Reaction Details |
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Target | Urokinase-type plasminogen activator |
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Ligand | BDBM50358883 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_790764 (CHEMBL1926217) |
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Ki | 15100±n/a nM |
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Citation | Shi, Y; O'Connor, SP; Sitkoff, D; Zhang, J; Shi, M; Bisaha, SN; Wang, Y; Li, C; Ruan, Z; Lawrence, RM; Klei, HE; Kish, K; Liu, EC; Seiler, SM; Schweizer, L; Steinbacher, TE; Schumacher, WA; Robl, JA; Macor, JE; Atwal, KS; Stein, PD Arylsulfonamidopiperidone derivatives as a novel class of factor Xa inhibitors. Bioorg Med Chem Lett21:7516-21 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Urokinase-type plasminogen activator |
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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: | MRALLARLLLCVLVVSDSKGSNELHQVPSNCDCLNGGTCVSNKYFSNIHWCNCPKKFGGQ
HCEIDKSKTCYEGNGHFYRGKASTDTMGRPCLPWNSATVLQQTYHAHRSDALQLGLGKHN
YCRNPDNRRRPWCYVQVGLKLLVQECMVHDCADGKKPSSPPEELKFQCGQKTLRPRFKII
GGEFTTIENQPWFAAIYRRHRGGSVTYVCGGSLISPCWVISATHCFIDYPKKEDYIVYLG
RSRLNSNTQGEMKFEVENLILHKDYSADTLAHHNDIALLKIRSKEGRCAQPSRTIQTICL
PSMYNDPQFGTSCEITGFGKENSTDYLYPEQLKMTVVKLISHRECQQPHYYGSEVTTKML
CAADPQWKTDSCQGDSGGPLVCSLQGRMTLTGIVSWGRGCALKDKPGVYTRVSHFLPWIR
SHTKEENGLAL
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BDBM50358883 |
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n/a |
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Name | BDBM50358883 |
Synonyms: | CHEMBL1923468 |
Type | Small organic molecule |
Emp. Form. | C28H29ClN4O5S |
Mol. Mass. | 569.072 |
SMILES | Clc1ccc2cc(ccc2c1)S(=O)(=O)N[C@H]1CCCN(CC(=O)N2C[C@@H]3C[C@H](C2)c2cccc(=O)n2C3)C1=O |r| |
Structure |
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