NCBI Taxonomy: 228638

Krameria grayi (ncbi_taxid: 228638)

found 151 associated metabolites at species taxonomy rank level.

Ancestor: Krameria

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].

   

beta-Sitosterol 3-O-beta-D-galactopyranoside

(2R,3R,4S,5S,6R)-2-(((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-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.4389659999999)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. beta-Sitosterol 3-O-beta-D-galactopyranoside is found in herbs and spices. beta-Sitosterol 3-O-beta-D-galactopyranoside is a constituent of Hibiscus sabdariffa (roselle) leaves. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

DUB OM HTO

(Z)-9-octadecenoic acid, methyl ester;methyl (Z)-9-octadecenoate;methyl cis-9-octadecenoate;methyl-cis-oleate

C19H36O2 (296.2715156)


Oleic acid methyl ester is a clear to amber liquid. Insoluble in water. (NTP, 1992) Methyl oleate is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of oleic acid with methanol. It is functionally related to an oleic acid. Methyl oleate is a natural product found in Anchietea pyrifolia, Lepidium meyenii, and other organisms with data available. Methyl oleate is a fatty acid methyl ester (FAME). Methyl oleate substantially improves the antioxidation ability but markedly impaired the antiwear capacity of zinc dialkyldithiophosphate (ZDDP)[1]. Methyl oleate is a fatty acid methyl ester (FAME). Methyl oleate substantially improves the antioxidation ability but markedly impaired the antiwear capacity of zinc dialkyldithiophosphate (ZDDP)[1].

   

Cycloartenol

(3R,6S,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-ol

C30H50O (426.386145)


Cycloartenol is found in alcoholic beverages. Cycloartenol is a constituent of Artocarpus integrifolia fruits and Solanum tuberosum (potato) Cycloartenol is a sterol precursor in photosynthetic organisms and plants. The biosynthesis of cycloartenol starts from the triterpenoid squalene. Its structure is also related to triterpenoid lanosterol Cycloartenol is a pentacyclic triterpenoid, a 3beta-sterol and a member of phytosterols. It has a role as a plant metabolite. It derives from a hydride of a lanostane. Cycloartenol is a natural product found in Euphorbia nicaeensis, Euphorbia boetica, and other organisms with data available. Constituent of Artocarpus integrifolia fruits and Solanum tuberosum (potato)

   

LICARIN A

2-methoxy-4-[(2S,3S)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C20H22O4 (326.1518012)


(-)-Licarin A is a natural product found in Magnolia dodecapetala, Magnolia kachirachirai, and other organisms with data available. Dehydrodiisoeugenol is a natural product found in Myristica fragrans with data available. Dehydrodiisoeugenol is isolated from Myristica fragrans Houtt, shows anti-inflammatory and anti-bacterial actions[1]. Dehydrodiisoeugenol inhibits LPS- stimulated NF-κB activation and cyclooxygenase (COX)-2 gene expression in murine macrophages[2]. Dehydrodiisoeugenol is isolated from Myristica fragrans Houtt, shows anti-inflammatory and anti-bacterial actions[1]. Dehydrodiisoeugenol inhibits LPS- stimulated NF-κB activation and cyclooxygenase (COX)-2 gene expression in murine macrophages[2]. Licarin A ((+)-Licarin A), a neolignan, significantly and dose-dependently reduces TNF-α production (IC50=12.6 μM) in dinitrophenyl-human serum albumin (DNP-HSA)-stimulated RBL-2H3 cells. Anti-allergic effects. Licarin A reduces TNF-α and PGD2 production, and COX-2 expression[1]. Licarin A ((+)-Licarin A), a neolignan, significantly and dose-dependently reduces TNF-α production (IC50=12.6 μM) in dinitrophenyl-human serum albumin (DNP-HSA)-stimulated RBL-2H3 cells. Anti-allergic effects. Licarin A reduces TNF-α and PGD2 production, and COX-2 expression[1].

