NCBI Taxonomy: 68538

Dictyoloma vandellianum (ncbi_taxid: 68538)

found 66 associated metabolites at species taxonomy rank level.

Ancestor: Dictyoloma

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].

   

Casimiroin

6-methoxy-9-methyl-2H,8H,9H-[1,3]dioxolo[4,5-h]quinolin-8-one

C12H11NO4 (233.0688046)


Casimiroin is found in pomes. Casimiroin is an alkaloid from the seed and bark of Casimiroa edulis (Mexican apple). Alkaloid from the seed and bark of Casimiroa edulis (Mexican apple). Casimiroin is found in pomes.

   

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].

   

7-Methoxyflindersine

7-Methoxyflindersine

C15H15NO3 (257.105188)


   

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].

   
   

2-(14-hydroxy-14,15-dimethylhexadecyl)-1h-quinolin-4-one

2-(14-hydroxy-14,15-dimethylhexadecyl)-1h-quinolin-4-one

C27H43NO2 (413.3293618)


   

2-[(3z)-hex-3-en-1-yl]-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

2-[(3z)-hex-3-en-1-yl]-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

C19H23NO (281.1779548)


   

(2s)-2-[(2s)-2-hydroxy-6-methylhept-5-en-2-yl]-7-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-5-carboxylic acid

(2s)-2-[(2s)-2-hydroxy-6-methylhept-5-en-2-yl]-7-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-5-carboxylic acid

C22H30O4 (358.214398)


   

2-(14-hydroxy-14,15-dimethylhexadecyl)-3-methoxy-1h-quinolin-4-one

2-(14-hydroxy-14,15-dimethylhexadecyl)-3-methoxy-1h-quinolin-4-one

C28H45NO3 (443.339926)


   

7-methoxy-2,2-dimethylpyrano[3,2-c]quinolin-5-ol

7-methoxy-2,2-dimethylpyrano[3,2-c]quinolin-5-ol

C15H15NO3 (257.105188)


   

methyl 3-[11'-(furan-3-yl)-3'-hydroxy-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

methyl 3-[11'-(furan-3-yl)-3'-hydroxy-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

C27H32O9 (500.2046222)


   

5-methoxy-2,8,8-trimethyl-6-(3-methylbut-2-en-1-yl)pyrano[2,3-f]chromen-4-one

5-methoxy-2,8,8-trimethyl-6-(3-methylbut-2-en-1-yl)pyrano[2,3-f]chromen-4-one

C21H24O4 (340.1674504)


   

2-[(14r)-14-hydroxy-14,15-dimethylhexadecyl]-3-methoxy-1h-quinolin-4-one

2-[(14r)-14-hydroxy-14,15-dimethylhexadecyl]-3-methoxy-1h-quinolin-4-one

C28H45NO3 (443.339926)


   

(2e)-6-[(1s,3ar,3br,5ar,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl]-2-methylhepta-2,6-dienal

(2e)-6-[(1s,3ar,3br,5ar,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl]-2-methylhepta-2,6-dienal

C30H46O2 (438.34976159999997)


   

2-(12-hydroxy-12-methyltridecyl)-3h-quinolin-4-one

2-(12-hydroxy-12-methyltridecyl)-3h-quinolin-4-one

C23H35NO2 (357.266765)


   

8-methoxy-2,2-dimethylpyrano[3,2-c]quinolin-5-ol

8-methoxy-2,2-dimethylpyrano[3,2-c]quinolin-5-ol

C15H15NO3 (257.105188)


   

(2r)-2-[(3z)-hex-3-en-1-yl]-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

(2r)-2-[(3z)-hex-3-en-1-yl]-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

C20H25NO2 (311.188519)


   

2-(hex-3-en-1-yl)-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

2-(hex-3-en-1-yl)-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

C20H25NO2 (311.188519)


   

methyl 3-[3'-(acetyloxy)-11'-(furan-3-yl)-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

methyl 3-[3'-(acetyloxy)-11'-(furan-3-yl)-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

C29H34O10 (542.2151864)


   

(2s)-2-[(3z)-hex-3-en-1-yl]-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

(2s)-2-[(3z)-hex-3-en-1-yl]-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

C20H25NO2 (311.188519)


   

methyl (2z)-3-[(1'r,2s,2's,3'r,6'r,7'r,10's,11's,14's)-11'-(furan-3-yl)-3'-hydroxy-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

methyl (2z)-3-[(1'r,2s,2's,3'r,6'r,7'r,10's,11's,14's)-11'-(furan-3-yl)-3'-hydroxy-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

C27H32O9 (500.2046222)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.386145)


   

2-(12-hydroxy-12-methyltridecyl)-3-methoxy-3h-quinolin-4-one

2-(12-hydroxy-12-methyltridecyl)-3-methoxy-3h-quinolin-4-one

C24H37NO3 (387.27732920000005)


   

methyl (2z)-3-[(1'r,2s,2's,6'r,7'r,10's,11's,14's)-3'-(acetyloxy)-11'-(furan-3-yl)-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

methyl (2z)-3-[(1'r,2s,2's,6'r,7'r,10's,11's,14's)-3'-(acetyloxy)-11'-(furan-3-yl)-2',3,3,6',10'-pentamethyl-4',13'-dioxo-12',15'-dioxaspiro[oxirane-2,5'-tetracyclo[8.5.0.0¹,¹⁴.0²,⁷]pentadecan]-6'-yl]prop-2-enoate

C29H34O10 (542.2151864)


   

2-(12-hydroxy-12-methyltridecyl)-3-methoxy-1h-quinolin-4-one

2-(12-hydroxy-12-methyltridecyl)-3-methoxy-1h-quinolin-4-one

C24H37NO3 (387.27732920000005)


   

2-[(3z)-hex-3-en-1-yl]-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

2-[(3z)-hex-3-en-1-yl]-8-methoxy-1h,2h,3h,4h-pyrido[1,2-a]quinolin-6-one

C20H25NO2 (311.188519)


   

2-(12-hydroxy-12-methyltridecyl)-1h-quinolin-4-one

2-(12-hydroxy-12-methyltridecyl)-1h-quinolin-4-one

C23H35NO2 (357.266765)


   

5-hydroxy-2,8,8-trimethyl-6-(3-methylbut-2-en-1-yl)pyrano[2,3-f]chromen-4-one

5-hydroxy-2,8,8-trimethyl-6-(3-methylbut-2-en-1-yl)pyrano[2,3-f]chromen-4-one

C20H22O4 (326.1518012)


   

2-[(14s)-14-hydroxy-14,15-dimethylhexadecyl]-1h-quinolin-4-one

2-[(14s)-14-hydroxy-14,15-dimethylhexadecyl]-1h-quinolin-4-one

C27H43NO2 (413.3293618)