N-[(1S)-1-Carboxy-3-phenylpropyl]-L-alanyl-L-proline hydrate (1:2)
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N-[(1S)-1-Carboxy-3-phenylpropyl]-L-alanyl-L-proline hydrate (1:2)
structure -
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CAS No:
84680-54-6
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Formula:
C18H24N2O5.2H2O
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Chemical Name:
N-[(1S)-1-Carboxy-3-phenylpropyl]-L-alanyl-L-proline hydrate (1:2)
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Synonyms:
L-Proline,N-[(1S)-1-carboxy-3-phenylpropyl]-L-alanyl-,hydrate (1:2);L-Proline,1-[N-(1-carboxy-3-phenylpropyl)-L-alanyl]-,dihydrate,(S)-;L-Proline,N-[(1S)-1-carboxy-3-phenylpropyl]-L-alanyl-,dihydrate;N-[(1S)-1-Carboxy-3-phenylpropyl]-L-alanyl-L-proline hydrate (1:2)
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CAS No:
Description
Enalaprilat is an angiotensin-converting enzyme (ACE) inhibitor with IC50 of 1.94 nM.Target: ACEEnalaprilat has high affinity for human endothelial ACE with IC50 of 1.94 nM in vitro binding assay by displacing a saturating concentration of [125I]351A, a radiolabeled lisinopril analogue from ACE binding sites, and shows bradykinin/angiotensin I selectivity ratio of 1.00 calculated from double displacement experiments [1]. Enalaprilat attenuates the IGF-I induced neonatal rat cardiac fibro
N-[(1S)-1-Carboxy-3-phenylpropyl]-L-alanyl-L-proline hydrate (1:2) Basic Attributes
384.42
384.189636
278-459-3
2933995300
Characteristics
109
1.32630
151-159°C
601°C at 760 mmHg
294.6ºC
1.579
H2O: soluble 14mg/mL at 60°C (warming for 5 minutes)
-20°C Freezer
Safety Information
NONH for all modes of transport
3
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . R36/37/38:Irritating to eyes, respiratory system and skin .
S22-S26-S36/37/39
TW3590600
Xi
P201, P202, P261, P264, P271, P280, P281, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
H315
N-[(1S)-1-Carboxy-3-phenylpropyl]-L-alanyl-L-proline hydrate (1:2) Use and Manufacturing
Active metabolite of Enalapril. A nonsulfhydryl dipeptide angiotensin converting enzyme (ACE) inhibitor.
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N-[(1S)-1-Carboxy-3-phenylpropyl]-L-alanyl-L-proline hydrate (1:2)
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