Exact Mass: 208.0847882

Exact Mass Matches: 208.0847882

Found 500 metabolites which its exact mass value is equals to given mass value 208.0847882, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Sinapaldehyde

2-Propenal, 3-(4-hydroxy-3,5-dimethoxyphenyl)-, (2E)-

C11H12O4 (208.0735552)


(E)-sinapaldehyde is a member of the class of cinnamaldehydes that is cinnamaldehyde substituted by a hydroxy group at position 4 and methoxy groups at positions 3 and 5. It has a role as an antifungal agent and a plant metabolite. It is a member of cinnamaldehydes, a dimethoxybenzene and a member of phenols. It is functionally related to an (E)-cinnamaldehyde. Sinapaldehyde is a natural product found in Stereospermum colais, Aralia bipinnata, and other organisms with data available. A member of the class of cinnamaldehydes that is cinnamaldehyde substituted by a hydroxy group at position 4 and methoxy groups at positions 3 and 5. D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D004791 - Enzyme Inhibitors Sinapaldehyde, also known as (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-propenal or (E)-sinapoyl aldehyde, is a member of the class of compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. Sinapaldehyde is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Sinapaldehyde can be synthesized from cinnamaldehyde. Sinapaldehyde can also be synthesized into 4-acetoxy-3,5-dimethoxy-trans-cinnamaldehyde. Sinapaldehyde can be found in a number of food items such as angelica, saskatoon berry, rubus (blackberry, raspberry), and lemon verbena, which makes sinapaldehyde a potential biomarker for the consumption of these food products. In Arabidopsis thaliana, this compound is part of the lignin biosynthesis pathway. The enzyme dihydroflavonol 4-reductase uses sinapaldehyde and NADPH to produce sinapyl alcohol and NADP+ . Annotation level-2 Sinapaldehyde exhibits moderate antibacterial against Methicillin resistant S. aureus (MRSA) and E. coli with MIC values of 128 and 128 μg/mL[1]. Sinapaldehyde exhibits moderate antibacterial against Methicillin resistant S. aureus (MRSA) and E. coli with MIC values of 128 and 128 μg/mL[1].

   

Chalcone

(E)-1,3-diphenylprop-2-en-1-one

C15H12O (208.0888102)


Chalcone is a member of the class of chalcones that is acetophenone in which one of the methyl hydrogens has been replaced by a benzylidene group. It has a role as a plant metabolite. It is a member of styrenes and a member of chalcones. Chalcone is a natural product found in Tilia tomentosa, Alpinia hainanensis, and other organisms with data available. An aromatic KETONE that forms the core molecule of CHALCONES. A member of the class of chalcones that is acetophenone in which one of the methyl hydrogens has been replaced by a benzylidene group. Annotation level-1 Acquisition and generation of the data is financially supported in part by CREST/JST. Chalcone is isolated from Glycyrrhiza uralensis and used to synthesize chalcone derivatives. Chalcone derivatives possess varied biological and pharmacological activity, including anti-inflammatory, antioxidative, antibacterial, anticancer, and anti-parasitic activities[1]. Chalcone is isolated from Glycyrrhiza uralensis and used to synthesize chalcone derivatives. Chalcone derivatives possess varied biological and pharmacological activity, including anti-inflammatory, antioxidative, antibacterial, anticancer, and anti-parasitic activities[1]. trans-Chalcone, isolated from Aronia melanocarpa skin, is a biphenolic core structure of flavonoids precursor. trans-Chalcone is a potent fatty acid synthase (FAS) and α-amylase inhibitor. trans-Chalcone causes cellcycle arrest and induces apoptosis in the breastcancer cell line MCF-7. trans-Chalcone has antifungal and anticancer activity[1][2][3]. trans-Chalcone, isolated from Aronia melanocarpa skin, is a biphenolic core structure of flavonoids precursor. trans-Chalcone is a potent fatty acid synthase (FAS) and α-amylase inhibitor. trans-Chalcone causes cellcycle arrest and induces apoptosis in the breastcancer cell line MCF-7. trans-Chalcone has antifungal and anticancer activity[1][2][3]. Chalcone. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=94-41-7 (retrieved 2024-09-27) (CAS RN: 94-41-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

L-Kynurenine

(AlphaS)-alpha,2-diamino-3-hydroxy-gamma-oxo-benzenebutanoic acid

C10H12N2O3 (208.0847882)


Kynurenine is a metabolite of the amino acid tryptophan used in the production of niacin. L-Kynurenine is a central compound of the tryptophan metabolism pathway since it can change into the neuroprotective agent kynurenic acid or to the neurotoxic agent quinolinic acid. The break-up of these endogenous compounds balance can be observable in many disorders such as stroke, epilepsy, multiple sclerosis, and amyotrophic lateral sclerosis. It can also occur in neurodegenerative disorders such as Parkinsons disease, Huntingtons, and Alzheimers disease; and in mental disorders such as schizophrenia and depression. Kynurenine is a metabolite of the amino acid tryptophan used in the production of niacin. [Raw Data] CBA10_Kynurenine_pos_10eV_1-2_01_666.txt [Raw Data] CBA10_Kynurenine_pos_30eV_1-2_01_668.txt [Raw Data] CBA10_Kynurenine_pos_40eV_1-2_01_669.txt [Raw Data] CBA10_Kynurenine_pos_20eV_1-2_01_667.txt [Raw Data] CBA10_Kynurenine_pos_50eV_1-2_01_670.txt L-Kynurenine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=2922-83-0 (retrieved 2024-07-01) (CAS RN: 2922-83-0). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). 2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid is an endogenous metabolite. L-Kynurenine is a metabolite of the amino acid L-tryptophan. L-Kynurenine is an aryl hydrocarbon receptor agonist.

   

Epibatidine

(+/-)-epibatidine

C11H13ClN2 (208.0767208)


D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics

   

(R)-2-Benzylsuccinate

(R)-2-AMINO-BUT-3-EN-1-OLHYDROCHLORIDE

C11H12O4 (208.0735552)


(R)-2-Benzylsuccinate is an aromatic compounds that is an intermediate in Benzoate degradation via CoA ligation. Biodegradation of aromatic compounds is a common process in anoxic environments. The many natural and synthetic aromatic compounds found in the environment are usually degraded by anaerobic microorganisms into only few central intermediates, prior to ring cleavage. Benzoyl-CoA is the most important of these intermediates since a large number of compounds, including chloro-, nitro-, and aminobenzoates, aromatic hydrocarbons, and phenolic compounds, are initially converted to benzoyl-CoA prior to ring reduction and cleavage. (R)-2-Benzylsuccinate can be generated from toluene via the enzyme benzylsuccinate synthase (EC 4.1.99.11). It is then converted to Benzylsuccinyl-CoA via the enzyme benzylsuccinate CoA-transferase BbsE subunit (EC 2.8.3.15). [HMDB] (R)-2-Benzylsuccinate is an aromatic compounds that is an intermediate in Benzoate degradation via CoA ligation. Biodegradation of aromatic compounds is a common process in anoxic environments. The many natural and synthetic aromatic compounds found in the environment are usually degraded by anaerobic microorganisms into only few central intermediates, prior to ring cleavage. Benzoyl-CoA is the most important of these intermediates since a large number of compounds, including chloro-, nitro-, and aminobenzoates, aromatic hydrocarbons, and phenolic compounds, are initially converted to benzoyl-CoA prior to ring reduction and cleavage. (R)-2-Benzylsuccinate can be generated from toluene via the enzyme benzylsuccinate synthase (EC 4.1.99.11). It is then converted to Benzylsuccinyl-CoA via the enzyme benzylsuccinate CoA-transferase BbsE subunit (EC 2.8.3.15). KEIO_ID B005

   

6-Methoxymellein

6-Methoxy-8-hydroxy-3-methyl-3,4-dihydroisocoumarin, (R)-(-)-isomer

C11H12O4 (208.0735552)


Isolated from Aspergillus caespitosus, Aspergillus variecolor and Sporormia bipartis. Reaches fungitoxic levels in stored infected carrot. Shows broad antimicrobial action. 6-Methoxymellein is found in wild carrot, root vegetables, and carrot. 6-Methoxymellein is found in carrot. 6-Methoxymellein is isolated from Aspergillus caespitosus, Aspergillus variecolor and Sporormia bipartis. Reaches fungitoxic levels in stored infected carrot. Shows broad antimicrobial action.

   

Formyl-5-hydroxykynurenamine

N-(2-(6-Hydroxy-5-methoxy-1H-indol-3-yl)ethyl)-acetamide

C10H12N2O3 (208.0847882)


Formyl-5-hydroxykynurenamine belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group and a phenyl group. Formyl-5-hydroxykynurenamine is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Formyl-5-hydroxykynurenamine can be biosynthesized from serotonin; which is mediated by the enzyme indoleamine 2,3-dioxygenase 1 [EC 1.13.11.52]. In humans, formyl-5-hydroxykynurenamine is involved in the tryptophan metabolism pathway. Formyl-5-hydroxykynurenamine is found in the tryptophan metabolism pathway. It is produced from serotonin through the action of indoleamine 2,3-dioxygenase [EC:1.13.11.52]. [HMDB]

   

1-Methoxyphenanthrene

Methyl 1-phenanthryl ether

C15H12O (208.08881019999998)


This compound belongs to the family of Phenanthrenes and Derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

   

Chalcone

phenyl (E)--2-phenylethenyl ketone

C15H12O (208.08881019999998)


Chalcone is an aromatic ketone that forms the central core for a variety of important biological compounds, which are known collectively as chalcones. They show antibacterial, antifungal, antitumor and anti-inflammatory properties. They are also intermediates in the biosynthesis of flavonoids, which are substances widespread in plants and with an array of biological activities. Chalcones are also intermediates in the Auwers synthesis of flavones.Chalcones can be prepared by an aldol condensation between a benzaldehyde and an acetophenone in the presence of sodium hydroxide as a catalyst. This reaction has been found to work in without any solvent at all - a solid-state reaction. The reaction between substituted benzaldehydes and acetophenones has been used to demonstrate green chemistry in undergraduate chemistry education. In a study investigating green chemistry synthesis, chalcones were also synthesized from the same starting materials in high temperature water (200 to 350 degree centigrade). Chalcone is an aromatic ketone that forms the central core for a variety of important biological compounds, which are known collectively as chalcones. They show antibacterial, antifungal, antitumor and anti-inflammatory properties. They are also intermediates in the biosynthesis of flavonoids, which are substances widespread in plants and with an array of biological activities. Chalcones are also intermediates in the Auwers synthesis of flavones.Chalcones can be prepared by an aldol condensation between a benzaldehyde and an acetophenone in the presence of sodium hydroxide as a catalyst. Chalcone is isolated from Glycyrrhiza uralensis and used to synthesize chalcone derivatives. Chalcone derivatives possess varied biological and pharmacological activity, including anti-inflammatory, antioxidative, antibacterial, anticancer, and anti-parasitic activities[1]. Chalcone is isolated from Glycyrrhiza uralensis and used to synthesize chalcone derivatives. Chalcone derivatives possess varied biological and pharmacological activity, including anti-inflammatory, antioxidative, antibacterial, anticancer, and anti-parasitic activities[1].

   

D-Kynurenine

(2R)-6-methoxy-2-phenyl-2,3-dihydrochromen-4-one

C10H12N2O3 (208.0847882)


Kynurenine, also known as 3-anthraniloylalanine, is a member of the class of compounds known as alkyl-phenylketones. Alkyl-phenylketones are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Kynurenine is slightly soluble (in water) and a moderately acidic compound (based on its pKa). Kynurenine can be found in a number of food items such as yellow zucchini, carrot, spinach, and broccoli, which makes kynurenine a potential biomarker for the consumption of these food products. Kynurenine is synthesized by the enzyme tryptophan dioxygenase, which is made primarily but not exclusively in the liver, and indoleamine 2,3-dioxygenase, which is made in many tissues in response to immune activation. Kynurenine and its further breakdown products carry out diverse biological functions, including dilating blood vessels during inflammation and regulating the immune response. Some cancers increase kynurenine production, which increases tumor growth . 2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid is an endogenous metabolite.

