NCBI Taxonomy: 756587

Senna garrettiana (ncbi_taxid: 756587)

found 34 associated metabolites at species taxonomy rank level.

Ancestor: Senna

Child Taxonomies: none taxonomy data.

3,3',4'5-Tetrahydroxystilbene

(E)-4-[2-(3,5Dihydroxyphenyl)ethenyl]1,2-benzenediol, 3,3a?4,5a?Tetrahydroxy-trans-stilbene

C14H12O4 (244.0736)


Piceatannol is a stilbenol that is trans-stilbene in which one of the phenyl groups is substituted by hydroxy groups at positions 3 and 4, while the other phenyl group is substituted by hydroxy groups at positions 3 and 5. It has a role as a protein kinase inhibitor, a tyrosine kinase inhibitor, an antineoplastic agent, a plant metabolite, a hypoglycemic agent, an apoptosis inducer and a geroprotector. It is a stilbenol, a member of resorcinols, a member of catechols and a polyphenol. It derives from a hydride of a trans-stilbene. Piceatannol is a natural product found in Vitis amurensis, Smilax bracteata, and other organisms with data available. Piceatannol is a polyhydroxylated stilbene extract from the seeds of Euphorbia lagascae, which inhibits protein tyrosine kinase Syk and induces apoptosis. (NCI) Piceatannol is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Wine grape (part of); Robinia pseudoacacia whole (part of); Tsuga canadensis bark (part of). 3,3,45-Tetrahydroxystilbene (or Piceatannol) is a phenolic stilbenoid. It is a metabolite of resveratrol found in red wine. A viral protein-tyrosine kinase (LMP2A) implicated in leukemia, non-Hodgkins lymphoma and other diseases associated with Epstein-Barr virus, was recently found to be blocked by picetannol in vitro (PMID 2590224). Therefore there is research interest in piceatannol as an anti-cancer and anti-EBV drug. Piceatannol can also act as an agonist for estrogen receptor alpha in human breast cancer cells (PMID: 16216908). [HMDB] 3,3,45-Tetrahydroxystilbene (or Piceatannol) is a phenolic stilbenoid. It is a metabolite of resveratrol found in red wine. A viral protein-tyrosine kinase (LMP2A) implicated in leukemia, non-Hodgkins lymphoma and other diseases associated with Epstein-Barr virus, was recently found to be blocked by picetannol in vitro (PMID 2590224). Therefore there is research interest in piceatannol as an anti-cancer and anti-EBV drug. Piceatannol can also act as an agonist for estrogen receptor alpha in human breast cancer cells (PMID: 16216908). A stilbenol that is trans-stilbene in which one of the phenyl groups is substituted by hydroxy groups at positions 3 and 4, while the other phenyl group is substituted by hydroxy groups at positions 3 and 5. C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C1967 - Tyrosine Kinase Inhibitor Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI)[1]. Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties[2]. Piceatannol induces apoptosis in DLBCL cell lines[3]. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells[4]. Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI)[1]. Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties[2]. Piceatannol induces apoptosis in DLBCL cell lines[3]. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells[4].

   

Chrysophanol

1,8-DIHYDROXY-3-METHYL-9,10-DIHYDROANTHRACENE-9,10-DIONE

C15H10O4 (254.0579)


Chrysophanic acid appears as golden yellow plates or brown powder. Melting point 196 °C. Slightly soluble in water. Pale yellow aqueous solutions turn red on addition of alkali. Solutions in concentrated sulfuric acid are red. (NTP, 1992) Chrysophanol is a trihydroxyanthraquinone that is chrysazin with a methyl substituent at C-3. It has been isolated from Aloe vera and exhibits antiviral and anti-inflammatory activity. It has a role as an antiviral agent, an anti-inflammatory agent and a plant metabolite. It is functionally related to a chrysazin. Chrysophanol is a natural product found in Rumex dentatus, Ageratina altissima, and other organisms with data available. See also: Frangula purshiana Bark (part of). A trihydroxyanthraquinone that is chrysazin with a methyl substituent at C-3. It has been isolated from Aloe vera and exhibits antiviral and anti-inflammatory activity. Constituent of Rumex, Rheum subspecies Chrysophanol is found in dock, garden rhubarb, and sorrel. Chrysophanol is found in dock. Chrysophanol is a constituent of Rumex, Rheum species D009676 - Noxae > D009153 - Mutagens Chrysophanol (Chrysophanic acid) is a natural anthraquinone, which inhibits EGF-induced phosphorylation of EGFR and suppresses activation of AKT and mTOR/p70S6K. Chrysophanol (Chrysophanic acid) is a natural anthraquinone, which inhibits EGF-induced phosphorylation of EGFR and suppresses activation of AKT and mTOR/p70S6K.

