NCBI Taxonomy: 38220

Coelogyne (ncbi_taxid: 38220)

found 114 associated metabolites at genus taxonomy rank level.

Ancestor: Coelogyninae

Child Taxonomies: Coelogyne cristata, Coelogyne naja, Coelogyne alba, Coelogyne magna, Coelogyne alata, Coelogyne renae, Coelogyne ovata, Coelogyne fusca, Coelogyne niana, Coelogyne elata, Coelogyne ovalis, Coelogyne alpina, Coelogyne chanii, Coelogyne latens, Coelogyne nitida, Coelogyne uncata, Coelogyne dayana, Coelogyne remota, Coelogyne cuprea, Coelogyne harana, Coelogyne blumea, Coelogyne carnea, Coelogyne lactea, Coelogyne nervosa, Coelogyne banksii, Coelogyne citrina, Coelogyne cornuta, Coelogyne viscosa, Coelogyne odorata, Coelogyne parvula, Coelogyne basalis, Coelogyne similis, Coelogyne tenella, Coelogyne rumphii, Coelogyne susanae, Coelogyne xyrekes, Coelogyne mossiae, Coelogyne usitana, Coelogyne oxyloba, Coelogyne scripta, Coelogyne pallida, Coelogyne kaliana, Coelogyne prasina, Coelogyne barbata, Coelogyne miniata, Coelogyne stricta, Coelogyne flavida, Coelogyne pallens, Coelogyne swaniana, Coelogyne cootesii, Coelogyne curranii, Coelogyne edentula, Coelogyne gracilis, Coelogyne porrecta, Coelogyne warrenii, Coelogyne coccinea, Coelogyne serratoi, Coelogyne cobbiana, Coelogyne corrugis, Coelogyne cupulata, Coelogyne woodiana, Coelogyne gibbsiae, Coelogyne carinata, Coelogyne haslamii, Coelogyne fragrans, Coelogyne selebica, Coelogyne speciosa, Coelogyne lacteola, Coelogyne apoensis, Coelogyne asperata, Coelogyne hampelii, Coelogyne tortilis, Coelogyne assamica, Coelogyne bulleyia, Coelogyne radicosa, Coelogyne wenzelii, Coelogyne testacea, Coelogyne beccarii, Coelogyne flexuosa, Coelogyne veitchii, Coelogyne velutina, Coelogyne flaccida, Coelogyne glumacea, Coelogyne cumingii, Coelogyne uniflora, Coelogyne longipes, Coelogyne acuifera, Coelogyne chinensis, Coelogyne latifolia, Coelogyne vernicosa, Coelogyne chen-tsii, Coelogyne schaiblei, Coelogyne smithiana, Coelogyne gibbifera, Coelogyne karoensis, Coelogyne virescens, Coelogyne strongiae, Coelogyne guamensis, Coelogyne mayeriana, Coelogyne pandurata, Coelogyne pterogyne, Coelogyne verrucosa, Coelogyne pulverula, Coelogyne protracta, Coelogyne tomentosa, Coelogyne bigibbosa, Coelogyne bracteosa, Coelogyne dentiloba, Coelogyne sulphurea, Coelogyne fimbriata, Coelogyne trinervis, Coelogyne imbricata, Coelogyne corymbosa, Coelogyne occultata, Coelogyne peltastes, Coelogyne calcicola, Coelogyne prolifera, Coelogyne breviscapa, Coelogyne wenshanica, Coelogyne filiformis, Coelogyne havilandii, Coelogyne javieriana, Coelogyne microchila, Coelogyne spathulata, Coelogyne arachnites, Coelogyne williamsii, Coelogyne yuccifolia, Coelogyne exasperata, Coelogyne celebensis, Coelogyne magniflora, Coelogyne incrassata, Coelogyne sanderiana, Coelogyne cuspilabia, Coelogyne jeffwoodii, Coelogyne lancilabia, Coelogyne complanata, Coelogyne stachyodes, Coelogyne transversa, Coelogyne articulata, Coelogyne schultesii, Coelogyne luzonensis, Coelogyne pantlingii, Coelogyne stenochila, Coelogyne luchanense, Coelogyne ventricosa, Coelogyne amplissima, Coelogyne bicamerata, Coelogyne kelamensis, Coelogyne multiflora, Coelogyne phaiostele, Coelogyne tricallosa, Coelogyne punctulata, Coelogyne fuscescens, Coelogyne erectilabia, Coelogyne leveilleana, Coelogyne pulcherrima, Coelogyne saccolabium, Coelogyne cruciformis, Coelogyne dewildeorum, Coelogyne dewindtiana, Coelogyne graminoides, Coelogyne joclemensii, Coelogyne lycastoides, Coelogyne tiomanensis, Coelogyne cantonensis, Coelogyne auricularis, Coelogyne tuberculata, Coelogyne lawrenceana, Coelogyne bilamellata, Coelogyne chloroptera, Coelogyne eberhardtii, Coelogyne macdonaldii, Coelogyne gardneriana, Coelogyne brachyptera, Coelogyne lentiginosa, Coelogyne rochussenii, Coelogyne papillilabia, Coelogyne benguetensis, Coelogyne linearifolia, Coelogyne mandarinorum, Coelogyne cymbidioides, Coelogyne lagarophylla, Coelogyne graciliscapa, Coelogyne monilirachis, Coelogyne plicatissima, Coelogyne rhabdobulbon, Coelogyne septemnervia, Coelogyne pachystachya, Coelogyne schilleriana, Coelogyne odoratissima, unclassified Coelogyne, Coelogyne entomophobia, Coelogyne alaticallosa, Coelogyne quadratiloba, Coelogyne graminifolia, Coelogyne panchaseensis, Coelogyne confertiflora, Coelogyne diabloviridis, Coelogyne sulawesiensis, Coelogyne septemcostata, Coelogyne trusmadiensis, Coelogyne pseudoscripta, Coelogyne kouytcheensis, Coelogyne missionariorum, Coelogyne pseudowenzelii, Coelogyne longpasiaensis, Coelogyne kamborangensis, Coelogyne foerstermannii, Coelogyne pallidiflavens, Coelogyne pangasinanensis, Coelogyne tenasserimensis, Coelogyne convallariiformis, Coelogyne lawrenceana x Coelogyne mooreana

