NCBI Taxonomy: 378295

Curcuma heyneana (ncbi_taxid: 378295)

found 159 associated metabolites at species taxonomy rank level.

Ancestor: Curcuma

Child Taxonomies: none taxonomy data.

Germacrone

3,7-Cyclodecadien-1-one, 3,7-dimethyl-10-(1-methylethylidene)-, (E,E)-

C15H22O (218.1670562)


(E,E)-germacrone is a germacrane sesquiterpenoid that has formula C15H22O. It is a natural product found in traditional medicinal plants of the family Zingiberaceae. The compound exhibits a range of pharmacological activities including anti-inflammatory, anticancer, antiviral, anti-androgenic, antioxidant, antimicrobial, antifungal, neuroprotective and insecticidal activities. It has a role as a volatile oil component, an antiviral agent, an insecticide, an anti-inflammatory agent, an antioxidant, an antineoplastic agent, an apoptosis inducer, an autophagy inducer, an antimicrobial agent, an androgen antagonist, a neuroprotective agent, a plant metabolite, an antifungal agent, an antitussive, an antifeedant and a hepatoprotective agent. It is a germacrane sesquiterpenoid and an olefinic compound. Germacrone is a natural product found in Rhododendron calostrotum, Rhododendron nivale, and other organisms with data available. A germacrane sesquiterpenoid that has formula C15H22O. It is a natural product found in traditional medicinal plants of the family Zingiberaceae. The compound exhibits a range of pharmacological activities including anti-inflammatory, anticancer, antiviral, anti-androgenic, antioxidant, antimicrobial, antifungal, neuroprotective and insecticidal activities. Germacrone is a member of the class of compounds known as germacrane sesquiterpenoids. Germacrane sesquiterpenoids are sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups. Germacrone is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Germacrone can be found in common thyme and turmeric, which makes germacrone a potential biomarker for the consumption of these food products. Germacrone is an antiviral isolate of Geranium macrorrhizum . Germacrone is extracted from Rhizoma Curcuma. Germacrone inhibits influenza virus infection[1]. Germacrone is extracted from Rhizoma Curcuma. Germacrone inhibits influenza virus infection[1].

   

Curcumenol

(3S,3aS,6R,8aS)-3,8-Dimethyl-5-(propan-2-ylidene)-2,3,4,5,6,8a-hexahydro-1H-3a,6-epoxyazulen-6-ol

C15H22O2 (234.1619712)


Curcumenol is a sesquiterpenoid. (3S,3aS,6R,8aS)-3,8-Dimethyl-5-(propan-2-ylidene)-2,3,4,5,6,8a-hexahydro-1H-3a,6-epoxyazulen-6-ol is a natural product found in Curcuma longa and Curcuma phaeocaulis with data available. D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors > D065692 - Cytochrome P-450 CYP3A Inhibitors 4-Epicurcumenol is a constituent of rhizomes of Curcuma zedoaria (zedoary). Curcumenol ((+)-Curcumenol) is a potent CYP3A4 inhibitor with an IC50 of 12.6 μM, which is one of constituents in the plants of medicinally important genus of Curcuma zedoaria, with neuroprotection, anti-inflammatory, anti-tumor and hepatoprotective activities. Curcumenol ((+)-Curcumenol) suppresses Akt-mediated NF-κB activation and p38 MAPK signaling pathway in LPS-stimulated BV-2 microglial cells[1][2]. Curcumenol ((+)-Curcumenol) is a potent CYP3A4 inhibitor with an IC50 of 12.6 μM, which is one of constituents in the plants of medicinally important genus of Curcuma zedoaria, with neuroprotection, anti-inflammatory, anti-tumor and hepatoprotective activities. Curcumenol ((+)-Curcumenol) suppresses Akt-mediated NF-κB activation and p38 MAPK signaling pathway in LPS-stimulated BV-2 microglial cells[1][2].

