Chemical Formula: C17H18O3

Chemical Formula C17H18O3

Found 95 metabolite its formula value is C17H18O3

4-tert-Butylphenyl salicylate

Benzoic acid, 2-hydroxy-, 4-(1,1-dimethylethyl)phenyl ester

C17H18O3 (270.1255878)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates Migration residue from food packaging. Migration residue from food packaging

   
   

4-cinnamyl-2,3-dimethoxyphenol

4-cinnamyl-2,3-dimethoxyphenol

C17H18O3 (270.1255878)


   

(E)-3,5,4'-Trimethoxystilbene

1,3-dimethoxy-5-[2-(4-methoxyphenyl)ethenyl]benzene

C17H18O3 (270.1255878)


   

Resveratrol trimethyl ether

3,5,4-Trimethoxy-trans-stilbene

C17H18O3 (270.1255878)


Trans-Trimethoxyresveratrol is a derivative of Resveratrol (RSV),and it may be a more potent anti-inflammatory, antiangiogenic and vascular-disrupting agent when compared with resveratrol. In vitro: The in vitro study of resveratrol and trans-Trimethoxyresveratrol showed rather weak cytotoxic effects on three cancer cell lines (HepG2, MCF-7, and MDA-MB-231), which contradicted a previous study reporting that resveratrol inhibited MCF-7 cells with an IC50 of about 10 μM. This discrepancy might be explained by the fact that the measurements were made 24 h after drug treatment, whereas the measurements of the previous study were taken 6 days after. The fact that the cytotoxic effect of trans-Trimethoxyresveratrol was lower than that of resveratrol is surprising, because in many studies, trans-Trimethoxyresveratrol is the most active analogue of resveratrol , although resveratrol shows much stronger antioxidant effects than that of trans-Trimethoxyresveratrol.[1] In vivo: Zebrafish embryos offer great advantage over their adults as well as other in vivo models because of the external development and optical transparency during their first few days, making them invaluable in the inspection of developmental processes. These unique advantages can even be made more useful when specific cell types are labeled with fluorescent probes. Zebrafish embryo in vivo, suggests that trans-Trimethoxyresveratrol has both more potent antiangiogenic activity and more importantly, stronger specific cytotoxic effects on endothelial cells than does resveratrol.[1] Trans-Trimethoxyresveratrol is a derivative of Resveratrol (RSV),and it may be a more potent anti-inflammatory, antiangiogenic and vascular-disrupting agent when compared with resveratrol. In vitro: The in vitro study of resveratrol and trans-Trimethoxyresveratrol showed rather weak cytotoxic effects on three cancer cell lines (HepG2, MCF-7, and MDA-MB-231), which contradicted a previous study reporting that resveratrol inhibited MCF-7 cells with an IC50 of about 10 μM. This discrepancy might be explained by the fact that the measurements were made 24 h after drug treatment, whereas the measurements of the previous study were taken 6 days after. The fact that the cytotoxic effect of trans-Trimethoxyresveratrol was lower than that of resveratrol is surprising, because in many studies, trans-Trimethoxyresveratrol is the most active analogue of resveratrol , although resveratrol shows much stronger antioxidant effects than that of trans-Trimethoxyresveratrol.[1] In vivo: Zebrafish embryos offer great advantage over their adults as well as other in vivo models because of the external development and optical transparency during their first few days, making them invaluable in the inspection of developmental processes. These unique advantages can even be made more useful when specific cell types are labeled with fluorescent probes. Zebrafish embryo in vivo, suggests that trans-Trimethoxyresveratrol has both more potent antiangiogenic activity and more importantly, stronger specific cytotoxic effects on endothelial cells than does resveratrol.[1]

   
   

Heliophenanthrone

Heliophenanthrone

C17H18O3 (270.1255878)


   

2,4-dimethoxy-5-(3-phenylprop-2-enyl)phenol

2,4-dimethoxy-5-(3-phenylprop-2-enyl)phenol

C17H18O3 (270.1255878)


   

O=C1C(O)=C(C)C(=O)c2c1c1c(C(C)(C)CCC1)cc2

O=C1C(O)=C(C)C(=O)c2c1c1c(C(C)(C)CCC1)cc2

C17H18O3 (270.1255878)


   

9,10-Dihydro-3,4,7-trimethoxyphenanthrene

9,10-Dihydro-3,4,7-trimethoxyphenanthrene

C17H18O3 (270.1255878)


   

Isomucronustyrene

Isomucronustyrene

C17H18O3 (270.1255878)


   
   

3,4,6-Trimethoxystilbene

3,4,6-Trimethoxystilbene

C17H18O3 (270.1255878)


