Reaction Details |
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Target | Transthyretin |
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Ligand | BDBM50197883 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2187564 (CHEMBL5099646) |
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Kd | 9.9±n/a nM |
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Citation | Pinheiro, F; Pallarès, I; Peccati, F; Sánchez-Morales, A; Varejão, N; Bezerra, F; Ortega-Alarcon, D; Gonzalez, D; Osorio, M; Navarro, S; Velázquez-Campoy, A; Almeida, MR; Reverter, D; Busqué, F; Alibés, R; Sodupe, M; Ventura, S Development of a Highly Potent Transthyretin Amyloidogenesis Inhibitor: Design, Synthesis, and Evaluation. J Med Chem65:14673-14691 (2022) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Transthyretin |
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Name: | Transthyretin |
Synonyms: | ATTR | PALB | Prealbumin | TBPA | TTHY_HUMAN | TTR | Transthyretin (TTR) |
Type: | Enzyme |
Mol. Mass.: | 15884.31 |
Organism: | Homo sapiens (Human) |
Description: | P02766 |
Residue: | 147 |
Sequence: | MASHRLLLLCLAGLVFVSEAGPTGTGESKCPLMVKVLDAVRGSPAINVAVHVFRKAADDT
WEPFASGKTSESGELHGLTTEEEFVEGIYKVEIDTKSYWKALGISPFHEHAEVVFTANDS
GPRRYTIAALLSPYSYSTTAVVTNPKE
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BDBM50197883 |
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n/a |
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Name | BDBM50197883 |
Synonyms: | CHEBI:78538 | FX-1006 | Tafamidis | US10377729, Compound Tafamidis | Vyndaqel |
Type | Small organic molecule |
Emp. Form. | C14H7Cl2NO3 |
Mol. Mass. | 308.116 |
SMILES | OC(=O)c1ccc2nc(oc2c1)-c1cc(Cl)cc(Cl)c1 |
Structure |
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