CHEBI:62110 - 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime

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ChEBI Name 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime ChEBI ID CHEBI:62110 ChEBI ASCII Name 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime Definition An oxime O-ether consisting of progesterone having an O-(carboxymethyl)oxime group at the 3-position and a hydroxy group at the 17α-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 C23H33NO5 Net Charge 0 Average Mass 403.51180 Monoisotopic Mass 403.23587 InChI InChI=1S/C23H33NO5/c1-14(25)23(28)11-8-19-17-5-4-15-12-16(24-29-13-20(26)27)6-9-21(15,2)18(17)7-10-22(19,23)3/h12,17-19,28H,4-11,13H2,1-3H3,(H,26,27)/t17-,18+,19+,21+,22+,23+/m1/s1 InChIKey NMRMMCZURGCYED-JZTHCNPZSA-N SMILES [H][C@@]12CCC3=CC(CC[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2([H])CC[C@]1(O)C(C)=O)=NOCC(O)=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 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime (CHEBI:62110) has functional parent progesterone 3-O-(carboxymethyl)oxime (CHEBI:62042) 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime (CHEBI:62110) is a 17α-hydroxy steroid (CHEBI:35342) 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime (CHEBI:62110) is a 20-oxo steroid (CHEBI:36885) 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime (CHEBI:62110) is a monocarboxylic acid (CHEBI:25384) 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime (CHEBI:62110) is a oxime O-ether (CHEBI:36816) 17-hydroxyprogesterone 3-O-(carboxymethyl)oxime (CHEBI:62110) is a tertiary α-hydroxy ketone (CHEBI:139592) IUPAC Name {[(17-hydroxy-20-oxopregn-4-en-3-ylidene)amino]oxy}acetic acid Synonyms Sources P4-3-CMO-17-ol ChEBI progesterone-17-ol-3-carboxymethyloxime ChEBI progesterone-17-ol-3-CMO ChEBI Registry Number Type Source 2188864 Reaxys Registry Number Reaxys Citation Type Source 18791859 PubMed citation Europe PMC Last Modified 06 February 2018