   

4-Hydrocinnamoyl-2,2,5-trimethyl-4-cyclopentene-1,3-dione

4-Hydrocinnamoyl-2,2,5-trimethyl-4-cyclopentene-1,3-dione

C17H18O3 (270.1255878)


   

4-Hydroxy-7-methoxy-8-methylflavan

4-Hydroxy-7-methoxy-8-methylflavan

C17H18O3 (270.1255878)


   

7-Hydroxy-5-methoxy-6-methylflavan

7-Hydroxy-5-methoxy-6-methylflavan

C17H18O3 (270.1255878)


   

(2S)-5-Methoxy-6-methylflavan-7-ol

(2S)-5-Methoxy-6-methylflavan-7-ol

C17H18O3 (270.1255878)


   

(R)-5-Hydroxy-2,4-dimethoxydalbergiquinol

(R)-5-Hydroxy-2,4-dimethoxydalbergiquinol

C17H18O3 (270.1255878)


   

9-Hydroxy-6,7-dimethoxydalbergiquinol

9-Hydroxy-6,7-dimethoxydalbergiquinol

C17H18O3 (270.1255878)


   

Tephrowatsin E

(2S) -2alpha-Phenyl-5,7-dimethoxychroman

C17H18O3 (270.1255878)


   

cis-trismethoxy Resveratrol

1,3-dimethoxy-5-[(1Z)-2-(4-methoxyphenyl)ethenyl]-benzene

C17H18O3 (270.1255878)


   
   

3,4-Dihydro-5-methoxy-6-methyl-2-phenyl-2H-1-benzopyran-7-ol

3,4-Dihydro-5-methoxy-6-methyl-2-phenyl-2H-1-benzopyran-7-ol

C17H18O3 (270.1255878)


   
   

(2S)-4,7-dihydroxy-6,8-dimethylflavane|(2S)-7,4-dihydroxy-6,8-dimethylflavane

(2S)-4,7-dihydroxy-6,8-dimethylflavane|(2S)-7,4-dihydroxy-6,8-dimethylflavane

C17H18O3 (270.1255878)


   

3,5-Dimethyl-4-(methoxymethyl)-9-methoxynaphtho[2,3-b]furan

3,5-Dimethyl-4-(methoxymethyl)-9-methoxynaphtho[2,3-b]furan

C17H18O3 (270.1255878)


   
   

2,3,5-Trimethoxy-9,10-dihydrophenanthrene

2,3,5-Trimethoxy-9,10-dihydrophenanthrene

C17H18O3 (270.1255878)


   

2,3,7-Trimethoxy-9,10-dihydrophenanthrene

2,3,7-Trimethoxy-9,10-dihydrophenanthrene

C17H18O3 (270.1255878)


   

(-)-4-hydroxy-7-methoxy-8-methylflavan

(-)-4-hydroxy-7-methoxy-8-methylflavan

C17H18O3 (270.1255878)


   

4bbeta,7-Dihydroxy-1-methyl-8-methylene-1,3,4a(10a)-gibbatrien-10-one

4bbeta,7-Dihydroxy-1-methyl-8-methylene-1,3,4a(10a)-gibbatrien-10-one

C17H18O3 (270.1255878)


   

(3R,4S)-3-(2-methoxyphenyl)-7-methyl-3,4-dihydro-2H-chromen-4-ol|conferol B

(3R,4S)-3-(2-methoxyphenyl)-7-methyl-3,4-dihydro-2H-chromen-4-ol|conferol B

C17H18O3 (270.1255878)


   

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

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

C17H18O3 (270.1255878)


   

9,10-Dihydro-2,5,6-trimethoxyphenanthrene

9,10-Dihydro-2,5,6-trimethoxyphenanthrene

C17H18O3 (270.1255878)


   
   
   

2-Methoxy-6,6-dimethyl-6H-dibenzo[b,d]pyran-9-methanol

2-Methoxy-6,6-dimethyl-6H-dibenzo[b,d]pyran-9-methanol

C17H18O3 (270.1255878)


   

(Z)-8-acetoxy-1,2-epoxy-9,14-pentadecadiene-4,6-diyne

(Z)-8-acetoxy-1,2-epoxy-9,14-pentadecadiene-4,6-diyne

C17H18O3 (270.1255878)


   

2(S)-3-hydroxy-1-(4-hydroxyphenyl)-5-phenyl-1-pentanone

2(S)-3-hydroxy-1-(4-hydroxyphenyl)-5-phenyl-1-pentanone

C17H18O3 (270.1255878)


   
   