   

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

   

Zerumbone

(2E,6E,10E)-2,6,9,9-tetramethylcycloundeca-2,6,10-trien-1-one

C15H22O (218.1670562)


Zerumbone is a sesquiterpenoid and cyclic ketone that is (1E,4E,8E)-alpha-humulene which is substituted by an oxo group at the carbon atom attached to two double bonds. It is obtained by steam distillation from a type of edible ginger, Zingiber zerumbet Smith, grown particularly in southeast Asia. It has a role as an anti-inflammatory agent, a plant metabolite and a glioma-associated oncogene inhibitor. It is a sesquiterpenoid and a cyclic ketone. It derives from a hydride of an alpha-humulene. Zerumbone is a natural product found in Curcuma amada, Curcuma longa, and other organisms with data available. Zerumbone is found in herbs and spices. Zerumbone is a constituent of the rhizomes of wild ginger (Zingiber zerumbet) Constituent of the rhizomes of wild ginger (Zingiber zerumbet). Zerumbone is found in herbs and spices. Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes of Zingiber zerumbet Smith. Zerumbone potently inhibits the activation of Epstein-Barr virus with an IC50 of 0.14 mM. Zerumbone has anti-cancer, antioxidant, anti-inflammatory and anti-proliferative activity[1][2]. Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes of Zingiber zerumbet Smith. Zerumbone potently inhibits the activation of Epstein-Barr virus with an IC50 of 0.14 mM. Zerumbone has anti-cancer, antioxidant, anti-inflammatory and anti-proliferative activity[1][2].

   

Dehydrocurdione

(6E,10S)-6,10-dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione

C15H22O2 (234.1619712)


Dehydrocurdione is a germacrane sesquiterpenoid. (6E,10S)-6,10-dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione is a natural product found in Curcuma aromatica, Curcuma longa, and other organisms with data available. Dehydrocurdione is found in turmeric. Dehydrocurdione is from Curcuma zedoaria (zedoary From Curcuma zedoaria (zedoary). Dehydrocurdione is found in turmeric.

   

Curcumin

InChI=1\C21H20O6\c1-26-20-11-14(5-9-18(20)24)3-7-16(22)13-17(23)8-4-15-6-10-19(25)21(12-15)27-2\h3-13,22,24-25H,1-2H3\b7-3+,8-4+,16-13

C21H20O6 (368.125982)


C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C1967 - Tyrosine Kinase Inhibitor COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials relative retention time with respect to 9-anthracene Carboxylic Acid is 1.286 D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics C471 - Enzyme Inhibitor > C1323 - Cyclooxygenase Inhibitor D000893 - Anti-Inflammatory Agents D000970 - Antineoplastic Agents D018501 - Antirheumatic Agents D004791 - Enzyme Inhibitors D004396 - Coloring Agents Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS relative retention time with respect to 9-anthracene Carboxylic Acid is 1.290 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.289 [Raw Data] CBA71_Curcumin_neg_10eV.txt [Raw Data] CBA71_Curcumin_neg_30eV.txt [Raw Data] CBA71_Curcumin_neg_40eV.txt [Raw Data] CBA71_Curcumin_pos_30eV.txt [Raw Data] CBA71_Curcumin_pos_20eV.txt [Raw Data] CBA71_Curcumin_pos_40eV.txt [Raw Data] CBA71_Curcumin_neg_50eV.txt [Raw Data] CBA71_Curcumin_pos_10eV.txt [Raw Data] CBA71_Curcumin_pos_50eV.txt [Raw Data] CBA71_Curcumin_neg_20eV.txt Curcumin (Diferuloylmethane), a natural phenolic compound, is a p300/CREB-binding protein-specific inhibitor of acetyltransferase, represses the acetylation of histone/nonhistone proteins and histone acetyltransferase-dependent chromatin transcription. Curcumin shows inhibitory effects on NF-κB and MAPKs, and has diverse pharmacologic effects including anti-inflammatory, antioxidant, antiproliferative and antiangiogenic activities. Curcumin induces stabilization of Nrf2 protein through Keap1 cysteine modification. Curcumin (Diferuloylmethane), a natural phenolic compound, is a p300/CREB-binding protein-specific inhibitor of acetyltransferase, represses the acetylation of histone/nonhistone proteins and histone acetyltransferase-dependent chromatin transcription. Curcumin shows inhibitory effects on NF-κB and MAPKs, and has diverse pharmacologic effects including anti-inflammatory, antioxidant, antiproliferative and antiangiogenic activities. Curcumin induces stabilization of Nrf2 protein through Keap1 cysteine modification.