   

9,10-Dihydro-2,3,5,7-Phenanthrenetetrol

2,3,5,7-Tetrahydroxy-9,10-dihydrophenanthrene

C14H12O4 (244.0736)


9,10-Dihydro-2,3,5,7-Phenanthrenetetrol is found in root vegetables. 9,10-Dihydro-2,3,5,7-Phenanthrenetetrol is isolated from Dioscorea bulbifera (air potato). Isolated from Dioscorea bulbifera (air potato). 9,10-Dihydro-2,3,5,7-Phenanthrenetetrol is found in root vegetables.

   

Piceatannol

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

C14H12O4 (244.0736)


Piceatannol, also known as (Z)-3,5,3,4-tetrahydroxystilbene, 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. Piceatannol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Piceatannol can be synthesized from cis-stilbene. Piceatannol can also be synthesized into cis-astringin. Piceatannol can be found in common grape and grape wine, which makes piceatannol a potential biomarker for the consumption of these food products. Piceatannol is a stilbenoid, a type of phenolic compound .

   

Cassigarol A

Cassigarol A

C28H24O8 (488.1471)


   

Chrysophanic acid

Chrysophanic acid

C15H10O4 (254.0579)


relative retention time with respect to 9-anthracene Carboxylic Acid is 1.321 D009676 - Noxae > D009153 - Mutagens relative retention time with respect to 9-anthracene Carboxylic Acid is 1.322 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.318 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.324 Chrysophanol (Chrysophanic acid) is a natural anthraquinone, which inhibits EGF-induced phosphorylation of EGFR and suppresses activation of AKT and mTOR/p70S6K. Chrysophanol (Chrysophanic acid) is a natural anthraquinone, which inhibits EGF-induced phosphorylation of EGFR and suppresses activation of AKT and mTOR/p70S6K.

   

Piceatannol

1,2-Benzenediol, {4-[2-(3,} 5-dihydroxyphenyl)ethenyl]-, (E)-

C14H12O4 (244.0736)


C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C1967 - Tyrosine Kinase Inhibitor Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI)[1]. Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties[2]. Piceatannol induces apoptosis in DLBCL cell lines[3]. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells[4]. Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI)[1]. Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties[2]. Piceatannol induces apoptosis in DLBCL cell lines[3]. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells[4].

   

9,10-Dihydro-2,3,5,7-Phenanthrenetetrol

2,3,5,7-Tetrahydroxy-9,10-dihydrophenanthrene

C14H12O4 (244.0736)


   

Crysophanol

Chrysophanic acid (1,8-dihydroxy-3-methylanthraquinone)

C15H10O4 (254.0579)


D009676 - Noxae > D009153 - Mutagens Chrysophanol (Chrysophanic acid) is a natural anthraquinone, which inhibits EGF-induced phosphorylation of EGFR and suppresses activation of AKT and mTOR/p70S6K. Chrysophanol (Chrysophanic acid) is a natural anthraquinone, which inhibits EGF-induced phosphorylation of EGFR and suppresses activation of AKT and mTOR/p70S6K.

