Chemical Formula: C20H34O
Chemical Formula C20H34O
Found 221 metabolite its formula value is C20H34O
Tetraprenol
Geranylgeraniol is an orally acitve vitamin K2 sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model[1][2][3][4]. Geranylgeraniol is an orally acitve vitamin K2 sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model[1][2][3][4].
(ent-16alpha)-16-Kauranol
(ent-16alpha)-16-Kauranol is found in fats and oils. (ent-16alpha)-16-Kauranol is isolated from sunflowers. Isolated from sunflowers. ent-16a-Kauranol is found in fats and oils.
Tuberculosinol
(3S,6E,10E)-1,6,10,14-Phytatetraen-3-ol
(3S,6E,10E)-1,6,10,14-Phytatetraen-3-ol is found in herbs and spices. (3S,6E,10E)-1,6,10,14-Phytatetraen-3-ol is a constituent of Jasmine oil Constituent of Jasmine oil. (3S,6E,10E)-1,6,10,14-Phytatetraen-3-ol is found in tea and herbs and spices.
Cyclooctat-9-en-7-ol
(1S,4E,8E,12E)-2,2,5,9,13-Pentamethylcyclopentadeca-4,8,12-trien-1-ol
18-Deoxysagittarol
18-Deoxysagittarol is found in root vegetables. 18-Deoxysagittarol is a constituent of Sagittaria sagittifolia (arrowhead). Constituent of Sagittaria sagittifolia (arrowhead). 18-Deoxysagittarol is found in root vegetables.
(3E,7E)-dolabella-3,7-dien-18-ol
A tricyclic diterpene with formula C20H32 which is produced by a diterpene cyclase gene expressed in roots of Arabidopsis.
Nezukol
An isopimarane diterpenoid that is isopimarane in which the ethyl subtituent at position 13 has undergone formal dehydrogenation to the corresponding vinyl group, and in which the hydrogen at position 8 has been replaced by a hydroxy group. It has been found in the leaves of several plants, including Cryptomeria japonica and Isodon rubescens.
Serratol
Serratol is found in herbs and spices. Serratol is a constituent of Boswellia serrata (Indian olibanum). Constituent of Boswellia serrata (Indian olibanum). Serratol is found in herbs and spices.
8alpha-13(16),14-Labdadien-8-ol
8alpha-13(16),14-Labdadien-8-ol is a constituent of the needles of Pinus sylvestris (Scotch pine). Constituent of the needles of Pinus sylvestris (Scotch pine)
ent-Kauran-16-beta-ol
Ent-kauran-16-beta-ol is a member of the class of compounds known as kaurane diterpenoids. Kaurane diterpenoids are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Ent-kauran-16-beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Ent-kauran-16-beta-ol can be found in sunflower, which makes ent-kauran-16-beta-ol a potential biomarker for the consumption of this food product.
Manoyl oxide
Manoyl oxide, also known as (-)-ent-13-epi-manoyl oxide, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Manoyl oxide is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Manoyl oxide can be found in pot marjoram, which makes manoyl oxide a potential biomarker for the consumption of this food product.
Manool
Manool, also known as (+)-manool, is a member of the class of compounds known as diterpenoids. Diterpenoids are terpene compounds formed by four isoprene units. Manool is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Manool can be found in common sage, which makes manool a potential biomarker for the consumption of this food product. Manool is a diterpene from Salvia officinalis. Manool induces selective cytotoxicity in cancer cells. Manool arrests the cancer cells at the G(2)/M phase of the cell cycle[1][2]. Manool is a diterpene from Salvia officinalis. Manool induces selective cytotoxicity in cancer cells. Manool arrests the cancer cells at the G(2)/M phase of the cell cycle[1][2].