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].

   

beta-Sitosterol

(3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H50O (414.3861)


beta-Sitosterol, a main dietary phytosterol found in plants, may have the potential for prevention and therapy for human cancer. Phytosterols are plant sterols found in foods such as oils, nuts, and vegetables. Phytosterols, in the same way as cholesterol, contain a double bond and are susceptible to oxidation, and are characterized by anti-carcinogenic and anti-atherogenic properties (PMID:13129445, 11432711). beta-Sitosterol is a phytopharmacological extract containing a mixture of phytosterols, with smaller amounts of other sterols, bonded with glucosides. These phytosterols are commonly derived from the South African star grass, Hypoxis rooperi, or from species of Pinus and Picea. The purported active constituent is termed beta-sitosterol. Additionally, the quantity of beta-sitosterol-beta-D-glucoside is often reported. Although the exact mechanism of action of beta-sitosterols is unknown, it may be related to cholesterol metabolism or anti-inflammatory effects (via interference with prostaglandin metabolism). Compared with placebo, beta-sitosterol improved urinary symptom scores and flow measures (PMID:10368239). A plant food-based diet modifies the serum beta-sitosterol concentration in hyperandrogenic postmenopausal women. This finding indicates that beta-sitosterol can be used as a biomarker of exposure in observational studies or as a compliance indicator in dietary intervention studies of cancer prevention (PMID:14652381). beta-Sitosterol induces apoptosis and activates key caspases in MDA-MB-231 human breast cancer cells (PMID:12579296). Sitosterol is a member of the class of phytosterols that is stigmast-5-ene substituted by a beta-hydroxy group at position 3. It has a role as a sterol methyltransferase inhibitor, an anticholesteremic drug, an antioxidant, a plant metabolite and a mouse metabolite. It is a 3beta-sterol, a stigmastane sterol, a 3beta-hydroxy-Delta(5)-steroid, a C29-steroid and a member of phytosterols. It derives from a hydride of a stigmastane. Active fraction of Solanum trilobatum; reduces side-effects of radiation-induced toxicity. Beta-Sitosterol is a natural product found in Elodea canadensis, Ophiopogon intermedius, and other organisms with data available. beta-Sitosterol is one of several phytosterols (plant sterols) with chemical structures similar to that of cholesterol. Sitosterols are white, waxy powders with a characteristic odor. They are hydrophobic and soluble in alcohols. beta-Sitosterol is found in many foods, some of which are ginseng, globe artichoke, sesbania flower, and common oregano. C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Beta-Sitosterol (purity>98\\%) is a plant sterol. Beta-Sitosterol (purity>98\\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1]. Beta-Sitosterol (purity>98\%) is a plant sterol. Beta-Sitosterol (purity>98\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1].

