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Merck
CN

M3504

Sigma-Aldrich

L-Methioninamide hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C5H12N2OS · HCl
CAS Number:
Molecular Weight:
184.69
MDL number:
UNSPSC Code:
12352200
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SMILES string

Cl.CSCC[C@H](N)C(N)=O

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W L Starnes et al.
European journal of biochemistry, 124(2), 363-370 (1982-05-17)
Human liver alanine aminopeptidase (EC 3.4.11.14; L-alpha-aminoacyl-peptide hydrolase) catalyzes the stepwise hydrolysis of methionyl-lysyl-bradykinin to yield methionine, lysine, and the limit nonapeptide, bradykinin which is resistant to further hydrolytic cleavage by this enzyme. Alanine aminopeptidase also catalyzes the hydrolysis of
M M Jones et al.
Anticancer research, 11(1), 449-453 (1991-01-01)
Six compounds containing a thioether group were examined as agents for the reduction of the nephrotoxicity caused by cisplatin (CDDP) in the rat. Of these, five were able to reduce the CDDP- induced nephrotoxicity when administered simultaneously with CDDP (8.0
András Láng et al.
Proteins, 58(3), 571-588 (2004-12-24)
The conformational space of the most biologically significant backbone folds of a suitable methionine peptide model was explored by density functional computational method. Using a medium [6-31G(d)] and a larger basis set [6-311++G(2d,2p)], the systematic exploration of low-energy backbone structures

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