   

Zedoarondiol

3,8-dihydroxy-3,8-dimethyl-5-propan-2-ylidene-1,2,3a,4,7,8a-hexahydroazulen-6-one

C15H24O3 (252.1725354)


1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-decahydroazulen-6-one is a sesquiterpenoid. Zedoarondiol is a natural product found in Curcuma aeruginosa, Curcuma aromatica, and other organisms with data available. Zedoarondiol is found in turmeric. Zedoarondiol is a constituent of Curcuma zedoaria (zedoary) Constituent of Curcuma zedoaria (zedoary). Zedoarondiol is found in turmeric.

   

Isocurcumenol

2-methyl-6-methylidene-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undecan-8-ol

C15H22O2 (234.1619712)


Isocurcumenol is a constituent of Curcuma zedoaria (zedoary). Constituent of Curcuma zedoaria (zedoary) Isocurcumenol, an estrogen receptor alpha (ERα) inhibitor isolated from Curcuma zedoaria Rhizomes, possesses anti-tumor acticity, with IC50 values of 99.1μg/mL and 178.2 μg/mL in DLA and KB cells, respectively[1][2]. Isocurcumenol, an estrogen receptor alpha (ERα) inhibitor isolated from Curcuma zedoaria Rhizomes, possesses anti-tumor acticity, with IC50 values of 99.1μg/mL and 178.2 μg/mL in DLA and KB cells, respectively[1][2].

   

Procurcumenol

3-hydroxy-3,8-dimethyl-5-(propan-2-ylidene)-1,2,3,3a,4,5,6,8a-octahydroazulen-6-one

C15H22O2 (234.1619712)


Procurcumenol is found in herbs and spices. Procurcumenol is a constituent of the dried rhizomes of Curcuma zedoaria (zedoary) and Curcuma longa (turmeric). Constituent of the dried rhizomes of Curcuma zedoaria (zedoary) and Curcuma longa (turmeric). Procurcumenol is found in turmeric and herbs and spices.

   

Curcumanolide A

6-methyl-9-(prop-1-en-2-yl)-3-(propan-2-ylidene)-1-oxaspiro[4.4]nonan-2-one

C15H22O2 (234.1619712)


Constituent of the crude drug zedoary (Curcuma zedoaria). Curcumanolide B is from Curcuma zedoaria (zedoary).

   

(1E,6E)-1,7-Bis(3-methoxy-4-hydroxyphenyl)-5-hydroxy-1,4,6-heptatriene-3-one

(1E,6E)-1,7-Bis(3-methoxy-4-hydroxyphenyl)-5-hydroxy-1,4,6-heptatriene-3-one

C21H20O6 (368.125982)


   

(2Z,6Z,10Z)-2,6,9,9-Tetramethylcycloundeca-2,6,10-trien-1-one

(2Z,6Z,10Z)-2,6,9,9-Tetramethylcycloundeca-2,6,10-trien-1-one

C15H22O (218.1670562)


   

Germacrone

3,7-dimethyl-10-(propan-2-ylidene)cyclodeca-3,7-dien-1-one

C15H22O (218.1670562)


   

Isocurcumenol

3S-(3alpha,3aalpha,6alpha,8abeta)-Octahydro-3-methyl-8-methylene-5-(1-methylethylidene)- 6H-3a,6-epoxyazulen-6-ol

C15H22O2 (234.1619712)


Isocurcumenol is a natural product found in Curcuma zedoaria, Curcuma harmandii, and other organisms with data available. Isocurcumenol, an estrogen receptor alpha (ERα) inhibitor isolated from Curcuma zedoaria Rhizomes, possesses anti-tumor acticity, with IC50 values of 99.1μg/mL and 178.2 μg/mL in DLA and KB cells, respectively[1][2]. Isocurcumenol, an estrogen receptor alpha (ERα) inhibitor isolated from Curcuma zedoaria Rhizomes, possesses anti-tumor acticity, with IC50 values of 99.1μg/mL and 178.2 μg/mL in DLA and KB cells, respectively[1][2].

   

Stigmasterol

Stigmasterol

C29H48O (412.37049579999996)


Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong.

   

Aerugidiol

(3S,3aR,8aR)-3,8a-dihydroxy-3,8-dimethyl-5-propan-2-ylidene-1,2,3a,4-tetrahydroazulen-6-one

C15H22O3 (250.1568862)


Aerugidiol is a natural product found in Curcuma aeruginosa, Curcuma zedoaria, and Curcuma heyneana with data available.