   

Methyl linoleate

Methyl linoleate, United States Pharmacopeia (USP) Reference Standard

C19H34O2 (294.2558664)


Methyl linoleate is a fatty acid methyl ester of linoleic acid. It has been isolated from Neolitsea daibuensis. It has a role as a plant metabolite. It is functionally related to a linoleic acid. Methyl linoleate is a natural product found in Tussilago farfara, Azadirachta indica, and other organisms with data available. Methyl linoleate belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. A fatty acid methyl ester of linoleic acid. It has been isolated from Neolitsea daibuensis. Methyl linoleate, a major active constituent of Sageretia thea?fruit (HFSF), is a major anti-melanogenic compound. Methyl linoleate downregulates microphthalmia-associated transcription factor (MITF)?and tyrosinase-related proteins[1]. Methyl linoleate, a major active constituent of Sageretia thea?fruit (HFSF), is a major anti-melanogenic compound. Methyl linoleate downregulates microphthalmia-associated transcription factor (MITF)?and tyrosinase-related proteins[1].

   

Oryzanol A

7,7,12,16-Tetramethyl-15-(6-methylhept-5-en-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid

C40H58O4 (602.4334868)


Oryzanol A is found in cereals and cereal products. Oryzanol A is from rice bran oil (Oryza sativa

   

Dehydrodiisoeugenol

2-methoxy-4-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C20H22O4 (326.1518012)


   

Methyl linolenate

Methyl octadeca-9,12,15-trienoic acid

C19H32O2 (292.24021719999996)


   

Conocarpan

(+)-Conocarpan

C18H18O2 (266.1306728)


   

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].

   

Methyl linolenate

Methyl linolenate

C19H32O2 (292.24021719999996)


Methyl linolenate prevents the oxidation or pre-oxidation of unsaturated fatty acid methyl esters. Methyl linolenate prevents the oxidation or pre-oxidation of unsaturated fatty acid methyl esters.

   

Cycloartenol

9beta,19-cyclolanost-24-en-3beta-ol

C30H50O (426.386145)


   

Daucosterol

(2R,3R,4S,5S,6R)-2-(((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-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.4389659999999)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. A steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

Oryzanol A

7,7,12,16-tetramethyl-15-(6-methylhept-5-en-2-yl)pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C40H58O4 (602.4334868)


D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents D009676 - Noxae > D000963 - Antimetabolites From rice bran oil (Oryza sativa). Oryzanol A is found in cereals and cereal products, rice, and fats and oils. γ-Oryzanol is a potent DNA methyltransferases (DNMTs) inhibitor in the striatum of mice. γ-Oryzanol significantly inhibits the activities of DNMT1 (IC50=3.2 μM), DNMT3a (IC50=22.3 μM).

   

Methyl linoleate

Methyl octadeca-9,12-dienoate

C19H34O2 (294.2558664)


D009676 - Noxae > D016877 - Oxidants > D010545 - Peroxides Mixture with CNB89-S (*FEMA 3411*) is used as a flavouring ingredient. Methyl linoleate is found in many foods, some of which are white mustard, cloves, soft-necked garlic, and flaxseed. Methyl linoleate, a major active constituent of Sageretia thea?fruit (HFSF), is a major anti-melanogenic compound. Methyl linoleate downregulates microphthalmia-associated transcription factor (MITF)?and tyrosinase-related proteins[1]. Methyl linoleate, a major active constituent of Sageretia thea?fruit (HFSF), is a major anti-melanogenic compound. Methyl linoleate downregulates microphthalmia-associated transcription factor (MITF)?and tyrosinase-related proteins[1].

   
   

4-{5-[(1E)-prop-1-en-1-yl]-1-benzofuran-2-yl}benzene-1,3-diol

4-{5-[(1E)-prop-1-en-1-yl]-1-benzofuran-2-yl}benzene-1,3-diol

C17H14O3 (266.0942894)


   

Rataniaphenol I

Rataniaphenol I

C18H16O3 (280.10993859999996)


A member of the class of benzofurans that is 1-benzofuran substituted by a 2-hydroxy-4-methoxyphenyl group at position 2 and a prop-1-en-1-yl group at position 5. It is a lignan derivative isolated from the roots of Krameria lappacea.

   

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].