   

UNII:AQ51A12T8K

Ethyl beta-D-glucopyranoside

C8H16O6 (208.0946836)


   

Caffeic acid ethyl ester

2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester

C11H12O4 (208.0735552)


Caffeic acid ethyl ester, also known as (E)-ethyl 3,4-dihydroxycinnamate or (E)-ethyl caffeate, belongs to coumaric acids and derivatives class of compounds. Those are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. Caffeic acid ethyl ester is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Caffeic acid ethyl ester can be found in eggplant and vinegar, which makes caffeic acid ethyl ester a potential biomarker for the consumption of these food products. Ethyl caffeate is an ester of an hydroxycinnamic acid, a naturally occurring organic compound . Ethyl trans-caffeate is an ethyl ester resulting from the formal condensation of the carboxy group of trans-caffeic acid with ethanol. It has a role as an anti-inflammatory agent and an antineoplastic agent. It is an alkyl caffeate ester and an ethyl ester. It is functionally related to a trans-caffeic acid. Ethyl caffeate is a natural product found in Cichorium endivia, Cichorium pumilum, and other organisms with data available. Ethyl Caffeate is a natural phenolic compound isolated from Bidens pilosa. Ethyl caffeate suppresses NF-κB activation and its downstream inflammatory mediators, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2) in vitro or in mouse skin[1]. Ethyl Caffeate is a natural phenolic compound isolated from Bidens pilosa. Ethyl caffeate suppresses NF-κB activation and its downstream inflammatory mediators, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2) in vitro or in mouse skin[1].

   

Anthriscinol

1-(7-methoxy-2H-1,3-benzodioxol-5-yl)prop-2-en-1-ol

C11H12O4 (208.0735552)


Anthriscinol is found in herbs and spices. Anthriscinol is a constituent of Myristica fragrans (nutmeg). Constituent of Myristica fragrans (nutmeg). Anthriscinol is found in herbs and spices. Anthriscinol is a member of benzodioxoles.

   

3-(3,4-Dimethoxyphenyl)-2-propenoic acid

InChI=1/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13)/b6-4

C11H12O4 (208.0735552)


3,4-dimethoxycinnamic acid is a methoxycinnamic acid that is trans-cinnamic acid substituted by methoxy groups at positions 3 and 4 respectively. It is functionally related to a trans-cinnamic acid. 3,4-Dimethoxycinnamic acid is a natural product found in Sibiraea angustata, Verbesina gigantea, and other organisms with data available. 3-(3,4-Dimethoxyphenyl)-2-propenoic acid is found in beverages. 3-(3,4-Dimethoxyphenyl)-2-propenoic acid is found in kava (Piper methysticum). FDA advises against use of kava in food due to potential risk of severe liver damage (2002 Found in kava (Piper methysticum). FDA advises against use of kava in food due to potential risk of severe liver damage (2002) (E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. (E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1].

   

2-Propenoic acid, 3-(3,5-dimethoxyphenyl)-

2-Propenoic acid, 3-(3,5-dimethoxyphenyl)-

C11H12O4 (208.0735552)


   

Dambonitol

(1R,2s,3S,4R,5s,6S)-4,6-dimethoxycyclohexane-1,2,3,5-tetrol

C8H16O6 (208.0946836)


Latex used for manufacture of chewing gum. Latex used for manuf. of chewing gum.

   

Ethyl alpha-glucopyranoside

(2R,3R,4S,5S,6R)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol

C8H16O6 (208.0946836)


Ethyl beta-D-glucopyranoside is a constituent of Citrus peels, the fresh root cortex of Manihot esculenta (cassava), and other plant subspecies. Ethyl beta-D-glucopyranoside is found in many foods, some of which are root vegetables, citrus, alcoholic beverages, and fruits. Constituent of Citrus peels, the fresh root cortex of Manihot esculenta (cassava) and other plant subspecies Ethyl beta-D-glucopyranoside is found in many foods, some of which are root vegetables, citrus, alcoholic beverages, and fruits.

   

3-(3-Methoxy-4,5-methylenedioxyphenyl)-2-propen-1-ol

(2Z)-3-(7-methoxy-2H-1,3-benzodioxol-5-yl)prop-2-en-1-ol

C11H12O4 (208.0735552)


3-(3-Methoxy-4,5-methylenedioxyphenyl)-2-propen-1-ol is found in herbs and spices. 3-(3-Methoxy-4,5-methylenedioxyphenyl)-2-propen-1-ol is a constituent of Myristica fragrans (nutmeg). Constituent of Myristica fragrans (nutmeg). 3-(3-Methoxy-4,5-methylenedioxyphenyl)-2-propen-1-ol is found in herbs and spices.

   

5-(3',4'-Dihydroxyphenyl)-gamma-valerolactone

(5R)-5-[(3,4-Dihydroxyphenyl)methyl]dihydro-2(3H)-furanone

C11H12O4 (208.0735552)


5-(3,4-Dihydroxyphenyl)-gamma-valerolactone (CAS: 21618-92-8) is a cocoa metabolite from gut microflora. It is found in urine. 5-(3,4-Dihydroxyphenyl)-gamma-valerolactone is a flavonoid metabolite.

   

Furapiole

8-methoxy-11-methyl-4,6,10-trioxatricyclo[7.3.0.0³,⁷]dodeca-1,3(7),8-triene

C11H12O4 (208.0735552)


Furapiole is found in herbs and spices. Furapiole is a constituent of Anethum sowa (Indian dill) Constituent of Anethum sowa (Indian dill). Furapiole is found in herbs and spices.

   

1-(2-Methoxy-3,4-methylenedioxyphenyl)-1-propanone

1-(2-Methoxy-3,4-methylenedioxyphenyl)-1-propanone

C11H12O4 (208.0735552)


1-(2-Methoxy-3,4-methylenedioxyphenyl)-1-propanone is found in herbs and spices. 1-(2-Methoxy-3,4-methylenedioxyphenyl)-1-propanone is a constituent of Anethum sowa (Indian dill). Constituent of Anethum sowa (Indian dill). 1-(2-Methoxy-3,4-methylenedioxyphenyl)-1-propanone is found in herbs and spices.

   

5-(3',5'-Dihydroxyphenyl)-gamma-valerolactone

5-(3,5-Dihydroxyphenyl)-gamma-valerolactone

C11H12O4 (208.0735552)


5-(3,5-Dihydroxyphenyl)-gamma-valerolactone is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

4-Aminobenzoyl-(beta)-alanine

3-[(4-aminophenyl)formamido]propanoic acid

C10H12N2O3 (208.0847882)


4-Aminobenzoyl-(beta)-alanine is a metabolite of balsalazide. Balsalazide is an anti-inflammatory drug used in the treatment of inflammatory bowel disease. It is sold under the name Colazal in the US and Colazide in the UK. It is also sold in generic form in the US by several generic manufacturers. It is usually administered as the disodium salt. Balsalazide releases mesalazine, also known as 5-aminosalicylic acid, or 5-ASA, in the large intestine. (Wikipedia)

   

5-(3',4'-Dihydroxyphenyl)-γ-valerolactone

5-(3,4-Dihydroxybenzyl)dihydro-2(3H)-furanone

C11H12O4 (208.0735552)


A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

Ethyl glucoside

2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol

C8H16O6 (208.0946836)


Constituent of Citrus peels, the fresh root cortex of Manihot esculenta (cassava) and other plant subspecies Ethyl beta-D-glucopyranoside is found in many foods, some of which are root vegetables, citrus, alcoholic beverages, and fruits.

   

(+)-Epibatidine

2-(6-chloropyridin-3-yl)-7-azabicyclo[2.2.1]heptane

C11H13ClN2 (208.0767208)


D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics

   

3-Methyl-1-propylxanthine

3-methyl-1-propyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione

C9H12N4O2 (208.0960212)


   
   

Propanedioic acid, (2-phenylethyl)-

Propanedioic acid, (2-phenylethyl)-

C11H12O4 (208.0735552)


   

7-Ethyltheophylline

7-ethyl-1,3-dimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione

C9H12N4O2 (208.0960212)


   

Allobarbital

4,6-dihydroxy-5,5-bis(prop-2-en-1-yl)-2,5-dihydropyrimidin-2-one

C10H12N2O3 (208.0847882)


N - Nervous system > N05 - Psycholeptics > N05C - Hypnotics and sedatives > N05CA - Barbiturates, plain C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic > C67084 - Barbiturate

   

Dihydroxyphenyl-valerolactone

(-)-5-(3,4-Dihydroxyphenyl)-gamma-valerolactone

C11H12O4 (208.0735552)


   

Isobutylxanthine

1-(2-methylpropyl)-2,3,6,7-tetrahydro-1H-purine-2,6-dione

C9H12N4O2 (208.0960212)


   

Sinapaldehyde

3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enal

C11H12O4 (208.0735552)


   

2',6'-O-Diacetyloninin

(1R,2S)-1-(7,8-dihydropteridin-6-yl)propane-1,2-diol

C9H12N4O2 (208.0960212)


2,6-o-diacetyloninin belongs to pteridines and derivatives class of compounds. Those are polycyclic aromatic compounds containing a pteridine moiety, which consists of a pyrimidine fused to a pyrazine ring to form pyrimido(4,5-b)pyrazine. 2,6-o-diacetyloninin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 2,6-o-diacetyloninin can be found in soy bean, which makes 2,6-o-diacetyloninin a potential biomarker for the consumption of this food product.

   

Methyl ferulate

Methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid

C11H12O4 (208.0735552)


Methyl ferulate, also known as methyl ferulic acid, belongs to coumaric acids and derivatives class of compounds. Those are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. Methyl ferulate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Methyl ferulate can be found in garden onion, which makes methyl ferulate a potential biomarker for the consumption of this food product. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2]. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2].

   

Ethyl beta-D-fructofuranoside

(2R,3S,4S,5R)-2-ethoxy-2,5-bis(hydroxymethyl)oxolane-3,4-diol

C8H16O6 (208.0946836)


Ethyl beta-d-fructofuranoside is a member of the class of compounds known as C-glycosyl compounds. C-glycosyl compounds are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond. Ethyl beta-d-fructofuranoside is soluble (in water) and a very weakly acidic compound (based on its pKa). Ethyl beta-d-fructofuranoside can be found in common wheat, which makes ethyl beta-d-fructofuranoside a potential biomarker for the consumption of this food product.

   

Kynurenine

L-Kynurenine

C10H12N2O3 (208.0847882)


L-Kynurenine is a metabolite of the amino acid L-tryptophan. L-Kynurenine is an aryl hydrocarbon receptor agonist.

   

Eleutheroside C

(2S,3R,4S,5R,6R)-2-ETHOXY-6-(HYDROXYMETHYL)OXANE-3,4,5-TRIOL

C8H16O6 (208.0946836)


Eleutheroside C is a natural product found in Justicia adhatoda, Rubus niveus, and Agave amica with data available.

   

Methyl

2-propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, methyl ester, (2E)-

C11H12O4 (208.0735552)


Trans-methylferulate is a cinnamate ester that is the methyl ester of ferulic acid. It has been isolated from Pisonia aculeata. It has a role as a plant metabolite. It is a cinnamate ester, a methyl ester and a member of guaiacols. It is functionally related to a ferulic acid. Methyl ferulate is a natural product found in Iris milesii, Coreopsis grandiflora, and other organisms with data available. See also: Black Cohosh (part of). A cinnamate ester that is the methyl ester of ferulic acid. It has been isolated from Pisonia aculeata. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2]. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2].

   
   
   
   

(4R)-5-Hydroxy-4-methoxy-alpha-tetralone

(4R)-5-Hydroxy-4-methoxy-alpha-tetralone

C11H12O4 (208.0735552)


   
   
   
   
   
   
   

Methyl ferulate

(E)-Methyl-4-hydroxy-3-methoxycinnamate

C11H12O4 (208.0735552)


Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2]. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2].

   

Methylferulic acid

3,4-Dimethoxycinnamic acid

C11H12O4 (208.0735552)


3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1].

