R&D Systems Inc. Tocris Bioscience Boston Biochem

JMV 390-1

Cat. No. 2575

JMV 390-1 N-[(2R)-4-Hydroxyamino)-1,4-dioxo-2-(phenylmethyl)butyl]-Ile-Leu

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Chemical Name: N-[(2R)-4-Hydroxyamino)-1,4-dioxo-2­-(phenylmethyl)butyl]-L-isoleucyl-L-leucine

Biological Activity

Inhibitor of the major neurotensin and neuromedin N degrading enzymes (IC50 values are 31, 40, 52 and 58 for endopeptidase 24.15, endopeptidase 24.11, leucine aminopeptidase and endopeptidase 24.16 respectively). Exhibits analgesic effects in various nociception assays.

Technical Data

M.Wt:
449.54
Formula:
C23H35N3O6
Sequence:
XIL (Modifications: X-1 = N-[(2R)-4-Hydroxyamino)-1,4-di­oxo-2-(phenylmethyl)butyl])
Solubility:
Soluble to 0.80 mg/ml in sodium bicarbonate (0.01M)
Storage:
Store at -20°C
CAS No:
148473-36-3

The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.

Certificate of Analysis / Safety Data Sheet

Certificate of Analysis: View current batch
Safety Data Sheet: View Safety Data Sheet

References

Kitabgi et al (1992) Effects of thiorphan, bestatin and a novel metallopeptidase inhibitor JMV 390-1 on the recovery of neurotensin and neuromedin N released from mouse hypothalamus. Neurosci.Lett. 142 200. PMID: 1454216.

Doulut et al (1993) Synthesis and analgesic effects of N-[3-[(hydroxyamino) carbonyl]-1-oxo-2(R)-benzylpropyl]-L-isoleucyl-L-leucine, a new potent inhibitor of multiple neurotensin/neuromedin N degrading enzymes. J.Med.Chem. 36 1369. PMID: 8496905.

Menard et al (1996) The cytotoxic activity of Bacillus anthracis lethal factor is inhibited by leukotriene A4 hydrolase and metallopeptidase inhibitors. Biochem.J. 320 687. PMID: 8973585.

If you know of a relevant citation for this product please let us know.

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Keywords: JMV 390-1, supplier, JMV390-1, endopeptidases, 24.15, 24.11, 24.16, inhibitors, neurotensin, neuromedin, n, analgesics

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