207386-83-2
Chemical Structure
Hippuryl-His-Leu-OH hydrate
Synonym(s): N-Benzoyl-Gly-His-Leu hydrate
- CAS No.: 207386-83-2
- Formula:C21H27N5O5.xH2O
- Molecular Weight:429.47 (free acid)
SMILES: O=C(N[C@H](C(O)=O)CC(C)C)[C@@H](NC(CNC(C1=CC=CC=C1)=O)=O)CC2=CN=CN2.[x].O
Biological Activity: Hippuryl-His-Leu-OH (N-Benzoyl-Gly-His-Leu) hydrate is a specific substrate for angiotensin-converting enzyme ACE I and is a molecular tool used for ACE activity detection in in vitro experiments. Hippuryl-His-Leu-OH hydrate is hydrolyzed by ACE through competitive binding. Under ACE catalysis, Hippuryl-His-Leu-OH hydrate undergoes hydrolysis to produce hippuric acid (HA). The amount of HA produced can be used to quantitatively assess ACE activity or screen for ACE inhibitors. The His-Leu released from Hippuryl-His-Leu-OH hydrate can also react with o-phthalaldehyde or Fluorescamine (HY-D0715) for fluorescence detection. Hippuryl-His-Leu-OH hydrate can be applied to the in vitro screening of ACE inhibitors for hypertension and cardiovascular diseases, and is also used in the study of changes in ACE activity during physiological and pathological processes such as renal compensatory hypertrophy[1][2][3].
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Hippuryl-His-Leu-OH hydrate | 99.88% | Hippuryl-His-Leu-OH (N-Benzoyl-Gly-His-Leu) hydrate is a specific substrate for angiotensin-converting enzyme ACE I and is a molecular tool used for ACE activity detection in in vitro experiments. Hippuryl-His-Leu-OH hydrate is hydrolyzed by ACE through competitive binding. Under ACE catalysis, Hippuryl-His-Leu-OH hydrate undergoes hydrolysis to produce hippuric acid (HA). The amount of HA produced can be used to quantitatively assess ACE activity or screen for ACE inhibitors. The His-Leu released from Hippuryl-His-Leu-OH hydrate can also react with o-phthalaldehyde or Fluorescamine (HY-D0715) for fluorescence detection. Hippuryl-His-Leu-OH hydrate can be applied to the in vitro screening of ACE inhibitors for hypertension and cardiovascular diseases, and is also used in the study of changes in ACE activity during physiological and pathological processes such as renal compensatory hypertrophy. | ||||||||||||||||||||
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- [1]. Komolafe K, et al. African locust bean (Parkia biglobosa, Jacq Benth) leaf extract affects mitochondrial redox chemistry and inhibits angiotensin-converting enzyme in vitro[J]. Clinical Phytoscience, 2017, 3(1): 19.
- [2]. Inoue K, et al. Screening assay of angiotensin-converting enzyme inhibitory activity from complex natural colourants and foods using high-throughput LC-MS/MS. Food Chem. 2011 Jun 15;126(4):1909-15. [Content Brief]
- [3]. Babić N, et al. Angiotensin converting enzyme activity in compensatory renal hypertrophy. Bosn J Basic Med Sci. 2007 Feb;7(1):79-83. [Content Brief]
Keywords