(1R*,1aR*,4S*,4aR*,5aR*,8aR*)-4-isopropyl-1,8a-dimethyl-5-methylenetetradecahydrophenathren-1-ol
(1R*,2E,4R*,7E,11S*,12R*)-18-hydroxy-2,7-dolabelladiene|18-hydroxy-2,7-dolabelladiene
2-[dodecahydro-1,4b,8,8-tetramethylphenanthren-2(1H)-ylidene]ethanol|taepeenin L
(5R,10R,13E)-8(9),13-labdadien-15-ol|ent-Labda-8,E-13-dien-15-ol
13-epi-homoverrucosan-5beta-ol|13-Epihomoverrucosan-5beta-ol
4,6-Bis(4-methylpent-3-en-1-yl)-6-methylcyclohexa-1,3-diene-carbaldehyde
9,11a-Methano-11aH-cyclohepta[a]naphthalen-8-ol, tetradecahydro-4,4,9,11b-tetramethyl-
15,16-dihydro-17-hydroxy-9-epi-ent-7,15-isopimaradiene
(10S,14R)-(-)-isoagath-12-en-15-ol|(14R)-isoagath-12-en-15-ol|(14S)-isoagath-12-en-15-ol|1.1.4ar.7c.8ac-Pentamethyl-8c-hydroxymethyl-(4btH.10atH)-Delta6-dodekahydro-phenanthren|14-Hydroxymethyl-8beta,13-dimethylpodocarpan|isoanticopal-12-en-15-ol
Manool
A labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 14 and carries an S-hydroxy group at position 13. Manool is a labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 14 and carries an R-hydroxy group at position 13. It has a role as an antineoplastic agent, a plant metabolite and an antibacterial agent. It is a labdane diterpenoid and a tertiary alcohol. Manool is a natural product found in Halocarpus biformis, Cedrus atlantica, and other organisms with data available. A labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 14 and carries an R-hydroxy group at position 13. Manool is a diterpene from Salvia officinalis. Manool induces selective cytotoxicity in cancer cells. Manool arrests the cancer cells at the G(2)/M phase of the cell cycle[1][2]. Manool is a diterpene from Salvia officinalis. Manool induces selective cytotoxicity in cancer cells. Manool arrests the cancer cells at the G(2)/M phase of the cell cycle[1][2].
C20H34O_2-Penten-1-ol, 5-[(1S,4aS,8aS)-decahydro-5,5,8a-trimethyl-2-methylene-1-naphthalenyl]-3-methyl-, (2E)
5-(1-methoxybutan-2-yl)isolongifol-5-ene
(3S,6E,10E)-1,6,10,14-Phytatetraen-3-ol
18-Deoxysagittarol
Serratol
A cembrane diterpenoid obtained by regio- and stereoselective hydration of the exocyclic double bond of cembrene C.
Geranyl geraniol
Geranylgeraniol is an orally acitve vitamin K2 sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model[1][2][3][4]. Geranylgeraniol is an orally acitve vitamin K2 sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model[1][2][3][4].
1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol
(+)-Copalol
A labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 13 (the latter with E-stereochemistry) and carries a hydroxy group at the terminal C-15 position.
(-)-Ent-copalol
A labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 13 (the latter with E-stereochemistry) and carries a hydroxy group at the terminal C-15 position.
FLUOROLINK(R) D
A diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. A geranylgeraniol in which all four double bonds have E- (trans-) geometry. Geranylgeraniol, also known as tetraprenol or (2e,6e,10e)-geranylgeraniol, is a member of the class of compounds known as acyclic diterpenoids. Acyclic diterpenoids are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle. Thus, geranylgeraniol is considered to be an isoprenoid lipid molecule. Geranylgeraniol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Geranylgeraniol can be found in flaxseed, which makes geranylgeraniol a potential biomarker for the consumption of this food product. Geranylgeraniol is a diterpene alcohol which plays a role in several important biological processes. It is an intermediate in the biosynthesis of other diterpenes and of vitamins E and K. It also used in the post-translational modification known as geranylgeranylation. Geranylgeraniol is a pheromone for bumblebees and a variety of other insects . Geranylgeraniol is an orally acitve vitamin K2 sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model[1][2][3][4]. Geranylgeraniol is an orally acitve vitamin K2 sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model[1][2][3][4].
Syn-copalol
A labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 13 (the latter with E-stereochemistry) and carries a hydroxy group at the terminal C-15 position.
(13S)-vitexifolin A
A labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 14 and carries an S-hydroxy group at position 13.
(13R)-edaxadiene
An edaxadiene in which the carbon bearing the hydroxy group has R configuration.
2-[(1R,3E,7E,11E)-4,8,12-trimethyltetradeca-3,7,11-trien-1-yl]propan-2-ol
(1R,4S,5aR,8aS,10bR)-1,4,5a,8a-tetramethyl-2,3,3a,5,6,7,8,9,10,10a,10b,10c-dodecahydro-1H-pyren-4-ol
(4R,4aS,7R,8R,8aS)-4-ethenyl-4,4,4,7,8a-pentamethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2-oxolane]
2-((1S,3aR,5E,9E,12aS)-3a,6,10-trimethyl-1,2,3,3a,4,7,8,11,12,12a-decahydrocyclopenta[11]annulen-1-yl)propan-2-ol
A natural product found in Dilophus spiralis.
