Reaction Details |
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Target | Cathepsin L2 |
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Ligand | BDBM103349 |
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Substrate/Competitor | n/a |
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Meas. Tech. | In Vitro Inhibition Assay |
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Ki | 1900±0.0 nM |
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Citation | Quibell, M; Watts, JP; Flinn, NS Furo[3, 2-B] pyrrol-3-ones as cathespin S inhibitors US Patent US8552202 Publication Date 10/8/2013 |
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More Info.: | Get all data from this article, Assay Method |
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Cathepsin L2 |
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Name: | Cathepsin L2 |
Synonyms: | CATL2 | CATL2_HUMAN | CTSL2 | CTSU | CTSV | Cathepsin U | Cathepsin V |
Type: | Enzyme |
Mol. Mass.: | 37341.06 |
Organism: | Homo sapiens (Human) |
Description: | O60911 |
Residue: | 334 |
Sequence: | MNLSLVLAAFCLGIASAVPKFDQNLDTKWYQWKATHRRLYGANEEGWRRAVWEKNMKMIE
LHNGEYSQGKHGFTMAMNAFGDMTNEEFRQMMGCFRNQKFRKGKVFREPLFLDLPKSVDW
RKKGYVTPVKNQKQCGSCWAFSATGALEGQMFRKTGKLVSLSEQNLVDCSRPQGNQGCNG
GFMARAFQYVKENGGLDSEESYPYVAVDEICKYRPENSVANDTGFTVVAPGKEKALMKAV
ATVGPISVAMDAGHSSFQFYKSGIYFEPDCSSKNLDHGVLVVGYGFEGANSNNSKYWLVK
NSWGPEWGSNGYVKIAKDKNNHCGIATAASYPNV
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BDBM103349 |
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n/a |
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Name | BDBM103349 |
Synonyms: | US8552202, Compound 1 |
Type | Small organic molecules |
Emp. Form. | C21H26N2O4 |
Mol. Mass. | 370.4421 |
SMILES | O=C(N[C@@H](C1CCCCC1)C(=O)N1CC[C@H]2OCC(=O)[C@@H]12)c1ccccc1 |r| |
Structure |
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