NCBI Taxonomy: 53728

Ratibida columnifera (ncbi_taxid: 53728)

found 174 associated metabolites at species taxonomy rank level.

Ancestor: Ratibida

Child Taxonomies: none taxonomy data.

Isoalantolactone

Naphtho(2,3-b)furan-2(3H)-one, decahydro-8a-methyl-3,5-bis(methylene)-, (3aR-(3a alpha,4a alpha,8a beta,9a alpha))-

C15H20O2 (232.14632200000003)


Isoalantolactone is a sesquiterpene lactone of the eudesmanolide group. It has been isolated from Inula helenium. It has a role as an apoptosis inducer, an antifungal agent and a plant metabolite. It is a sesquiterpene lactone and a eudesmane sesquiterpenoid. Isoalantolactone is a natural product found in Eupatorium cannabinum, Critonia quadrangularis, and other organisms with data available. Isoalantolactone is found in herbs and spices. Isoalantolactone is a constituent of the essential oil of Inula helenium (elecampane) Constituent of the essential oil of Inula helenium (elecampane). Isoalantolactone is found in herbs and spices. Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent. Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent.

   

Pinocembrin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (S)-(-)-

C15H12O4 (256.0735552)


Pinocembrin is a dihydroxyflavanone in which the two hydroxy groups are located at positions 5 and 7. A natural product found in Piper sarmentosum and Cryptocarya chartacea. It has a role as an antioxidant, an antineoplastic agent, a vasodilator agent, a neuroprotective agent and a metabolite. It is a dihydroxyflavanone and a (2S)-flavan-4-one. Pinocembrin is a natural product found in Prunus leveilleana, Alpinia rafflesiana, and other organisms with data available. Pinocembrin is found in mexican oregano and is isolated from many plants including food plants. Pinocembrin belongs to the family of flavanones. These are compounds containing a flavan-3-one moiety, which structure is characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. A dihydroxyflavanone in which the two hydroxy groups are located at positions 5 and 7. A natural product found in Piper sarmentosum and Cryptocarya chartacea. Isolated from many plants including food plants. (S)-Pinocembrin is found in mexican oregano and pine nut. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1].

   

Stigmasterol

(3S,8S,9S,10R,13R,14S,17R)-17-((2R,5S,E)-5-ethyl-6-methylhept-3-en-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

C29H48O (412.37049579999996)


Stigmasterol is a phytosterol, meaning it is steroid derived from plants. As a food additive, phytosterols have cholesterol-lowering properties (reducing cholesterol absorption in intestines), and may act in cancer prevention. Phytosterols naturally occur in small amount in vegetable oils, especially soybean oil. One such phytosterol complex, isolated from vegetable oil, is cholestatin, composed of campesterol, stigmasterol, and brassicasterol, and is marketed as a dietary supplement. Sterols can reduce cholesterol in human subjects by up to 15\\%. The mechanism behind phytosterols and the lowering of cholesterol occurs as follows : the incorporation of cholesterol into micelles in the gastrointestinal tract is inhibited, decreasing the overall amount of cholesterol absorbed. This may in turn help to control body total cholesterol levels, as well as modify HDL, LDL and TAG levels. Many margarines, butters, breakfast cereals and spreads are now enriched with phytosterols and marketed towards people with high cholesterol and a wish to lower it. Stigmasterol is found to be associated with phytosterolemia, which is an inborn error of metabolism. Stigmasterol is a 3beta-sterol that consists of 3beta-hydroxystigmastane having double bonds at the 5,6- and 22,23-positions. It has a role as a plant metabolite. It is a 3beta-sterol, a stigmastane sterol, a 3beta-hydroxy-Delta(5)-steroid and a member of phytosterols. It derives from a hydride of a stigmastane. Stigmasterol is a natural product found in Ficus auriculata, Xylopia aromatica, and other organisms with data available. Stigmasterol is a steroid derivative characterized by the hydroxyl group in position C-3 of the steroid skeleton, and unsaturated bonds in position 5-6 of the B ring, and position 22-23 in the alkyl substituent. Stigmasterol is found in the fats and oils of soybean, calabar bean and rape seed, as well as several other vegetables, legumes, nuts, seeds, and unpasteurized milk. See also: Comfrey Root (part of); Saw Palmetto (part of); Plantago ovata seed (part of). Stigmasterol is an unsaturated plant sterol occurring in the plant fats or oils of soybean, calabar bean, and rape seed, and in a number of medicinal herbs, including the Chinese herbs Ophiopogon japonicus (Mai men dong) and American Ginseng. Stigmasterol is also found in various vegetables, legumes, nuts, seeds, and unpasteurized milk. A 3beta-sterol that consists of 3beta-hydroxystigmastane having double bonds at the 5,6- and 22,23-positions. C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol

   

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].

