NCBI Taxonomy: 186945

Cremanthodium ellisii (ncbi_taxid: 186945)

found 58 associated metabolites at species taxonomy rank level.

Ancestor: Cremanthodium

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].

   

Isorhoifolin

5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C27H30O14 (578.163548)


Isorhoifolin is a natural product found in Astragalus onobrychis, Phillyrea latifolia, and other organisms with data available. Isorhoifolin is found in citrus. Isorhoifolin is isolated from leaves of Citrus paradisi (grapefruit) and other plant species. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2]. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2].

   

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].

   

Scolimoside

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromone

C27H30O15 (594.158463)


Luteolin 7-rutinoside is a natural product found in Saussurea medusa, Trachycarpus fortunei, and other organisms with data available. Luteolin-7-rutinoside has both anti-arthritic and antifungal activities, can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection.

   

Isorhoifolin

5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-2-yl)oxy]-4H-chromen-4-one

C27H30O14 (578.163548)


Isolated from leaves of Citrus paradisi (grapefruit) and other plant subspecies Isorhoifolin is found in many foods, some of which are sweet orange, citrus, dill, and lemon. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2]. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2].

   

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].

   

Isorhoifolin

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4H-chromen-4-one

C27H30O14 (578.163548)


Apigenin 8-c-rhamnosyl-glucoside, also known as isorhoifoline or apigenin-7-O-rutinoside, is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Apigenin 8-c-rhamnosyl-glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Apigenin 8-c-rhamnosyl-glucoside can be found in oat, which makes apigenin 8-c-rhamnosyl-glucoside a potential biomarker for the consumption of this food product. Isorhoifolin is found in citrus. Isorhoifolin is isolated from leaves of Citrus paradisi (grapefruit) and other plant species. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2]. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2].

   

7beta-Hydroxysitosterol

7beta-Hydroxysitosterol

C29H50O2 (430.38106)


A natural product found in Melia toosendan.

   

(1r,3as,3bs,4s,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7-diol

(1r,3as,3bs,4s,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7-diol

C29H50O2 (430.38106)


   

4-[1-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

4-[1-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

C18H18O2 (266.1306728)


   

7β-hydroxysitosterol

7β-hydroxy-sitosterol

C29H50O2 (430.38106)


{"Ingredient_id": "HBIN013115","Ingredient_name": "7\u03b2-hydroxysitosterol","Alias": "7\u03b2-hydroxy-sitosterol","Ingredient_formula": "C29H50O2","Ingredient_Smile": "CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "39602;34524","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

(3s,5s)-6-[(1s,2s,3s,4s,5s,6s)-5-(acetyloxy)-2-hydroxy-6-methyl-4-[(2-methylpropanoyl)oxy]-7-oxabicyclo[4.1.0]heptan-3-yl]-2-hydroxy-2-methyl-5-[(2-methylpropanoyl)oxy]hept-6-en-3-yl 2-methylpropanoate

(3s,5s)-6-[(1s,2s,3s,4s,5s,6s)-5-(acetyloxy)-2-hydroxy-6-methyl-4-[(2-methylpropanoyl)oxy]-7-oxabicyclo[4.1.0]heptan-3-yl]-2-hydroxy-2-methyl-5-[(2-methylpropanoyl)oxy]hept-6-en-3-yl 2-methylpropanoate

C29H46O11 (570.3039966)


   

(3s,5s)-2-[(1s,2s,3s,4r,5s,6s)-3-(acetyloxy)-4,6-dihydroxy-4-methyl-2,5-bis[(2-methylpropanoyl)oxy]cyclohexyl]-5,6-dihydroxy-6-methylhept-1-en-3-yl 2-methylpropanoate

(3s,5s)-2-[(1s,2s,3s,4r,5s,6s)-3-(acetyloxy)-4,6-dihydroxy-4-methyl-2,5-bis[(2-methylpropanoyl)oxy]cyclohexyl]-5,6-dihydroxy-6-methylhept-1-en-3-yl 2-methylpropanoate