   

5-[2-(3,4-dihydroxyphenyl)ethyl]benzene-1,3-diol

5-[2-(3,4-dihydroxyphenyl)ethyl]benzene-1,3-diol

C14H14O4 (246.0892)


   

(2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol

(2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol

C28H20O8 (484.1158)


   

(2s,3s)-2-[3,4-bis(acetyloxy)phenyl]-3-[3,5-bis(acetyloxy)phenyl]-4-[(1e)-2-[3,4-bis(acetyloxy)phenyl]ethenyl]-2,3-dihydro-1-benzofuran-6-yl acetate

(2s,3s)-2-[3,4-bis(acetyloxy)phenyl]-3-[3,5-bis(acetyloxy)phenyl]-4-[(1e)-2-[3,4-bis(acetyloxy)phenyl]ethenyl]-2,3-dihydro-1-benzofuran-6-yl acetate

C42H36O15 (780.2054)


   

(2r,10s)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6,13,14-tetrol

(2r,10s)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6,13,14-tetrol

C28H24O8 (488.1471)


   

3-(acetyloxy)-5-(2-{3-[3,4-bis(acetyloxy)phenyl]-2-[3,5-bis(acetyloxy)phenyl]-2,3-dihydro-1,4-benzodioxin-6-yl}ethenyl)phenyl acetate

3-(acetyloxy)-5-(2-{3-[3,4-bis(acetyloxy)phenyl]-2-[3,5-bis(acetyloxy)phenyl]-2,3-dihydro-1,4-benzodioxin-6-yl}ethenyl)phenyl acetate

C40H34O14 (738.1948)


   

pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,12,13,17,19-hexol

pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,12,13,17,19-hexol

C21H16O6 (364.0947)


   

15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.0³,⁸.0⁹,²².0¹⁶,²¹]docosa-3,5,7,9(22),10,12,16,18,20-nonaene-5,7,11,18,19-pentol

15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.0³,⁸.0⁹,²².0¹⁶,²¹]docosa-3,5,7,9(22),10,12,16,18,20-nonaene-5,7,11,18,19-pentol

C28H22O7 (470.1365)


   

2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol

2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol

C28H20O8 (484.1158)


   

3-(acetyloxy)-5-{2-[4,6,10,11-tetrakis(acetyloxy)-15,22-dioxapentacyclo[12.8.0.0²,⁷.0⁸,¹³.0¹⁶,²¹]docosa-2,4,6,8,10,12,16,18,20-nonaen-18-yl]ethenyl}phenyl acetate

3-(acetyloxy)-5-{2-[4,6,10,11-tetrakis(acetyloxy)-15,22-dioxapentacyclo[12.8.0.0²,⁷.0⁸,¹³.0¹⁶,²¹]docosa-2,4,6,8,10,12,16,18,20-nonaen-18-yl]ethenyl}phenyl acetate

C40H32O14 (736.1792)


   

pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,11,13,18,19-hexol

pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,11,13,18,19-hexol

C21H16O6 (364.0947)


   

4-[(2r,3r)-3-(3,5-dihydroxyphenyl)-7-[(1e)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol

4-[(2r,3r)-3-(3,5-dihydroxyphenyl)-7-[(1e)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol

C28H22O8 (486.1315)


   

2-[3,4-bis(acetyloxy)phenyl]-3-[3,5-bis(acetyloxy)phenyl]-4-{2-[3,4-bis(acetyloxy)phenyl]ethenyl}-2,3-dihydro-1-benzofuran-6-yl acetate

2-[3,4-bis(acetyloxy)phenyl]-3-[3,5-bis(acetyloxy)phenyl]-4-{2-[3,4-bis(acetyloxy)phenyl]ethenyl}-2,3-dihydro-1-benzofuran-6-yl acetate

C42H36O15 (780.2054)


   

3-(acetyloxy)-5-[(1e)-2-[(1s,14s)-4,6,10,11-tetrakis(acetyloxy)-15,22-dioxapentacyclo[12.8.0.0²,⁷.0⁸,¹³.0¹⁶,²¹]docosa-2,4,6,8,10,12,16,18,20-nonaen-18-yl]ethenyl]phenyl acetate

3-(acetyloxy)-5-[(1e)-2-[(1s,14s)-4,6,10,11-tetrakis(acetyloxy)-15,22-dioxapentacyclo[12.8.0.0²,⁷.0⁸,¹³.0¹⁶,²¹]docosa-2,4,6,8,10,12,16,18,20-nonaen-18-yl]ethenyl]phenyl acetate

