Reaction Details |
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Target | Indoleamine 2,3-dioxygenase 1 |
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Ligand | BDBM50335098 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1280717 (CHEMBL3097526) |
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IC50 | >500000±n/a nM |
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Citation | Fung, SP; Wang, H; Tomek, P; Squire, CJ; Flanagan, JU; Palmer, BD; Bridewell, DJ; Tijono, SM; Jamie, JF; Ching, LM Discovery and characterisation of hydrazines as inhibitors of the immune suppressive enzyme, indoleamine 2,3-dioxygenase 1 (IDO1). Bioorg Med Chem21:7595-603 (2013) [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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BDBM50335098 |
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n/a |
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Name | BDBM50335098 |
Synonyms: | 6-Nitro-benzothiazol-2-ylamine | 6-nitrobenzo[d]thiazol-2-amine | CHEMBL318275 |
Type | Small organic molecule |
Emp. Form. | C7H5N3O2S |
Mol. Mass. | 195.199 |
SMILES | Nc1nc2ccc(cc2s1)[N+]([O-])=O |
Structure |
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