Reaction Details |
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Target | Indoleamine 2,3-dioxygenase 1 |
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Ligand | BDBM494756 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Enzyme Assay |
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IC50 | 50.3±n/a nM |
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Citation | Liu, K; Achab, A; Biju, P; Cernak, TA; Deng, Y; Fradera, X; Guo, L; Han, Y; He, S; Kozlowski, J; Li, D; Li, G; Pu, Q; Shi, Z; Yu, W; Zhang, H Substituted n′-hydroxycarbamimidoyl-1,2,5-oxadiazole compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors US Patent US10988487 Publication Date 4/27/2021 |
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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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BDBM494756 |
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n/a |
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Name | BDBM494756 |
Synonyms: | N-(4-fluorobicyclo[4.2.0]octa- 1(6),2,4-trien-7-yl)-N'-hydroxy-4- ((2-(sulfamoylamino)ethyl)amino)- 1,2,5-oxadiazole-3-carboximidamide | US10988487, Example 152 |
Type | Small organic molecule |
Emp. Form. | C13H16FN7O4S |
Mol. Mass. | 385.374 |
SMILES | NS(=O)(=O)NCCNc1nonc1\C(NC1Cc2ccc(F)cc12)=N\O |
Structure |
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