ChemicalBook--->CAS DataBase List--->100938-10-1

100938-10-1

100938-10-1 Structure

100938-10-1 Structure
IdentificationBack Directory
[Name]

AMASTATIN HYDROCHLORIDE
[CAS]

100938-10-1
[Synonyms]

AMASTATIN
AMASTATIN HCL
AMASTATIN HYDROCHLORIDE
AMASTATIN HYDROCHLORIDE HYDRATE
H-(2S,3R)-AHMH-VAL-VAL-ASP-OH HCL
Amastatin hydrate hydrochloride
4-formylphenyl-O-β-d-allopyranoside
N((2S 3R)3-AMINO-2-HXY-5-ME.HEXANOYL)-L&
Amastatinhydrochloridebiochemikasynthetic
(2S,3R)-[3-AMINO-2-HYDROXY-5-METHYLHEXANOYL]-VAL-VAL-ASP-OH HCL
[(2S,3R)-3-AMINO-2-HYDROXY-5-METHYLHEXANOYL]-VAL-VAL-ASP HYDROCHLORIDE
(2s,3r)-3-amino-2-hydroxy-5-methylhexanoyl-val-val-asp hydrochloride hydrate
(2S,3R)-3-Amino-2-hydroxy-5-methylhexanoyl-Val-Val-Asp hydrate hydrochloride
(Amino-2-hydroxy-5-methyl-hexanoyl)-L-valyl-L-valyl-L-aspartic acid hydrochloride salt
L-Aspartic acid,N-[(2S,3R)-3-amino-2-hydroxy-5-methyl-1-oxohexyl]-L-valyl-L-valyl-,monohydrochloride (9CI)
[EINECS(EC#)]

999-999-2
[Molecular Formula]

C21H39ClN4O8
[MDL Number]

MFCD00058071
[MOL File]

100938-10-1.mol
[Molecular Weight]

511.01
Chemical PropertiesBack Directory
[Melting point ]

202-205 °C
[storage temp. ]

-20°C
[solubility ]

methanol: 5 mg/mL, clear, colorless
[form ]

White to off-white powder.
[color ]

White to off-white
[biological source]

synthetic (organic)
[BRN ]

8888370
Safety DataBack Directory
[WGK Germany ]

3
[F ]

10
[HS Code ]

2924190090
Hazard InformationBack Directory
[Uses]

Amastatin is a slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of human serum AP-A (glutamyl AP; IC50 = 0.54 μg/ml) but not of AP-B (arginine AP). It also inhibits AP-N (AP-M, alanyl AP; Ki = 20-200 nM), leucyl-cystinyl AP (Ki = 20-220 nM), and endoplasmic reticulum AP 1 (Ki = 41.8 μM). Amastatin is without effect on trypsin, papain, chymotrypsin, elastase, pepsin, or thermolysin.[Cayman Chemical]
[General Description]

Chemical structure: peptide
[Biochem/physiol Actions]

It inhibits cytosolic leucine aminopeptidase (EC.3.4.11.1), microsomal aminopeptidase M (EC.3.4.11.2) and bacterial leucine aminopeptidase (EC.3.4.11.10). It is less effective against aminopeptidase A (EC 3.4.11.7), the enzyme that converts angiotensin II to angiotensin III. Potentiates the CNS effects of vasopressin and oxytocin in vivo.Effective concentration: 1-10 μM.
[storage]

Store at -20°C
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