7 results for "ADAM Inhibitors" in Products

ADAM Inhibitors

ADAMs (a disintegrin and metalloproteases) are a family of transmembrane metalloproteinases that function as proteases and/or adhesion molecules. They are members of the M12B adamalysin protease subfamily, which also includes reprolysins and ADAMTs. There have been 25 human ADAM genes identified to date, 21 of them are functional, and 13 have proteolytic activity. The ADAMs with proteolytic activity are ADAMDEC-1, ADAM-8, 9, 10, 12, 15, 17, 19, 20, 21, 28, 30 and 33, while ADAM-2, 7, 11, 18, ...

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Selective ADAM10 metalloprotease inhibitor

Chemical Name: (2R)-N-[(1S)-2,2-Dimethyl-1-[(methylamino)carbonyl]propyl]-2-[(1S)-1-(N-hydroxyformamido)ethyl]-5-phenylpentanamide
Purity: ≥98%
Selective ADAM10 metalloprotease inhibitor
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Potent ADAM10 and ADAM17 inhibitor

Chemical Name: Phenylmethyl N-[(5S)-5-[[(2R,3S)-3-(formylhydroxyamino)-2-(2-methylpropyl)-1-oxohexyl]amino]-6-oxo-6-(2-thiazolylamino)hexyl]carbamate
Purity: ≥98%
Potent ADAM10 and ADAM17 inhibitor
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ADAM-17 (TACE) and MMP inhibitor

Alternate Names: TNF-α processing inhibitor-0
Chemical Name: N-[(2R)-2-[2-(Hydroxyamino)-2-oxoethyl]-4-methyl-1-oxopentyl]-3-(2-naphthalenyl)-L-alanyl-L-alaninamide
Purity: ≥95%
ADAM-17 (TACE) and MMP inhibitor
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Adam 17 (TACE) and MMP inhibitor; orally bioavailable

Chemical Name: (3S)-4-[[4-(2-Butyn-1-yloxy)phenyl]sulfonyl]-N-hydroxy-2,2-dimethyl-3-thiomorpholinecarboxamide
Purity: ≥98%
Adam 17 (TACE) and MMP inhibitor; orally bioavailable
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ADAM-17 (TACE) and MMP inhibitor

Chemical Name: N-[(2R)-2-[2-(Hydroxyamino)-2-oxoethyl]-4-methyl-1-oxopentyl]-3-methyl-L-valyl-N-(2-aminoethyl)-L-alaninamide
Purity: ≥95%
ADAM-17 (TACE) and MMP inhibitor
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ADAM-17 (TACE) and MMP inhibitor

Chemical Name: N-[(2R)-2-[2-(Hydroxyamino)-2-oxoethyl]-4-methyl-1-oxopentyl]-3-(2-naphthalenyl)-L-alanyl-N-(2-aminoethyl)-L-alaninamide
Purity: ≥95%
ADAM-17 (TACE) and MMP inhibitor
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Potent ADAMTS7 and ADAMTS12 inhibitor

Chemical Name: 5,6-Difluoro-N-[[(4S)-4-(1-methyl-1H-pyrazol-5-yl)-2,5-dioxo-4-imidazolidinyl]methyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamide
Purity: ≥98%
Potent ADAMTS7 and ADAMTS12 inhibitor
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