CHEBI:23757 - dihydrophaseic acid

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ChEBI Name dihydrophaseic acid
ChEBI ID CHEBI:23757
Definition An apo carotenoid sesquiterpenoid that is phaseic acid in which the keto group has been reduced to the corresponding alcohol such that the two hydroxy groups are on opposite sides of the 6-membered ring.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C15H22O5
Net Charge 0
Average Mass 282.33218
Monoisotopic Mass 282.14672
InChI InChI=1S/C15H22O5/c1-10(6-12(17)18)4-5-15(19)13(2)7-11(16)8-14(15,3)20-9-13/h4-6,11,16,19H,7-9H2,1-3H3,(H,17,18)/b5-4+,10-6-/t11-,13+,14+,15-/m0/s1
InChIKey XIVFQYWMMJWUCD-VSTJRZLJSA-N
SMILES CC(\C=C\[C@]1(O)[C@@]2(C)CO[C@]1(C)C[C@@H](O)C2)=C\C(O)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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 dihydrophaseic acid (CHEBI:23757) has functional parent phaseic acid (CHEBI:28205)
dihydrophaseic acid (CHEBI:23757) has role metabolite (CHEBI:25212)
dihydrophaseic acid (CHEBI:23757) is a α,β-unsaturated monocarboxylic acid (CHEBI:79020)
dihydrophaseic acid (CHEBI:23757) is a 6-hydroxy monocarboxylic acid (CHEBI:35971)
dihydrophaseic acid (CHEBI:23757) is a apo carotenoid sesquiterpenoid (CHEBI:36758)
dihydrophaseic acid (CHEBI:23757) is a cyclic ether (CHEBI:37407)
dihydrophaseic acid (CHEBI:23757) is a secondary alcohol (CHEBI:35681)
dihydrophaseic acid (CHEBI:23757) is a tertiary alcohol (CHEBI:26878)
IUPAC Name
(2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]oct-8-yl]-3-methylpenta-2,4-dienoic acid
Synonym Source
(-)-Dihydrophaseic acid KEGG COMPOUND
Manual Xrefs Databases
C15971 KEGG COMPOUND
CPD-7726 MetaCyc
HMDB0038660 HMDB
LMPR0103050005 LIPID MAPS
View more database links
Registry Numbers Types Sources
41756-77-8 CAS Registry Number HMDB
6770423 Beilstein Registry Number Beilstein
6770423 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
14646201 PubMed citation Europe PMC
19782241 PubMed citation Europe PMC
22664582 PubMed citation Europe PMC
Last Modified
27 June 2014