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CHEBI:41285 - [(R)-1-L-prolylpyrrolidin-2-yl]boronic acid

Default Structure
ChEBI IDCHEBI:41285
ChEBI Name[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid
Stars
ASCII Name[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid
DefinitionAn N-acylpyrrolidine obtained by formal condenstion of the carboxy group of L-proline and the secondary amino group of (R)-pyrrolidine-2-carboxylic acid.
Last Modified7 January 2015
DownloadsMolfile
FormulaC9H17BN2O3
Net Charge0
Average Mass212.058
Monoisotopic Mass212.13322
SMILES[H][C@@]1(B(O)O)CCCN1C(=O)[C@]1([H])CCCN1
InChIInChI=1S/C9H17BN2O3/c13-9(7-3-1-5-11-7)12-6-2-4-8(12)10(14)15/h7-8,11,14-15H,1-6H2/t7-,8-/m0/s1
InChIKeyXSBZZZGVAIXJLD-YUMQZZPRSA-N
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
EC 3.4.* (hydrolases acting on peptide bond) inhibitor  A hydrolase inhibitor that interferes with the action of any hydrolase acting on peptide bonds (peptidase), EC 3.4.*.*).
ChEBI Ontology
Outgoing Relation(s)
[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid (CHEBI:41285) has role EC 3.4.* (hydrolases acting on peptide bond) inhibitor (CHEBI:60258)
[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid (CHEBI:41285) is a N-acylpyrrolidine (CHEBI:46766)
[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid (CHEBI:41285) is a L-proline derivative (CHEBI:84186)
[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid (CHEBI:41285) is a boronic acids (CHEBI:38269)
IUPAC Name 
[(2R)-1-L-prolylpyrrolidin-2-yl]boronic acid
Synonym  Source
Pro-boroProChEBI
Manual XrefsDatabases
BPRPDBeChem
Registry NumbersSources
Reaxys:14528096Reaxys
Citations