Reaction Details |
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Target | Indoleamine 2,3-dioxygenase 1 |
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Ligand | BDBM50520449 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1880241 (CHEMBL4381635) |
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IC50 | 42±n/a nM |
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Citation | Peng, YH; Liao, FY; Tseng, CT; Kuppusamy, R; Li, AS; Chen, CH; Fan, YS; Wang, SY; Wu, MH; Hsueh, CC; Chang, JY; Lee, LC; Shih, C; Shia, KS; Yeh, TK; Hung, MS; Kuo, CC; Song, JS; Wu, SY; Ueng, SH Unique Sulfur-Aromatic Interactions Contribute to the Binding of Potent Imidazothiazole Indoleamine 2,3-Dioxygenase Inhibitors. J Med Chem63:1642-1659 (2020) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Indoleamine 2,3-dioxygenase 1 |
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Name: | Indoleamine 2,3-dioxygenase 1 |
Synonyms: | I23O1_HUMAN | IDO | IDO-1 | IDO1 | INDO | Indoleamine 2,3-Dioxygenasae (IDO) | Indoleamine 2,3-dioxygenase | Indoleamine-pyrrole 2,3-dioxygenase |
Type: | Enzyme |
Mol. Mass.: | 45330.80 |
Organism: | Homo sapiens (Human) |
Description: | P14902 |
Residue: | 403 |
Sequence: | MAHAMENSWTISKEYHIDEEVGFALPNPQENLPDFYNDWMFIAKHLPDLIESGQLRERVE
KLNMLSIDHLTDHKSQRLARLVLGCITMAYVWGKGHGDVRKVLPRNIAVPYCQLSKKLEL
PPILVYADCVLANWKKKDPNKPLTYENMDVLFSFRDGDCSKGFFLVSLLVEIAAASAIKV
IPTVFKAMQMQERDTLLKALLEIASCLEKALQVFHQIHDHVNPKAFFSVLRIYLSGWKGN
PQLSDGLVYEGFWEDPKEFAGGSAGQSSVFQCFDVLLGIQQTAGGGHAAQFLQDMRRYMP
PAHRNFLCSLESNPSVREFVLSKGDAGLREAYDACVKALVSLRSYHLQIVTKYILIPASQ
QPKENKTSEDPSKLEAKGTGGTDLMNFLKTVRSTTEKSLLKEG
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BDBM50520449 |
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n/a |
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Name | BDBM50520449 |
Synonyms: | CHEMBL4459210 |
Type | Small organic molecule |
Emp. Form. | C18H15ClN4OS |
Mol. Mass. | 370.856 |
SMILES | Clc1cccc(NC(=O)NCc2cnc3scc(C#CC4CC4)n23)c1 |
Structure |
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