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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Urokinase-type plasminogen activator | ||
| Ligand | BDBM50103200 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_1461148 (CHEMBL3395473) | ||
| Ki | >14060±n/a nM | ||
| Citation |  Corte, JR; Fang, T; Hangeland, JJ; Friends, TJ; Rendina, AR; Luettgen, JM; Bozarth, JM; Barbera, FA; Rossi, KA; Wei, A; Ramamurthy, V; Morin, PE; Seiffert, DA; Wexler, RR; Quan, ML Pyridine and pyridinone-based factor XIa inhibitors. Bioorg Med Chem Lett25:925-30 (2015) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Urokinase-type plasminogen activator | |||
| Name: | Urokinase-type plasminogen activator | ||
| Synonyms: | 3.4.21.73 | PLAU | U-plasminogen activator | UROK_HUMAN | Urokinase | Urokinase-type plasminogen activator (uPA) | Urokinase-type plasminogen activator chain B | Urokinase-type plasminogen activator long chain A | Urokinase-type plasminogen activator short chain A | Urokinase-type plasminogen activator/surface receptor | uPA | ||
| Type: | Enzyme | ||
| Mol. Mass.: | 48528.62 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | P00749 | ||
| Residue: | 431 | ||
| Sequence: |
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| BDBM50103200 | |||
| n/a | |||
| Name | BDBM50103200 | ||
| Synonyms: | CHEMBL3393386 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C28H32N6O | ||
| Mol. Mass. | 468.5933 | ||
| SMILES | NC[C@H]1CC[C@@H](CC1)C(=O)N[C@@H](Cc1ccccc1)c1cc(ccn1)-c1ccc2c(N)n[nH]c2c1 |r,wU:2.1,wD:5.8,11.12,(2.94,9.71,;2.94,8.48,;1.61,7.7,;1.62,6.16,;.29,5.39,;-1.05,6.16,;-1.05,7.7,;.28,8.47,;-2.38,5.38,;-2.38,4.15,;-3.72,6.15,;-5.05,5.38,;-6.39,6.15,;-7.72,5.38,;-9.06,6.15,;-10.39,5.37,;-10.39,3.83,;-9.05,3.07,;-7.72,3.84,;-5.05,3.84,;-3.72,3.07,;-3.71,1.53,;-5.05,.76,;-6.38,1.53,;-6.38,3.07,;-2.38,.77,;-2.38,-.77,;-1.03,-1.55,;.3,-.77,;1.76,-1.24,;2.15,-2.41,;2.66,.02,;1.76,1.24,;.3,.77,;-1.03,1.55,)| | ||
| Structure | 
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