CHEBI:141059 - (S)-2,5,5-trimethylthiazolidine-4-carboxylic acid

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ChEBI Name (S)-2,5,5-trimethylthiazolidine-4-carboxylic acid
ChEBI ID CHEBI:141059
ChEBI ASCII Name (S)-2,5,5-trimethylthiazolidine-4-carboxylic acid
Definition A trimethyl-substituted thiazolidine carboxylic acid derived by cleavage of and loss of C=O from the azetidine ring of penicillanic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C7H13NO2S
Net Charge 0
Average Mass 175.24900
Monoisotopic Mass 175.06670
InChI InChI=1S/C7H13NO2S/c1-4-8-5(6(9)10)7(2,3)11-4/h4-5,8H,1-3H3,(H,9,10)/t4?,5-/m0/s1
InChIKey MQQSPQRNCBFBSG-AKGZTFGVSA-N
SMILES CC1N[C@@H](C(O)=O)C(C)(C)S1
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 (S)-2,5,5-trimethylthiazolidine-4-carboxylic acid (CHEBI:141059) has functional parent penicillanic acid (CHEBI:37806)
(S)-2,5,5-trimethylthiazolidine-4-carboxylic acid (CHEBI:141059) is a monocarboxylic acid (CHEBI:25384)
(S)-2,5,5-trimethylthiazolidine-4-carboxylic acid (CHEBI:141059) is a thiazolidines (CHEBI:35622)
IUPAC Name
(4S)-2,5,5-trimethyl-1,3-thiazolidine-4-carboxylic acid
Synonym Source
(S)-2,5,5-Trimethyl-thiazolidine-4-carboxylic acid ChEMBL
Registry Numbers Types Sources
4462 Beilstein Registry Number Beilstein
4462 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
7716788 PubMed citation Europe PMC
Last Modified
24 November 2014