NCBI Taxonomy: 198827

Iris tenuifolia (ncbi_taxid: 198827)

found 110 associated metabolites at species taxonomy rank level.

Ancestor: Iris

Child Taxonomies: none taxonomy data.

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 (414.386145)


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].

   

Betavulgarin

7-(2-hydroxyphenyl)-9-methoxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-8-one

C17H12O6 (312.06338519999997)


Betavulgarin, also known as 2-hydroxy-5-methoxy-6,7-methylenedioxyisoflavone, is a member of the class of compounds known as isoflavones. Isoflavones are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom. Thus, betavulgarin is considered to be a flavonoid lipid molecule. Betavulgarin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Betavulgarin can be found in chickpea, common beet, and red beetroot, which makes betavulgarin a potential biomarker for the consumption of these food products.

   

UNII:AQ51A12T8K

Ethyl beta-D-glucopyranoside

C8H16O6 (208.0946836)


   

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.

   

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.

   

Irisone B

9-hydroxy-7-(2-hydroxyphenyl)-2H,8H-[1,3]dioxolo[4,5-g]chromen-8-one

C16H10O6 (298.047736)


Irisone b, also known as 2,5-dihydroxy-6,7-methylenedioxyisoflavone, is a member of the class of compounds known as isoflavones. Isoflavones are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom. Thus, irisone b is considered to be a flavonoid lipid molecule. Irisone b is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Irisone b can be found in common beet, which makes irisone b a potential biomarker for the consumption of this food product.

   

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 (414.386145)


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].

   

Irisone A

5-Hydroxy-2-methoxy-6,7-methylenedioxyisoflavone

C17H12O6 (312.06338519999997)


   

Ethyl glucoside

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

C8H16O6 (208.0946836)


   

Betavulgarin

7-(2-hydroxyphenyl)-9-methoxy-pyrano[2,3-f][1,3]benzodioxol-8-one

C17H12O6 (312.06338519999997)


A hydroxyisoflavone that is isoflavone substituted by a hydroxy group at position 2, a methoxy group at position 5 and a methylenedioxy group across positions 6 and 7 respectively.

   

Irisone B

5,2-Dihydroxy-6,7-methylenedioxyisoflavone

C16H10O6 (298.047736)


   

Izalpinin

3,5-Dihydroxy-7-methoxyflavone

C16H12O5 (284.0684702)


   

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 (414.386145)


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].

   

1,3,6-trihydroxy-2-methoxy-10h-5,11-dioxatetraphen-12-one

1,3,6-trihydroxy-2-methoxy-10h-5,11-dioxatetraphen-12-one

C17H12O7 (328.05830019999996)


   

(11r)-11-(2,3-dihydroxyphenyl)-2-hydroxy-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

(11r)-11-(2,3-dihydroxyphenyl)-2-hydroxy-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

C16H12O7 (316.05830019999996)


   

(3s,3as,5bs,11as,13ar)-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

(3s,3as,5bs,11as,13ar)-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

C30H48O (424.37049579999996)


   

(2s)-2-(2,3-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one

(2s)-2-(2,3-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-2,3-dihydro-1-benzopyran-4-one

C17H16O7 (332.0895986)


   

(2s)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

(2s)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C16H14O6 (302.0790344)


   

(1s,9s)-11,13-dimethoxy-8,16-dioxatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadeca-2,4,6,10,12,14-hexaen-6-ol

(1s,9s)-11,13-dimethoxy-8,16-dioxatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadeca-2,4,6,10,12,14-hexaen-6-ol

C17H16O5 (300.0997686)


   

5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C17H16O6 (316.0946836)


   

(2s)-5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

(2s)-5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C17H16O6 (316.0946836)


   

(11s)-11-(2,3-dihydroxyphenyl)-2-hydroxy-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

(11s)-11-(2,3-dihydroxyphenyl)-2-hydroxy-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