7-methoxy-2,8-dimethyl-9,10-dihydrophenantherene-3,6-diol|neonthrene

7-methoxy-2,8-dimethyl-9,10-dihydrophenantherene-3,6-diol|neonthrene

C17H18O3 (270.1255878)


   

(3S,4S)-8-methyl-3-(prop-1-en-2-yl)-3,4-dihydro-1H-benzo[h]isochromene-4,10-diol|cichorin C

(3S,4S)-8-methyl-3-(prop-1-en-2-yl)-3,4-dihydro-1H-benzo[h]isochromene-4,10-diol|cichorin C

C17H18O3 (270.1255878)


   
   

2-(1-Phenyl-2-propenyl)-4,5-dimethoxyphenol

2-(1-Phenyl-2-propenyl)-4,5-dimethoxyphenol

C17H18O3 (270.1255878)


   

5,7-Dimethoxyflavan

5,7-Dimethoxyflavan

C17H18O3 (270.1255878)


   

Sargasal II|Sargasal-II

Sargasal II|Sargasal-II

C17H18O3 (270.1255878)


   

Di-Me ether-3,4,5-Trimethylnaphtho[2,3-b]furan-6,8-diol

Di-Me ether-3,4,5-Trimethylnaphtho[2,3-b]furan-6,8-diol

C17H18O3 (270.1255878)


   

Isoneocryptotanshinone II

Isoneocryptotanshinone II

C17H18O3 (270.1255878)


   

7-hydroxy-3-(4-methoxybenzyl)-chroman|7-hydroxy-3-(4-methoxybenzyl)chroman

7-hydroxy-3-(4-methoxybenzyl)-chroman|7-hydroxy-3-(4-methoxybenzyl)chroman

C17H18O3 (270.1255878)


   

2,5-Dihydroxy-3-isoprenyl-6-(3-methylbut-3-en-1-ynyl)benzaldehyde|2,5-dihydroxy-3-isopropenyl-6-(3-methylbut-3-en-1-ynyl)benzaldehyde

2,5-Dihydroxy-3-isoprenyl-6-(3-methylbut-3-en-1-ynyl)benzaldehyde|2,5-dihydroxy-3-isopropenyl-6-(3-methylbut-3-en-1-ynyl)benzaldehyde

C17H18O3 (270.1255878)


   
   

safynol-2-O-isobutyrate

safynol-2-O-isobutyrate

C17H18O3 (270.1255878)


   

(E)-3,5,4-Trimethoxystilbene

Benzene,1,3-dimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]-

C17H18O3 (270.1255878)


(E)-3,5,4-Trimethoxystilbene is a natural product found in Dalea versicolor, Streptomyces avermitilis, and other organisms with data available. Trans-Trimethoxyresveratrol is a derivative of Resveratrol (RSV),and it may be a more potent anti-inflammatory, antiangiogenic and vascular-disrupting agent when compared with resveratrol. In vitro: The in vitro study of resveratrol and trans-Trimethoxyresveratrol showed rather weak cytotoxic effects on three cancer cell lines (HepG2, MCF-7, and MDA-MB-231), which contradicted a previous study reporting that resveratrol inhibited MCF-7 cells with an IC50 of about 10 μM. This discrepancy might be explained by the fact that the measurements were made 24 h after drug treatment, whereas the measurements of the previous study were taken 6 days after. The fact that the cytotoxic effect of trans-Trimethoxyresveratrol was lower than that of resveratrol is surprising, because in many studies, trans-Trimethoxyresveratrol is the most active analogue of resveratrol , although resveratrol shows much stronger antioxidant effects than that of trans-Trimethoxyresveratrol.[1] In vivo: Zebrafish embryos offer great advantage over their adults as well as other in vivo models because of the external development and optical transparency during their first few days, making them invaluable in the inspection of developmental processes. These unique advantages can even be made more useful when specific cell types are labeled with fluorescent probes. Zebrafish embryo in vivo, suggests that trans-Trimethoxyresveratrol has both more potent antiangiogenic activity and more importantly, stronger specific cytotoxic effects on endothelial cells than does resveratrol.[1] Trans-Trimethoxyresveratrol is a derivative of Resveratrol (RSV),and it may be a more potent anti-inflammatory, antiangiogenic and vascular-disrupting agent when compared with resveratrol. In vitro: The in vitro study of resveratrol and trans-Trimethoxyresveratrol showed rather weak cytotoxic effects on three cancer cell lines (HepG2, MCF-7, and MDA-MB-231), which contradicted a previous study reporting that resveratrol inhibited MCF-7 cells with an IC50 of about 10 μM. This discrepancy might be explained by the fact that the measurements were made 24 h after drug treatment, whereas the measurements of the previous study were taken 6 days after. The fact that the cytotoxic effect of trans-Trimethoxyresveratrol was lower than that of resveratrol is surprising, because in many studies, trans-Trimethoxyresveratrol is the most active analogue of resveratrol , although resveratrol shows much stronger antioxidant effects than that of trans-Trimethoxyresveratrol.[1] In vivo: Zebrafish embryos offer great advantage over their adults as well as other in vivo models because of the external development and optical transparency during their first few days, making them invaluable in the inspection of developmental processes. These unique advantages can even be made more useful when specific cell types are labeled with fluorescent probes. Zebrafish embryo in vivo, suggests that trans-Trimethoxyresveratrol has both more potent antiangiogenic activity and more importantly, stronger specific cytotoxic effects on endothelial cells than does resveratrol.[1]