C29H48O12 (588.3145608)


   

4-[(3s,4z)-5-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

4-[(3s,4z)-5-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

C18H18O2 (266.1306728)


   

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]phenanthrene-4,7-diol

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]phenanthrene-4,7-diol

C29H50O2 (430.38106)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

C27H30O15 (594.158463)


   

2-[3-(acetyloxy)-4,6-dihydroxy-4-methyl-2,5-bis[(2-methylpropanoyl)oxy]cyclohexyl]-5,6-dihydroxy-6-methylhept-1-en-3-yl 2-methylpropanoate

2-[3-(acetyloxy)-4,6-dihydroxy-4-methyl-2,5-bis[(2-methylpropanoyl)oxy]cyclohexyl]-5,6-dihydroxy-6-methylhept-1-en-3-yl 2-methylpropanoate

C29H48O12 (588.3145608)


   

(1s,2r,3s,4s,5s,6s)-3-(acetyloxy)-5-[(3r,5s)-3,6-dihydroxy-6-methyl-5-[(2-methylpropanoyl)oxy]hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate

(1s,2r,3s,4s,5s,6s)-3-(acetyloxy)-5-[(3r,5s)-3,6-dihydroxy-6-methyl-5-[(2-methylpropanoyl)oxy]hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate

C30H48O12 (600.3145608)


   

(1s,2r,3s,4s,5s,6s)-3-(acetyloxy)-5-[(3s,5s)-5,6-dihydroxy-6-methyl-3-[(2-methylpropanoyl)oxy]hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate

(1s,2r,3s,4s,5s,6s)-3-(acetyloxy)-5-[(3s,5s)-5,6-dihydroxy-6-methyl-3-[(2-methylpropanoyl)oxy]hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl (2z)-2-methylbut-2-enoate

C30H48O12 (600.3145608)


   

3-(acetyloxy)-5-{3,6-dihydroxy-6-methyl-5-[(2-methylpropanoyl)oxy]hept-1-en-2-yl}-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl 2-methylbut-2-enoate

3-(acetyloxy)-5-{3,6-dihydroxy-6-methyl-5-[(2-methylpropanoyl)oxy]hept-1-en-2-yl}-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl 2-methylbut-2-enoate

C30H48O12 (600.3145608)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-2-yl)oxy]chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-2-yl)oxy]chromen-4-one

C27H30O15 (594.158463)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.386145)


   

4-[(3r,4z)-5-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

4-[(3r,4z)-5-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

C18H18O2 (266.1306728)


   

3-(acetyloxy)-5-{5,6-dihydroxy-6-methyl-3-[(2-methylpropanoyl)oxy]hept-1-en-2-yl}-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl 2-methylbut-2-enoate

3-(acetyloxy)-5-{5,6-dihydroxy-6-methyl-3-[(2-methylpropanoyl)oxy]hept-1-en-2-yl}-2,6-dihydroxy-2-methyl-4-[(2-methylpropanoyl)oxy]cyclohexyl 2-methylbut-2-enoate

C30H48O12 (600.3145608)


   

6-[5-(acetyloxy)-2-hydroxy-6-methyl-4-[(2-methylpropanoyl)oxy]-7-oxabicyclo[4.1.0]heptan-3-yl]-2-hydroxy-2-methyl-5-[(2-methylpropanoyl)oxy]hept-6-en-3-yl 2-methylpropanoate

6-[5-(acetyloxy)-2-hydroxy-6-methyl-4-[(2-methylpropanoyl)oxy]-7-oxabicyclo[4.1.0]heptan-3-yl]-2-hydroxy-2-methyl-5-[(2-methylpropanoyl)oxy]hept-6-en-3-yl 2-methylpropanoate

C29H46O11 (570.3039966)


   

4-[(4z)-5-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

4-[(4z)-5-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol

C18H18O2 (266.1306728)