   

5,8-Dihydroxy-4-methoxy-1-tetralone

5,8-Dihydroxy-4-methoxy-1-tetralone

C11H12O4 (208.0735552)


   

8-Hydroxy-6-methoxy-3-methyl-3,4-dihydroisocoumarin

8-Hydroxy-6-methoxy-3-methyl-3,4-dihydroisocoumarin

C11H12O4 (208.0735552)


   

2,3-Dihydro-7-methoxy-2-methyl-5,6-methylenedioxybenzofuran

2,3-Dihydro-7-methoxy-2-methyl-5,6-methylenedioxybenzofuran

C11H12O4 (208.0735552)


   

Methyl cis-ferulate

Methyl cis-ferulate

C11H12O4 (208.0735552)


   

Ethyl glucoside

2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol

C8H16O6 (208.0946836)


   

5-Hydroxymethylmellein

5-Hydroxymethylmellein

C11H12O4 (208.0735552)


   

5,5-Diallylbarbituric acid

5,5-Diallylbarbituric acid

C10H12N2O3 (208.0847882)


N - Nervous system > N05 - Psycholeptics > N05C - Hypnotics and sedatives > N05CA - Barbiturates, plain C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic > C67084 - Barbiturate

   

3-Methyl-6-hydroxy-8-methoxy-3,4-dihydroisocoumarin

3-Methyl-6-hydroxy-8-methoxy-3,4-dihydroisocoumarin

C11H12O4 (208.0735552)


   
   

3-(3,4-dihydroxyphenyl)-2-propen-1-ethanoate

3-(3,4-dihydroxyphenyl)-2-propen-1-ethanoate

C11H12O4 (208.0735552)


   

7-Me ether-2,3-Dihydro-5,7-dihydroxy-2-methyl-4H-1-benzopyran-4-one

7-Me ether-2,3-Dihydro-5,7-dihydroxy-2-methyl-4H-1-benzopyran-4-one

C11H12O4 (208.0735552)


   

trans-2,4-Dimethoxycinnamic acid

trans-2,4-Dimethoxycinnamic acid

C11H12O4 (208.0735552)


   
   

3,4-Dihydro-3,4,8-trihydroxy-3-methyl-1(2H)-naphthalenone

3,4-Dihydro-3,4,8-trihydroxy-3-methyl-1(2H)-naphthalenone

C11H12O4 (208.0735552)


   
   

ethyl beta-D-fructopyranoside

ethyl beta-D-fructopyranoside

C8H16O6 (208.0946836)


   

D-gluco-3,4,5-Trihydroxy-2,6-dimethoxy-hexanal|O2,O6-dimethyl-D-glucose

D-gluco-3,4,5-Trihydroxy-2,6-dimethoxy-hexanal|O2,O6-dimethyl-D-glucose

C8H16O6 (208.0946836)


   

3,6-dimethoxy-1,2,4,5-cyclohexanetetrol

3,6-dimethoxy-1,2,4,5-cyclohexanetetrol

C8H16O6 (208.0946836)


   

methyl 3-(4-methoxyphenoxy)prop-2-enoate

methyl 3-(4-methoxyphenoxy)prop-2-enoate

C11H12O4 (208.0735552)


   

Methyl 3-(4-methoxyphenyl)-3-oxopropionate

Methyl 3-(4-methoxyphenyl)-3-oxopropionate

C11H12O4 (208.0735552)


   
   

O2,O4-dimethyl-D-galactose

O2,O4-dimethyl-D-galactose

C8H16O6 (208.0946836)


   

3,6-Anhydro-L-galactose-dimethylacetal|3,6-Anhydro-L-galaktose-dimethylacetal

3,6-Anhydro-L-galactose-dimethylacetal|3,6-Anhydro-L-galaktose-dimethylacetal

C8H16O6 (208.0946836)


   

4-Hydroxy-5-methylmellein

4-Hydroxy-5-methylmellein

C11H12O4 (208.0735552)


   

2,3-Di-O-methyl-D-mannopyranose|2,3-di-O-methyl-D-mannose|2,3-di-O-methylmannopyranose|O2,O3-dimethyl-D-mannose

2,3-Di-O-methyl-D-mannopyranose|2,3-di-O-methyl-D-mannose|2,3-di-O-methylmannopyranose|O2,O3-dimethyl-D-mannose

C8H16O6 (208.0946836)


   
   
   

2-amino-5-oxo-5-pyridin-2-ylpentanoic acid

2-amino-5-oxo-5-pyridin-2-ylpentanoic acid

C10H12N2O3 (208.0847882)


   

3-Acetoxy-2-phenylpropanoic acid

3-Acetoxy-2-phenylpropanoic acid

C11H12O4 (208.0735552)


   

Me ether,Et ester-2-Formyl-6-hydroxybenzoic acid

Me ether,Et ester-2-Formyl-6-hydroxybenzoic acid

C11H12O4 (208.0735552)


   
   

phosphoric acid hex-4t-enyl ester dimethyl ester

phosphoric acid hex-4t-enyl ester dimethyl ester

C8H17O4P (208.0864412)


   

3-methyl-5,7-dimethoxyphthalide

3-methyl-5,7-dimethoxyphthalide

C11H12O4 (208.0735552)


   

methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C11H12O4 (208.0735552)


   

SCHEMBL14601942

SCHEMBL14601942

C8H16O6 (208.0946836)


   

(1E)-3-methyl-6-(1-methyl-2-methoxycarbonylvinyl)-alpha-pyrone

(1E)-3-methyl-6-(1-methyl-2-methoxycarbonylvinyl)-alpha-pyrone

C11H12O4 (208.0735552)


   

6,7-dimethoxychroman-4-one

6,7-dimethoxychroman-4-one

C11H12O4 (208.0735552)


   

3-allyl-3a,5,6,6a-tetrahydro-2,3a-dihydroxypentalene-1,4-dione|xialenon E

3-allyl-3a,5,6,6a-tetrahydro-2,3a-dihydroxypentalene-1,4-dione|xialenon E

C11H12O4 (208.0735552)


   

5,5-Oxybis(1,5-dihydro-3-methyl-2H-pyrrole-2-one)

5,5-Oxybis(1,5-dihydro-3-methyl-2H-pyrrole-2-one)

C10H12N2O3 (208.0847882)


   
   
   

3,4-Dihydro-6,8-dihydroxy-3,5-dimethyl-1H-2-benzopyran-1-one

3,4-Dihydro-6,8-dihydroxy-3,5-dimethyl-1H-2-benzopyran-1-one

C11H12O4 (208.0735552)


   

5,7-dimethoxy-6-methylisobenzofuran-1(3H)-one

5,7-dimethoxy-6-methylisobenzofuran-1(3H)-one

C11H12O4 (208.0735552)


   

SCHEMBL12518140

SCHEMBL12518140

C8H16O6 (208.0946836)


   
   

4-Acetyl-2-methoxyphenyl acetate

4-Acetyl-2-methoxyphenyl acetate

C11H12O4 (208.0735552)


   
   

methyl (E)-3-(4-hydroxy-2-methoxyphenyl)propenoate|Methylisoferulat

methyl (E)-3-(4-hydroxy-2-methoxyphenyl)propenoate|Methylisoferulat

C11H12O4 (208.0735552)


   
   

1-Chloro-3-(2-chloropropan-2-yl)-1-methylcyclohexane

1-Chloro-3-(2-chloropropan-2-yl)-1-methylcyclohexane

C10H18Cl2 (208.07854880000002)


   

1-(2,4-dihydroxy-6-methoxy-phenyl)-but-2(E)-en-1-one

1-(2,4-dihydroxy-6-methoxy-phenyl)-but-2(E)-en-1-one

C11H12O4 (208.0735552)


   

2-Propenoic acid, 3-(2,5-dimethoxyphenyl)-

2-Propenoic acid, 3-(2,5-dimethoxyphenyl)-

C11H12O4 (208.0735552)


   

2,3-di-O-methyl-D-glucose|2.3-Di-O-methyl-beta-D-glucose|2.3-Di-O-methyl-D-glucose|2.3-Dimethyl-d-glucose|D-gluco-4,5,6-Trihydroxy-2,3-dimethoxy-hexanal|O2,O3-dimethyl-D-glucose

2,3-di-O-methyl-D-glucose|2.3-Di-O-methyl-beta-D-glucose|2.3-Di-O-methyl-D-glucose|2.3-Dimethyl-d-glucose|D-gluco-4,5,6-Trihydroxy-2,3-dimethoxy-hexanal|O2,O3-dimethyl-D-glucose

C8H16O6 (208.0946836)


   

2-Acetoxy-3-phenylpropanoic acid

2-Acetoxy-3-phenylpropanoic acid

C11H12O4 (208.0735552)


   
   

SCHEMBL15631938

SCHEMBL15631938

C8H16O6 (208.0946836)


   

4-METHYLCATECHOL DIACETATE

4-METHYLCATECHOL DIACETATE

C11H12O4 (208.0735552)


   

(3S,4R)-4,8-dihydroxy-3-methoxy-3,4-dihydro-1(2H)-naphthalenone

(3S,4R)-4,8-dihydroxy-3-methoxy-3,4-dihydro-1(2H)-naphthalenone

C11H12O4 (208.0735552)


   

Ethyl b-D-fructopyranoside

Ethyl b-D-fructopyranoside

C8H16O6 (208.0946836)


   

ethyl 3-(2,5-dihydroxyphenyl)prop-2-enoate

ethyl 3-(2,5-dihydroxyphenyl)prop-2-enoate

C11H12O4 (208.0735552)


   

Methyl kakuol

1-(6-Methoxy-2H-1,3-benzodioxol-5-yl)propan-1-one

C11H12O4 (208.0735552)


1-(6-Methoxy-2H-1,3-benzodioxol-5-yl)propan-1-one is a natural product found in Piper marginatum with data available.

   

nigerapyrone E

nigerapyrone E

C11H12O4 (208.0735552)


A member of the class of 2-pyranones that is 2H-pyran-2-one substituted by a methoxy group at position 4, a methyl group at position 3 and a 3-oxobut-1-en-1-yl group at position 6. It has been isolated from an endophytic fungus Aspergillus niger.

   
   
   

7-hydroxy-5-methoxy-4,6-dimethylphthalide

7-hydroxy-5-methoxy-4,6-dimethylphthalide

C11H12O4 (208.0735552)


   

2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester

2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester

C11H12O4 (208.0735552)


   

2-(2-Hydroxy-4-methoxyphenyl)ethenyl acetate

2-(2-Hydroxy-4-methoxyphenyl)ethenyl acetate

C11H12O4 (208.0735552)


   
   

8-hydroxy-3-methoxy-3-methylisochroman-1-one

8-hydroxy-3-methoxy-3-methylisochroman-1-one

C11H12O4 (208.0735552)


   

thyl beta-D-fructofuranoside

thyl beta-D-fructofuranoside

C8H16O6 (208.0946836)


   

6,7-Dimethoxy-3,4-dihydro-2H-1-benzopyran-2-one

6,7-Dimethoxy-3,4-dihydro-2H-1-benzopyran-2-one

C11H12O4 (208.0735552)


   
   
   

3-Ethyl-6-methoxy-7-hydroxyisobenzofuran-1(3H)-one

3-Ethyl-6-methoxy-7-hydroxyisobenzofuran-1(3H)-one

C11H12O4 (208.0735552)


   
   

Pyrenocin A|pyrenocine A

Pyrenocin A|pyrenocine A

C11H12O4 (208.0735552)


   
   
   

3-methyl-1-(2,4,5-trihydroxyphenyl)but-2-en-1-one

3-methyl-1-(2,4,5-trihydroxyphenyl)but-2-en-1-one

C11H12O4 (208.0735552)


   

6-Me-D-3-O-Methylmannose

6-Me-D-3-O-Methylmannose

C8H16O6 (208.0946836)


   

2,2-Dimethyl-6,7-dihydroxy-4-chromanone

2,2-Dimethyl-6,7-dihydroxy-4-chromanone

C11H12O4 (208.0735552)


   

4-acetoxybenzyl acetate

4-acetoxybenzyl acetate

C11H12O4 (208.0735552)


   

6-hydroxy-3-methylisochroman-5-carboxylic acid

6-hydroxy-3-methylisochroman-5-carboxylic acid

C11H12O4 (208.0735552)


   
   

2,3-Dihydroxy-8-undecene-4,6-diynoic acid

2,3-Dihydroxy-8-undecene-4,6-diynoic acid

C11H12O4 (208.0735552)


   

DL-Alanine, 3-(benzoylamino)-

DL-Alanine, 3-(benzoylamino)-

C10H12N2O3 (208.0847882)


   

D-galacto-3,5,6-Trihydroxy-2,4-dimethoxy-hexanal|O2,O4-dimethyl-D-galactose

D-galacto-3,5,6-Trihydroxy-2,4-dimethoxy-hexanal|O2,O4-dimethyl-D-galactose

C8H16O6 (208.0946836)


