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...Chemogenomics]]{{·}} [[Drug design]]{{·}} [[Drug discovery]]{{·}} [[Enzyme inhibitor]]{{·}} [[Ligand efficiency]]{{·}} [[Mechanism of action]]{{·}} [[New che

* ''Steroid [[enzyme inhibitor|synthesis inhibitor]]s:'' [[Danazol]]

| group3 = [[Enzyme]]<br /><small>([[enzyme inhibitor|inhibitor]]s)</small>

| group2 = [[Enzyme inhibitor]]s | group1 = [[5-alpha-reductase inhibitor|5α-Reductase]]

| group1 = [[Spindle poison|SP]]s/[[mitotic inhibitor|MI]]s<BR>([[M phase]]) | group2 = [[DNA replication]]<BR>inhibitor

| group1 = [[Spindle poison|SP]]s/[[mitotic inhibitor|MI]]s<br />([[M phase]]) | group2 = [[DNA replication]]<br />inhibitor

| group2 = [[Reuptake inhibitor|Reuptake<br>inhibitor]]s | group3 = [[Enzyme inhibitor|Enzyme<br>inhibitor]]s

| group2 = [[Reuptake inhibitor]]s | group3 = [[Enzyme inhibitor]]s

* [[Enzyme inhibitor|Enzyme inhibition]]

...n tienilic acid being covalently linked to the enzyme, thus inhibiting the enzyme irreversibly. ...known (could be multiple). However tienilic acid is a good mechanism based inhibitor of CYP2C9 and seems to inactivate it stoichiometrically. Progress in proteo

...tonin antagonist and reuptake inhibitor|Serotonin Antagonists and Reuptake Inhibitor]]s ([[Trazodone]], [[Nefazodone]]){{•}} [[Typical antipsychotic|Typical A | group2 = [[Reuptake_inhibitor|Reuptake<br>Inhibitor]]s

...<ref name="entrez">{{cite web | title = Entrez Gene: IDE insulin-degrading enzyme| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView& ...تيد]]ات تستطيع الارتباط بجزيئات ال[[زنك]] مما نتج عنه مركب جديد يسمى ( IDE inhibitor 1 ) يمنع نشاط إنزيم خفض فاعلية االأنسولين .

| group10 = [[Prolyl endopeptidase]] [[enzyme inhibition|inhibitors]] * [[C16 (PKR inhibitor)|C16]]

| group2 = [[Dopamine reuptake inhibitor|Reuptake inhibitors]] | group5 = [[Enzyme inhibitor]]s

| class1 = [[Dihydrofolate reductase]] [[enzyme inhibitor|inhibitor]] (16.7%)

| group2 = [[Reuptake_inhibitor|Reuptake<br>Inhibitor]]s | group3 = [[Enzyme_inhibitor|Enzyme<br>Inhibitor]]s

...7118): a highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes ...i = 10.1021/op900226j | title = Preparation of Saxagliptin, a Novel DPP-IV Inhibitor | year = 2009 | pages = 091016152805096 | author8 = Scott A. Savage, Gregor

{{enzyme ...Crystal structure of the Homo sapiens kynureninase-3-hydroxyhippuric acid inhibitor complex: insights into the molecular basis of kynureninase substrate specif

| Mechanism_of_action = [[Enzyme inhibitor]]

...alc: A development of a database analysis that provides putative metabolic enzyme reactions for ligand-based drug design | journal = Computational Biology an * [[Enzyme inhibitor]]s