CHEBI:134582 - (4S)-4,16-dihydroxyretinoic acid

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ChEBI Name (4S)-4,16-dihydroxyretinoic acid ChEBI ID CHEBI:134582 ChEBI ASCII Name (4S)-4,16-dihydroxyretinoic acid Definition A retinoid that is all-trans-retinoic acid which has been hydroxylated at the 4-pro-S position and at the 16 position. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C20H28O4 Net Charge 0 Average Mass 332.435 Monoisotopic Mass 332.19876 InChI InChI=1S/C20H28O4/c1-14(6-5-7-15(2)12-19(23)24)8-9-17-16(3)18(22)10-11-20(17,4)13-21/h5-9,12,18,21-22H,10-11,13H2,1-4H3,(H,23,24)/b7-5+,9-8+,14-6+,15-12+/t18-,20+/m0/s1 InChIKey DGCPGJKPROZYMN-RGKDZJHZSA-N SMILES [C@@]1(C)(CO)CC[C@@H](C(=C1\C=C\C(=C\C=C\C(=C\C(=O)O)\C)\C)C)O Roles Classification Chemical Role(s): Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) View more via ChEBI Ontology ChEBI Ontology Outgoing (4S)-4,16-dihydroxyretinoic acid (CHEBI:134582) has functional parent all-trans-4-hydroxyretinoic acid (CHEBI:63795) (4S)-4,16-dihydroxyretinoic acid (CHEBI:134582) is a monocarboxylic acid (CHEBI:25384) (4S)-4,16-dihydroxyretinoic acid (CHEBI:134582) is a primary alcohol (CHEBI:15734) (4S)-4,16-dihydroxyretinoic acid (CHEBI:134582) is a retinoid (CHEBI:26537) (4S)-4,16-dihydroxyretinoic acid (CHEBI:134582) is a secondary allylic alcohol (CHEBI:134396) (4S)-4,16-dihydroxyretinoic acid (CHEBI:134582) is conjugate acid of (4S)-4,16-dihydroxyretinoate (CHEBI:134233) Incoming (4S)-4,16-dihydroxyretinoate (CHEBI:134233) is conjugate base of (4S)-4,16-dihydroxyretinoic acid (CHEBI:134582) IUPAC Name (4S)-4,16-dihydroxyretinoic acid Synonym Source all-trans-(4S,16)-dihydroxyretinoic acid ChEBI Citation Type Source 23071109 PubMed citation Europe PMC Last Modified 17 February 2017