ChemicalBook--->CAS DataBase List--->67655-94-1

67655-94-1

67655-94-1 Structure

67655-94-1 Structure
IdentificationBack Directory
[Name]

AMASTATIN
[CAS]

67655-94-1
[Synonyms]

AMASTATIN
Aids059868
Aids-059868
s*))-(s-(r*
AMASTATIN, STREPTOMYCES SPECIES
[(2S,3R)-3-Amino-2-hydroxy-5-methylhexanoyl]-Val-val-Asp
(2S,3R)-3-AMINO-2-HYDROXY-5-METHYLHEXANOYL-VAL-VAL-ASP-OH
(AMINO-2-HYDROXY-5-METHYL-HEXANOYL)-L-VALYL-L-VALYL-L-ASPARTIC ACID
N-[(2S,3R)-3-Amino-2-hydroxy-5-methylhexanoyl]-L-Val-L-Val-L-Asp-OH
[(2S,3R)-3-AMINO-2-HYDROXY-5-METHYLHEXANOYL]-L-VALYL-L-VALYL-L-ASPARTIC ACID
l-asparticacid,n-(n-(3-amino-2-hydroxy-5-methyl-1-oxohexyl)-l-valyl)-l-valyl)
N-[(2S,3R)-3-AMINO-2-HYDROXY-5-METHYLHEXANOYL]-L-VALYL-L-VALYL-L-ASPARTIC ACID
N-[(2S,3R)-3-Amino-2-hydroxy-5-methyl-1-oxohexyl]-L-valyl-L-valyl-L-aspartic acid
L-Aspartic acid, N-[(2S,3R)-3-amino-2-hydroxy-5-methyl-1-oxohexyl]-L-valyl-L-valyl-
N-[N-[N-[(2S,3R)-3-Amino-2-hydroxy-5-methyl-1-oxohexyl]-L-valyl]-L-valyl]-L-aspartic acid
S-(R*,S*)]-N-[N-[N-(3-Amino-2-hydroxy-5-methyl-1-oxohexyl)-L-valyl]-L-valyl]-L-aspartic acid
[Molecular Formula]

C21H38N4O8
[MDL Number]

MFCD00038400
[MOL File]

67655-94-1.mol
[Molecular Weight]

474.55
Chemical PropertiesBack Directory
[Boiling point ]

795℃
[density ]

1.228
[Fp ]

435℃
[form ]

powder
[color ]

White
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[HS Code ]

29241900
Hazard InformationBack Directory
[Uses]

Amastatin is A slow, tightly bound, competitive inhibitor of aminopeptidase (AP) with an IC50 of 0.54 μg/mL for AP-A[1][2].
[Definition]

ChEBI: A tetrapeptide comprising (2S,3R)-3-amino-2-hydroxy-5-methylhexanoyl, L-valyl, L-valyl and L-aspartic acid units joined in sequence
[References]

[1] Aoyagi T, et al. Amastatin, an inhibitor of aminopeptidase A, produced by actinomycetes. J Antibiot (Tokyo). 1978 Jun;31(6):636-8. DOI:10.7164/antibiotics.31.636
[2] Wilkes SH, et al. The slow, tight binding of bestatin and amastatin to aminopeptidases. J Biol Chem. 1985 Oct 25;260(24):13154-62. PMID:2865258
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