   

Lupeyl acetate

[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate

C32H52O2 (468.3967092)


Lupeol acetate is an organic molecular entity. It has a role as a metabolite. Lupeol acetate is a natural product found in Euphorbia dracunculoides, Euphorbia larica, and other organisms with data available. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].

   

dinatin

Scutellarein 6-methyl ether

C16H12O6 (300.06338519999997)


Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM.

   

Lupeol acetate

1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl acetate

C32H52O2 (468.3967092)


   

Hispidulin

4H-1-Benzopyran-4-one, 5, 7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-

C16H12O6 (300.06338519999997)


Hispidulin is a monomethoxyflavone that is scutellarein methylated at position 6. It has a role as an apoptosis inducer, an anti-inflammatory agent, an antioxidant, an anticonvulsant, an antineoplastic agent and a plant metabolite. It is a trihydroxyflavone and a monomethoxyflavone. It is functionally related to a scutellarein. Hispidulin (4,5,7-trihydroxy-6-methoxyflavone) is a potent benzodiazepine (BZD) receptor ligand with positive allosteric properties. Hispidulin is a natural product found in Eupatorium cannabinum, Eupatorium perfoliatum, and other organisms with data available. See also: Arnica montana Flower (part of). A monomethoxyflavone that is scutellarein methylated at position 6. 6-methylscutellarein, also known as 4,5,7-trihydroxy-6-methoxyflavone or dinatin, is a member of the class of compounds known as 6-o-methylated flavonoids. 6-o-methylated flavonoids are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. Thus, 6-methylscutellarein is considered to be a flavonoid lipid molecule. 6-methylscutellarein is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 6-methylscutellarein can be found in a number of food items such as italian oregano, common sage, sunflower, and common thyme, which makes 6-methylscutellarein a potential biomarker for the consumption of these food products. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM.

   

Lupeol acetate

Acetic acid (1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-eicosahydro-cyclopenta[a]chrysen-9-yl ester

C32H52O2 (468.3967092)


Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].

   

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].

   

dinatin

4H-1-Benzopyran-4-one, 5, 7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-

C16H12O6 (300.06338519999997)


Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM.

   

pinocembrine

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)-

C15H12O4 (256.0735552)


4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)- is a natural product found in Alpinia nutans, Alpinia zerumbet, and Boesenbergia rotunda with data available.

   

Pinocembrin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (S)-(-)-

C15H12O4 (256.0735552)


(2s)-pinocembrin, also known as 5,7-dihydroxyflavanone or dihydrochrysin, is a member of the class of compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. Thus, (2s)-pinocembrin is considered to be a flavonoid lipid molecule (2s)-pinocembrin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (2s)-pinocembrin can be found in a number of food items such as acorn, lentils, mulberry, and sorghum, which makes (2s)-pinocembrin a potential biomarker for the consumption of these food products. (s)-pinocembrin, also known as 5,7-dihydroxyflavanone or dihydrochrysin, is a member of the class of compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3 (s)-pinocembrin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (s)-pinocembrin is a bitter tasting compound found in mexican oregano and tarragon, which makes (s)-pinocembrin a potential biomarker for the consumption of these food products. relative retention time with respect to 9-anthracene Carboxylic Acid is 1.069 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.067 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.071 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.070 5,7-Dihydroxyflavanone is a natural product found in Pinus contorta var. latifolia, Piper nigrum, and other organisms with data available. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1].

   

Isoalantolactone

Isoalantolactone

C15H20O2 (232.14632200000003)


relative retention time with respect to 9-anthracene Carboxylic Acid is 1.234 Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent. Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent.

   

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].