   

Procurcumenol

InChI=1/C15H22O2/c1-9(2)12-8-13-11(5-6-15(13,4)17)10(3)7-14(12)16/h7,11,13,17H,5-6,8H2,1-4H3/t11-,13-,15-/m0/s1

C15H22O2 (234.1619712)


Procurcumenol is a sesquiterpenoid. Procurcumenol is a natural product found in Curcuma aromatica, Curcuma longa, and other organisms with data available.

   

Curcumenol

Curcumenol

C15H22O2 (234.1619712)


Constituent of Curcuma zedoaria (zedoary) and Curcuma longa (turmeric). Curcumenol is found in turmeric and herbs and spices. Curcumenol ((+)-Curcumenol) is a potent CYP3A4 inhibitor with an IC50 of 12.6 μM, which is one of constituents in the plants of medicinally important genus of Curcuma zedoaria, with neuroprotection, anti-inflammatory, anti-tumor and hepatoprotective activities. Curcumenol ((+)-Curcumenol) suppresses Akt-mediated NF-κB activation and p38 MAPK signaling pathway in LPS-stimulated BV-2 microglial cells[1][2]. Curcumenol ((+)-Curcumenol) is a potent CYP3A4 inhibitor with an IC50 of 12.6 μM, which is one of constituents in the plants of medicinally important genus of Curcuma zedoaria, with neuroprotection, anti-inflammatory, anti-tumor and hepatoprotective activities. Curcumenol ((+)-Curcumenol) suppresses Akt-mediated NF-κB activation and p38 MAPK signaling pathway in LPS-stimulated BV-2 microglial cells[1][2].

   

Guaidiol

1,4-dimethyl-7-(prop-1-en-2-yl)-decahydroazulene-1,4-diol

C15H26O2 (238.1932696)


   

Curcumanolide A

6-methyl-9-(prop-1-en-2-yl)-3-(propan-2-ylidene)-1-oxaspiro[4.4]nonan-2-one

C15H22O2 (234.1619712)


   

Zedoarondiol

1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-decahydroazulen-6-one

C15H24O3 (252.1725354)


   

Zerumbone

(2E,6E,10E)-2,6,9,9-tetramethylcycloundeca-2,6,10-trien-1-one

C15H22O (218.1670562)


Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes of Zingiber zerumbet Smith. Zerumbone potently inhibits the activation of Epstein-Barr virus with an IC50 of 0.14 mM. Zerumbone has anti-cancer, antioxidant, anti-inflammatory and anti-proliferative activity[1][2]. Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes of Zingiber zerumbet Smith. Zerumbone potently inhibits the activation of Epstein-Barr virus with an IC50 of 0.14 mM. Zerumbone has anti-cancer, antioxidant, anti-inflammatory and anti-proliferative activity[1][2].

   

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

   

germacron

3,7-Cyclodecadien-1-one, 3,7-dimethyl-10-(1-methylethylidene)-, (E,E)-

C15H22O (218.1670562)


Germacrone is extracted from Rhizoma Curcuma. Germacrone inhibits influenza virus infection[1]. Germacrone is extracted from Rhizoma Curcuma. Germacrone inhibits influenza virus infection[1].

   

(6E,10S)-3-isopropylidene-6,10-dimethylcyclodec-6-ene-1,4-dione

(6E,10S)-6,10-dimethyl-3-propan-2-ylidene-cyclodec-6-ene-1,4-dione

C15H22O2 (234.1619712)


   

cyperusol C

cyperusol C

C15H26O2 (238.1932696)


A natural product found in Sanicula lamelligera.

   

erumbone

(2E,6E,10E)-2,6,9,9-tetramethylcycloundeca-2,6,10-trien-1-one

C15H22O (218.1670562)


