Reaction Details |
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Target | Tryptase delta |
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Ligand | BDBM50217813 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_210701 (CHEMBL817298) |
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IC50 | 4.0±n/a nM |
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Citation | Slusarchyk, WA; Bolton, SA; Hartl, KS; Huang, MH; Jacobs, G; Meng, W; Ogletree, ML; Pi, Z; Schumacher, WA; Seiler, SM; Sutton, JC; Treuner, U; Zahler, R; Zhao, G; Bisacchi, GS Synthesis of potent and highly selective inhibitors of human tryptase. Bioorg Med Chem Lett12:3235-8 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Tryptase delta |
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Name: | Tryptase delta |
Synonyms: | Delta-tryptase | HmMCP-3-like tryptase III | Mast cell mMCP-7-like | TPSD1 | TRYD_HUMAN | Tryptase delta | Tryptase-3 |
Type: | PROTEIN |
Mol. Mass.: | 26578.73 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_104777 |
Residue: | 242 |
Sequence: | MLLLAPQMLSLLLLALPVLASPAYVAPAPGQALQQTGIVGGQEAPRSKWPWQVSLRVRGP
YWMHFCGGSLIHPQWVLTAAHCVEPDIKDLAALRVQLREQHLYYQDQLLPVSRIIVHPQF
YIIQTGADIALLELEEPVNISSHIHTVTLPPASETFPPGMPCWVTGWGDVDNNVHLPPPY
PLKEVEVPVVENHLCNAEYHTGLHTGHSFQIVRDDMLCAGSENHDSCQGDSGGPLVCKVN
GT
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BDBM50217813 |
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n/a |
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Name | BDBM50217813 |
Synonyms: | CHEMBL302058 |
Type | Small organic molecule |
Emp. Form. | C21H36N6O6 |
Mol. Mass. | 468.5471 |
SMILES | [#6]-[#6](-[#6])-[#6](-[#8]-[#6](=O)-[#7]-1-[#6]-[#6]-[#7](-[#6]-[#6]-1)-[#6](=O)-[#7]-1-[#6@@H](-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6]-1=O)-[#6](-[#8])=O)-[#6](-[#6])-[#6] |
Structure |
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