   

Stigmasterin

(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methyl-hept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H48O (412.37049579999996)


C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol

   

AI3-31148

Naphtho[2,3-b]furan-2(3H)-one, decahydro-8a-methyl-3,5-bis(methylene)-, [3aR-(3a.alpha.,4a.alpha.,8a.beta.,9a.alpha.)]-

C15H20O2 (232.14632200000003)


Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent. Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent.

   

Lupeol acetate

1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl acetate

C32H52O2 (468.3967092)


Lupeyl acetate, also known as lupeyl acetic acid, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Lupeyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Lupeyl acetate can be found in burdock, date, and fig, which makes lupeyl acetate a potential biomarker for the consumption of these food products. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].

   

Isohelenin

Naphtho(2,3-b)furan-2(3H)-one, decahydro-8a-methyl-3,5-bis(methylene)-, (3aR-(3a alpha,4a alpha,8a beta,9a alpha))-

C15H20O2 (232.14632200000003)


Isoalantolactone is a sesquiterpene lactone of the eudesmanolide group. It has been isolated from Inula helenium. It has a role as an apoptosis inducer, an antifungal agent and a plant metabolite. It is a sesquiterpene lactone and a eudesmane sesquiterpenoid. Isoalantolactone is a natural product found in Eupatorium cannabinum, Critonia quadrangularis, and other organisms with data available. A sesquiterpene lactone of the eudesmanolide group. It has been isolated from Inula helenium. Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent. Isoalantolactone is an apoptosis inducer, which also acts as an alkylating agent.

   

7-(but-2-enoyl)-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

7-(but-2-enoyl)-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

C20H28O7 (380.1834938)


   

10,12-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

10,12-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

C17H28O4 (296.19874880000003)


   

(3r,3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2e)-2-methylbut-2-enoate

(3r,3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2e)-2-methylbut-2-enoate

C20H28O7 (380.1834938)


   

6-ethenyl-6-methyl-3-methylidene-5-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-2-one

6-ethenyl-6-methyl-3-methylidene-5-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-2-one

C15H20O2 (232.14632200000003)


   

(3r,3as,6s,7s,8s,8ar)-7-hydroxy-7-[(3r)-3-hydroxybutanoyl]-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3r,3as,6s,7s,8s,8ar)-7-hydroxy-7-[(3r)-3-hydroxybutanoyl]-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H30O7 (382.199143)


   

(3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H26O6 (362.17292960000003)


   

(3r,3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2e)-2-methylbut-2-enoate

(3r,3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2e)-2-methylbut-2-enoate

C20H28O6 (364.1885788)


   

(2's,3ar,5s,7ar)-2',6-dimethyl-3-methylidene-4,7a-dihydro-3ah-spiro[1-benzofuran-5,1'-cyclopentan]-2-one

(2's,3ar,5s,7ar)-2',6-dimethyl-3-methylidene-4,7a-dihydro-3ah-spiro[1-benzofuran-5,1'-cyclopentan]-2-one

C15H20O2 (232.14632200000003)


   

(2's,6r)-2',3,5-trimethylspiro[1-benzofuran-6,1'-cyclopentan]-2-one

(2's,6r)-2',3,5-trimethylspiro[1-benzofuran-6,1'-cyclopentan]-2-one

C15H18O2 (230.1306728)


   

(2e,6e,10s)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-1-yl acetate

(2e,6e,10s)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-1-yl acetate

C17H28O4 (296.19874880000003)


   

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

(3ar,4ar,5s,9ar)-4a,5-dimethyl-3-methylidene-3ah,4h,5h,6h,7h,9h,9ah-naphtho[2,3-b]furan-2-one

(3ar,4ar,5s,9ar)-4a,5-dimethyl-3-methylidene-3ah,4h,5h,6h,7h,9h,9ah-naphtho[2,3-b]furan-2-one

C15H20O2 (232.14632200000003)


   

(1r,2r,4s,5s,6s,7s,8r,11r)-6-[(3r)-3-ethoxybutanoyl]-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

(1r,2r,4s,5s,6s,7s,8r,11r)-6-[(3r)-3-ethoxybutanoyl]-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

C22H32O8 (424.20970719999997)


   

(3ar,5s,6s,7ar)-6-ethenyl-6-methyl-3-methylidene-5-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-2-one