   

3-methyl-5-methoxy-8-hydroxy-3,4-dihydroisocoumarin

3-methyl-5-methoxy-8-hydroxy-3,4-dihydroisocoumarin

C11H12O4 (208.0735552)


   

4-(4-hydroxy-3-methoxyphenyl)but-3-enoic acid

4-(4-hydroxy-3-methoxyphenyl)but-3-enoic acid

C11H12O4 (208.0735552)


   

O-methylsilvaticol

O-methylsilvaticol

C11H12O4 (208.0735552)


   

4-Me ether,Ac-2,4-Dihydroxy-6-methylbenzaldehyde-

4-Me ether,Ac-2,4-Dihydroxy-6-methylbenzaldehyde-

C11H12O4 (208.0735552)


   

6-Demethylkigelin

6-Demethylkigelin

C11H12O4 (208.0735552)


   

4-methyl-1,1,3,3-tetraoxo-2,2-bicyclopentyl

4-methyl-1,1,3,3-tetraoxo-2,2-bicyclopentyl

C11H12O4 (208.0735552)


   

SPHYQDXGWOASKY-UHFFFAOYSA-

SPHYQDXGWOASKY-UHFFFAOYSA-

C11H12O4 (208.0735552)


   

methyl 2-methoxy-5-hydroxycinnamic acid

methyl 2-methoxy-5-hydroxycinnamic acid

C11H12O4 (208.0735552)


   

3-allyl-3a,5,6,6a-tetrahydro-2,6a-dihydroxypentalene-1,4-dione|xialenon D

3-allyl-3a,5,6,6a-tetrahydro-2,6a-dihydroxypentalene-1,4-dione|xialenon D

C11H12O4 (208.0735552)


   

6,7-Dimethoxy-2H-1-benzopyran-2-one

6,7-Dimethoxy-2H-1-benzopyran-2-one

C11H12O4 (208.0735552)


   
   
   

3-acetoxybenzyl acetate

3-acetoxybenzyl acetate

C11H12O4 (208.0735552)


   

2,5-Diacetoxytoluene

2,5-Diacetoxytoluene

C11H12O4 (208.0735552)


   

1,3,7,8-Tetramethylxanthine

1,3,7,8-Tetramethylxanthine

C9H12N4O2 (208.0960212)


   

methyl 3-(4-methoxyphenyl)-2-oxopropanoate

methyl 3-(4-methoxyphenyl)-2-oxopropanoate

C11H12O4 (208.0735552)


   

AI3-23713

2-propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, methyl ester, (2E)-

C11H12O4 (208.0735552)


Trans-methylferulate is a cinnamate ester that is the methyl ester of ferulic acid. It has been isolated from Pisonia aculeata. It has a role as a plant metabolite. It is a cinnamate ester, a methyl ester and a member of guaiacols. It is functionally related to a ferulic acid. Methyl ferulate is a natural product found in Iris milesii, Coreopsis grandiflora, and other organisms with data available. See also: Black Cohosh (part of). Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2]. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2].

   

3,4-Dimethoxycinnamic acid

3,4-Dimethoxycinnamic acid

C11H12O4 (208.0735552)


Annotation level-1 Acquisition and generation of the data is financially supported in part by CREST/JST. (E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. (E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1].

   

3,5-Dimethoxycinnamic acid

3,5-Dimethoxycinnamic acid

C11H12O4 (208.0735552)


Annotation level-1 Acquisition and generation of the data is financially supported in part by CREST/JST.

   

Kynurenine

(2R)-6-methoxy-2-phenyl-2,3-dihydrochromen-4-one

C10H12N2O3 (208.0847882)


A ketone that is alanine in which one of the methyl hydrogens is substituted by a 2-aminobenzoyl group. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.061 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.060 2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid is an endogenous metabolite. L-Kynurenine is a metabolite of the amino acid L-tryptophan. L-Kynurenine is an aryl hydrocarbon receptor agonist.

   

(E)-3-(3,4-dimethoxyphenyl)prop-2-enoic acid

NCGC00095522-05!(E)-3-(3,4-dimethoxyphenyl)prop-2-enoic acid

C11H12O4 (208.0735552)


   

Dimethoxycinnamic acid

3,4-Dimethoxycinnamic acid

C11H12O4 (208.0735552)


3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1].

   

C10H12N2O3_N-(2-Aminobenzoyl)alanine

NCGC00384567-01_C10H12N2O3_N-(2-Aminobenzoyl)alanine

C10H12N2O3 (208.0847882)


   

C11H12O4_1H-2-Benzopyran-1-one, 3,4-dihydro-6-hydroxy-8-methoxy-3-methyl

Pyrenocin A - NCGC00169582-02_C11H12O4_1H-2-Benzopyran-1-one, 3,4-dihydro-6-hydroxy-8-methoxy-3-methyl-

C11H12O4 (208.0735552)


   

L-Kynurenine

L-Kynurenine

C10H12N2O3 (208.0847882)


A kynurenine that has L configuration. MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; YGPSJZOEDVAXAB-QMMMGPOBSA-N_STSL_0006_L-Kynurenine_2000fmol_180416_S2_LC02_MS02_52; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. L-Kynurenine is a metabolite of the amino acid L-tryptophan. L-Kynurenine is an aryl hydrocarbon receptor agonist.

   

2-Benzylsuccinic acid

2-Benzylsuccinic acid

C11H12O4 (208.0735552)


A dicarboxylic acid consisting of succinic acid carrying a 2-benzyl substituent.

   

Benzylsuccinic acid

2-benzylbutanedioic acid

C11H12O4 (208.0735552)


   

2-[(2-aminobenzoyl)amino]propanoic acid

2-[(2-aminobenzoyl)amino]propanoic acid

C10H12N2O3 (208.0847882)


   

Sinapoyl aldehyde

Sinapoyl aldehyde

C11H12O4 (208.0735552)


Annotation level-1

   

Pyrenocin A putative

Pyrenocin A putative

C11H12O4 (208.0735552)


   

Dimethylcaffeic acid

3,4-Dimethoxycinnamic acid, predominantly trans

C11H12O4 (208.0735552)


(E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. (E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1].

   

Kynurenine; LC-tDDA; CE10

Kynurenine; LC-tDDA; CE10

C10H12N2O3 (208.0847882)


   

Kynurenine; LC-tDDA; CE20

Kynurenine; LC-tDDA; CE20

C10H12N2O3 (208.0847882)


   

Kynurenine; LC-tDDA; CE30

Kynurenine; LC-tDDA; CE30

C10H12N2O3 (208.0847882)


   

Kynurenine; LC-tDDA; CE40

Kynurenine; LC-tDDA; CE40

C10H12N2O3 (208.0847882)


   
   

2-[(2-aminobenzoyl)amino]propanoic acid_major

2-[(2-aminobenzoyl)amino]propanoic acid_major

C10H12N2O3 (208.0847882)


   

3,4-Dimethoxycinnamic Acid_major

3,4-Dimethoxycinnamic Acid_major

C11H12O4 (208.0735552)


   

4-hydroxy-3-methoxy-Cinnamic acid

4-hydroxy-3-methoxy-Cinnamic acid

C11H12O4 (208.0735552)


   

2,5-Dimethoxycinnamic acid

31H-4,21-(Methano[1,3]benzenomethano)-26,30-metheno-25H-dibenzo[q,z][1,4,7,10,13,16]hexaoxacycloheptacosin,6,7,9,10,12,13,15,16,18,19-decahydro-32,35-dimethoxy-

C11H12O4 (208.0735552)


   

8-METHYLCAFFEINE

1,3,7,8-Tetramethylxanthine

C9H12N4O2 (208.0960212)


   

5-(3,4-Dihydroxyphenyl)-gamma-valerolactone

5-(3,4-Dihydroxybenzyl)dihydro-2(3H)-furanone

C11H12O4 (208.0735552)


   

Dambonite

(1R,2s,3S,4R,5s,6S)-4,6-dimethoxycyclohexane-1,2,3,5-tetrol

C8H16O6 (208.0946836)


   

Furapiole

8-methoxy-11-methyl-4,6,10-trioxatricyclo[7.3.0.0^{3,7}]dodeca-1(9),2,7-triene

C11H12O4 (208.0735552)


   

1-(2-Methoxy-3,4-methylenedioxyphenyl)-1-propanone

1-(2-Methoxy-3,4-methylenedioxyphenyl)-1-propanone

C11H12O4 (208.0735552)


   

3'-Methoxy-4',5'-methylenedioxycinnamyl alcohol

3'-Methoxy-4',5'-methylenedioxycinnamyl alcohol

C11H12O4 (208.0735552)


   

Anthriscinol

1-(7-methoxy-2H-1,3-benzodioxol-5-yl)prop-2-en-1-ol

C11H12O4 (208.0735552)


   

5-[(3,5-dihydroxyphenyl)methyl]oxolan-2-one

5-(3',5'-Dihydroxyphenyl)-gamma-valerolactone

C11H12O4 (208.0735552)


   

1-(Benzyloxy)-3-ethynylbenzene

1-(Benzyloxy)-3-ethynylbenzene

C15H12O (208.08881019999998)


   

Benzyl trans-3-fluorocyclobutanecarboxylate

Benzyl trans-3-fluorocyclobutanecarboxylate

C12H13FO2 (208.089953)


   

methyl (E)-5-(4-fluorophenyl)pent-2-enoate

methyl (E)-5-(4-fluorophenyl)pent-2-enoate

C12H13FO2 (208.089953)


   

ETHYL 4-OXO-4,5,6,7-TETRAHYDRO-1H-INDAZOLE-3-CARBOXYLATE

ETHYL 4-OXO-4,5,6,7-TETRAHYDRO-1H-INDAZOLE-3-CARBOXYLATE

C10H12N2O3 (208.0847882)


   

Pikamilone

Pikamilone

C10H12N2O3 (208.0847882)


Picamilon is an orally active derivative of γ-aminobutyric acid that has nootropic effect. Picamilon improves the epilepsy model in rats and promotes correction of functional disorders of the pancreas during Alloxan (HY-W017227)-induced diabetes mellitus in rats[1][2][3].

   

1,4-Bis(dicyanomethylene)cyclohexane

1,4-Bis(dicyanomethylene)cyclohexane

C12H8N4 (208.0748928)


   
   

1-(5-Nitro-2-pyridinyl)piperazine

1-(5-Nitro-2-pyridinyl)piperazine

C9H12N4O2 (208.0960212)


   

3-([1,1-BIPHENYL]-4-YL)ACRYLALDEHYDE

3-([1,1-BIPHENYL]-4-YL)ACRYLALDEHYDE

C15H12O (208.08881019999998)


   
   
   

4,5-Dimethyl-2-nitroacetanilide

4,5-Dimethyl-2-nitroacetanilide

C10H12N2O3 (208.0847882)


   
   

4-(1,3-dioxolan-2-yl)-N-hydroxybenzenecarboximidamide

4-(1,3-dioxolan-2-yl)-N-hydroxybenzenecarboximidamide

C10H12N2O3 (208.0847882)


   

Methyl 5-acetyl-2-methoxybenzoate

Methyl 5-acetyl-2-methoxybenzoate

C11H12O4 (208.0735552)


   

1-[4-(ALLYLOXY)-2,6-DIHYDROXYPHENYL]ETHAN-1-ONE

1-[4-(ALLYLOXY)-2,6-DIHYDROXYPHENYL]ETHAN-1-ONE

C11H12O4 (208.0735552)


   

(2S,3R)-3AMINO-4-CYCLOBUTYL-2-HYDROXYBUTANAMIDE HYDROCHLORIDE

(2S,3R)-3AMINO-4-CYCLOBUTYL-2-HYDROXYBUTANAMIDE HYDROCHLORIDE

C8H17ClN2O2 (208.0978492)


   
   

1-(2-Fluorophenyl)cyclopentanecarboxylic acid

1-(2-Fluorophenyl)cyclopentanecarboxylic acid

C12H13FO2 (208.089953)


   

[(5-Ethyl-3-thienyl)ethynyl](trimethyl)silane

[(5-Ethyl-3-thienyl)ethynyl](trimethyl)silane

C11H16SSi (208.0741936)


   

(4-PHENYLTHIOPHENYL)DIPHENYLSULFONIUMTRIFLATE

(4-PHENYLTHIOPHENYL)DIPHENYLSULFONIUMTRIFLATE

C11H12O4 (208.0735552)


