Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
twitter

MetaCyc Compound Class: a sesquiterpenoid

Synonyms: a sesquiterpene

Superclasses: a lipid an isoprenoid a terpenoid
a secondary metabolite a terpenoid

Summary:
Terpenoids make up a very large family of natural products containing more than 50,000 structurally diverse compounds. They are categorized by the number of C5 isoprene units as follows:

Hemiterpenoids (one C5 unit), monoterpenoids (C10; two C5 units), sesquiterpenoids (C15; three C5 units), diterpenoids (C20; four C5 units), sesterterpenoids (C25; five C5 units), triterpenoids (C30; six C5 units), sesquarterpenoids (C35; seven C5 units), and tetraterpenoids (C40; eight C5 units).

Child Classes: a δ-selinene (1) , abscisic acid (8) , α-curcumene (2) , α-selinene (2) , β-phellandrene (2) , germacrene A (1) , sesquisabinene (2)

Instances:
α-acoradiene ,
α-calacorene ,
α-chamigrene ,
α-copaene ,
α-cubebene ,
α-eudesmol ,
α-guaiene ,
α-himachalene ,
α-humulene ,
α-longipinene ,
α-patchoulene ,
α-phellandrene ,
α-ylangene ,
α-zingiberene ,
β-acoradiene ,
β-cedrene ,
β-copaene ,
β-elemene ,
β-eudesmol ,
β-gurjunene ,
β-himachalene ,
β-isocomene ,
β-longipinene ,
β-patchoulene ,
β-santalol ,
β-selinene ,
β-sesquiphellandrene ,
β-ylangene ,
δ-cadinol ,
δ-guaiene ,
Δ6-protoilludene ,
γ-calacorene ,
γ-curcumene ,
γ-himachalene ,
γ-humulene ,
γ-patchoulene ,
ω, mono-trans, poly-cis-heptaprenyl diphosphate ,
ω, mono-trans, poly-cis-hexaprenyl diphosphate ,
ω, mono-trans, poly-cis-nonaprenyl diphosphate ,
ω, mono-trans, poly-cis-octaprenyl diphosphate ,
ω, mono-trans, poly-cis-undecaprenyl diphosphate ,
ω, mono-trans,deca-cis-dodecaprenyl diphosphate ,
ω, mono-trans,octa-cis-decaprenyl diphosphate ,
τ-muurolene ,
(+)-α-amorphene ,
(+)-α-barbatene ,
(+)-α-bulgarene ,
(+)-α-cadinene ,
(+)-α-muurolene ,
(+)-α-santalene ,
(+)-α-santalol ,
(+)-β-amorphene ,
(+)-β-barbatene ,
(+)-β-bulgarene ,
(+)-β-cadinene ,
(+)-β-caryophyllene ,
(+)-β-chamigrene ,
(+)-β-muurolene ,
(+)-δ-amorphene ,
(+)-γ-amorphene ,
(+)-γ-bulgarene ,
(+)-γ-cadinene ,
(+)-γ-gurjunene ,
(+)-γ-muurolene ,
(+)-5-epi-aristolochene ,
(+)-cis-abscisic aldehyde ,
(+)-endo-β-bergamotene ,
(+)-epi-α-bisabolol ,
(+)-epi-β-santalene ,
(+)-epi-isozizaene ,
(+)-exo-β-bergamotene ,
(+)-trans-abscisic aldehyde ,
(+)-caryolan-1-ol ,
(+)-costunolide ,
(+)-cubenene ,
(+)-epicubenol ,
(+)-germacrene D ,
(+)-isoitalicene ,
(+)-sativene ,
(+)-selina-4,11-diene ,
(+)-thujopsene ,
(+)-valencene ,
(-)-α-bisabolol ,
(-)-α-cedrene ,
(-)-α-cuprenene ,
(-)-α-gurjunene ,
(-)-α-isocomene ,
(-)-β-caryophyllene ,
(-)-β-cubebene ,
(-)-β-curcumene ,
(-)-β-elemene ,
(-)-β-santalene ,
(-)-γ-cadinene ,
(-)-4-epieremophilene ,
(-)-endo-α-bergamotene ,
(-)-epi-β-santalene ,
(-)-exo-α-bergamotene ,
(-)-cuparene ,
(-)-cyperene ,
(-)-germacrene D ,
(-)-patchoulol ,