(3ar,5s,6s,7ar)-6-ethenyl-6-methyl-3-methylidene-5-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-2-one

C15H20O2 (232.14632200000003)


   

7-(but-2-enoyl)-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylbut-2-enoate

7-(but-2-enoyl)-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H28O7 (380.1834938)


   

7-(but-2-enoyl)-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

7-(but-2-enoyl)-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

C19H28O7 (368.1834938)


   

7-hydroxy-7-(3-methoxybutanoyl)-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl 2-methylbutanoate

7-hydroxy-7-(3-methoxybutanoyl)-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl 2-methylbutanoate

C21H30O8 (410.194058)


   

(3ar,6r,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

(3ar,6r,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

C20H26O7 (378.1678446)


   

(2e,6e,8r,10s)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-1-yl acetate

(2e,6e,8r,10s)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-1-yl acetate

C17H28O4 (296.19874880000003)


   

(3ar,5r,6s,7s,8s,8ar)-5,7-dihydroxy-7-(3-hydroxybutanoyl)-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

(3ar,5r,6s,7s,8s,8ar)-5,7-dihydroxy-7-(3-hydroxybutanoyl)-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

C20H30O8 (398.194058)


   

(3ar,6s,7s,8s,8ar)-7-hydroxy-7-(3-methoxybutanoyl)-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

(3ar,6s,7s,8s,8ar)-7-hydroxy-7-(3-methoxybutanoyl)-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

C21H32O7 (396.2147922)


   

(1s,2r,4s,5s,6s,7s,8r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

(1s,2r,4s,5s,6s,7s,8r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

C20H24O7 (376.1521954)


   

7-(but-2-enoyl)-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

7-(but-2-enoyl)-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H26O6 (362.17292960000003)


   

6-(3-ethoxybutanoyl)-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

6-(3-ethoxybutanoyl)-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

C22H32O8 (424.20970719999997)


   

(2's,3ar,5s,7ar)-2'-methyl-3,6-dimethylidene-tetrahydrospiro[1-benzofuran-5,1'-cyclopentan]-2-one

(2's,3ar,5s,7ar)-2'-methyl-3,6-dimethylidene-tetrahydrospiro[1-benzofuran-5,1'-cyclopentan]-2-one

C15H20O2 (232.14632200000003)


   

6-(but-2-enoyl)-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

6-(but-2-enoyl)-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

C20H24O7 (376.1521954)


   

(1r,2r,4s,5s,6s,7s,8r,11r)-6-hydroxy-6-[(3s)-3-hydroxybutanoyl]-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

(1r,2r,4s,5s,6s,7s,8r,11r)-6-hydroxy-6-[(3s)-3-hydroxybutanoyl]-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

C20H28O8 (396.1784088)


   

(3ar,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3ar,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H26O6 (362.17292960000003)


   

(3ar,6r,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl 2-methylbutanoate

(3ar,6r,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl 2-methylbutanoate

C20H26O7 (378.1678446)


   

(3as,4s,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3as,4s,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

(1r,2r,4s,5s,6s,7s,8r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

(1r,2r,4s,5s,6s,7s,8r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

C20H24O7 (376.1521954)


   

(3r,3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

(3r,3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

C19H28O6 (352.1885788)


   

7-(but-2-enoyl)-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

7-(but-2-enoyl)-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

(3r,3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3r,3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H28O7 (380.1834938)


   

8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-one

8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-one

C15H24O3 (252.1725354)


   

(3ar,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

(3ar,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H26O6 (362.17292960000003)


   

6-hydroxy-6-(3-hydroxybutanoyl)-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

6-hydroxy-6-(3-hydroxybutanoyl)-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

C20H28O8 (396.1784088)


   

(6e,8r,10s)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-one

(6e,8r,10s)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-one

C15H24O3 (252.1725354)


   

7-hydroxy-7-(3-hydroxybutanoyl)-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylbut-2-enoate

7-hydroxy-7-(3-hydroxybutanoyl)-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H30O7 (382.199143)


   

(3ar,4s,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3ar,4s,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

C20H28O7 (380.1834938)


   

7-(but-2-enoyl)-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

7-(but-2-enoyl)-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

C19H28O6 (352.1885788)


