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Results 1 - 10 of 55 > >>
EC Number
Inhibitors
Commentary
Structure
(E)-N'-(4-butyl-2-methylphenyl)-N-hydroxyformimidamide
HET0016, almost completely abolishes hypotonic solutions- or 2,4,6-trinitrophenol-induced enhancement of receptor-activated cationic current I(TRPC6)
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(E)-N'-(4-butyl-2-methylphenyl)-N-hydroxyformimidamide
HET0016, diminishes TRPC6-like channel activity in myocytes
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1,1-dichloroethene
50% of BMO activity is irreversibly lost after oxidation of approximately 25 nmol/mg protein
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1,2-cis-dichloroethene
50% of BMO activity is lost after oxidation of 120 nmol/mg protein
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1,2-trans-dichloroethene
50% of BMO activity is lost after oxidation of 20 nmol/mg protein
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1,7-octadiyne
inhibits oxidation of methyl tert-butyl ether; putative mechanism-based inactivator, strongly inhibitory at 0.1% (v/v)
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1-octyne
acts as a mechanism-based inhibitor of AlkB
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1-octyne
irreversible inhibition, oxidation product hexylketene or its equivalent, covalently binds to AlkB
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11-dodecynoic acid
completely inhibited lauric acid omega-hydroxylation
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17-octadecynoic acid
almost completely abolishes hypotonic solutions- or 2,4,6-trinitrophenol-induced enhancement of receptor-activated cationic current I(TRPC6)
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Results 1 - 10 of 55 > >>