   

AI3-03520

9,12-Octadecadienoic acid (9Z,12Z)-, methyl ester

C19H34O2 (294.2558664)


Methyl linoleate, a major active constituent of Sageretia thea?fruit (HFSF), is a major anti-melanogenic compound. Methyl linoleate downregulates microphthalmia-associated transcription factor (MITF)?and tyrosinase-related proteins[1]. Methyl linoleate, a major active constituent of Sageretia thea?fruit (HFSF), is a major anti-melanogenic compound. Methyl linoleate downregulates microphthalmia-associated transcription factor (MITF)?and tyrosinase-related proteins[1].

   

rataniaphenol II

rataniaphenol II

C18H16O2 (264.1150236)


A member of the class of benzofurans that is 1-benzofuran substituted by a 4-hydroxyphenyl group at position 2, a methyl group at position 3 and a prop-1-en-1-yl group at position 5. It is a lignan derivative isolated from the roots of Krameria lappacea.

   

5-methoxy-2-[5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

5-methoxy-2-[5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

C18H16O3 (280.10993859999996)


   

4-{1-hydroxy-2-[4-(prop-1-en-1-yl)phenoxy]propyl}phenol

4-{1-hydroxy-2-[4-(prop-1-en-1-yl)phenoxy]propyl}phenol

C18H20O3 (284.14123700000005)


   

2-[5-(3-hydroxyprop-1-en-1-yl)-1-benzofuran-2-yl]-5-methoxyphenol

2-[5-(3-hydroxyprop-1-en-1-yl)-1-benzofuran-2-yl]-5-methoxyphenol

C18H16O4 (296.1048536)


   

4-[(2r,3r)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[(2r,3r)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

2-(4-methoxyphenyl)-3-methyl-5-(prop-1-en-1-yl)-1-benzofuran

2-(4-methoxyphenyl)-3-methyl-5-(prop-1-en-1-yl)-1-benzofuran

C19H18O2 (278.1306728)


   

4-{5-[(1e)-3-hydroxyprop-1-en-1-yl]-1-benzofuran-2-yl}-3-methoxyphenol

4-{5-[(1e)-3-hydroxyprop-1-en-1-yl]-1-benzofuran-2-yl}-3-methoxyphenol

C18H16O4 (296.1048536)


   

4-[5-(2-hydroxypropyl)-3-methyl-1-benzofuran-2-yl]phenol

4-[5-(2-hydroxypropyl)-3-methyl-1-benzofuran-2-yl]phenol

C18H18O3 (282.1255878)


   

4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C18H18O2 (266.1306728)


   

4-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

(1s,3r,6s,8r,11s,12s,15r,16r)-7,7,12,16-tetramethyl-15-[(2r)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(1s,3r,6s,8r,11s,12s,15r,16r)-7,7,12,16-tetramethyl-15-[(2r)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C39H56O4 (588.4178376)


   

4-[5-(3-hydroxyprop-1-en-1-yl)-1-benzofuran-2-yl]-3-methoxyphenol

4-[5-(3-hydroxyprop-1-en-1-yl)-1-benzofuran-2-yl]-3-methoxyphenol

C18H16O4 (296.1048536)


   

4-{7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

4-{7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

C19H18O3 (294.1255878)


   

2-(4-methoxyphenyl)-5-[(1e)-prop-1-en-1-yl]-1-benzofuran

2-(4-methoxyphenyl)-5-[(1e)-prop-1-en-1-yl]-1-benzofuran

C18H16O2 (264.1150236)


   

2-(4-methoxyphenyl)-5-(prop-1-en-1-yl)-1-benzofuran

2-(4-methoxyphenyl)-5-(prop-1-en-1-yl)-1-benzofuran

C18H16O2 (264.1150236)


   

4-(2-{2-methoxy-5-[(1e)-prop-1-en-1-yl]phenyl}prop-2-en-1-yl)phenol

4-(2-{2-methoxy-5-[(1e)-prop-1-en-1-yl]phenyl}prop-2-en-1-yl)phenol

C19H20O2 (280.146322)


   

4-[5-(prop-1-en-1-yl)-1-benzofuran-2-yl]benzene-1,3-diol

4-[5-(prop-1-en-1-yl)-1-benzofuran-2-yl]benzene-1,3-diol

C17H14O3 (266.0942894)


   

