A1501
N-Acetyl-D-methionine
~99%, suitable for ligand binding assays
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关于此项目
经验公式（希尔记法）:
C7H13NO3S
化学文摘社编号:
分子量:
191.25
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
216-144-4
MDL number:
Beilstein/REAXYS Number:
1725553
产品名称
N-Acetyl-D-methionine, ~99%
InChI key
XUYPXLNMDZIRQH-ZCFIWIBFSA-N
InChI
1S/C7H13NO3S/c1-5(9)8-6(7(10)11)3-4-12-2/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)/t6-/m1/s1
SMILES string
CSCC[C@@H](NC(C)=O)C(O)=O
assay
~99%
form
powder or crystals
technique(s)
ligand binding assay: suitable
color
white
mp
102.3-103.6 °C
storage temp.
−20°C
Quality Level
Application
N-Acetyl-D-methionine may be used as a substrate to identify, differentiate and characterized N-acylamino acid racemase(s) and N-acyl-D-amino acid amidohydrolase(s).
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Wen-Ching Wang et al.
Journal of molecular biology, 342(1), 155-169 (2004-08-18)
N-acylamino acid racemase (NAAAR) catalyzes the racemization of N-acylamino acids and can be used in concert with an aminoacylase to produce enantiopure alpha-amino acids, a process that has potential industrial applications. Here we have cloned and characterized an NAAAR homologue
Pei-Hsun Lin et al.
European journal of biochemistry, 269(19), 4868-4878 (2002-10-02)
An N-acyl-d-amino acid amidohydrolase (N-D-AAase) was identified in cell extracts of a strain, Iso1, isolated from an environment containing N-acetyl-d-methionine. The bacterium was classified as Variovorax paradoxus by phylogenetic analysis. The gene was cloned and sequenced. The gene consisted of
N-acetylmethionine and biotin as photocleavable protective groups for ruthenium polypyridyl complexes.
Roosmarijn E Goldbach et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(36), 9924-9929 (2011-07-29)
D R Sheff et al.
The Journal of biological chemistry, 264(19), 11491-11496 (1989-07-05)
Genes for the various isoactins define two classes of actin. Class I actin genes code for Met-Asp(Glu)-actin, and class II actin genes code for Met-X-Asp(Glu)-actin where X is usually cysteine. Amino termini of both are removed in an acetylation-dependent processing
M Mályusz et al.
Renal physiology and biochemistry, 17(6), 307-315 (1994-11-01)
Hippurate is known to be synthesized from benzoate and glycine in the liver and kidney. It takes part in renal ammoniagenesis by modulating the activity of gamma-glutamyl transpeptidase (gamma GT). Due to its chemical structure, however, hippurate might also serve
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