M3504
L-Methioninamide hydrochloride
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About This Item
Empirical Formula (Hill Notation):
C5H12N2OS · HCl
CAS Number:
Molecular Weight:
184.69
UNSPSC Code:
12352200
MDL number:
SMILES string
Cl.CSCC[C@H](N)C(N)=O
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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
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
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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