PDB ID: 1MU8
Hetero Atom Contents
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| Code | Name | Style | Show | Link | |
|---|---|---|---|---|---|
| CDB | 2-(6-chloro-3-{[2,2-difluoro-2-(2-pyridinyl)ethyl]amino}-2-oxo-1(2h)-pyrazinyl)-N-[(2-fluoro-3-methyl-6-pyridinyl)methyl]acetamide | PoSSuM |
| Code | Name | Show |
|---|---|---|
| TYS | O-sulfo-L-tyrosine |
| Code | Name | Emphasize |
|---|
| Code | Name | Show |
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Download interaction data: 1MU8
Structure summary
| Code : | 1MU8 PDBj RCSB PDB PDBe | ||||||||||||||||||||||||||||||||||||
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| Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||||||||||||||||||||||||||
| Title : | thrombin-hirugen_l-378,650 | ||||||||||||||||||||||||||||||||||||
| Release Data : | 2004-04-06 | ||||||||||||||||||||||||||||||||||||
| Compound : |
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| Source : |
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| Authors : | Burgey, C.S., Robinson, K.A., Lyle, T.A., Sanderson, P.E., Lewis, S.D., Lucas, B.J., Krueger, J.A., Singh, R., Miller-Stein, C., White, R.B., Wong, B., Lyle, E.A., Williams, P.D., Coburn, C.A., Dorsey, B.D., Barrow, J.C., Stranieri, M.T., Holahan, M.A., Sitko, G.R., Cook, J.J., McMasters, D.R., McDonough, C.M., Sanders, W.M., Wallace, A.A., Clayton, F.C., Bohn, D., Leonard, Y.M., Detwiler Jr., T.J., Lynch Jr., J.J., Yan, Y., Chen, Z., Kuo, L., Gardell, S.J., Shafer, J.A., Vacca, J.P.J. | ||||||||||||||||||||||||||||||||||||
| Keywords : | thrombin-hirugen, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX | ||||||||||||||||||||||||||||||||||||
| Exp. method : | X-RAY DIFFRACTION ( 2.0 Å ) | ||||||||||||||||||||||||||||||||||||
| Citation : |
Metabolism-directed optimization of 3-aminopyrazinone acetamide thrombin inhibitors. Development of an orally bioavailable series containing P1 and P3 pyridines.
Burgey, C.S.,Robinson, K.A.,Lyle, T.A.
et al.
PubMed: 12570369 |
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Reaction
| Chain : | B | ||||||||
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| UniProt : | P00734 (THRB_HUMAN) | ||||||||
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| Chain : | C |
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| UniProt : | P28506 (HIR2B_HIRME) |
| Reaction : | - |