   

2,4-dimethoxycinnamic acid

3-(2,4-Dimethoxyphenyl)acrylic acid

C11H12O4 (208.0735552)


   

Benzyl methyl malonate

Benzyl methyl malonate

C11H12O4 (208.0735552)


   

1-Benzyl-3-Methylimidazolium Chloride

1-Benzyl-3-Methylimidazolium Chloride

C11H13ClN2 (208.0767208)


   
   

4-(3-METHOXYPHENYL)-4-OXOBUTYRIC ACID

4-(3-METHOXYPHENYL)-4-OXOBUTYRIC ACID

C11H12O4 (208.0735552)


   

6-Methoxy-3-chromanecarboxylic acid

6-Methoxy-3-chromanecarboxylic acid

C11H12O4 (208.0735552)


   
   

METHYL 2-HYDROXY-3-PROPIONYLBENZOATE

METHYL 2-HYDROXY-3-PROPIONYLBENZOATE

C11H12O4 (208.0735552)


   

N-Acetyl-2-(4-nitrophenyl)ethylamine

N-Acetyl-2-(4-nitrophenyl)ethylamine

C10H12N2O3 (208.0847882)


   

8-Methoxy-chroman-3-carboxylic acid

8-Methoxy-chroman-3-carboxylic acid

C11H12O4 (208.0735552)


   

2-(4-acetylphenoxy)propanoic acid

2-(4-acetylphenoxy)propanoic acid

C11H12O4 (208.0735552)


   

Butanedioic acid,1-(2-phenylhydrazide)

Butanedioic acid,1-(2-phenylhydrazide)

C10H12N2O3 (208.0847882)


   

3-[(4-aminophenyl)carbamoyl]propanoic acid

3-[(4-aminophenyl)carbamoyl]propanoic acid

C10H12N2O3 (208.0847882)


   

(3-Formyl-5-isopropoxyphenyl)boronic acid

(3-Formyl-5-isopropoxyphenyl)boronic acid

C10H13BO4 (208.09068480000002)


   

(3-FORMYL-4-ISOPROPOXYPHENYL)BORONIC ACID

(3-FORMYL-4-ISOPROPOXYPHENYL)BORONIC ACID

C10H13BO4 (208.09068480000002)


   

Methyl 4-methoxybenzoylacetate

Methyl 4-methoxybenzoylacetate

C11H12O4 (208.0735552)


   

2-(5-(METHOXYCARBONYL)-2-METHYLPHENYL)ACETIC ACID

2-(5-(METHOXYCARBONYL)-2-METHYLPHENYL)ACETIC ACID

C11H12O4 (208.0735552)


   
   

Dimethyl 4-methylisophthalate

Dimethyl 4-methylisophthalate

C11H12O4 (208.0735552)


   

2-[(R)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

2-[(R)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

C11H13ClN2 (208.0767208)


   

2-[(S)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

2-[(S)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

C11H13ClN2 (208.0767208)


   

3-[(S)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

3-[(S)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

C11H13ClN2 (208.0767208)


   

4-[(S)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

4-[(S)-amino(cyclopropyl)methyl]benzonitrile,hydrochloride

C11H13ClN2 (208.0767208)


   

2-PHENYL-MALONIC ACID MONOETHYL ESTER

2-PHENYL-MALONIC ACID MONOETHYL ESTER

C11H12O4 (208.0735552)


   

ethyl 2-acetamidopyridine-4-carboxylate

ethyl 2-acetamidopyridine-4-carboxylate

C10H12N2O3 (208.0847882)


   

5,7-Dimethoxychroman-4-one

5,7-Dimethoxychroman-4-one

C11H12O4 (208.0735552)


   

[4-(Methoxycarbonyl)-3,5-dimethylphenyl]boronic acid

[4-(Methoxycarbonyl)-3,5-dimethylphenyl]boronic acid

C10H13BO4 (208.09068480000002)


   
   

3-Methyl-7-propylxanthine

3-Methyl-7-propylxanthine

C9H12N4O2 (208.0960212)


   

(2S,3R)-3-AMINO-2-HYDROXYHEXANOICACID

(2S,3R)-3-AMINO-2-HYDROXYHEXANOICACID

C8H16O6 (208.0946836)


   

Methyl 4-(2-methoxy-2-oxoethyl)benzoate

Methyl 4-(2-methoxy-2-oxoethyl)benzoate

C11H12O4 (208.0735552)


   

1,4-Benzodioxin-2-carboxylic acid, 2,3-dihydro-, ethyl ester, (2S)-

1,4-Benzodioxin-2-carboxylic acid, 2,3-dihydro-, ethyl ester, (2S)-

C11H12O4 (208.0735552)


   

2-HYDROXY-5,6,7,8-TETRAHYDRO-[1,6]NAPHTHYRIDINE-3-CARBOXYLIC ACID METHYL ESTER

2-HYDROXY-5,6,7,8-TETRAHYDRO-[1,6]NAPHTHYRIDINE-3-CARBOXYLIC ACID METHYL ESTER

C10H12N2O3 (208.0847882)


   

(E)-5-(BUT-2-ENYL)-2,3,4-TRIHYDROXYBENZALDEHYDE

(E)-5-(BUT-2-ENYL)-2,3,4-TRIHYDROXYBENZALDEHYDE

C11H12O4 (208.0735552)


   

METHYL 2-(3-FORMYLPHENOXY)PROPIONATE

METHYL 2-(3-FORMYLPHENOXY)PROPIONATE

C11H12O4 (208.0735552)


   

{[(BENZYLAMINO)CARBONYL]AMINO}ACETIC ACID

{[(BENZYLAMINO)CARBONYL]AMINO}ACETIC ACID

C10H12N2O3 (208.0847882)


   

4-(3-nitrophenyl)morpholine

4-(3-nitrophenyl)morpholine

C10H12N2O3 (208.0847882)


   

4-ethoxycarbonylmethylphenylboronic acid

4-ethoxycarbonylmethylphenylboronic acid

C10H13BO4 (208.09068480000002)


   

(4-((CYCLOPROPYLMETHYL)THIO)PHENYL)BORONIC ACID

(4-((CYCLOPROPYLMETHYL)THIO)PHENYL)BORONIC ACID

C10H13BO2S (208.07292680000003)


   

Benzamide,N-(2-amino-2-oxoethyl)-4-methoxy

Benzamide,N-(2-amino-2-oxoethyl)-4-methoxy

C10H12N2O3 (208.0847882)


   

(5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDIN-4-YL)-HYDRAZINE

(5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDIN-4-YL)-HYDRAZINE

C11H12O4 (208.0735552)


   
   

isoferulic acid methyl ester

isoferulic acid methyl ester

C11H12O4 (208.0735552)


   

2,3-Dimethoxycinnamic acid

2,3-Dimethoxy cinnamic acid

C11H12O4 (208.0735552)


   

4-(4-Methoxyphenyl)-4-oxobutanoic acid

4-(4-Methoxyphenyl)-4-oxobutanoic acid

C11H12O4 (208.0735552)


   

Methyl 3-(2-methoxyphenyl)-3-oxopropanoate

Methyl 3-(2-methoxyphenyl)-3-oxopropanoate

C11H12O4 (208.0735552)


   

Acetamide,N-(2,5-dimethyl-4-nitrophenyl)-

Acetamide,N-(2,5-dimethyl-4-nitrophenyl)-

C10H12N2O3 (208.0847882)


   

8-chloro-6-hydroxy methyl caprylate

8-chloro-6-hydroxy methyl caprylate

C9H17ClO3 (208.0866162)


   

2-[(2-methylphenyl)methyl]propanedioic acid

2-[(2-methylphenyl)methyl]propanedioic acid

C11H12O4 (208.0735552)


   

3-Pyridazinecarboxamide, 6-(4-morpholinyl)-

3-Pyridazinecarboxamide, 6-(4-morpholinyl)-

C9H12N4O2 (208.0960212)


   

2,6-DIETHYL-4-METHYLANILINE

2,6-DIETHYL-4-METHYLANILINE

C10H12N2O3 (208.0847882)


   

1-(4-Fluorophenyl)cyclopentanecarboxylic acid

1-(4-Fluorophenyl)cyclopentanecarboxylic acid

C12H13FO2 (208.089953)


   
   

2-ACETYLAMINO-3-PYRIDIN-3-YL-PROPIONIC ACID

2-ACETYLAMINO-3-PYRIDIN-3-YL-PROPIONIC ACID

C10H12N2O3 (208.0847882)


   

3H-2-Benzopyran-3-one,1,4-dihydro-6,7-dimethoxy-

3H-2-Benzopyran-3-one,1,4-dihydro-6,7-dimethoxy-

C11H12O4 (208.0735552)


   

(S)-Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate

(S)-Methyl 2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetate

C11H12O4 (208.0735552)


   

Dimethyl 5-methylisophthalate

Dimethyl 5-methylisophthalate

C11H12O4 (208.0735552)


   

3-hydroxybenzoylacetic acid ethyl ester

3-hydroxybenzoylacetic acid ethyl ester

C11H12O4 (208.0735552)


   

2,2-di-(prop-2-ynyl)-malonic acid dimethyl ester

2,2-di-(prop-2-ynyl)-malonic acid dimethyl ester

C11H12O4 (208.0735552)


   
   
   

6-Morpholinonicotinic acid

6-Morpholinonicotinic acid

C10H12N2O3 (208.0847882)


   

4-(2-METHOXYCARBONYLETHYL)PHENYLBORONIC ACID

4-(2-METHOXYCARBONYLETHYL)PHENYLBORONIC ACID

C10H13BO4 (208.09068480000002)


   

METHYL 3-(3-BORONOPHENYL)PROPIONATE

METHYL 3-(3-BORONOPHENYL)PROPIONATE

C10H13BO4 (208.09068480000002)


   

Acetic acid,2-(2-formylphenoxy)-, ethyl ester

Acetic acid,2-(2-formylphenoxy)-, ethyl ester

C11H12O4 (208.0735552)


   

SG 209

N-[2-(Acetoxy)ethyl]-3-pyridinecarboxamide

C10H12N2O3 (208.0847882)


   

Acetamide,N-(2,4-dimethyl-6-nitrophenyl)-

Acetamide,N-(2,4-dimethyl-6-nitrophenyl)-

C10H12N2O3 (208.0847882)


   

1-(2-HYDROXY-ETHOXYMETHYL)-5-TRIFLUOROMETHYL-1H-PYRIMIDINE-2,4-DIONE

1-(2-HYDROXY-ETHOXYMETHYL)-5-TRIFLUOROMETHYL-1H-PYRIMIDINE-2,4-DIONE

C7H16N2O3S (208.0881586)


   

2-(4-Morpholinyl)isonicotinic acid

2-(4-Morpholinyl)isonicotinic acid

C10H12N2O3 (208.0847882)


   

5-ACETYLAMINO-3-NITRO 1,2-XYLIN

5-ACETYLAMINO-3-NITRO 1,2-XYLIN

C10H12N2O3 (208.0847882)


   
   

1-(3-Nitropyridin-2-yl)piperazine

1-(3-Nitropyridin-2-yl)piperazine

C9H12N4O2 (208.0960212)


   

Ethyl N-(3-pyridinylcarbonyl)glycinate

Ethyl N-(3-pyridinylcarbonyl)glycinate

C10H12N2O3 (208.0847882)


   

4-(Acetoxymethyl)benzoic acid methyl ester

4-(Acetoxymethyl)benzoic acid methyl ester

C11H12O4 (208.0735552)


   

Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate

Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxylate

C11H12O4 (208.0735552)


   

8a-(Trifluoromethyl)hexahydropyrrolo[1,2-a]pyrimidin-6(7H)-one

8a-(Trifluoromethyl)hexahydropyrrolo[1,2-a]pyrimidin-6(7H)-one

C8H11F3N2O (208.08234319999997)


   

2,5-Methano-5H,9H-pyrimido[2,1-b][1,5,3]dioxazepin-9-one,2,3-dihydro-3-(hydroxymethyl)-8-methyl-, (2R,3R,5R)-

2,5-Methano-5H,9H-pyrimido[2,1-b][1,5,3]dioxazepin-9-one,2,3-dihydro-3-(hydroxymethyl)-8-methyl-, (2R,3R,5R)-

C10H12N2O3 (208.0847882)


