EC Number   |
Inhibitors |
Structure |
|---|
    2.7.7.23 | (2S,4R)-N-(4-((6,7-dimethoxyquinazolin-4-yl)amino)phenyl)-4-hydroxypyrrolidine-2-carboxamide |
- |
   |
| 2.7.7.23 | (3-hydroxyphenyl)[4-(5,6,7,8-tetrahydroquinazolin-4-ylamino)phenyl]methanone |
30% inhibition at 0.05 mM |
|
| 2.7.7.23 | (4-(6,7-dimethoxyquinazolin-4-yl)piperazin-1-yl)(phenyl)-methanone |
- |
|
| 2.7.7.23 | (S)-N-(4-((6,7-dimethoxyquinazolin-4-yl)amino)phenyl)pyrrolidine-2-carboxamide |
- |
|
| 2.7.7.23 | (Z)-4-(4-(benzyloxy)benzylidene)-2-(naphthalen-1-yl)oxazol-5(4H)-one |
i.e. Oxa33, synthesis of a specific GlmU inhibitor, molecular docking study, the inhibitor binds to an allosteric site of the uridyltransferase domain, overview. Oxa33 fails to inhibit cell growth even at concentrations as high as 0.150 mM. Tyr150, Glu250 and Arg 253 are in hydrogen bonding with carbonyl oxygen over the oxazole ring, while Leu144, Pro147, Phe148, Tyr150, Ala233, Ala236 and Leu247 participate in strong hydrophobic interactions with Oxa33 |
|
| 2.7.7.23 | 1-(3-hydroxybenzoyl)-4-(thieno[3,2-d]pyrimidin-4-ylamino)pyridinium |
38% inhibition at 0.05 mM |
|
| 2.7.7.23 | 1-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]dihydropyrimidine-2,4(1H,3H)-dione |
- |
|
| 2.7.7.23 | 1-[2,4-dimethoxy-5-(10H-phenoxazin-10-ylsulfonyl) phenylamino]-2-(-4-pyridyl)-1-ethanone |
commercial inhibitor |
|
| 2.7.7.23 | 2,3-dihydroxy-5-nitrophenyl 2-acetamido-2-deoxy-alpha-D-xylo-hexopyranoside |
forms with UNAcP hydrogen bonds, Pi-cation and hydrophobic interactions |
|
| 2.7.7.23 | 2-(3-((4-((6,7-dimethoxyquinazolin-4-yl)amino)phenyl)carbamoyl)phenoxy)acetic acid |
34% inhibition at 0.05 mM |
|