   

beta-Sitosterol 3-O-beta-D-galactopyranoside

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.439)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. beta-Sitosterol 3-O-beta-D-galactopyranoside is found in herbs and spices. beta-Sitosterol 3-O-beta-D-galactopyranoside is a constituent of Hibiscus sabdariffa (roselle) leaves. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

Lusianthridin

2,5-Dihydroxy-7-methoxy-9,10-dihydrophenanthrene (14)

C15H14O3 (242.0943)


7-methoxy-9,10-dihydrophenanthrene-2,5-diol is a dihydrophenanthrene. 7-Methoxy-9,10-dihydrophenanthrene-2,5-diol is a natural product found in Dendrobium loddigesii, Pleione bulbocodioides, and other organisms with data available.

   
   

Flavidin

9,10-Dihydro-5H-phenanthro[4,5-bcd]pyran-2,7-diol

C15H12O3 (240.0786)


   
   

3-O-Methylbatatasin III

Phenol, 3-methoxy-5-[2-(3-methoxyphenyl)ethyl]-

C16H18O3 (258.1256)


3-O-methylbatatasin III is a stilbenoid. 3-O-Methylbatatasin III is a natural product found in Coelogyne ovalis, Pleione bulbocodioides, and other organisms with data available. 3'-O-Methylbatatasin III shows spasmolytic activity[1]. 3'-O-Methylbatatasin III shows spasmolytic activity[1].

   

Orchinol

2,4-Dimethoxy-7-hydroxy-9,10-dihydrophenanthrene

C16H16O3 (256.1099)


   

Batatasin III

1-(3-Hydroxy-5-methoxyphenyl)-2-(3-hydroxyphenyl)ethane

C15H16O3 (244.1099)


Batatasin III is a stilbenoid. batatasin III is a natural product found in Bulbophyllum reptans, Cymbidium aloifolium, and other organisms with data available. Batatasin III is found in root vegetables. Batatasin III is a constituent of Dioscorea batatas (Chinese yam) Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT signals. Batatasin III has anti-cancer activities[1]. Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT signals. Batatasin III has anti-cancer activities[1]. Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT signals. Batatasin III has anti-cancer activities[1].

   

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

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

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].

   

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].

   

Coelonin

2,7-Dihydroxy-4-methoxy-9,10-dihydrophenanthrene

C15H14O3 (242.0943)


4-Methoxy-9,10-dihydrophenanthrene-2,7-diol is a natural product found in Bulbophyllum reptans, Cymbidium aloifolium, and other organisms with data available.

   

Pholidotol A

2,3-Dihydroxy-5-methoxy-3,4-methylenedioxydihydrostilbene

C16H16O5 (288.0998)


   

Bulbophylol B

Bulbophylol B

C16H14O5 (286.0841)


   

Pholidotol B

2-Hydroxy-5-methoxy-3,4,3,4-dimethylene-dioxydihydrostilbene

C17H16O6 (316.0947)


   

Gymconpin C

Gymconpin C

C30H26O6 (482.1729)


   

Coeloginanthrin

Coeloginanthrin

C16H14O5 (286.0841)


   

Coeloginin

Coeloginin

C17H14O6 (314.079)


   

erianthridin

erianthridin

C16H16O4 (272.1049)


   

sitosterol

17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H50O (414.3861)


A member of the class of phytosterols that is stigmast-5-ene substituted by a beta-hydroxy group at position 3. C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Beta-Sitosterol (purity>98\\%) is a plant sterol. Beta-Sitosterol (purity>98\\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1]. Beta-Sitosterol (purity>98\%) is a plant sterol. Beta-Sitosterol (purity>98\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1].