   

methyl (2-acetylphenoxy)acetate

methyl (2-acetylphenoxy)acetate

C11H12O4 (208.0735552)


   
   

Methyl 3-(3-methoxyphenyl)-3-oxopropanoate

Methyl 3-(3-methoxyphenyl)-3-oxopropanoate

C11H12O4 (208.0735552)


   

2-TERT-BUTYL-6-CHLORO-IMIDAZO[1,2-A]PYRIDINE

2-TERT-BUTYL-6-CHLORO-IMIDAZO[1,2-A]PYRIDINE

C11H13ClN2 (208.0767208)


   

7-Methoxychroman-3-carboxylic acid

7-Methoxychroman-3-carboxylic acid

C11H12O4 (208.0735552)


   

Butanedioic acid,2-(2-methylphenyl)-

Butanedioic acid,2-(2-methylphenyl)-

C11H12O4 (208.0735552)


   

Methanediol, 1-phenyl-,1,1-diacetate

Methanediol, 1-phenyl-,1,1-diacetate

C11H12O4 (208.0735552)


   

4-(4-nitrophenyl)morpholine

4-(4-nitrophenyl)morpholine

C10H12N2O3 (208.0847882)


   
   

methyl 2-(2′-hydroxy phenyl)-3-methoxy acrylate

methyl 2-(2′-hydroxy phenyl)-3-methoxy acrylate

C11H12O4 (208.0735552)


   

desoxypeganine hydrochloride

desoxypeganine hydrochloride

C11H13ClN2 (208.0767208)


   

(6-FLUORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-ACETIC ACID

(6-FLUORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-ACETIC ACID

C12H13FO2 (208.089953)


   

3-BIPHENYL-4-YLPROP-2-YN-1-OL

3-BIPHENYL-4-YLPROP-2-YN-1-OL

C15H12O (208.08881019999998)


   

b-Alanine,N-[(phenylamino)carbonyl]-

b-Alanine,N-[(phenylamino)carbonyl]-

C10H12N2O3 (208.0847882)


   

[4-(Propoxycarbonyl)phenyl]boronic acid

[4-(Propoxycarbonyl)phenyl]boronic acid

C10H13BO4 (208.09068480000002)


   
   

(3-(2-ETHOXY-2-OXOETHYL)PHENYL)BORONIC ACID

(3-(2-ETHOXY-2-OXOETHYL)PHENYL)BORONIC ACID

C10H13BO4 (208.09068480000002)


   

1-(4-fluorophenyl)-4-methylpentane-1,3-dione

1-(4-fluorophenyl)-4-methylpentane-1,3-dione

C12H13FO2 (208.089953)


   

3-(4-Acetylphenoxy)propanoic acid

3-(4-Acetylphenoxy)propanoic acid

C11H12O4 (208.0735552)


   

5-fluoro-3-((trimethylsilyl)ethynyl)pyridin-2-amine

5-fluoro-3-((trimethylsilyl)ethynyl)pyridin-2-amine

C10H13FN2Si (208.08319899999998)


   

tert-Butyl 3-aminoazetidine-1-carboxylate hydrochloride

tert-Butyl 3-aminoazetidine-1-carboxylate hydrochloride

C8H17ClN2O2 (208.0978492)


   

Benzoic acid,4-[[(dimethylamino)carbonyl]amino]-

Benzoic acid,4-[[(dimethylamino)carbonyl]amino]-

C10H12N2O3 (208.0847882)


   

benzyl hydrogen succinate

benzyl hydrogen succinate

C11H12O4 (208.0735552)


   

2,6-DIMETHOXYCINNAMIC ACID

2,6-DIMETHOXYCINNAMIC ACID

C11H12O4 (208.0735552)


   

2-([1,3]DIOXOLAN-2-YLMETHOXY)-BENZALDEHYDE

2-([1,3]DIOXOLAN-2-YLMETHOXY)-BENZALDEHYDE

C11H12O4 (208.0735552)


   

1,3,5-Triazin-2-amine,4,6-bis(2-propen-1-yloxy)-

1,3,5-Triazin-2-amine,4,6-bis(2-propen-1-yloxy)-

C9H12N4O2 (208.0960212)


   
   

6-methoxy-3,4-dihydro-2H-chromene-2-carboxylic acid

6-methoxy-3,4-dihydro-2H-chromene-2-carboxylic acid

C11H12O4 (208.0735552)


   

Methyl 3-(p-methoxyphenyl)-2,3-epoxypropionate

Methyl 3-(p-methoxyphenyl)-2,3-epoxypropionate

C11H12O4 (208.0735552)


   

(3-Formyl-5-propoxyphenyl)boronic acid

(3-Formyl-5-propoxyphenyl)boronic acid

C10H13BO4 (208.09068480000002)


   

ETHYL5-OXO-1,2,3,5-TETRAHYDROIMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLATE

ETHYL5-OXO-1,2,3,5-TETRAHYDROIMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLATE

C10H12N2O3 (208.0847882)


   

3-Phenylpyrido[2,3-e][1,2,4]triazine

3-Phenylpyrido[2,3-e][1,2,4]triazine

C12H8N4 (208.0748928)


   

Benzamide,4-nitro-N-propyl-

Benzamide,4-nitro-N-propyl-

C10H12N2O3 (208.0847882)


   

(E)-3-(4-Amino-3,5-dimethylphenyl)acrylonitrile hydrochloride

(E)-3-(4-Amino-3,5-dimethylphenyl)acrylonitrile hydrochloride

C11H13ClN2 (208.0767208)


   

4-(2-Oxiranylmethoxy)benzoic Acid Methyl Ester

4-(2-Oxiranylmethoxy)benzoic Acid Methyl Ester

C11H12O4 (208.0735552)


   
   

Benzenemethanol, a-(2-phenylethynyl)-

Benzenemethanol, a-(2-phenylethynyl)-

C15H12O (208.08881019999998)


   

ethyl O-acetylsalicylate

ethyl O-acetylsalicylate

C11H12O4 (208.0735552)


   

3-(Cyclopropylmethyl)thiophenylboronic acid

3-(Cyclopropylmethyl)thiophenylboronic acid

C10H13BO2S (208.07292680000003)


   

(3-(CYCLOBUTYLTHIO)PHENYL)BORONIC ACID

(3-(CYCLOBUTYLTHIO)PHENYL)BORONIC ACID

C10H13BO2S (208.07292680000003)


   

ETHYL 1-(4-FLUOROPHENYL)CYCLOPROPANECARBOXYLATE

ETHYL 1-(4-FLUOROPHENYL)CYCLOPROPANECARBOXYLATE

C12H13FO2 (208.089953)


   

1-(3-Fluorophenyl)cyclopentanecarboxylic acid

1-(3-Fluorophenyl)cyclopentanecarboxylic acid

C12H13FO2 (208.089953)


   

DIMETHYL 2-METHYLISOPHTHALATE

DIMETHYL 2-METHYLISOPHTHALATE

C11H12O4 (208.0735552)


   

2-ACETOXY-3-PHENYL-PROPIONIC ACID

2-ACETOXY-3-PHENYL-PROPIONIC ACID

C11H12O4 (208.0735552)


   

3-(4-Nitrophenoxy)pyrrolidine

3-(4-Nitrophenoxy)pyrrolidine

C10H12N2O3 (208.0847882)


   

6,6-DIMETHYL-4-OXO-4,5,6,7-TETRAHYDRO-1-BENZOFURAN-3-CARBOXYLIC ACID

6,6-DIMETHYL-4-OXO-4,5,6,7-TETRAHYDRO-1-BENZOFURAN-3-CARBOXYLIC ACID

C11H12O4 (208.0735552)


   
   
   

5-methyl-3-phenyl-1-benzofuran

5-methyl-3-phenyl-1-benzofuran

C15H12O (208.08881019999998)


   

3-(3-acetoxyphenyl)propionic acid

3-(3-acetoxyphenyl)propionic acid

C11H12O4 (208.0735552)


   

3-(2-ACETOXYPHENYL)PROPANOIC ACID

3-(2-ACETOXYPHENYL)PROPANOIC ACID

C11H12O4 (208.0735552)


   

methyl 2-(4-formylphenoxy)propanoate

methyl 2-(4-formylphenoxy)propanoate

C11H12O4 (208.0735552)


   

Glycine,N-[4-(acetylamino)phenyl]-

Glycine,N-[4-(acetylamino)phenyl]-

C10H12N2O3 (208.0847882)


   

[4-(Isopropoxycarbonyl)phenyl]boronic acid

[4-(Isopropoxycarbonyl)phenyl]boronic acid

C10H13BO4 (208.09068480000002)


   

3-Isopropoxycarbonylphenylboronic acid

3-Isopropoxycarbonylphenylboronic acid

C10H13BO4 (208.09068480000002)


   

1H-INDOLE-3-METHANAMINE, 5-CHLORO-N,N-DIMETHYL-

1H-INDOLE-3-METHANAMINE, 5-CHLORO-N,N-DIMETHYL-

C11H13ClN2 (208.0767208)


   

2-BENZO[1,3]DIOXOL-5-YL-PROPIONIC ACID METHYL ESTER

2-BENZO[1,3]DIOXOL-5-YL-PROPIONIC ACID METHYL ESTER

C11H12O4 (208.0735552)


   

4-HYDROXY-2,2-DIMETHYL-2,3-DIHYDROBENZOFURAN-6-CARBOXYLIC ACID

4-HYDROXY-2,2-DIMETHYL-2,3-DIHYDROBENZOFURAN-6-CARBOXYLIC ACID

C11H12O4 (208.0735552)


   

Methyl 2-(2-methoxy-2-oxoethyl)benzoate

Benzeneacetic acid,2-(methoxycarbonyl)-, methyl ester

C11H12O4 (208.0735552)


   
   

dimethyl bicyclo[2.2.1]hepta-2,5-diene-5,6-dicarboxylate

dimethyl bicyclo[2.2.1]hepta-2,5-diene-5,6-dicarboxylate

C11H12O4 (208.0735552)


   

3-(4-methoxycarbonylphenyl)propanoic acid

3-(4-methoxycarbonylphenyl)propanoic acid

C11H12O4 (208.0735552)


   
   

4-Chloro-2-(2-methyl-2-propanyl)-1H-pyrrolo[2,3-b]pyridine

4-Chloro-2-(2-methyl-2-propanyl)-1H-pyrrolo[2,3-b]pyridine

C11H13ClN2 (208.0767208)


   

1-methoxy-2-(2-phenylethynyl)benzene

1-methoxy-2-(2-phenylethynyl)benzene

C15H12O (208.08881019999998)


   

1-(2-(3-METHOXYPHENYL)ETHYNYL)BENZENE

1-(2-(3-METHOXYPHENYL)ETHYNYL)BENZENE

C15H12O (208.08881019999998)


   

3-(Cyclopropylmethoxy)-4-hydroxybenzoic acid

3-(Cyclopropylmethoxy)-4-hydroxybenzoic acid

C11H12O4 (208.0735552)


   

ethyl 4-methoxybenzoylformate

ethyl 4-methoxybenzoylformate

C11H12O4 (208.0735552)


   

Dimethyl 2-methylterephthalate

Dimethyl 2-methylterephthalate

C11H12O4 (208.0735552)


   
   

N-(2,3-Dimethyl-6-nitrophenyl)acetamide

N-(2,3-Dimethyl-6-nitrophenyl)acetamide

C10H12N2O3 (208.0847882)


   

6-(BENZYLOXY)-9-(1S,3R,4S)-4-(BENZYLOXY)-3-(BENZYOXYMETHYL)-2-METHYLENECYCLOPENTYL)-9H-PURIN-2-AMINE

6-(BENZYLOXY)-9-(1S,3R,4S)-4-(BENZYLOXY)-3-(BENZYOXYMETHYL)-2-METHYLENECYCLOPENTYL)-9H-PURIN-2-AMINE

C11H13ClN2 (208.0767208)


   

3-Phenylpentanedioic acid

3-Phenylpentanedioic acid

C11H12O4 (208.0735552)


   

2-(Benzoyloxy)-2-methylpropanoic acid

2-(Benzoyloxy)-2-methylpropanoic acid

C11H12O4 (208.0735552)


   

1H-Indole-3-methanamine,6-chloro-N,N-dimethyl-

1H-Indole-3-methanamine,6-chloro-N,N-dimethyl-

C11H13ClN2 (208.0767208)


   

