Therapeutic Targets Database
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TTD Drug ID: DAP000198

Drug Information
NameL-Proline
SynonymsCHEBI:17203; Proline (VAN); 81710_SIGMA; bmse000047; CHEMBL54922; nchembio.186-comp54; DB02853; AC1Q71B7; Proline [USAN:INN]; 147-85-3; Carboxypyrrolidine; 81709_SIGMA; L-alpha-Pyrrolidinecarboxylic acid; 608998_ALDRICH; (-)-Proline; 2-Pyrrolidinecarboxylic acid, (S)-; C00148; FEMA Number 3319; L-Pyrrolidine-2-carboxylic acid; FEMA No. 3319; A01B5B63-CC3D-4796-A7B4-C2DE26A6FA93; (S)-Proline; P0481; 18875-45-1; nchembio816-comp9; TL80073505; AB1002323; NCGC00014017; (S)-2-Carboxypyrrolidine; CB 1707; 2-pyrrolidinecarboxylic acid; W331902_ALDRICH; EINECS 205-702-2; Proline (USP); (S)-Pyrrolidine-2-carboxylic acid; P8865_SIAL; LS-2381; AmbotzHAA1126; pro; (2S)-pyrrolidine-2-carboxylic acid; L-(2,3-3H)Proline; P0380_SIAL; L-proline; proline; AC1L3RTC; (-)-Proline (S)-2-Carboxypyrrolidine; H-Pro-OH; MolPort-001-757-108; PRO (IUPAC abbreviation); UNII-9DLQ4CIU6V; L-Prolin; Prolinum [Latin]; 4607-28-7; AI3-26710; Prolina [Spanish]; HSDB 1210; P5607_SIGMA; (L)-PROLINE; NCGC00097126-01; NSC-97923; 81709_FLUKA; P8865_SIGMA; (-)-2-Pyrrolidinecarboxylic acid; (S)-2-Pyrrolidinecarboxylic acid; AC-11190; 4305-67-3; 81710_FLUKA; (-)-(S)-Proline; L-Proline, labeled with carbon-14; L-Proline (JAN); CID145742; Proline, L-; D00035; NSC 46703; L-Proline-15N; 37159-97-0; DB00172; Prolinum; L-(-)-Proline; prolina
IndicationDietary supplement
[ICD9: 260-269   ICD10: E40-E46]
Approved    [1]
Dietary supplement
[ICD9: 260-269   ICD10: E40-E46]
Approved    [2]
Structure

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InChI1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1
InChIKeyONIBWKKTOPOVIA-BYPYZUCNSA-N
Canonical SMILESC1CC(NC1)C(=O)O    
Isomeric SMILESC1C[C@H](NC1)C(=O)O
Therapeutic ClassDietary supplement
CAS NumberCAS 147-85-3
FormulaC5H9NO2
PubChem Compound IDCID 145742.
PubChem Substance IDSID 3448.
ChEBI17203;
TargetPeptidyl-prolyl cis-trans isomerase ABinder[2]
Peptidyl-prolyl cis-trans isomerase BBinder[1]
Ref 1Escherichia coli cyclophilin B binds a highly distorted form of trans-prolyl peptide isomer. Eur J Biochem. 2004 Sep;271(18):3794-803. To Reference
Ref 2Mechanistic insight into the role of transition-state stabilization in cyclophilin A. J Am Chem Soc. 2009 Jan 14;131(1):147-52. To Reference



 

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