   

Phenol, 3-[2-(4-hydroxyphenyl)ethyl]-5-methoxy-

Phenol, 3-[2-(4-hydroxyphenyl)ethyl]-5-methoxy-

C15H16O3 (244.1099)


   

2-methoxy-9,10-dihydrophenanthrene-4,5-diol

2-methoxy-9,10-dihydrophenanthrene-4,5-diol

C15H14O3 (242.0943)


   

Phochinenin G

Phochinenin G

C30H26O6 (482.1729)


   

CHEMBL564527

CHEMBL564527

C30H26O6 (482.1729)


   

Oxoflavidin

Oxoflavidin

C15H10O4 (254.0579)


   

Phochinenin B

Phochinenin B

C30H24O6 (480.1573)


   

Phochinenin D

Phochinenin D

C30H26O6 (482.1729)


   

Phochinenin A

Phochinenin A

C30H26O6 (482.1729)


   

Daucosterol

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.439)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. A steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

Phochinenin I

Phochinenin I

C30H28O6 (484.1886)


   

7-Methoxy-9,10-dihydrophenanthrene-3,5-diol

7-Methoxy-9,10-dihydrophenanthrene-3,5-diol

C15H14O3 (242.0943)


   

Phochinenin H

Phochinenin H

C30H26O6 (482.1729)


   

Phochinenin K

Phochinenin K

C30H28O6 (484.1886)


   

Phochinenin J

Phochinenin J

C30H28O6 (484.1886)


   

Phochinenin E

Phochinenin E

C30H26O6 (482.1729)


   

7-[4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy]-2-methoxy-9,10-dihydrophenanthren-4-ol

7-[4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy]-2-methoxy-9,10-dihydrophenanthren-4-ol

C30H28O6 (484.1886)


   

Dotriacontanol

Dotriacontan-1-ol

C32H66O (466.5113)


   

Phochinenin C

Phochinenin C

C30H26O6 (482.1729)


   

Gymconopin C

Gymconopin C

C30H26O6 (482.1729)


Gymconopin C is a natural product found in Pholidota chinensis, Bletilla formosana, and other organisms with data available.

   

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.

   

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].

   

3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol

NCGC00385266-01!3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol

C15H16O3 (244.1099)


   

7-methoxy-9,10-dihydrophenanthrene-2,5-diol

NCGC00385352-01!7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C15H14O3 (242.0943)


   

4-methoxy-9,10-dihydrophenanthrene-2,7-diol

4-methoxy-9,10-dihydrophenanthrene-2,7-diol

C15H14O3 (242.0943)


   

Batatasin III

3-[2-(3-Hydroxyphenyl)ethyl]-5-methoxyphenol, 9CI

C15H16O3 (244.1099)


   

FOH 32:0

Dotriacontan-1-ol

C32H66O (466.5113)


   

Phoyunbene C

Phoyunbene C

C16H16O4 (272.1049)


A stilbenoid that is trans-stilbene substituted by hydroxy groups at positions 3 and 3 and methoxy groups at positions 2 and 5. Isolated from Pholidota yunnanensis, it exhibits inhibitory activity on nitric oxide production.

   

Harzol

(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methyl-heptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H50O (414.3861)


C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Beta-Sitosterol (purity>98\\%) is a plant sterol. Beta-Sitosterol (purity>98\\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1]. Beta-Sitosterol (purity>98\%) is a plant sterol. Beta-Sitosterol (purity>98\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1].

   

56684-87-8

3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol

C16H18O3 (258.1256)


3'-O-Methylbatatasin III shows spasmolytic activity[1]. 3'-O-Methylbatatasin III shows spasmolytic activity[1].

   

CHEBI:28678

4,7-dihydroxy-2-methoxy-9,10-dihydrophenanthrene

C15H14O3 (242.0943)


   

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].

   

Phenol, 4-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy-

4-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxyphenol

C16H18O4 (274.1205)


Gigantol is a natural product that could be isolated from Cymbidium giganteum. Gigantol is a potent inhibitor of the spontaneous contractions of the guinea-pig ileum[1].

   

Phoyunbene D

Phoyunbene D

C17H18O4 (286.1205)


A stilbenoid that is trans-stilbene substituted by a hydroxy group at position 3 and methoxy groups at positions 2, 3 and 5. Isolated from Pholidota yunnanensis, it exhibits inhibitory effects on production of nitric oxide.

   

Dotriacontan-1-ol

Dotriacontan-1-ol

C32H66O (466.5113)


An ultra-long-chain primary fatty alcohol that is dotriacontane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group.

