Reaction Details |
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Target | Procathepsin L |
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Ligand | BDBM50175213 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_326940 (CHEMBL854328) |
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Ki | 6400±n/a nM |
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Citation | Martina, E; Stiefl, N; Degel, B; Schulz, F; Breuning, A; Schiller, M; Vicik, R; Baumann, K; Ziebuhr, J; Schirmeister, T Screening of electrophilic compounds yields an aziridinyl peptide as new active-site directed SARS-CoV main protease inhibitor. Bioorg Med Chem Lett15:5365-9 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Procathepsin L |
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Name: | Procathepsin L |
Synonyms: | CATL1_HUMAN | CTSL | CTSL CTSL1 | CTSL1 | Cathepsin L | Cathepsin L1 | Cathepsin L1 heavy chain | Cathepsin L1 light chain | MEP | Major excreted protein | cathepsin L preproprotein |
Type: | Enzyme |
Mol. Mass.: | 37557.19 |
Organism: | Homo sapiens (Human) |
Description: | Purchased from Calbiochem (San Diego, CA). |
Residue: | 333 |
Sequence: | MNPTLILAAFCLGIASATLTFDHSLEAQWTKWKAMHNRLYGMNEEGWRRAVWEKNMKMIE
LHNQEYREGKHSFTMAMNAFGDMTSEEFRQVMNGFQNRKPRKGKVFQEPLFYEAPRSVDW
REKGYVTPVKNQGQCGSCWAFSATGALEGQMFRKTGRLISLSEQNLVDCSGPQGNEGCNG
GLMDYAFQYVQDNGGLDSEESYPYEATEESCKYNPKYSVANDTGFVDIPKQEKALMKAVA
TVGPISVAIDAGHESFLFYKEGIYFEPDCSSEDMDHGVLVVGYGFESTESDNNKYWLVKN
SWGEEWGMGGYVKMAKDRRNHCGIASAASYPTV
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BDBM50175213 |
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n/a |
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Name | BDBM50175213 |
Synonyms: | (2S,3S)-dibenzyl 1-((S)-2-(tert-butoxycarbonyl)-2-(piperidin-1-yl)acetyl)aziridine-2,3-dicarboxylate | CHEMBL198858 |
Type | Small organic molecule |
Emp. Form. | C30H37N3O7 |
Mol. Mass. | 551.6307 |
SMILES | CC(C)(C)OC(=O)N[C@@H](N1CCCCC1)C(=O)N1[C@@H]([C@H]1C(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |
Structure |
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