CHEBI:62416 - dammarenediol-II

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ChEBI Name dammarenediol-II
ChEBI ID CHEBI:62416
Definition A tetracyclic triterpenoid that is dammarane which has a double bond between positions 24 and 25, and is substituted by hydroxy groups at the 3β- and 20- positions.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C30H52O2
Net Charge 0
Average Mass 444.73270
Monoisotopic Mass 444.39673
InChI InChI=1S/C30H52O2/c1-20(2)10-9-16-30(8,32)22-13-18-28(6)21(22)11-12-24-27(5)17-15-25(31)26(3,4)23(27)14-19-29(24,28)7/h10,21-25,31-32H,9,11-19H2,1-8H3/t21-,22+,23+,24-,25+,27+,28-,29-,30+/m1/s1
InChIKey NLHQJXWYMZLQJY-TXNIMPHESA-N
SMILES [H][C@@]1(CC[C@]2(C)[C@]1([H])CC[C@]1([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]21C)[C@@](C)(O)CCC=C(C)C
Metabolite of Species Details
Aglaia abbreviata (IPNI:576946-1) Found in stem (BTO:0001300). 95% ethanolic extract of air-dried stems See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing dammarenediol-II (CHEBI:62416) has parent hydride dammarane (CHEBI:36488)
dammarenediol-II (CHEBI:62416) has role metabolite (CHEBI:25212)
dammarenediol-II (CHEBI:62416) is a secondary alcohol (CHEBI:35681)
dammarenediol-II (CHEBI:62416) is a tertiary alcohol (CHEBI:26878)
dammarenediol-II (CHEBI:62416) is a tetracyclic triterpenoid (CHEBI:26893)
Incoming (20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) has functional parent dammarenediol-II (CHEBI:62416)
IUPAC Name
(3β)-dammar-24-ene-3,20-diol
Synonyms Sources
(20S)-dammar-24-ene-3β,20-diol ChEBI
(20S)-dammarenediol ChEBI
3β-glucodammar-24-ene-3,20-diol ChemIDplus
8-methyl-18-nor-lanost-24-en-3β,20-diol ChEBI
8-methyl-18-nor-lanost-24-ene-3β,20-diol ChEBI
dammar-24-ene-20(SS),3β-diol ChEBI
dammar-24-ene-3β,20-diol ChemIDplus
dammarenediol ChemIDplus
dammarenediol II ChemIDplus
dammarenediol-II UniProt
Registry Numbers Types Sources
14351-29-2 CAS Registry Number ChemIDplus
2511034 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16962103 PubMed citation Europe PMC
17088293 PubMed citation Europe PMC
2828553 PubMed citation Europe PMC
8124758 PubMed citation Europe PMC
Last Modified
01 November 2018