C40H32O14 (736.1792)


   

3-(acetyloxy)-5-[(1e)-2-[(2r,3r)-3-[3,4-bis(acetyloxy)phenyl]-2-[3,5-bis(acetyloxy)phenyl]-2,3-dihydro-1,4-benzodioxin-6-yl]ethenyl]phenyl acetate

3-(acetyloxy)-5-[(1e)-2-[(2r,3r)-3-[3,4-bis(acetyloxy)phenyl]-2-[3,5-bis(acetyloxy)phenyl]-2,3-dihydro-1,4-benzodioxin-6-yl]ethenyl]phenyl acetate

C40H34O14 (738.1948)


   

(1s,9r)-pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,11,13,18,19-hexol

(1s,9r)-pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,11,13,18,19-hexol

C21H16O6 (364.0947)


   

10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6,13,14-tetrol

10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6,13,14-tetrol

C28H24O8 (488.1471)


   

5-[2-(3,4-dihydroxyphenyl)-4-[(1e)-2-(3,4-dihydroxyphenyl)ethenyl]-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol

5-[2-(3,4-dihydroxyphenyl)-4-[(1e)-2-(3,4-dihydroxyphenyl)ethenyl]-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol

C28H22O8 (486.1315)


   

3-[2-(3-hydroxyphenyl)ethyl]phenol

3-[2-(3-hydroxyphenyl)ethyl]phenol

C14H14O2 (214.0994)


   

4-[(2r,3r)-3-(3,5-dihydroxyphenyl)-7-[(1z)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol

4-[(2r,3r)-3-(3,5-dihydroxyphenyl)-7-[(1z)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol

C28H22O8 (486.1315)


   

(1s,9s)-pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,11,13,18,20-hexol

(1s,9s)-pentacyclo[7.6.6.0²,⁷.0¹⁰,¹⁵.0¹⁶,²¹]henicosa-2,4,6,10,12,14,16,18,20-nonaene-3,5,11,13,18,20-hexol

C21H16O6 (364.0947)


   

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

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

C14H14O3 (230.0943)


   

(1s,15r)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.0³,⁸.0⁹,²².0¹⁶,²¹]docosa-3,5,7,9(22),10,12,16,18,20-nonaene-5,7,11,18,19-pentol

(1s,15r)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.0³,⁸.0⁹,²².0¹⁶,²¹]docosa-3,5,7,9(22),10,12,16,18,20-nonaene-5,7,11,18,19-pentol

C28H22O7 (470.1365)


   

(1r,14r)-19-[(1e)-2-(3,5-dihydroxyphenyl)ethenyl]-15,22-dioxapentacyclo[12.8.0.0²,⁷.0⁸,¹³.0¹⁶,²¹]docosa-2,4,6,8,10,12,16,18,20-nonaene-4,5,9,11-tetrol

(1r,14r)-19-[(1e)-2-(3,5-dihydroxyphenyl)ethenyl]-15,22-dioxapentacyclo[12.8.0.0²,⁷.0⁸,¹³.0¹⁶,²¹]docosa-2,4,6,8,10,12,16,18,20-nonaene-4,5,9,11-tetrol

C28H20O8 (484.1158)


   

(2s,10s)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6,13,14-tetrol

(2s,10s)-10-(3,4-dihydroxyphenyl)-2-[(3,5-dihydroxyphenyl)methyl]tricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4,6,13,14-tetrol

C28H24O8 (488.1471)


   

(1r,15s)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.0³,⁸.0⁹,²².0¹⁶,²¹]docosa-3,5,7,9(22),10,12,16,18,20-nonaene-5,7,11,18,19-pentol

(1r,15s)-15-(3,4-dihydroxyphenyl)pentacyclo[11.8.1.0³,⁸.0⁹,²².0¹⁶,²¹]docosa-3,5,7,9(22),10,12,16,18,20-nonaene-5,7,11,18,19-pentol

C28H22O7 (470.1365)