Reaction Details |
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Target | Cathepsin D |
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Ligand | BDBM50022582 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_44971 |
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IC50 | 3200±n/a nM |
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Citation | Bühlmayer, P; Caselli, A; Fuhrer, W; Göschke, R; Rasetti, V; Rüeger, H; Stanton, JL; Criscione, L; Wood, JM Synthesis and biological activity of some transition-state inhibitors of human renin. J Med Chem31:1839-46 (1988) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Cathepsin D |
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Name: | Cathepsin D |
Synonyms: | CATD_BOVIN | CTSD |
Type: | PROTEIN |
Mol. Mass.: | 42158.92 |
Organism: | Bos taurus |
Description: | ChEMBL_1458606 |
Residue: | 387 |
Sequence: | VIRIPLHKFTSIRRTMSEAAGVLIAKGPISKYATGEPAVRQGPIPELLKNYMDAQYYGEI
GIGTPPQCFTVVFDTGSANLWVPSIHCKLLDIACWTHRKYNSDKSSTYVKNGTTFDIHYG
SGSLSGYLSQDTVSVPCNPSSSSPGGVTVQRQTFGEAIKQPGVVFIAAKFDGILGMAYPR
ISVNNVLPVFDNLMQQKLVDKNVFSFFLNRDPKAQPGGELMLGGTDSKYYRGSLMFHNVT
RQAYWQIHMDQLDVGSSLTVCKGGCEAIVDTGTSLIVGPVEEVRELQKAIGAVPLIQGEY
MIPCEKVSSLPEVTVKLGGKDYALSPEDYALKVSQAETTVCLSGFMGMDIPPPGGPLWIL
GDVFIGRYYTVFDRDQNRVGLAEAARL
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BDBM50022582 |
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n/a |
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Name | BDBM50022582 |
Synonyms: | CHEMBL53139 | Diastereomer-5-[2-[2-Benzyl-3-(2-methyl-propane-2-sulfonyl)-propionylamino]-3-(3H-imidazol-4-yl)-propionylamino]-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid butylamide |
Type | Small organic molecule |
Emp. Form. | C39H63N5O6S |
Mol. Mass. | 730.012 |
SMILES | CCCCNC(=O)[C@@H](CC(O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)C(Cc1ccccc1)CS(=O)(=O)C(C)(C)C)C(C)C |
Structure |
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