3-(4-hydroxy-3-methoxyphenyl)-2-methylprop-2-enoic acid

3-(4-hydroxy-3-methoxyphenyl)-2-methylprop-2-enoic acid

C11H12O4 (208.0735552)


   

6-Morpholinopyridine-2-carboxylic Acid

6-Morpholinopyridine-2-carboxylic Acid

C10H12N2O3 (208.0847882)


   

2-Methyl-3-[(3,4-methylenedioxy)phenyl]propionic acid

2-Methyl-3-[(3,4-methylenedioxy)phenyl]propionic acid

C11H12O4 (208.0735552)


   
   

ethyl 4-oxo-6,7-dihydro-5H-1-benzofuran-3-carboxylate

ethyl 4-oxo-6,7-dihydro-5H-1-benzofuran-3-carboxylate

C11H12O4 (208.0735552)


   

Ethyl 1,4-benzodioxan-2-carboxylate

Ethyl 1,4-benzodioxan-2-carboxylate

C11H12O4 (208.0735552)


   

N-(2,4-dimethyl-5-nitrophenyl)acetamide

N-(2,4-dimethyl-5-nitrophenyl)acetamide

C10H12N2O3 (208.0847882)


   

CARBAMIC ACID, N-4-PYRIDINYL-, ETHYL ESTER

CARBAMIC ACID, N-4-PYRIDINYL-, ETHYL ESTER

C10H12N2O3 (208.0847882)


   

Ethyl vanillin acetate

Ethyl vanillin acetate

C11H12O4 (208.0735552)


   

beta-(4-Acetoxyphenyl)propionic acid

beta-(4-Acetoxyphenyl)propionic acid

C11H12O4 (208.0735552)


   

4-[(E)-2-Phenylvinyl]benzaldehyde

4-[(E)-2-Phenylvinyl]benzaldehyde

C15H12O (208.08881019999998)


   

N-(7-amino-2,3-dihydro-1,4-benzodioxin-6-yl)acetamide

N-(7-amino-2,3-dihydro-1,4-benzodioxin-6-yl)acetamide

C10H12N2O3 (208.0847882)


   

2-Phenylglutaric acid

2-Phenylglutaric acid

C11H12O4 (208.0735552)


   

POLY(PROPYLENE GLUTARATE)

POLY(PROPYLENE GLUTARATE)

C8H16O6 (208.0946836)


   

1-(N-methylcarbamimidoyl)-1-phenylthiourea

1-(N-methylcarbamimidoyl)-1-phenylthiourea

C9H12N4S (208.07826319999998)


   

ETHYL 3-METHOXYBENZOYLFORMATE

ETHYL 3-METHOXYBENZOYLFORMATE

C11H12O4 (208.0735552)


   

Pyrrolo[3,4-b]pyrrole, octahydro-1-(trifluoroacetyl)- (9CI)

Pyrrolo[3,4-b]pyrrole, octahydro-1-(trifluoroacetyl)- (9CI)

C8H11F3N2O (208.08234319999997)


   

1,3-dioxan-5-ol,1,3-dioxolan-4-ylmethanol

1,3-dioxan-5-ol,1,3-dioxolan-4-ylmethanol

C8H16O6 (208.0946836)


   

2-Morpholinonicotinic acid

2-Morpholinonicotinic acid

C10H12N2O3 (208.0847882)


   

4-(2-aminoanilino)-4-oxobutanoic acid

4-(2-aminoanilino)-4-oxobutanoic acid

C10H12N2O3 (208.0847882)


   

DIETHYL (2-OXOBUTYL)PHOSPHONATE

DIETHYL (2-OXOBUTYL)PHOSPHONATE

C8H17O4P (208.0864412)


   
   

methyl 2-(4-formyl-3-hydroxyphenyl)propanoate

methyl 2-(4-formyl-3-hydroxyphenyl)propanoate

C11H12O4 (208.0735552)


   

5-(4-fluorophenyl)pent-5-enoic acid

5-(4-fluorophenyl)pent-5-enoic acid

C12H13FO2 (208.089953)


   

[2R,4R,5R]-5-hydroxy-2-phenyl-[1,3]dioxane-4-carbaldehyde

[2R,4R,5R]-5-hydroxy-2-phenyl-[1,3]dioxane-4-carbaldehyde

C11H12O4 (208.0735552)


   
   

(S)-2-Benzylsuccinic acid

(S)-2-Benzylsuccinic acid

C11H12O4 (208.0735552)


   

4-(1H-pyrrole-1-yl)benzylamine

4-(1H-pyrrole-1-yl)benzylamine

C11H13ClN2 (208.0767208)


   

5-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)furan-2-carbaldehyde

5-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)furan-2-carbaldehyde

C10H13BO4 (208.09068480000002)


   

methyl 6-methoxy-2,3-dihydro-1-benzofuran-2-carboxylate

methyl 6-methoxy-2,3-dihydro-1-benzofuran-2-carboxylate

C11H12O4 (208.0735552)


   

Boronic acid,[4-(1,3-dioxan-2-yl)phenyl]-(9CI)

Boronic acid,[4-(1,3-dioxan-2-yl)phenyl]-(9CI)

C10H13BO4 (208.09068480000002)


   

ethyl 2-(methylcarbamoyl)pyridine-4-carboxylate

ethyl 2-(methylcarbamoyl)pyridine-4-carboxylate

C10H12N2O3 (208.0847882)


   

4-(4-MORPHOLINYL)-PICOLINIC ACID

4-(4-MORPHOLINYL)-PICOLINIC ACID

C10H12N2O3 (208.0847882)


   

Ethanone,2-(acetyloxy)-1-(4-methoxyphenyl)-

Ethanone,2-(acetyloxy)-1-(4-methoxyphenyl)-

C11H12O4 (208.0735552)


   

ethyl (4-formylphenoxy)acetate

ethyl (4-formylphenoxy)acetate

C11H12O4 (208.0735552)


   

3-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-propionic acid

3-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-propionic acid

C11H12O4 (208.0735552)


   

D-kynurenine

D-kynurenine

C10H12N2O3 (208.0847882)


A kynurenine that has D configuration. D-kynurenine, a metabolite of D-tryptophan, can serve as the bioprecursor of kynurenic acid (KYNA) and 3-hydroxykynurenine. D-Kynurenine is an agonist for G protein-coupled receptor, GPR109B. D-Kynurenine is a substrate in a fluorometric assay of D-amino acid oxidase. D-kynurenine promotes epithelial-to-mesenchymal transition via activating aryl hydrocarbon receptor (AHR)[1][2][3][4].

   

Methyl 3-(4-methoxyphenyl)oxirane-2-carboxylate

Methyl 3-(4-methoxyphenyl)oxirane-2-carboxylate

C11H12O4 (208.0735552)


   

4-morpholin-4-ylpyridine-3-carboxylic acid

4-morpholin-4-ylpyridine-3-carboxylic acid

C10H12N2O3 (208.0847882)


   

Benzeneacetic acid, 4-(ethoxycarbonyl)

Benzeneacetic acid, 4-(ethoxycarbonyl)

C11H12O4 (208.0735552)


   

METHYL 2-OXO-5,6,7,8-TETRAHYDRO-2H-CHROMENE-3-CARBOXYLATE

METHYL 2-OXO-5,6,7,8-TETRAHYDRO-2H-CHROMENE-3-CARBOXYLATE

C11H12O4 (208.0735552)


   

4-(ALLYLOXY)-3-METHOXYBENZOIC ACID

4-(ALLYLOXY)-3-METHOXYBENZOIC ACID

C11H12O4 (208.0735552)


   

3-(Benzo[D][1,3]Dioxol-6-Yl)Propane-Hydrazide

3-(Benzo[D][1,3]Dioxol-6-Yl)Propane-Hydrazide

C10H12N2O3 (208.0847882)


   

acetoxyethyl trimethoxysilane

acetoxyethyl trimethoxysilane

C7H16O5Si (208.0766966)


   

4-ACETOXYMETHYLPHENYLACETIC ACID

4-ACETOXYMETHYLPHENYLACETIC ACID

C11H12O4 (208.0735552)


   

5-MORPHOLIN-4-YL-NICOTINIC ACID

5-MORPHOLIN-4-YL-NICOTINIC ACID

C10H12N2O3 (208.0847882)


   
   

ethyl 2-(3-formylphenoxy)acetate

ethyl 2-(3-formylphenoxy)acetate

C11H12O4 (208.0735552)


   

3-(2-METHYL-1,3-DIOXOLAN-2-YL)PHENYLBORONIC ACID

3-(2-METHYL-1,3-DIOXOLAN-2-YL)PHENYLBORONIC ACID

C10H13BO4 (208.09068480000002)


   

2-(2-Methyl-1,3-dioxolan-2-yl)phenylboronic acid

2-(2-Methyl-1,3-dioxolan-2-yl)phenylboronic acid

C10H13BO4 (208.09068480000002)


   

3-(Propoxycarbonyl)Phenylboronic Acid

3-(Propoxycarbonyl)Phenylboronic Acid

C10H13BO4 (208.09068480000002)


   

3-N-Boc-AminoazetidineHCl

3-N-Boc-AminoazetidineHCl

C8H17ClN2O2 (208.0978492)


   

(2-ethoxy-3-formyl-5-methylphenyl)boronic acid

(2-ethoxy-3-formyl-5-methylphenyl)boronic acid

C10H13BO4 (208.09068480000002)


   

1H-Indene-4-carboxylicacid,2,3,5,6,7,7a-hexahydro-7a-methyl-1,5-dioxo-(9CI)

1H-Indene-4-carboxylicacid,2,3,5,6,7,7a-hexahydro-7a-methyl-1,5-dioxo-(9CI)

C11H12O4 (208.0735552)


   

1-(6-Nitropyridin-3-yl)piperazin

1-(6-Nitropyridin-3-yl)piperazin

C9H12N4O2 (208.0960212)


   

4,5-Dimethoxybenzocyclobutene-1-carboxylic acid

4,5-Dimethoxybenzocyclobutene-1-carboxylic acid

C11H12O4 (208.0735552)


   

N-carbamoylphenylalanine

N-carbamoylphenylalanine

C10H12N2O3 (208.0847882)


   

2-Butyl-5,6-dihydro-1H-imidazo[4,5-D]pyridazine-4,7-dione

2-Butyl-5,6-dihydro-1H-imidazo[4,5-D]pyridazine-4,7-dione

C9H12N4O2 (208.0960212)


   

4-Acetyl-3-methoxy-5-methylbenzoic acid

4-Acetyl-3-methoxy-5-methylbenzoic acid

C11H12O4 (208.0735552)


   
   

7-Ethyltheophylline

7-Ethyltheophylline

C9H12N4O2 (208.0960212)


   

Ethyl beta-D-fructofuranoside

Ethyl beta-D-fructofuranoside

C8H16O6 (208.0946836)


   

Monoisopropyl phthalate

Monoisopropyl phthalate

C11H12O4 (208.0735552)


A phthalic acid monoester obtained by formal condensation of one of the carboxy groups of phthalic acid with the hydroxy group of isopropanol.

   

cis-Chalcone

cis-Chalcone

C15H12O (208.08881019999998)


The cis-stereoisomer of chalcone.

   

1-methyl-3-propyl-7H-purine-2,6-dione

1-methyl-3-propyl-7H-purine-2,6-dione

C9H12N4O2 (208.0960212)


   

5-(3-Pyridinylmethyl)-1,3,5-triazinane-2-thione

5-(3-Pyridinylmethyl)-1,3,5-triazinane-2-thione

C9H12N4S (208.07826319999998)


   

4-Methoxy-4-oxo-3-phenylbutanoic acid

4-Methoxy-4-oxo-3-phenylbutanoic acid

C11H12O4 (208.0735552)


   
   

Norrimazole carboxylic acid

Norrimazole carboxylic acid

C10H12N2O3 (208.0847882)


   

Methyl ethyl phthalate

Methyl ethyl phthalate

C11H12O4 (208.0735552)


   
   

Benzo-1,3-dioxole-5-methanol propanoate

Benzo-1,3-dioxole-5-methanol propanoate

C11H12O4 (208.0735552)


   

1-(4-Trimethylsilyloxyphenyl)ethanone

1-(4-Trimethylsilyloxyphenyl)ethanone

C11H16O2Si (208.09195160000002)


   
   

3-Carboxymethyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one

3-Carboxymethyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one

C10H12N2O3 (208.0847882)


   
   

(+/-)-epibatidine

(1R,2R,4S)-2-(6-Chloropyridin-3-yl)-7-azabicyclo[2.2.1]heptane

C11H13ClN2 (208.0767208)


D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics

   

[(3R)-7-nitro-1,2,3,4-tetrahydroisoquinolin-3-yl]methanol

[(3R)-7-nitro-1,2,3,4-tetrahydroisoquinolin-3-yl]methanol

C10H12N2O3 (208.0847882)


   

3-(Benzoylamino)-L-Alanine

3-(Benzoylamino)-L-Alanine

C10H12N2O3 (208.0847882)


   
   

102-37-4

(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid ethyl ester

C11H12O4 (208.0735552)


Ethyl Caffeate is a natural phenolic compound isolated from Bidens pilosa. Ethyl caffeate suppresses NF-κB activation and its downstream inflammatory mediators, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2) in vitro or in mouse skin[1]. Ethyl Caffeate is a natural phenolic compound isolated from Bidens pilosa. Ethyl caffeate suppresses NF-κB activation and its downstream inflammatory mediators, inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2) in vitro or in mouse skin[1].

