Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Inhibitors

show results
Don't show organism specific information (fast!)
Search organism in taxonomic tree (slow, choose "exact" as search mode, e.g. "mammalia" for rat,human,monkey,...)
(Not possible to combine with the first option)
Refine your search
Image of 2D Structure
Search for synonyms (with exact matching search term)

Search term:

Results 1 - 4 of 4
download as CSV
download all results as CSV
EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B284-[[4-(2-butynyloxy)phenyl]sulfonyl]-N-hydroxy-2,2-dimethyl-(3S)-thiomorpholinecarboxamide i.e. TMI-1, complete inhibition at 0.01 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B28adamastat sulfonamide inhibitor, binds to the active site of the ADAM15 metalloproteinase domain with a calculated binding energy of -9.0 kcal/mol.In the preferred binding mode, the biphenyl amino side chain of the inhibitor resides in the deep amphipathic S1' amino acid recognition pocket of the ADAM15 catalytic domain. Adamastat significantly inhibits the viability of UM-UC-9 and UM-UC-6 cells at 10 microM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B28GI254023 40% inhibition at 0.1 mM Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.B28more not inhibitory: TIMP1, TIMP3, marimastat, TAPI2 Go to the Ligand Summary Page
Results 1 - 4 of 4
download as CSV
download all results as CSV