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MMP inhibitor
BML-PI115-0005 5 mg 63.00 USD
BML-PI115-0025 25 mg 258.00 USD
Potent inhibitor of human stromelysin-1 (MMP-3), Ki=0.13 µM. Also inhibits MMP-1, MMP-2, MMP-7, MMP-8, MMP-9, MMP-10, MMP-12 (metalloelastase), MMP-13, MMP-14, and MMP-20.

Product Specification

Alternative Name:N-Isobutyl-N-(4-methoxyphenylsulfonyl)glycyl hydroxamic acid
Purity:≥99% (TLC)
Appearance:White solid.
Solubility:Soluble in DMSO (30mg/ml) or 100% ethanol (8mg/ml).
Long Term Storage:Ambient
BML-PI115 v2
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BML-PI115 v2

Product Literature References

Catalytic domain of MMP20 (Enamelysin) - the NMR structure of a new matrix metalloproteinase: Y. Arendt et al.; FEBS Lett. 581, 4723 (2007), Abstract;
A high-affinity carbohydrate-containing inhibitor of matrix metalloproteinases: V. Calderone; Chem. Med. Chem 1, 598 (2006), Abstract;
Crystal structure of the catalytic domain of human matrix metalloproteinase 10: I. Bertini et al.; J. Mol. Biol. 336, 707 (2004), Abstract;
Sulfonamide-based hydroxamic acids as potent inhibitors of mouse macrophage metalloelastase: A. Y. Jeng et al.; Bioorg. Med. Chem. Lett. 8, 897 (1998), Abstract;
Discovery of CGS 27023A, a non-peptidic, potent, and orally active stromelysin inhibitor that blocks cartilage degradation in rabbits: L. J. MacPherson et al.; J. Med. Chem. 40, 2525 (1997), Abstract;
NNGH is a potent inhibitor of MMPs: Unpublished data, BIOMOL Internatinal, LP; (0),

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