   

(3as,6r,7s,8s,8ar)-7-hydroxy-7-[(3s)-3-methoxybutanoyl]-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

(3as,6r,7s,8s,8ar)-7-hydroxy-7-[(3s)-3-methoxybutanoyl]-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

C21H30O8 (410.194058)


   

6-(but-2-enoyl)-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

6-(but-2-enoyl)-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl 2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

(3r,3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

(3r,3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylpropanoate

C19H28O7 (368.1834938)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.386145)


   

(3as,4s,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

(3as,4s,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-4,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

2',6-dimethyl-3-methylidene-4,7a-dihydro-3ah-spiro[1-benzofuran-5,1'-cyclopentan]-2-one

2',6-dimethyl-3-methylidene-4,7a-dihydro-3ah-spiro[1-benzofuran-5,1'-cyclopentan]-2-one

C15H20O2 (232.14632200000003)


   

(3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3as,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-1-yl acetate

8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-1-yl acetate

C17H28O4 (296.19874880000003)


   

(1s,5s,9r)-9-isopropyl-1-methyl-6-methylidenespiro[4.5]decan-1-ol

(1s,5s,9r)-9-isopropyl-1-methyl-6-methylidenespiro[4.5]decan-1-ol

C15H26O (222.1983546)


   

7-(but-2-enoyl)-7-hydroxy-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl 2-methylbutanoate

7-(but-2-enoyl)-7-hydroxy-6-methyl-3-methylidene-2,5-dioxo-tetrahydro-3ah-cyclohepta[b]furan-8-yl 2-methylbutanoate

C20H26O7 (378.1678446)


   

7-(but-2-enoyl)-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

7-(but-2-enoyl)-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H26O7 (378.1678446)


   

2'-methyl-3,6-dimethylidene-tetrahydrospiro[1-benzofuran-5,1'-cyclopentan]-2-one

2'-methyl-3,6-dimethylidene-tetrahydrospiro[1-benzofuran-5,1'-cyclopentan]-2-one

C15H20O2 (232.14632200000003)


   

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

(3ar,5r,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-5,7-dihydroxy-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

C20H28O7 (380.1834938)


   

(1s,2r,4s,5s,6s,7s,8r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

(1s,2r,4s,5s,6s,7s,8r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5-methyl-11-methylidene-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

C20H24O7 (376.1521954)


   

5,7-dihydroxy-7-(3-hydroxybutanoyl)-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

5,7-dihydroxy-7-(3-hydroxybutanoyl)-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl 2-methylbutanoate

C20H30O8 (398.194058)


   

(3r,3as,6s,7s,8s,8ar)-7-hydroxy-7-[(3s)-3-hydroxybutanoyl]-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3r,3as,6s,7s,8s,8ar)-7-hydroxy-7-[(3s)-3-hydroxybutanoyl]-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H30O7 (382.199143)


   

(3as,5r,6s,7s,8s,8ar)-5,7-dihydroxy-7-[(3s)-3-hydroxybutanoyl]-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

(3as,5r,6s,7s,8s,8ar)-5,7-dihydroxy-7-[(3s)-3-hydroxybutanoyl]-6-methyl-3-methylidene-2-oxo-hexahydrocyclohepta[b]furan-8-yl (2r)-2-methylbutanoate

C20H30O8 (398.194058)


   

(3r,3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

(3r,3as,6s,7s,8s,8ar)-7-[(2e)-but-2-enoyl]-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H28O6 (364.1885788)


   

7-(but-2-enoyl)-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylbut-2-enoate

7-(but-2-enoyl)-7-hydroxy-3,6-dimethyl-2-oxo-hexahydro-3h-cyclohepta[b]furan-8-yl 2-methylbut-2-enoate

C20H28O6 (364.1885788)


   

(1r,2r,4s,5s,6s,7s,8r,11r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

(1r,2r,4s,5s,6s,7s,8r,11r)-6-[(2e)-but-2-enoyl]-6-hydroxy-5,11-dimethyl-10-oxo-3,9-dioxatricyclo[6.3.0.0²,⁴]undecan-7-yl (2z)-2-methylbut-2-enoate

C20H26O7 (378.1678446)