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Article title matches
- Category:Potent antiviral inhibitor grl-02031 (67 bytes)
1: List of pages with the keyword Potent antiviral inhibitor grl-02031 - Category:Potent antiviral inhibitor grl-0519a (67 bytes)
1: List of pages with the keyword Potent antiviral inhibitor grl-0519a - Category:Potent inhibitor (47 bytes)
1: List of pages with the keyword Potent inhibitor - Category:Potent antitumor effect (54 bytes)
1: List of pages with the keyword Potent antitumor effect - Category:Potent (37 bytes)
1: List of pages with the keyword Potent - Category:Potent selective phosphinic inhibitor (68 bytes)
1: List of pages with the keyword Potent selective phosphinic inhibitor - Category:Syk catalytic domain in complex with a potent triazolopyridine based inhibitor (109 bytes)
1: ...he keyword Syk catalytic domain in complex with a potent triazolopyridine based inhibitor - Category:Potent selective (47 bytes)
1: List of pages with the keyword Potent selective
Page text matches
- Acetylcholinesterase (8,905 bytes)
3: ...rus (OP) poisons is attributed primarily to their potent AChE inhibitors.
24: ....wikipedia.org/wiki/Nerve_agent nerve agents] are potent inhibitors which rapidly phosphonylate AChE and t... - Sandbox Tst (3,047 bytes)
11: ...rve agents is attributed primarily to their being potent AChE inhibitors.
14: ....wikipedia.org/wiki/Nerve_agent nerve agents] are potent inhibitors which rapidly phosphonylate AChE and t...
18: ...ene> are within hydrogen-bonding distance of four potential donors from catalytic subsites of the enzyme, ... - NADH quinone oxidoreductase (NQO1) with inhibitor dicoumarol (8,927 bytes)
2: ...quinone oxidoreductase (NQO1) in complex with its potent inhibitor dicoumarol ==
7: ...igure3 copy.jpg|border|center|300px]] is the most potent competitive inhibitor of NQO1. Dicoumarol compete... - 117e (5,307 bytes)
24: ...is positioned where Wat1 is in the wild-type: the potent Wat1 nucleophile is replaced by a carboxylate co-... - 1zzz (4,899 bytes)
24: The crystal structures of three highly potent and selective low-molecular weight rigid peptidyl... - Sandbox 781 (8,140 bytes)
9: ...ive classes of natural nucleoside inhibitors with potent antibacterial activity: the liposidomycins/capraz... - 2boh (5,419 bytes)
26: ...dole nucleus led to the discovery of a remarkably potent factor Xa inhibitor displaying a K(i) value of 0.... - 2cn0 (7,541 bytes)
26: ...espectively. All newly prepared inhibitors showed potent biological activity, with inhibitory constants (K... - 2cni (5,849 bytes)
24: ...ctural insights that have led to the discovery of potent benzimidazole aryl sulfonamide o-substituted deri... - 2cnh (5,858 bytes)
24: ...ctural insights that have led to the discovery of potent benzimidazole aryl sulfonamide o-substituted deri... - 2cng (5,901 bytes)
24: ...ctural insights that have led to the discovery of potent benzimidazole aryl sulfonamide o-substituted deri... - 2cne (5,882 bytes)
24: ...ctural insights that have led to the discovery of potent benzimidazole aryl sulfonamide o-substituted deri... - 2cnf (5,828 bytes)
24: ...ctural insights that have led to the discovery of potent benzimidazole aryl sulfonamide o-substituted deri... - 1gkc (6,218 bytes)
26: ...present structure enables us to aid the design of potent and specific inhibitors for this important cardio... - 1gkd (6,279 bytes)
26: ...present structure enables us to aid the design of potent and specific inhibitors for this important cardio... - 1rbo (4,633 bytes)
24: ...be isolated. Analogues of these intermediates are potent inhibitors of the enzyme. We have studied the int... - 9big (3,481 bytes)
14: ...blon ligands, we discovered AK-1690 as the first, potent and selective PROTAC STAT6 degrader. AK-1690 effe...
16: Discovery of AK-1690: A Potent and Highly Selective STAT6 PROTAC Degrader.,Kanes... - 9bik (4,099 bytes)
16: Discovery of GNE-6893, a Potent, Selective, Orally Bioavailable Small Molecule In... - 1vdf (4,605 bytes)
11: ...lay a role in the pathogenesis of osteoarthritis. Potent suppressor of apoptosis in both primary chondrocy... - 1h7r (4,687 bytes)
24: ...he hereditary disease type I tyrosinaemia and its potent inhibition of ALAD also has implications for the ...
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