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Key Documents

A6508

Sigma-Aldrich

L-Aspartic acid β-hydroxamate

>98%

Synonym(s):

AAH, HDX, LAH

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About This Item

Empirical Formula (Hill Notation):
C4H8N2O4
CAS Number:
Molecular Weight:
148.12
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

Product Name

L-Aspartic acid β-hydroxamate, serine racemase inhibitor

Quality Level

Assay

>98%

form

powder

color

white to yellow

application(s)

detection

storage temp.

−20°C

SMILES string

N[C@@H](CC(=O)NO)C(O)=O

InChI

1S/C4H8N2O4/c5-2(4(8)9)1-3(7)6-10/h2,10H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1

InChI key

ZBYVTTSIVDYQSO-REOHCLBHSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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N Thomasset et al.
International journal of cancer, 49(3), 421-424 (1991-09-30)
D and L isomers of aspartic acid beta-hydroxamate (respectively DAH and LAH) were compared for their in vitro and in vivo activity against the murine leukemia L5178Y and their tolerance in vivo in DBA/2 mice. DAH and LAH displayed comparable
Lidia Mingorance et al.
PLoS pathogens, 14(9), e1007284-e1007284 (2018-09-19)
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Hepatitis C virus (HCV) infection is a major biomedical problem worldwide. Although new direct antiviral agents (DAAs) have been developed for the treatment of chronic HCV infection, the potential emergence of resistant virus variants and the difficulties to implement their

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