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TargetProgrammed cell death 1 ligand 1 [19-238]/protein 1 [25-167]
LigandBDBM446472
Substrate/Competitorn/a
Meas. Tech.Homogeneous Time-Resolved Fluorescence (HTRF) PD-1/PD-L1 Binding Assay
IC50<10±n/a nM
Citation Wu, LLi, JYao, W Heterocyclic compounds as immunomodulators US Patent US10669271 Publication Date 6/2/2020
More Info.:Get all data from this article,  Assay Method
 
Programmed cell death 1 ligand 1 [19-238]/protein 1 [25-167]
Name:Programmed cell death 1 ligand 1 [19-238]/protein 1 [25-167]
Synonyms:PD-1/PD-L1
Type:Protein
Mol. Mass.:n/a
Description:n/a
Components:This complex has 2 components.
Component 1
Name:Programmed cell death protein 1 [25-167]
Synonyms:PD1 | PDCD1 | PDCD1_HUMAN | Programmed cell death protein 1 (25-167) | Programmed cell death protein 1 (aa25-167) | Protein PD-1 | hPD-1
Type:Enzyme Catalytic Domain
Mol. Mass.:15954.64
Organism:Homo sapiens (Human)
Description:Q15116 (aa25-167)
Residue:143
Sequence:
LDSPDRPWNPPTFSPALLVVTEGDNATFTCSFSNTSESFVLNWYRMSPSNQTDKLAAFPE
DRSQPGQDCRFRVTQLPNGRDFHMSVVRARRNDSGTYLCGAISLAPKAQIKESLRAELRV
TERRAEVPTAHPSPSPRPAGQFQ
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Component 2
Name:Programmed cell death 1 ligand 1 [19-238]
Synonyms:B7H1 | CD274 | PD-L1 | PD1L1_HUMAN | PDCD1 ligand 1 | PDCD1L1 | PDCD1LG1 | PDL1 | Programmed cell death 1 ligand 1 (aa19-238) | Programmed death ligand 1 | hPD-L1
Type:Enzyme Catalytic Domain
Mol. Mass.:25191.31
Organism:Homo sapiens (Human)
Description:Q9NZQ7 (aa19-238)
Residue:220
Sequence:
FTVTVPKDLYVVEYGSNMTIECKFPVEKQLDLAALIVYWEMEDKNIIQFVHGEEDLKVQH
SSYRQRARLLKDQLSLGNAALQITDVKLQDAGVYRCMISYGGADYKRITVKVNAPYNKIN
QRILVVDPVTSEHELTCQAEGYPKAEVIWTSSDHQVLSGKTTTTNSKREEKLFNVTSTLR
INTTTNEIFYCTFRRLDPEENHTAELVIPELPLAHPPNER
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BDBM446472
n/a
NameBDBM446472
Synonyms:(R)-1-((7-cyano-2-(3′-(2-(difluoromethyl)-7-((3-hydroxypyrrolidin-1-yl)methyl)pyrido[3,2-d]pyrimidin-4-ylamino)-2,2′-dimethylbiphenyl-3-yl)benzo[d]oxazol-5-yl)methyl)-N,N-dimethylpiperidine-4-carboxamide | US10669271, Example 25 | US11124511, Example 25
TypeSmall organic molecule
Emp. Form.C44H45F2N9O3
Mol. Mass.785.8834
SMILESCN(C)C(=O)C1CCN(Cc2cc(C#N)c3oc(nc3c2)-c2cccc(c2C)-c2cccc(Nc3nc(nc4cc(CN5CC[C@@H](O)C5)cnc34)C(F)F)c2C)CC1 |r|
Structure
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