A1501

N-Acetyl-D-methionin

Name: N-Acetyl-<SC>D</SC>-methionin
Brand: SIGMA
Price: 462 EUR

~99%, suitable for ligand binding assays

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A1501-5G

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Über diesen Artikel

Empirische Formel (Hill-System):

C₇H₁₃NO₃S

CAS-Nummer:

1509-92-8

Molekulargewicht:

191.25

NACRES:

NA.26

PubChem Substance ID:

24890549

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

216-144-4

MDL number:

MFCD00069962

Beilstein/REAXYS Number:

1725553

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Unterstützung erhalten

Produktname

N-Acetyl-D-methionin, ~99%

assay

~99%

Quality Level

200

form

powder or crystals

technique(s)

ligand binding assay: suitable

color

white

mp

102.3-103.6 °C

storage temp.

−20°C

SMILES string

CSCC[C@@H](NC(C)=O)C(O)=O

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

InChI key

XUYPXLNMDZIRQH-ZCFIWIBFSA-N

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Dieser Artikel	A6376	P1380	A0876
Sigma-Aldrich A1501 N-Acetyl-D-methionine	Sigma-Aldrich A6376 N-Acetyl-L-tryptophan	Sigma-Aldrich P1380 L-Proline β-naphthylamide hydrochloride	Sigma-Aldrich A0876 N-Acetyl-D-leucine
form powder or crystals	form powder	form powder	form powder
technique(s) ligand binding assay: suitable	technique(s) ligand binding assay: suitable	technique(s) ligand binding assay: suitable	technique(s) cell culture \| mammalian: suitable, ligand binding assay: suitable
assay ~99%	assay ≥99% (TLC)	assay ≥99%	assay ≥99% (TLC)
storage temp. −20°C	storage temp. 2-8°C	storage temp. −20°C	storage temp. −20°C
color white	color white to off-white	color white to off-white	color white
mp 102.3-103.6 °C	mp -	mp -	mp -

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).

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Identification and characterization of a new gene from Variovorax paradoxus Iso1 encoding N-acyl-D-amino acid amidohydrolase responsible for D-amino acid production.

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

Structural basis for catalytic racemization and substrate specificity of an N-acylamino acid racemase homologue from Deinococcus radiodurans.

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

A bulky platinum triamine complex that reacts faster with guanosine 5'-monophosphate than with N-acetylmethionine.

Rebecca D Sandlin et al.

Journal of inorganic biochemistry, 104(2), 214-216 (2009-11-13)

A bulky platinum triamine complex, [Pt(Me(5)dien)(NO(3))]NO(3) (Me(5)dien=N,N,N',N',N''-pentamethyldiethylenetriamine) has been prepared and reacted in D(2)O with N-acetylmethionine (N-AcMet) and guanosine 5'-monophosphate (5'-GMP); the reactions have been studied using (1)H NMR spectroscopy. Reaction with 5'-GMP leads to two rotamers of [Pt(Me(5)dien)(5'-GMP-N7)](+). Reaction

Ammonia production from hippurate by the rat kidney in vitro.

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

Identification of N-acetylmethionine as the product released during the NH2-terminal processing of a pseudo-class I actin.

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

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