   

E-Resveratrol trimethyl ether

E-Resveratrol trimethyl ether

C17H18O3 (270.1255878)


Annotation level-1

   

Violastyrene_major

Violastyrene_major

C17H18O3 (270.1255878)


   
   

UV absorber NL 3

Benzoic acid, 2-hydroxy-, 4-(1,1-dimethylethyl)phenyl ester

C17H18O3 (270.1255878)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates

   

trans-trismethoxy Resveratrol-d4

trans-trismethoxy Resveratrol-d4

C17H18O3 (270.1255878)


   

METHYL 2-METHYL-4-BENZYLOXYPHENYLACETATE

METHYL 2-METHYL-4-BENZYLOXYPHENYLACETATE

C17H18O3 (270.1255878)


   

3-(2-Methoxy-5-methylphenyl)-3-phenylpropanoic acid

3-(2-Methoxy-5-methylphenyl)-3-phenylpropanoic acid

C17H18O3 (270.1255878)


   

ETHYL (2-METHOXY-BIPHENYL-3-YL)-ACETATE

ETHYL (2-METHOXY-BIPHENYL-3-YL)-ACETATE

C17H18O3 (270.1255878)


   

3-[2-(Benzyloxy)-5-methoxyphenyl]propanal

3-[2-(Benzyloxy)-5-methoxyphenyl]propanal

C17H18O3 (270.1255878)


   

(2,4-diethoxyphenyl)-phenylmethanone

(2,4-diethoxyphenyl)-phenylmethanone

C17H18O3 (270.1255878)


   

Benzenepropanoic acid, .beta.-hydroxy-.beta.-phenyl-, ethyl ester

Benzenepropanoic acid, .beta.-hydroxy-.beta.-phenyl-, ethyl ester

C17H18O3 (270.1255878)


   

3-HYDROXY-3-(4-METHOXY-PHENYL)-2-METHYL-1-PHENYL-PROPAN-1-ONE

3-HYDROXY-3-(4-METHOXY-PHENYL)-2-METHYL-1-PHENYL-PROPAN-1-ONE

C17H18O3 (270.1255878)


   

4-BENZYLOXY-2-METHOXY-3-METHYLACETOPHENONE

4-BENZYLOXY-2-METHOXY-3-METHYLACETOPHENONE

C17H18O3 (270.1255878)


   

4-(4-Phenylbutoxy)benzoic acid

4-(4-Phenylbutoxy)benzoic acid

C17H18O3 (270.1255878)


   

1,5-bis(4-hydroxyphenyl)pentan-3-one

1,5-bis(4-hydroxyphenyl)pentan-3-one

C17H18O3 (270.1255878)


   

1-[4-(4-PROPOXY-PHENOXY)-PHENYL]-ETHANONE

1-[4-(4-PROPOXY-PHENOXY)-PHENYL]-ETHANONE

C17H18O3 (270.1255878)


   

3-(2,3-DIMETHYLPHENOXYMETHYL)-4-METHOXYBENZALDEHYDE

3-(2,3-DIMETHYLPHENOXYMETHYL)-4-METHOXYBENZALDEHYDE

C17H18O3 (270.1255878)


   

(4-methoxyphenyl) 4-propylbenzoate

(4-methoxyphenyl) 4-propylbenzoate

C17H18O3 (270.1255878)


   

Benzenebutanoicacid, 4-(phenylmethoxy)-

Benzenebutanoicacid, 4-(phenylmethoxy)-

C17H18O3 (270.1255878)


   

1-(4-Hydroxy-3-methoxyphenyl)-3-(4-methylphenyl)propan-2-one

1-(4-Hydroxy-3-methoxyphenyl)-3-(4-methylphenyl)propan-2-one

C17H18O3 (270.1255878)


   