Zerumbone is a sesquiterpenoid and cyclic ketone that is (1E,4E,8E)-alpha-humulene which is substituted by an oxo group at the carbon atom attached to two double bonds. It is obtained by steam distillation from a type of edible ginger, Zingiber zerumbet Smith, grown particularly in southeast Asia. It has a role as an anti-inflammatory agent, a plant metabolite and a glioma-associated oncogene inhibitor. It is a sesquiterpenoid and a cyclic ketone. It derives from a hydride of an alpha-humulene. Zerumbone is a natural product found in Curcuma amada, Curcuma longa, and other organisms with data available. A sesquiterpenoid and cyclic ketone that is (1E,4E,8E)-alpha-humulene which is substituted by an oxo group at the carbon atom attached to two double bonds. It is obtained by steam distillation from a type of edible ginger, Zingiber zerumbet Smith, grown particularly in southeast Asia. Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes of Zingiber zerumbet Smith. Zerumbone potently inhibits the activation of Epstein-Barr virus with an IC50 of 0.14 mM. Zerumbone has anti-cancer, antioxidant, anti-inflammatory and anti-proliferative activity[1][2]. Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes of Zingiber zerumbet Smith. Zerumbone potently inhibits the activation of Epstein-Barr virus with an IC50 of 0.14 mM. Zerumbone has anti-cancer, antioxidant, anti-inflammatory and anti-proliferative activity[1][2].

   

Dehydrocurdione

(6E,10S)-6,10-dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione

C15H22O2 (234.1619712)


Dehydrocurdione is a germacrane sesquiterpenoid. (6E,10S)-6,10-dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione is a natural product found in Curcuma aromatica, Curcuma longa, and other organisms with data available.

   

3-hydroxy-3,8-dimethyl-5-(propan-2-ylidene)-1,2,3,3a,4,5,6,8a-octahydroazulen-6-one

3-hydroxy-3,8-dimethyl-5-(propan-2-ylidene)-1,2,3,3a,4,5,6,8a-octahydroazulen-6-one

C15H22O2 (234.1619712)


   

(3s,3as,5s,8as)-3a-hydroxy-3,3',3',8-tetramethyl-2,3,4,8a-tetrahydro-1h-spiro[azulene-5,2'-oxiran]-6-one

(3s,3as,5s,8as)-3a-hydroxy-3,3',3',8-tetramethyl-2,3,4,8a-tetrahydro-1h-spiro[azulene-5,2'-oxiran]-6-one

C15H22O3 (250.1568862)


   

(5r,6s,9s)-6-methyl-9-(prop-1-en-2-yl)-3-(propan-2-ylidene)-1-oxaspiro[4.4]nonan-2-one

(5r,6s,9s)-6-methyl-9-(prop-1-en-2-yl)-3-(propan-2-ylidene)-1-oxaspiro[4.4]nonan-2-one

C15H22O2 (234.1619712)


   

(2e)-2-{2-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]ethylidene}butanedial

(2e)-2-{2-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]ethylidene}butanedial

C20H30O2 (302.224568)


   

(5r,6r,9s)-3-(2-hydroxypropan-2-yl)-6-methyl-9-(prop-1-en-2-yl)-1-oxaspiro[4.4]non-3-en-2-one

(5r,6r,9s)-3-(2-hydroxypropan-2-yl)-6-methyl-9-(prop-1-en-2-yl)-1-oxaspiro[4.4]non-3-en-2-one

C15H22O3 (250.1568862)


   

(2z,4z,7z)-5-(2-hydroxypropan-2-yl)-2,8-dimethylcyclodeca-2,4,7-triene-1,6-dione

(2z,4z,7z)-5-(2-hydroxypropan-2-yl)-2,8-dimethylcyclodeca-2,4,7-triene-1,6-dione

C15H20O3 (248.14123700000002)


   

(4as,5r,7as)-7a-methyl-5-(prop-1-en-2-yl)-3-(propan-2-ylidene)-tetrahydro-4h-cyclopenta[b]pyran-2-one

(4as,5r,7as)-7a-methyl-5-(prop-1-en-2-yl)-3-(propan-2-ylidene)-tetrahydro-4h-cyclopenta[b]pyran-2-one

C15H22O2 (234.1619712)


   

(4as,5r,7ar)-7a-methyl-5-(prop-1-en-2-yl)-3-(propan-2-ylidene)-tetrahydro-4h-cyclopenta[b]pyran-2-one

(4as,5r,7ar)-7a-methyl-5-(prop-1-en-2-yl)-3-(propan-2-ylidene)-tetrahydro-4h-cyclopenta[b]pyran-2-one

C15H22O2 (234.1619712)


   

(2e)-2-{2-[(1s,4as,8ar)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]ethylidene}butanedial

(2e)-2-{2-[(1s,4as,8ar)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]ethylidene}butanedial

