13H12N2O2 (228.0899)


   

2-hydroxy-5-[(4-hydroxyphenyl)methyl]benzaldehyde

2-hydroxy-5-[(4-hydroxyphenyl)methyl]benzaldehyde

C14H12O3 (228.0786)


   

1-[5-(1h-indol-3-yl)-1,3-oxazol-2-yl]ethanol

1-[5-(1h-indol-3-yl)-1,3-oxazol-2-yl]ethanol

C13H12N2O2 (228.0899)


   

4,9-dimethoxynaphtho[2,3-b]furan

4,9-dimethoxynaphtho[2,3-b]furan

C14H12O3 (228.0786)


   

4-hydroxy-3-[(4-hydroxyphenyl)methyl]benzaldehyde

4-hydroxy-3-[(4-hydroxyphenyl)methyl]benzaldehyde

C14H12O3 (228.0786)


   

7-acetyl-4-methylazulene-1-carboxylic acid

7-acetyl-4-methylazulene-1-carboxylic acid

C14H12O3 (228.0786)


   

methyl 2-(hexa-2,4-diyn-1-yl)-6-hydroxybenzoate

methyl 2-(hexa-2,4-diyn-1-yl)-6-hydroxybenzoate

C14H12O3 (228.0786)


   

4-methoxy-6-[(1z)-2-phenylethenyl]pyran-2-one

4-methoxy-6-[(1z)-2-phenylethenyl]pyran-2-one

C14H12O3 (228.0786)


   

11,12-dimethoxy-2,6-diazatricyclo[7.3.1.0⁵,¹³]trideca-1,3,5(13),7,9,11-hexaene

11,12-dimethoxy-2,6-diazatricyclo[7.3.1.0⁵,¹³]trideca-1,3,5(13),7,9,11-hexaene

C13H12N2O2 (228.0899)


   

2-methoxy-6-(2-phenylethenyl)pyran-4-one

2-methoxy-6-(2-phenylethenyl)pyran-4-one

C14H12O3 (228.0786)


   

tocilizumab

tocilizumab

C14H12O3 (228.0786)


   

methyl 5-(2-phenylethenyl)furan-2-carboxylate

methyl 5-(2-phenylethenyl)furan-2-carboxylate

C14H12O3 (228.0786)