2-[(1R,3aR,4E,6R,12aS)-3a,6,10-trimethyl-2,3,6,7,8,11,12,12a-octahydro-1H-cyclopenta[11]annulen-1-yl]propan-2-ol
(13R)-manoyl oxide
A tricyclic labdane diterpenoid that is an intermediate in the biosynthesis of forskolin by Coleus forskohlii.
(1R,3aR,5E,12aR)-3a,6,10-trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-1-ol
9,13(R)-epoxylabd-14-ene
A tricyclic diterpenoid that is an intermediate in the biosynthesis of marrubiin by the medicinal plant Marrubium vulgare.
Penichrysol
A diterpenoid that is produced by the fungal chimeric terpene synthases, PTTS087 and PTTS136.
(1S,2E,7E,11E)-1,7,11-trimethyl-4-propan-2-ylcyclotetradeca-2,7,11-trien-1-ol
(1R,2E,7E,11E)-1,7,11-trimethyl-4-propan-2-ylcyclotetradeca-2,7,11-trien-1-ol
(1S,4S,4aS,7E,11Z,12aR)-4,7,11-trimethyl-1-propan-2-yl-2,3,4a,5,6,9,10,12a-octahydro-1H-benzo[10]annulen-4-ol
(1S,2E,4R,7E,11E)-1,7,11-trimethyl-4-propan-2-ylcyclotetradeca-2,7,11-trien-1-ol
(3E,7E,11E)-1-Hydroxy-1-isopropyl-4,8,12-trimethylcyclotetradecatriene
(1S,2E,6Z,10E,14S)-3,7,11-trimethyl-14-propan-2-ylcyclotetradeca-2,6,10-trien-1-ol
(1S,2Z,6Z,10E,14S)-3,7,11-trimethyl-14-propan-2-ylcyclotetradeca-2,6,10-trien-1-ol
(3E,7Z,11E)-4,8,12-trimethyl-1-propan-2-ylcyclotetradeca-3,7,11-trien-1-ol
geranyllinalool
A diterpenoid that is linalool in which one of the terminal methyl hydrogens is substituted by a geranyl group (the 6E,10E-geoisomer)
cis-Abienol
A labdane diterpenoid in which the labdane skeleton has double bonds at C-12 and C-14 (the former with Z-stereochemistry) and carries a hydroxy group at position C-8.
(R)-nephthenol
A cembrane diterpenoid obtained by regio- and stereoselective hydration of the exocyclic double bond of cembrene C.
(13R)-epi-8,13-epoxylabd-14-ene
A tricyclic diterpenoid that is isolated from plants and fungi and exhibits anti-bacterial protperties.
(13S)-edaxadiene
An edaxadiene in which the carbon bearing the hydroxy group has S configuration.
edaxadiene
A bicyclic halimane-type diterpenoid produced by the pathogen Mycobacterium tuberculosis as a defense against macrophage attack. The structure was revised in 2010, having been initially thought to be tricyclic. The compound was originally named nosyberkol after it was first isolated in 2004 from a sponge, Raspailia sp., collected from the Nosy Be island of Madagascar.
(5Z,8Z,11Z,14Z)-icosatetraen-1-ol
A long-chain primary fatty alcohol that is (5Z,8Z,11Z,14Z)-icosatetraene in which one of the methyl hydrogens at position 1 is replaced by a hydroxy group.
(Z,Z,Z)-geranylgeraniol
A geranylgeraniol in which all double bonds have Z- (cis-) geometry.
(1R,2E,4R,7E,11S,12R)-18-hydroxy-2,7-dolabelladiene
A natural product found in Dilophus spiralis.
fusaterpenol
A diterpenoid synthesised by a monofunctional diterpene synthase from Fusarium graminearum.
13-epi-manool
A labdane diterpenoid in which the labdane skeleton has double bonds at positions 8(17) and 14 and carries an S-hydroxy group at position 13.
neoverrucosan-5beta-ol
A diterpenoid isolated from the liverwort Mylia verrucosa.
rel-(1R,3E,7E,11R,12R)-12-Hydroxy-3,7-dolabelladiene
A natural product found in Dilophus spiralis.