CHEBI:59065 - 3,3,5-trimethylcyclohexanol

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ChEBI Name 3,3,5-trimethylcyclohexanol
Definition A secondary alcohol that is cyclohexanol substituted by two methyl groups at the 3-position and one methyl group at the 5-position. It exhibits inhibitory activity against HMG-CoA reductase ( EC
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C9H18O
Net Charge 0
Average Mass 142.23860
Monoisotopic Mass 142.13577
InChI InChI=1S/C9H18O/c1-7-4-8(10)6-9(2,3)5-7/h7-8,10H,4-6H2,1-3H3
Roles Classification
Biological Role(s): EC (hydroxymethylglutaryl-CoA reductase) inhibitor
Any EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD+ or NADP+ acceptor) inhibitor that inhibits HMG-CoA reductases. Hydroxymethylglutaryl-CoA reductase inhibitors have been shown to lower directly cholesterol synthesis. The Enzyme Commission designation is EC for the NADPH-dependent enzyme and EC for an NADH-dependent enzyme.
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ChEBI Ontology
Outgoing 3,3,5-trimethylcyclohexanol (CHEBI:59065) has role EC (hydroxymethylglutaryl-CoA reductase) inhibitor (CHEBI:35664)
3,3,5-trimethylcyclohexanol (CHEBI:59065) is a cyclohexanols (CHEBI:23480)
3,3,5-trimethylcyclohexanol (CHEBI:59065) is a secondary alcohol (CHEBI:35681)
Incoming cyclandelate (CHEBI:3988) has functional parent 3,3,5-trimethylcyclohexanol (CHEBI:59065)
Synonyms Sources
3,3,5-trimethyl-1-cyclohexanol NIST Chemistry WebBook
dihydroisophorol ChemIDplus
homomenthol NIST Chemistry WebBook
Registry Numbers Types Sources
116-02-9 CAS Registry Number ChemIDplus
116-02-9 CAS Registry Number NIST Chemistry WebBook
2203314 Beilstein Registry Number Beilstein
2203314 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
3768035 PubMed citation Europe PMC
6681959 PubMed citation Europe PMC
Last Modified
08 May 2014