C16H12O7 (316.05830019999996)


   

(3r,3ar,5ar,5br,7ar,11as,13as,13br)-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

(3r,3ar,5ar,5br,7ar,11as,13as,13br)-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

C30H48O (424.37049579999996)


   

(2s,3r)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

(2s,3r)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C17H16O7 (332.0895986)


   

(2r)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

(2r)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C16H14O6 (302.0790344)


   

3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

C30H48O (424.37049579999996)


   

5,7-dihydroxy-3-(2-hydroxyphenyl)-6-methoxychromen-4-one

5,7-dihydroxy-3-(2-hydroxyphenyl)-6-methoxychromen-4-one

C16H12O6 (300.06338519999997)


   

(2r,3r)-2-(2,3-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

(2r,3r)-2-(2,3-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C16H14O7 (318.0739494)


   

5,7-dihydroxy-6-methoxy-3-(2-methoxyphenyl)chromen-4-one

5,7-dihydroxy-6-methoxy-3-(2-methoxyphenyl)chromen-4-one

C17H14O6 (314.0790344)


   

3,5-dihydroxy-7-methoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

3,5-dihydroxy-7-methoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C16H14O5 (286.0841194)


   

(11r)-2-hydroxy-11-(2-hydroxyphenyl)-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

(11r)-2-hydroxy-11-(2-hydroxyphenyl)-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

C16H12O6 (300.06338519999997)


   

2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C16H14O6 (302.0790344)


   

(2r,3r)-3,5-dihydroxy-7-methoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

(2r,3r)-3,5-dihydroxy-7-methoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C16H14O5 (286.0841194)


   

2-hydroxy-11-(2-hydroxyphenyl)-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

2-hydroxy-11-(2-hydroxyphenyl)-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

C16H12O6 (300.06338519999997)


   

3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C17H16O7 (332.0895986)


   

7-(2,3-dihydroxyphenyl)-9-hydroxy-2h-[1,3]dioxolo[4,5-g]chromen-8-one

7-(2,3-dihydroxyphenyl)-9-hydroxy-2h-[1,3]dioxolo[4,5-g]chromen-8-one

C16H10O7 (314.042651)


   

11-(2,3-dihydroxyphenyl)-2-hydroxy-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

11-(2,3-dihydroxyphenyl)-2-hydroxy-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

C16H12O7 (316.05830019999996)


   

(3s,3as,5as,5bs,7ar,11as,13ar,13bs)-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

(3s,3as,5as,5bs,7ar,11as,13ar,13bs)-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one

C30H48O (424.37049579999996)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.386145)


   

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

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

C16H14O5 (286.0841194)


   

(1s,12s)-3-methoxy-5,7,11,19-tetraoxapentacyclo[10.7.1.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2(10),3,8,13,15,17-hexaen-17-ol

(1s,12s)-3-methoxy-5,7,11,19-tetraoxapentacyclo[10.7.1.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2(10),3,8,13,15,17-hexaen-17-ol

C17H14O6 (314.0790344)


   

(2r,3r)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

(2r,3r)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C17H16O7 (332.0895986)


   

2-(2,3-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

2-(2,3-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydro-1-benzopyran-4-one

C16H14O7 (318.0739494)


   

1-(6-hydroxy-4-methoxy-2h-1,3-benzodioxol-5-yl)-2-(2-hydroxyphenyl)ethane-1,2-dione

1-(6-hydroxy-4-methoxy-2h-1,3-benzodioxol-5-yl)-2-(2-hydroxyphenyl)ethane-1,2-dione

C16H12O7 (316.05830019999996)


   

(11s)-2-hydroxy-11-(2-hydroxyphenyl)-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

(11s)-2-hydroxy-11-(2-hydroxyphenyl)-4,6,10-trioxatricyclo[7.4.0.0³,⁷]trideca-1,3(7),8-trien-13-one

C16H12O6 (300.06338519999997)