2-(2,4-dimethoxyphenyl)-5-[(1e)-prop-1-en-1-yl]-1-benzofuran

2-(2,4-dimethoxyphenyl)-5-[(1e)-prop-1-en-1-yl]-1-benzofuran

C19H18O3 (294.1255878)


   

4-{2-hydroxy-2-[2-methoxy-5-(prop-1-en-1-yl)phenyl]propyl}phenol

4-{2-hydroxy-2-[2-methoxy-5-(prop-1-en-1-yl)phenyl]propyl}phenol

C19H22O3 (298.15688620000003)


   

(3r,6s,8r,11s,12s,15r,16r)-7,7,12,16-tetramethyl-15-[(2r)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

(3r,6s,8r,11s,12s,15r,16r)-7,7,12,16-tetramethyl-15-[(2r)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

C30H50O (426.386145)


   

2-methoxy-4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

2-methoxy-4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

4-[(1r,2r)-1-hydroxy-2-{4-[(1e)-prop-1-en-1-yl]phenoxy}propyl]phenol

4-[(1r,2r)-1-hydroxy-2-{4-[(1e)-prop-1-en-1-yl]phenoxy}propyl]phenol

C18H20O3 (284.14123700000005)


   

2-(2,4-dimethoxyphenyl)-5-(prop-1-en-1-yl)-1-benzofuran

2-(2,4-dimethoxyphenyl)-5-(prop-1-en-1-yl)-1-benzofuran

C19H18O3 (294.1255878)


   

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

C18H16O2 (264.1150236)


   

4-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

4-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

C19H18O3 (294.1255878)


   

2-{[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]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{[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]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C35H60O6 (576.4389659999999)


   

4-{2-[2-methoxy-5-(prop-1-en-1-yl)phenyl]prop-2-en-1-yl}phenol

4-{2-[2-methoxy-5-(prop-1-en-1-yl)phenyl]prop-2-en-1-yl}phenol

C19H20O2 (280.146322)


   

4-[(2s)-2-hydroxy-2-{2-methoxy-5-[(1e)-prop-1-en-1-yl]phenyl}propyl]phenol

4-[(2s)-2-hydroxy-2-{2-methoxy-5-[(1e)-prop-1-en-1-yl]phenyl}propyl]phenol

C19H22O3 (298.15688620000003)


   

(1s,3r,8r,11s,12s,15r,16r)-7,7,12,16-tetramethyl-15-[(2r)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-one

(1s,3r,8r,11s,12s,15r,16r)-7,7,12,16-tetramethyl-15-[(2r)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-one

C30H48O (424.37049579999996)


   

2-(4-methoxyphenyl)-3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran

2-(4-methoxyphenyl)-3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran

C19H18O2 (278.1306728)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.386145)


   

2-{5-[(1e)-3-hydroxyprop-1-en-1-yl]-1-benzofuran-2-yl}-5-methoxyphenol

2-{5-[(1e)-3-hydroxyprop-1-en-1-yl]-1-benzofuran-2-yl}-5-methoxyphenol

C18H16O4 (296.1048536)


   

2-methoxy-4-[(2r,3r)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

2-methoxy-4-[(2r,3r)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C20H22O4 (326.1518012)


   

2-methoxy-4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

2-methoxy-4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

7,7,12,16-tetramethyl-15-(6-methylhept-5-en-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-one

7,7,12,16-tetramethyl-15-(6-methylhept-5-en-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-one

C30H48O (424.37049579999996)


   

4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C18H18O2 (266.1306728)


   

(2r,3r)-2-(4-methoxyphenyl)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran

(2r,3r)-2-(4-methoxyphenyl)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran

C19H20O2 (280.146322)


   

4-{5-[(2r)-2-hydroxypropyl]-3-methyl-1-benzofuran-2-yl}phenol

4-{5-[(2r)-2-hydroxypropyl]-3-methyl-1-benzofuran-2-yl}phenol

C18H18O3 (282.1255878)


   

(4s,8r,9r)-8-[(1s)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione

(4s,8r,9r)-8-[(1s)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione

C15H16O8 (324.0845136)


   

2-(4-methoxyphenyl)-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran

2-(4-methoxyphenyl)-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran

C19H20O2 (280.146322)