C20H30O2 (302.224568)


   

(1s,2s,5s,8r)-2,6-dimethyl-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undec-6-en-8-ol

(1s,2s,5s,8r)-2,6-dimethyl-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undec-6-en-8-ol

C15H22O2 (234.1619712)


   

(1s,3as,4s,7r,8as)-1,4-dimethyl-7-(prop-1-en-2-yl)-octahydroazulene-1,4-diol

(1s,3as,4s,7r,8as)-1,4-dimethyl-7-(prop-1-en-2-yl)-octahydroazulene-1,4-diol

C15H26O2 (238.1932696)


   

(1s,3ar,8as)-1-hydroxy-1,4-dimethyl-7-(propan-2-ylidene)-3,3a,8,8a-tetrahydro-2h-azulen-6-one

(1s,3ar,8as)-1-hydroxy-1,4-dimethyl-7-(propan-2-ylidene)-3,3a,8,8a-tetrahydro-2h-azulen-6-one

C15H22O2 (234.1619712)


   

(1s,3as,4s,8as)-1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-hexahydroazulen-6-one

(1s,3as,4s,8as)-1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-hexahydroazulen-6-one

C15H24O3 (252.1725354)


   

(2z,4s,7r,8r)-4,7,8-trihydroxy-3,7-dimethyl-10-(propan-2-ylidene)cyclodec-2-en-1-one

(2z,4s,7r,8r)-4,7,8-trihydroxy-3,7-dimethyl-10-(propan-2-ylidene)cyclodec-2-en-1-one

C15H24O4 (268.1674504)


   

(1s,5r,8r)-2,6-dimethyl-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undec-6-en-8-ol

(1s,5r,8r)-2,6-dimethyl-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undec-6-en-8-ol

C15H22O2 (234.1619712)


   

(2z,4r,7s,8r)-4,7,8-trihydroxy-3,7-dimethyl-10-(propan-2-ylidene)cyclodec-2-en-1-one

(2z,4r,7s,8r)-4,7,8-trihydroxy-3,7-dimethyl-10-(propan-2-ylidene)cyclodec-2-en-1-one

C15H24O4 (268.1674504)


   

(1s,3ar,8ar)-1,3a-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-2,3,8,8a-tetrahydroazulen-6-one

(1s,3ar,8ar)-1,3a-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-2,3,8,8a-tetrahydroazulen-6-one

C15H22O3 (250.1568862)


   

6,10-dimethyl-3-(propan-2-ylidene)cyclodec-6-ene-1,4-dione

6,10-dimethyl-3-(propan-2-ylidene)cyclodec-6-ene-1,4-dione

C15H22O2 (234.1619712)


   

(1s,3as,4r,7s,8as)-1,4-dimethyl-7-(prop-1-en-2-yl)-octahydroazulene-1,4-diol

(1s,3as,4r,7s,8as)-1,4-dimethyl-7-(prop-1-en-2-yl)-octahydroazulene-1,4-diol

C15H26O2 (238.1932696)


   

(5r,6s,9s)-3-(2-hydroxypropan-2-yl)-6-methyl-9-(prop-1-en-2-yl)-1-oxaspiro[4.4]non-3-en-2-one

(5r,6s,9s)-3-(2-hydroxypropan-2-yl)-6-methyl-9-(prop-1-en-2-yl)-1-oxaspiro[4.4]non-3-en-2-one

C15H22O3 (250.1568862)


   

(1s,2s,5s,8r)-2-methyl-6-methylidene-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undecan-8-ol

(1s,2s,5s,8r)-2-methyl-6-methylidene-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undecan-8-ol

C15H22O2 (234.1619712)


   

(7z)-5-(2-hydroxypropan-2-yl)-2,8-dimethylcyclodeca-2,4,7-triene-1,6-dione

(7z)-5-(2-hydroxypropan-2-yl)-2,8-dimethylcyclodeca-2,4,7-triene-1,6-dione

C15H20O3 (248.14123700000002)


   

(3z)-5-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]-3-formylpent-3-enoic acid

(3z)-5-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]-3-formylpent-3-enoic acid

C20H30O3 (318.21948299999997)


   

(1s,2s,5s,8s)-2-methyl-6-methylidene-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undecan-8-ol