   

AIDS-021439

InChI=1\C11H12O4\c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2\h3-7H,1-2H3,(H,12,13)\b6-4

C11H12O4 (208.0735552)


(E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. (E)-3,4-Dimethoxycinnamic acid is the less active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1]. 3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway[1]. Anti-apoptotic effects[1].

   

(2S)-4-(2-aminophenyl)-2-azaniumyl-4-oxobutanoate

(2S)-4-(2-aminophenyl)-2-azaniumyl-4-oxobutanoate

C10H12N2O3 (208.0847882)


   

(2S,3R,6S)-3-fluoro-2,6-diaminopimelic acid

(2S,3R,6S)-3-fluoro-2,6-diaminopimelic acid

C7H13FN2O4 (208.085931)


   

(2S,3R,6S)-3-fluoro-2,6-diaminopimelate

(2S,3R,6S)-3-fluoro-2,6-diaminopimelate

C7H13FN2O4 (208.085931)


   

(2R,3S,6S)-3-Fluoro-2,6-diaminoheptanedioic acid

(2R,3S,6S)-3-Fluoro-2,6-diaminoheptanedioic acid

C7H13FN2O4 (208.085931)


   

(2R,3R,6S)-2,6-diamino-3-fluoroheptanedioic acid

(2R,3R,6S)-2,6-diamino-3-fluoroheptanedioic acid

C7H13FN2O4 (208.085931)


   

(2S,3S,6S)-2,6-diamino-3-fluoroheptanedioic acid

(2S,3S,6S)-2,6-diamino-3-fluoroheptanedioic acid

C7H13FN2O4 (208.085931)


   

(2S,3S,6S)-3-fluoro-2,6-diaminopimelate

(2S,3S,6S)-3-fluoro-2,6-diaminopimelate

C7H13FN2O4 (208.085931)


   

(2R,3S,6S)-3-fluoro-2,6-diaminopimelate

(2R,3S,6S)-3-fluoro-2,6-diaminopimelate

C7H13FN2O4 (208.085931)


   

(2R,3R,6S)-3-fluoro-2,6-diaminopimelate

(2R,3R,6S)-3-fluoro-2,6-diaminopimelate

C7H13FN2O4 (208.085931)


   

2,4-Dihydroxy-3-methyl-6-(2-oxopropyl)benzaldehyde

2,4-Dihydroxy-3-methyl-6-(2-oxopropyl)benzaldehyde

C11H12O4 (208.0735552)


A dihydroxybenzaldehyde that is 2,4-dihydroxybenzaldehyde in which the hydrogens at positions 3 and 6 have been replaced by a methyl and 2-oxopropyl groups, respectively.

   

3,6-di-O-methyl-beta-D-glucose

3,6-di-O-methyl-beta-D-glucose

C8H16O6 (208.0946836)


   

3,3-Dimethoxy-1-phenylpropane-1,2-dione

3,3-Dimethoxy-1-phenylpropane-1,2-dione

C11H12O4 (208.0735552)


An alpha-diketone that is 1-phenyl-1,2-propanedione substituted by two methoxy groups at position 3.

   

(3R,4S)-3-(6-chloro-3-pyridyl)-7-azabicyclo[2.2.1]heptane

(3R,4S)-3-(6-chloro-3-pyridyl)-7-azabicyclo[2.2.1]heptane

C11H13ClN2 (208.0767208)


D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics

   

2-hydroxy-N-propionylbenzohydrazide

2-hydroxy-N-propionylbenzohydrazide

C10H12N2O3 (208.0847882)


   

Ethyl beta-d-galactofuranoside

Ethyl beta-d-galactofuranoside

C8H16O6 (208.0946836)


   

1-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one

1-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one

C11H12O4 (208.0735552)


   
   

4-Formyl-2,5-dimethoxy-6-methyltropone

4-Formyl-2,5-dimethoxy-6-methyltropone

C11H12O4 (208.0735552)


   

4-(4-Methoxyphenyl)-4-methylthio-1-butene

4-(4-Methoxyphenyl)-4-methylthio-1-butene

C12H16OS (208.09218059999998)


   

1-Phenylbicyclo(3.2.2)nona-3,6,8-trien-2-one

1-Phenylbicyclo(3.2.2)nona-3,6,8-trien-2-one

C15H12O (208.08881019999998)


   
   

Formyl-5-hydroxykynurenamine

Formyl-5-hydroxykynurenamine

C10H12N2O3 (208.0847882)


A hydroxykynurenamine that is 5-hydroxykynurenamine with the hydrogen on the aryl amine replaced by a formyl group.

   

Benzylsuccinate

(R)-2-AMINO-BUT-3-EN-1-OLHYDROCHLORIDE

C11H12O4 (208.0735552)


The (R)-enantiomer of 2-benzylsuccinic acid.

   

3-(6-chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane

3-(6-chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane

C11H13ClN2 (208.0767208)


   

5-[(3,4-dihydroxyphenyl)methyl]oxolan-2-one

5-(3,4-Dihydroxybenzyl)dihydro-2(3H)-furanone

C11H12O4 (208.0735552)


   

3-Methyl-6-methoxy-8-hydroxy-3,4-dihydroisocoumarin

3-Methyl-6-methoxy-8-hydroxy-3,4-dihydroisocoumarin

C11H12O4 (208.0735552)


   
   

N-(4-Aminobenzoyl)-β-alanine

N-(4-Aminobenzoyl)-Beta-Alanine

C10H12N2O3 (208.0847882)


   

3-(3-Methoxy-4,5-methylenedioxyphenyl)-2-propen-1-ol

3-(3-Methoxy-4,5-methylenedioxyphenyl)-2-propen-1-ol

C11H12O4 (208.0735552)


   

2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-

2-Propenoic acid, 3-(3,4-dimethoxyphenyl)-

C11H12O4 (208.0735552)


   

L-kynurenine zwitterion

L-kynurenine zwitterion

C10H12N2O3 (208.0847882)


Zwitterionic form of L-kynurenine arising from transfer of a proton from the carboxy to the amino group; major species at pH 7.3.

   

caffeic acid ethyl ester

caffeic acid ethyl ester

C11H12O4 (208.0735552)


A natural product found in Solanum campaniforme.

   

trans-Chalcone

trans-Chalcone

C15H12O (208.08881019999998)


The trans-isomer of chalcone.

   

Ethyl alpha-glucose

Ethyl alpha-glucose

C8H16O6 (208.0946836)


   
   

Dimethoxyphenyl)propenoic acid

Dimethoxyphenyl)propenoic acid

C11H12O4 (208.0735552)


   

methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate

methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate

C11H12O4 (208.0735552)


   

6-(hydroxymethyl)-3,4-dimethoxyoxane-2,5-diol

6-(hydroxymethyl)-3,4-dimethoxyoxane-2,5-diol

C8H16O6 (208.0946836)


   

(2s,3z,3ar)-2-hydroxy-6a-(hydroxymethyl)-3-(prop-2-en-1-ylidene)-2h,3ah-cyclopenta[b]furan-4-one

(2s,3z,3ar)-2-hydroxy-6a-(hydroxymethyl)-3-(prop-2-en-1-ylidene)-2h,3ah-cyclopenta[b]furan-4-one

C11H12O4 (208.0735552)


   

(4s)-4,8-dihydroxy-5-methoxy-3,4-dihydro-2h-naphthalen-1-one

(4s)-4,8-dihydroxy-5-methoxy-3,4-dihydro-2h-naphthalen-1-one

C11H12O4 (208.0735552)


   

(3s)-5,7-dimethoxy-3-methyl-3h-2-benzofuran-1-one

(3s)-5,7-dimethoxy-3-methyl-3h-2-benzofuran-1-one

C11H12O4 (208.0735552)


   

(5e)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1z)-3-hydroxyprop-1-en-1-yl]furan-2-one

(5e)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1z)-3-hydroxyprop-1-en-1-yl]furan-2-one

C11H12O4 (208.0735552)


   

(5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one

(5z)-5-[(2e)-4-hydroxybut-2-en-1-ylidene]-3-[(1e)-3-hydroxyprop-1-en-1-yl]furan-2-one

C11H12O4 (208.0735552)


   

5-(but-2-enoyl)-4-methoxy-6-methylpyran-2-one

5-(but-2-enoyl)-4-methoxy-6-methylpyran-2-one

C11H12O4 (208.0735552)


   

(2s,3s)-3,7-dihydroxy-2,5-dimethyl-2,3-dihydro-1-benzopyran-4-one

(2s,3s)-3,7-dihydroxy-2,5-dimethyl-2,3-dihydro-1-benzopyran-4-one

C11H12O4 (208.0735552)


   

(3r,4s)-8-hydroxy-4-methoxy-3-methyl-3,4-dihydro-2-benzopyran-1-one

(3r,4s)-8-hydroxy-4-methoxy-3-methyl-3,4-dihydro-2-benzopyran-1-one

C11H12O4 (208.0735552)


   

(2r,3r,4s)-2-[(1s)-1-hydroxy-2,2-dimethoxyethyl]oxolane-3,4-diol

(2r,3r,4s)-2-[(1s)-1-hydroxy-2,2-dimethoxyethyl]oxolane-3,4-diol

C8H16O6 (208.0946836)


   
   

(4r)-4,6,8-trihydroxy-5-methyl-3,4-dihydro-2h-naphthalen-1-one

(4r)-4,6,8-trihydroxy-5-methyl-3,4-dihydro-2h-naphthalen-1-one

C11H12O4 (208.0735552)


   

3,6-dihydroxy-4-methoxy-5-methyl-2,3-dihydroinden-1-one

3,6-dihydroxy-4-methoxy-5-methyl-2,3-dihydroinden-1-one

C11H12O4 (208.0735552)


   

4-hydroxy-6-[(1e,3e)-5-hydroxypenta-1,3-dien-1-yl]-3-methylpyran-2-one

4-hydroxy-6-[(1e,3e)-5-hydroxypenta-1,3-dien-1-yl]-3-methylpyran-2-one

C11H12O4 (208.0735552)


   

(2e)-3-(3,4-dihydroxyphenyl)-2-methylbut-2-enoic acid

(2e)-3-(3,4-dihydroxyphenyl)-2-methylbut-2-enoic acid

C11H12O4 (208.0735552)


   

(1s,6s,12s)-12-hydroxy-8-oxatricyclo[4.3.3.0¹,⁶]dodec-4-ene-3,9-dione

(1s,6s,12s)-12-hydroxy-8-oxatricyclo[4.3.3.0¹,⁶]dodec-4-ene-3,9-dione

C11H12O4 (208.0735552)


   

2-hydroxyethyl 3-(4-hydroxyphenyl)prop-2-enoate

2-hydroxyethyl 3-(4-hydroxyphenyl)prop-2-enoate

C11H12O4 (208.0735552)


   
   

(1r,2r,3r,4r,5r,6s)-4,6-dimethoxycyclohexane-1,2,3,5-tetrol

(1r,2r,3r,4r,5r,6s)-4,6-dimethoxycyclohexane-1,2,3,5-tetrol

C8H16O6 (208.0946836)


   

ethyl β-d-galactopyranoside

ethyl β-d-galactopyranoside

C8H16O6 (208.0946836)