Reaction Details |
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Target | Trypsin-3 |
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Ligand | BDBM50387180 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_827953 (CHEMBL2051532) |
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Ki | 168000±n/a nM |
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Citation | Karle, M; Knecht, W; Xue, Y Discovery of benzothiazole guanidines as novel inhibitors of thrombin and trypsin IV. Bioorg Med Chem Lett22:4839-43 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Trypsin-3 |
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Name: | Trypsin-3 |
Synonyms: | Brain trypsinogen | Mesotrypsinogen | PRSS3 | PRSS4 | Serine protease 3 | Serine protease 4 | TRY3 | TRY3_HUMAN | TRY4 | Thrombin & trypsin | Trypsin | Trypsin III | Trypsin IV | Trypsin-3 |
Type: | PROTEIN |
Mol. Mass.: | 32532.52 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_216043 |
Residue: | 304 |
Sequence: | MCGPDDRCPARWPGPGRAVKCGKGLAAARPGRVERGGAQRGGAGLELHPLLGGRTWRAAR
DADGCEALGTVAVPFDDDDKIVGGYTCEENSLPYQVSLNSGSHFCGGSLISEQWVVSAAH
CYKTRIQVRLGEHNIKVLEGNEQFINAAKIIRHPKYNRDTLDNDIMLIKLSSPAVINARV
STISLPTTPPAAGTECLISGWGNTLSFGADYPDELKCLDAPVLTQAECKASYPGKITNSM
FCVGFLEGGKDSCQRDSGGPVVCNGQLQGVVSWGHGCAWKNRPGVYTKVYNYVDWIKDTI
AANS
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BDBM50387180 |
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n/a |
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Name | BDBM50387180 |
Synonyms: | CHEMBL2047998 |
Type | Small organic molecule |
Emp. Form. | C12H14N4O3S |
Mol. Mass. | 294.33 |
SMILES | CCOC(=O)Cn1c2ccc(O)cc2s\c1=N\C(N)=N |
Structure |
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