   

2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaene-6,13-diol

2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaene-6,13-diol

C15H12O3 (240.0786)


   

3-[2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

3-[2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

C15H14O3 (242.0943)


   

8-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H28O6 (484.1886)


   

(1s,3r,6s,7s,8s,11r,12s,15r,16r)-15-[(2r,5r)-5-ethyl-5,6-dimethylhept-6-en-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl (2z)-3-(4-hydroxyphenyl)prop-2-enoate

(1s,3r,6s,7s,8s,11r,12s,15r,16r)-15-[(2r,5r)-5-ethyl-5,6-dimethylhept-6-en-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl (2z)-3-(4-hydroxyphenyl)prop-2-enoate

C41H60O3 (600.4542)


   

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

C30H26O6 (482.1729)


   

3-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-5-methoxyphenol

3-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-5-methoxyphenol

C16H18O4 (274.1205)


   

15-(5-ethyl-5,6-dimethylhept-6-en-2-yl)-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl 3-(4-hydroxyphenyl)prop-2-enoate

15-(5-ethyl-5,6-dimethylhept-6-en-2-yl)-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl 3-(4-hydroxyphenyl)prop-2-enoate

C41H60O3 (600.4542)


   

6,13-dihydroxy-5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

6,13-dihydroxy-5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C16H12O5 (284.0685)


   

6,13-dihydroxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

6,13-dihydroxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C15H10O4 (254.0579)


   

3-[2-(2,3-dimethoxyphenyl)ethenyl]-5-methoxyphenol

3-[2-(2,3-dimethoxyphenyl)ethenyl]-5-methoxyphenol

C17H18O4 (286.1205)


   

5-[2-(3-hydroxyphenyl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

5-[2-(3-hydroxyphenyl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

C16H16O5 (288.0998)


   

3-[(1e)-2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

3-[(1e)-2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

C15H14O4 (258.0892)


   

2,5-dihydroxy-6,7-dimethoxyphenanthrene-4-carboxylic acid

2,5-dihydroxy-6,7-dimethoxyphenanthrene-4-carboxylic acid

C17H14O6 (314.079)


   

2',3-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-4,4',7,7'-tetrol

2',3-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-4,4',7,7'-tetrol

C30H26O6 (482.1729)


   

7-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy}-2-methoxy-9,10-dihydrophenanthren-4-ol

7-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy}-2-methoxy-9,10-dihydrophenanthren-4-ol

C30H28O6 (484.1886)


   

3,7'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2',4,5',7-tetrol

3,7'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2',4,5',7-tetrol

C30H26O6 (482.1729)


   

5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-6,13-diol

5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-6,13-diol

C16H14O4 (270.0892)


   

6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-13-ol

6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-13-ol

C16H14O3 (254.0943)


   

4,7-dimethoxy-9,10-dihydrophenanthrene-2,6-diol

4,7-dimethoxy-9,10-dihydrophenanthrene-2,6-diol

C16H16O4 (272.1049)


   

8-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.1729)


   

8-{2-hydroxy-6-[2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-{2-hydroxy-6-[2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.1729)


   

2-hydroxy-7-methoxyphenanthrene-1,4-dione

2-hydroxy-7-methoxyphenanthrene-1,4-dione

C15H10O4 (254.0579)


   

13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-6-ol

13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-6-ol

C16H14O3 (254.0943)


   

(2s,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

(2s,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

C31H28O7 (512.1835)


   

3-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

3-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H28O6 (484.1886)


   

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,1'-biphenanthrene]-2,2',7,7'-tetrol

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,1'-biphenanthrene]-2,2',7,7'-tetrol

C30H26O6 (482.1729)


   

8-[(7-hydroxy-5-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-[(7-hydroxy-5-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.1729)


   

5,13-dihydroxy-6,7-dimethoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),9,11(15),12-heptaen-3-one

5,13-dihydroxy-6,7-dimethoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),9,11(15),12-heptaen-3-one

C17H12O6 (312.0634)


   

3-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

3-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

C15H14O4 (258.0892)


   

(3ar)-3a,9-dihydroxy-7,10-dimethoxy-4,5-dihydropyren-1-one

(3ar)-3a,9-dihydroxy-7,10-dimethoxy-4,5-dihydropyren-1-one

C18H16O5 (312.0998)