(-)-vetispiradiene ,
(2E,6E)-farnesyl diphosphate ,
(2E,6Z)-farnesyl diphosphate ,
(2Z,6E)-farnesyl diphosphate ,
(2Z,6Z,10E)-tetraprenyl diphosphate ,
(2Z,6Z)-farnesyl diphosphate ,
(11R)-dihydroartemisinic aldehyde ,
(E,E)-germacrene B ,
(E)-α-bisabolene ,
(E)-β-farnesene ,
(E)-2-epi-β-caryophyllene ,
(E,E)-α-farnesene ,
(S)-β-bisabolene ,
(Z,E)-germacrene B ,
(E) γ-bisabolene ,
(Z) γ-bisabolene ,
(Z,E)-α-farnesene ,
1-deoxy-11β-hydroxypentalenate ,
1-deoxy-11-oxopentalenate ,
1-deoxy-capsidiol ,
1-deoxypentalenate ,
2-dehydrolubimin ,
3β-hydroxycostunolide ,
3β-hydroxyparthenolide ,
3-deoxy-capsidiol ,
3-hydroxy-15-dihydrolubimin ,
3-hydroxylubimin ,
4-(5,5-dimethylcyclohex-1-en-1-yl)cyclohex-1-ene-1-carbaldehyde ,
4-epi-α-acoradiene ,
6α-hydroxy-germacra-1(10),4,11(13)-trien-12-oate ,
7-epi-sesquithujene ,
7-epizingiberene ,
8β-hydroxy-germacra-1(10),4,11(13)-trien-12-oate ,
8-epi-cedrol ,
10-epi-γ-eudesmol ,
10-hydroxy-α-humulene ,
15-hydroxysolavetivone ,
cis-abscisic alcohol ,
cis-muurola-3,5-diene ,
cis-muurola-4(14),5-diene ,
trans,octacis-decaprenyl phosphate ,
trans-abscisic alcohol ,
amorpha-4,11-diene ,
aristolochene ,
artemisinate ,
artemisinic alcohol ,
artemisinic aldehyde ,
artemisinin ,
avermitilol ,
bicyclogermacrene ,
botrydial ,
cadalene ,
capsidiol ,
cedrol ,
cyclosativene ,
desoxyhemigossypol ,
desoxyhemigossypol-6-methyl ether ,
dihydroartemisinate ,
dihydroartemisinic acid hydroperoxide ,
germacra-1(10),4,11(13)-trien-12-al ,
germacra-1(10),4,11(13)-trien-12-oate ,
germacra-1(10),4,11(13)-trien-12-ol ,
germacrene C ,
gossypol ,
gossypol-6,6'-dimethyl ether ,
guaia-6,9-diene ,
hemigossypol ,
hemigossypol-6-methyl ether ,
intermedeol ,
isobazzanene ,
kunzeaol ,
lepidozene ,
longiborneol ,
longicyclene ,
lubimin ,
neopentalenolactone ,
neopentalenolactone D ,
neopentalenolactone E ,
neopentalenolactone F ,
nootkatene ,
parthenolide ,
pentalen-13-al ,
pentalen-13-ol ,
pentalenate ,
pentalenene ,
pentalenolactone ,
pentalenolactone D ,
pentalenolactone E ,
pentalenolactone F ,
PR-imine ,
PR-toxin ,
rishitin ,
rotundene ,
seli-3,7(11)-diene ,
sesquithujene ,
seychellene ,
sibirene ,
solavetivol ,
solavetivone ,
valerena-4,7(11)-diene ,
valerenate ,
viridiflorene ,
viridiflorol ,
zealexin A1 ,
zealexin A2 ,
zealexin A3 ,
zealexin B1 ,
zerumbone ,
[4-(5,5-dimethylcyclohex-1-en-1-yl)-cyclohex-1-en-1-yl] methanol

Unification Links: ChEBI:26658

Reactions known to consume the compound:

linoleate biosynthesis I (plants) :
oleoyl-CoA + a lipid + H+ → a lipid oleoyl-group + coenzyme A

Reactions known to produce the compound:

glutathione redox reactions I :
a lipid hydroperoxide + 2 glutathione + H+a lipid + glutathione disulfide + 2 H2O


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
Page generated by SRI International Pathway Tools version 18.5 on Fri Dec 19, 2014, BIOCYC14A.