Reaction Details |
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Target | Myeloblastin |
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Ligand | BDBM50270029 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_508142 (CHEMBL1004879) |
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IC50 | >50000±n/a nM |
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Citation | Méthot, N; Rubin, J; Guay, D; Beaulieu, C; Ethier, D; Reddy, TJ; Riendeau, D; Percival, MD Inhibition of the activation of multiple serine proteases with a cathepsin C inhibitor requires sustained exposure to prevent pro-enzyme processing. J Biol Chem282:20836-46 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Myeloblastin |
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Name: | Myeloblastin |
Synonyms: | Leukocyte proteinase 3 | MBN | PRTN3 | PRTN3_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 27816.30 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1463425 |
Residue: | 256 |
Sequence: | MAHRPPSPALASVLLALLLSGAARAAEIVGGHEAQPHSRPYMASLQMRGNPGSHFCGGTL
IHPSFVLTAAHCLRDIPQRLVNVVLGAHNVRTQEPTQQHFSVAQVFLNNYDAENKLNDVL
LIQLSSPANLSASVATVQLPQQDQPVPHGTQCLAMGWGRVGAHDPPAQVLQELNVTVVTF
FCRPHNICTFVPRRKAGICFGDSGGPLICDGIIQGIDSFVIWGCATRLFPDFFTRVALYV
DWIRSTLRRVEAKGRP
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BDBM50270029 |
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n/a |
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Name | BDBM50270029 |
Synonyms: | 2-Amino-N-[(S)-3-diazo-1-(4-iodo-benzyl)-2-oxo-propyl]-acetamide | CHEMBL450997 |
Type | Small organic molecule |
Emp. Form. | C12H13IN4O2 |
Mol. Mass. | 372.1617 |
SMILES | NCC(=O)N[C@@H](Cc1ccc(I)cc1)C(=O)[CH-][N+]#N |r| |
Structure |
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