3-ETHOXY-4-[(3-METHYLBENZYL)OXY]BENZALDEHYDE

3-ETHOXY-4-[(3-METHYLBENZYL)OXY]BENZALDEHYDE

C17H18O3 (270.1255878)


   

Methyl 3-(4-(benzyloxy)phenyl)propanoate

Methyl 3-(4-(benzyloxy)phenyl)propanoate

C17H18O3 (270.1255878)


   

2,4-dihydroxy-5-tert-butylbenzophenone

2,4-dihydroxy-5-tert-butylbenzophenone

C17H18O3 (270.1255878)


   

3-ETHOXY-4-[(2-METHYLBENZYL)OXY]BENZALDEHYDE

3-ETHOXY-4-[(2-METHYLBENZYL)OXY]BENZALDEHYDE

C17H18O3 (270.1255878)


   

3-(2,6-DIMETHYLPHENOXYMETHYL)-4-METHOXYBENZALDEHYDE

3-(2,6-DIMETHYLPHENOXYMETHYL)-4-METHOXYBENZALDEHYDE

C17H18O3 (270.1255878)


   

ETHYL (2-METHOXY-BIPHENYL-4-YL)-ACETATE

ETHYL (2-METHOXY-BIPHENYL-4-YL)-ACETATE

C17H18O3 (270.1255878)


   

[4-(1-methyl-1-phenylethyl)phenoxy]acetic acid

[4-(1-methyl-1-phenylethyl)phenoxy]acetic acid

C17H18O3 (270.1255878)


   

3-ETHOXY-4-[(4-METHYLBENZYL)OXY]BENZALDEHYDE

3-ETHOXY-4-[(4-METHYLBENZYL)OXY]BENZALDEHYDE

C17H18O3 (270.1255878)


   

4-BENZYLOXYPHENYLACETIC ACID ETHYL ESTER

4-BENZYLOXYPHENYLACETIC ACID ETHYL ESTER

C17H18O3 (270.1255878)


   

(4-tert-butylphenyl)-(2,4-dihydroxyphenyl)methanone

(4-tert-butylphenyl)-(2,4-dihydroxyphenyl)methanone

C17H18O3 (270.1255878)


   

4-Butoxy-4-biphenylcarboxylic acid

4-Butoxy-4-biphenylcarboxylic acid

C17H18O3 (270.1255878)


   

(2S)-2-(4-ethylphenoxy)-3-phenylpropanoic acid

(2S)-2-(4-ethylphenoxy)-3-phenylpropanoic acid

C17H18O3 (270.1255878)


   

Phenol, 2,4-dimethoxy-5-[(1R)-1-phenyl-2-propenyl]-

Phenol, 2,4-dimethoxy-5-[(1R)-1-phenyl-2-propenyl]-

C17H18O3 (270.1255878)


   
   

Conferol B

Conferol B

C17H18O3 (270.1255878)


A member of the class of isoflavans that is isoflavan with a hydroxy group at position 4, a methyl group at position 7 and a methoxy group at position 2 (the 3R,4S stereoisomer). It is isolated from Caragana conferta and exhibits significant anti-inflammatory activity in the respiratory burst assay.

   

4-tert-Butylphenyl salicylate

Benzoic acid,2-hydroxy-, 4-(1,1-dimethylethyl)phenyl ester

C17H18O3 (270.1255878)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates

   

(6r)-6-(4-oxo-6-phenylhex-2-en-1-yl)-5,6-dihydropyran-2-one

(6r)-6-(4-oxo-6-phenylhex-2-en-1-yl)-5,6-dihydropyran-2-one

C17H18O3 (270.1255878)


   

{2-methoxy-6,6-dimethylbenzo[c]chromen-9-yl}methanol

{2-methoxy-6,6-dimethylbenzo[c]chromen-9-yl}methanol

C17H18O3 (270.1255878)


   

(6s)-6-[(1z)-hepta-1,6-dien-1-yl]-1-[(2s)-oxiran-2-yl]octa-2,4-diyne-1,7-dione

(6s)-6-[(1z)-hepta-1,6-dien-1-yl]-1-[(2s)-oxiran-2-yl]octa-2,4-diyne-1,7-dione

C17H18O3 (270.1255878)


   

1,4-dimethoxy-2-[(1e)-2-(4-methoxyphenyl)ethenyl]benzene

1,4-dimethoxy-2-[(1e)-2-(4-methoxyphenyl)ethenyl]benzene

C17H18O3 (270.1255878)


   

2,6-dimethoxy-3-(3-phenylprop-2-en-1-yl)phenol

2,6-dimethoxy-3-(3-phenylprop-2-en-1-yl)phenol

C17H18O3 (270.1255878)