| Reaction Details |
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 | Report a problem with these data |
| Target | Cathepsin E |
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| Ligand | BDBM50427565 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_941701 (CHEMBL2330924) |
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| IC50 | 11000±n/a nM |
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| Citation |  Lorthiois, E; Breitenstein, W; Cumin, F; Ehrhardt, C; Francotte, E; Jacoby, E; Ostermann, N; Sellner, H; Kosaka, T; Webb, RL; Rigel, DF; Hassiepen, U; Richert, P; Wagner, T; Maibaum, J The discovery of novel potent trans-3,4-disubstituted pyrrolidine inhibitors of the human aspartic protease renin from in silico three-dimensional (3D) pharmacophore searches. J Med Chem56:2207-17 (2013) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Cathepsin E |
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| Name: | Cathepsin E |
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| Synonyms: | 3.4.23.34 | CATE_HUMAN | CTSE | Cathepsin E form I | Cathepsin E form II |
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| Type: | Enzyme |
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| Mol. Mass.: | 43298.99 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P14091 |
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| Residue: | 396 |
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| Sequence: | MKTLLLLLLVLLELGEAQGSLHRVPLRRHPSLKKKLRARSQLSEFWKSHNLDMIQFTESC
SMDQSAKEPLINYLDMEYFGTISIGSPPQNFTVIFDTGSSNLWVPSVYCTSPACKTHSRF
QPSQSSTYSQPGQSFSIQYGTGSLSGIIGADQVSVEGLTVVGQQFGESVTEPGQTFVDAE
FDGILGLGYPSLAVGGVTPVFDNMMAQNLVDLPMFSVYMSSNPEGGAGSELIFGGYDHSH
FSGSLNWVPVTKQAYWQIALDNIQVGGTVMFCSEGCQAIVDTGTSLITGPSDKIKQLQNA
IGAAPVDGEYAVECANLNVMPDVTFTINGVPYTLSPTAYTLLDFVDGMQFCSSGFQGLDI
HPPAGPLWILGDVFIRQFYSVFDRGNNRVGLAPAVP
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| BDBM50427565 |
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| n/a |
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| Name | BDBM50427565 |
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| Synonyms: | CHEMBL2322896 |
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| Type | Small organic molecule |
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| Emp. Form. | C24H25ClN2 |
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| Mol. Mass. | 376.922 |
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| SMILES | Clc1ccc(cc1)N(C[C@@H]1CNC[C@H]1Cc1ccccc1)c1ccccc1 |r| |
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| Structure | 
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