(1s,2s,5s,8s)-2-methyl-6-methylidene-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0¹,⁵]undecan-8-ol

C15H22O2 (234.1619712)


   

(1s,3ar,4r,8as)-1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-hexahydroazulen-6-one

(1s,3ar,4r,8as)-1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-hexahydroazulen-6-one

C15H24O3 (252.1725354)


   

(6e,10s)-6,10-dimethyl-3-(propan-2-ylidene)cyclodec-6-ene-1,4-dione

(6e,10s)-6,10-dimethyl-3-(propan-2-ylidene)cyclodec-6-ene-1,4-dione

C15H22O2 (234.1619712)


   

2-[2-(5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl)ethylidene]butanedial

2-[2-(5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl)ethylidene]butanedial

C20H30O2 (302.224568)


   

(5r,6s,9r)-6-methyl-9-(prop-1-en-2-yl)-3-(propan-2-ylidene)-1-oxaspiro[4.4]nonan-2-one

(5r,6s,9r)-6-methyl-9-(prop-1-en-2-yl)-3-(propan-2-ylidene)-1-oxaspiro[4.4]nonan-2-one

C15H22O2 (234.1619712)


   

(1's,2r,2's,5's,8'r)-2',3,3,6'-tetramethyl-11'-oxaspiro[oxirane-2,9'-tricyclo[6.2.1.0¹,⁵]undecan]-6'-en-8'-ol

(1's,2r,2's,5's,8'r)-2',3,3,6'-tetramethyl-11'-oxaspiro[oxirane-2,9'-tricyclo[6.2.1.0¹,⁵]undecan]-6'-en-8'-ol

C15H22O3 (250.1568862)


   

2',3,3,6'-tetramethyl-11'-oxaspiro[oxirane-2,9'-tricyclo[6.2.1.0¹,⁵]undecan]-6'-en-8'-ol

2',3,3,6'-tetramethyl-11'-oxaspiro[oxirane-2,9'-tricyclo[6.2.1.0¹,⁵]undecan]-6'-en-8'-ol

C15H22O3 (250.1568862)


   

(1r,3ar,4s,8as)-1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-hexahydroazulen-6-one

(1r,3ar,4s,8as)-1,4-dihydroxy-1,4-dimethyl-7-(propan-2-ylidene)-hexahydroazulen-6-one

C15H24O3 (252.1725354)


   

5-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]-3-formylpent-3-enoic acid

5-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]-3-formylpent-3-enoic acid

C20H30O3 (318.21948299999997)


   

3a-hydroxy-3,3',3',8-tetramethyl-2,3,4,8a-tetrahydro-1h-spiro[azulene-5,2'-oxiran]-6-one

3a-hydroxy-3,3',3',8-tetramethyl-2,3,4,8a-tetrahydro-1h-spiro[azulene-5,2'-oxiran]-6-one

C15H22O3 (250.1568862)


   

(3e)-4-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]but-3-en-2-one

(3e)-4-[(1s,4as,8as)-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]but-3-en-2-one

C18H28O (260.2140038)


   

(1s,3ar,8as)-1-hydroxy-4-(hydroxymethyl)-1-methyl-7-(propan-2-ylidene)-3,3a,8,8a-tetrahydro-2h-azulen-6-one

(1s,3ar,8as)-1-hydroxy-4-(hydroxymethyl)-1-methyl-7-(propan-2-ylidene)-3,3a,8,8a-tetrahydro-2h-azulen-6-one

C15H22O3 (250.1568862)


   

(1s,2s,5s,8r,9e)-9-(1-hydroxypropan-2-ylidene)-2,6-dimethyl-11-oxatricyclo[6.2.1.0¹,⁵]undec-6-en-8-ol

(1s,2s,5s,8r,9e)-9-(1-hydroxypropan-2-ylidene)-2,6-dimethyl-11-oxatricyclo[6.2.1.0¹,⁵]undec-6-en-8-ol

C15H22O3 (250.1568862)


   

(2z,4s,7s,8r)-4,7,8-trihydroxy-3,7-dimethyl-10-(propan-2-ylidene)cyclodec-2-en-1-one

(2z,4s,7s,8r)-4,7,8-trihydroxy-3,7-dimethyl-10-(propan-2-ylidene)cyclodec-2-en-1-one

C15H24O4 (268.1674504)