Reaction Details |
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Target | Cathepsin K |
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Ligand | BDBM109843 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Enzyme Inhibition Assay |
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Ki | 52±0.0 nM |
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Citation | Schudok, M; Wagner, M; Bauer, A; Kohlmann, A Spirocyclic nitriles as protease inhibitors US Patent US8609681 Publication Date 12/17/2013 |
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More Info.: | Get all data from this article, Assay Method |
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Cathepsin K |
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Name: | Cathepsin K |
Synonyms: | CATK_HUMAN | CTSK | CTSO | CTSO2 | Cathepsin O | Cathepsin O2 | Cathepsin X |
Type: | Enzyme |
Mol. Mass.: | 36975.68 |
Organism: | Homo sapiens (Human) |
Description: | P43235 |
Residue: | 329 |
Sequence: | MWGLKVLLLPVVSFALYPEEILDTHWELWKKTHRKQYNNKVDEISRRLIWEKNLKYISIH
NLEASLGVHTYELAMNHLGDMTSEEVVQKMTGLKVPLSHSRSNDTLYIPEWEGRAPDSVD
YRKKGYVTPVKNQGQCGSCWAFSSVGALEGQLKKKTGKLLNLSPQNLVDCVSENDGCGGG
YMTNAFQYVQKNRGIDSEDAYPYVGQEESCMYNPTGKAAKCRGYREIPEGNEKALKRAVA
RVGPVSVAIDASLTSFQFYSKGVYYDESCNSDNLNHAVLAVGYGIQKGNKHWIIKNSWGE
NWGNKGYILMARNKNNACGIANLASFPKM
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BDBM109843 |
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n/a |
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Name | BDBM109843 |
Synonyms: | US8609681, 49 |
Type | Small organic molecule |
Emp. Form. | C25H31F2N5O3 |
Mol. Mass. | 487.5421 |
SMILES | CC(F)(F)C[C@H](NC(=O)N1CCC2(CCN(Cc3ccccc3)C2=O)CC1)C(=O)NC1(CC1)C#N |r| |
Structure |
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