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

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ChEBI Name	[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid

ChEBI ID	CHEBI:41285

ChEBI ASCII Name	[(R)-1-L-prolylpyrrolidin-2-yl]boronic acid

Definition	An N-acylpyrrolidine obtained by formal condenstion of the carboxy group of L-proline and the secondary amino group of (R)-pyrrolidine-2-carboxylic acid.

Stars	This entity has been manually annotated by the ChEBI Team.

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Formula

C9H17BN2O3

Net Charge

Average Mass

212.05400

Monoisotopic Mass

212.13322

InChI

InChI=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

InChIKey

XSBZZZGVAIXJLD-YUMQZZPRSA-N

SMILES

OB(O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1

Roles Classification
Chemical Role(s):	Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid )

Biological Role(s):	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	[(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-boroPro	ChEBI

Registry Number	Type	Source
14528096	Reaxys Registry Number	Reaxys

Last Modified

07 January 2015