   

3,3'-dimethoxy-9,10-dihydro-[1,1'-biphenanthrene]-4,4',7,7'-tetrol

3,3'-dimethoxy-9,10-dihydro-[1,1'-biphenanthrene]-4,4',7,7'-tetrol

C30H24O6 (480.1573)


   

3-[(1e)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

3-[(1e)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

C15H14O3 (242.0943)


   

8-{2-hydroxy-6-[(1e)-2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-{2-hydroxy-6-[(1e)-2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.1729)


   

13-methoxy-3-oxo-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-6-yl acetate

13-methoxy-3-oxo-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-6-yl acetate

C18H14O5 (310.0841)


   

8-[(5-hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-[(5-hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.1729)


   

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C35H60O6 (576.439)


   

6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaene-5,13-diol

6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaene-5,13-diol

C16H14O4 (270.0892)


   

5,13-dihydroxy-6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),9,11(15),12-heptaen-3-one

5,13-dihydroxy-6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),9,11(15),12-heptaen-3-one

C16H10O5 (282.0528)


   

7,8-dimethoxy-9,10-dihydrophenanthrene-2,4,6-triol

7,8-dimethoxy-9,10-dihydrophenanthrene-2,4,6-triol

C16H16O5 (288.0998)


   

13-methoxy-2,15,17-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-6-ol

13-methoxy-2,15,17-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-6-ol

C16H14O5 (286.0841)


   

3-[2-(3-hydroxy-2-methoxyphenyl)ethenyl]-5-methoxyphenol

3-[2-(3-hydroxy-2-methoxyphenyl)ethenyl]-5-methoxyphenol

C16H16O4 (272.1049)


   

3a,9-dihydroxy-7,10-dimethoxy-4,5-dihydropyren-1-one

3a,9-dihydroxy-7,10-dimethoxy-4,5-dihydropyren-1-one

C18H16O5 (312.0998)


   

6,13-dihydroxy-5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,9,11(15),12-heptaen-3-one

6,13-dihydroxy-5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,9,11(15),12-heptaen-3-one

C16H10O5 (282.0528)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.3861)


   

2-hydroxy-7-methoxy-9,10-dihydrophenanthrene-1,4-dione

2-hydroxy-7-methoxy-9,10-dihydrophenanthrene-1,4-dione

C15H12O4 (256.0736)


   

3-{2-hydroxy-4-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

3-{2-hydroxy-4-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H28O6 (484.1886)


   

3,4-dimethoxy-9,10-dihydrophenanthrene-2,7-diol

3,4-dimethoxy-9,10-dihydrophenanthrene-2,7-diol

C16H16O4 (272.1049)


   

2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

C31H28O7 (512.1835)


   

5-[2-(2h-1,3-benzodioxol-5-yl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

5-[2-(2h-1,3-benzodioxol-5-yl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

C17H16O6 (316.0947)


   

4,5'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

4,5'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

C30H26O6 (482.1729)


   

6-hydroxy-13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

6-hydroxy-13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C16H12O4 (268.0736)


   

1-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

1-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

C30H26O6 (482.1729)


   

3-[(1z)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

3-[(1z)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

C15H14O3 (242.0943)


   

3-[2-(4-hydroxyphenyl)ethyl]-5-methoxyphenol

3-[2-(4-hydroxyphenyl)ethyl]-5-methoxyphenol

C15H16O3 (244.1099)


   

6,7-dimethoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-5,13-diol

6,7-dimethoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-5,13-diol

C17H16O5 (300.0998)


   

5-[2-(4-hydroxyphenyl)ethyl]-2-methoxyphenol

5-[2-(4-hydroxyphenyl)ethyl]-2-methoxyphenol

C15H16O3 (244.1099)


   

2',7-dimethoxy-9h,9'h,10h,10'h-[3,3'-biphenanthrene]-2,4',5,7'-tetrol

2',7-dimethoxy-9h,9'h,10h,10'h-[3,3'-biphenanthrene]-2,4',5,7'-tetrol

C30H26O6 (482.1729)


   

5,13-dihydroxy-6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

5,13-dihydroxy-6-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C16H12O5 (284.0685)


   

tocilizumab

tocilizumab

C14H12O3 (228.0786)