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N-Acetyl-L-proline

Catalog No. A0783 Name Sigma Aldrich
CAS Number 68-95-1 Website http://www.sigmaaldrich.com
M. F. C7H11NO3 Telephone 1-800-521-8956
M. W. 157.16714 Fax
Purity Email
Storage Chembase ID: 18291

SYNONYMS

IUPAC name
(2S)-1-acetylpyrrolidine-2-carboxylic acid
IUPAC Traditional name
acetylproline

DATABASE IDS

MDL Number MFCD00020837
PubChem SID 24890453
CAS Number 68-95-1
EC Number 200-698-9

PROPERTIES

Empirical Formula (Hill Notation) C7H11NO3
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
N-Acetyl-L-proline, an analog of the COOH-terminal dipeptide portion of preferred angiotensin-converting enzyme substrates, is use to probe the active site of angiotensin-converting enzyme(s). N-Acetyl-L-proline may be used to to identify, differentiate and characterized N-acyl-amino acid amidohydrolase(s)/aminoacylase(s). N-Acetyl-L-proline is used to study the physicochemical parameters of prolines.
N-acetyl-L-proline is an analog of the COOH-terminal dipeptide portion of preferred substrates of angiotensin-converting enzyme (ACE). It may be used in studies of the binding of substrates and inhibitors by ACE and to differentiate the specificities of various aminoacylases.
Description (简体中文)
Biochem/physiol Actions
N-acetyl-L-proline is an analog of the COOH-terminal dipeptide portion of preferred substrates of angiotensin-converting enzyme (ACE). It may be used in studies of the binding of substrates and inhibitors by ACE and to differentiate the specificities of various aminoacylases.

REFERENCES