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PD 1/PD L1

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PD 1/PD L1

Chemical Structure Cat. No. Product Name CAS No.
PD-1/PD-L1 Inhibitor 4 Chemical Structure
 BCP25721 PD-1/PD-L1 Inhibitor 4 1629655-94-2
BMS-8 Chemical Structure
 BCP45103 BMS-8 1675201-90-7
BMS-8 is a novel inhibitor of the PD-1/PD-L1 interaction by inducing PD-L1 dimerization through PD-1 interacting surface, binding at a hydrophobic cavity formed upon PD-L1 dimerization.
M351-056 Chemical Structure
 BCP44929 M351-056 M351-056
M351-056 is a novel VISTA (V-domain immunoglobulin suppressor of T-cell activation) agonist.
M351-110 Chemical Structure
 BCP44928 M351-110 M351-110
M351-110 is a novel VISTA (V-domain immunoglobulin suppressor of T-cell activation) agonist.
Evixapodlin Chemical Structure
 BCP43535 Evixapodlin 2374856-75-2
Evixapodlin is a programmed cell death ligand 1 (PD-L1) inhibitor.
PD-1/PD-L1-IN-10 Chemical Structure
 BCP43172 PD-1/PD-L1-IN-10 2487550-41-2
PD-1/PD-L1-IN-10 is an orally active PD-1/PD-L1 inhibitor (IC50 of 2.7 nM) with potent anticancer efficacy.
BMS202 HCl Chemical Structure
 BCP42693 BMS202 HCl BMS202HCl
BMS-202 is a PD-1/PD-L1 interaction inhibitor.
INCB086550 Chemical Structure
 BCP38993 INCB086550 INCB086550
INCB086550, a first-in-class oral inhibitor of PD-L1, as initial immune checkpoint inhibitor therapy in participants with select solid tumors
PD-1/PD-L1 Inhibitor 3 Chemical Structure
 BCP35838 PD-1/PD-L1 Inhibitor 3 1629654-95-0
PD-1/PD-L1 Inhibitor 3 is a Macrocyclic inhibitor of PD-1/PD-L1 interaction with IC50 of 5.6 nM.
AUNP-12 TFA Chemical Structure
 BCP35837 AUNP-12 TFA AUNP12TFA
AUNP-12 TFA is a peptide antagonist of the PD-1 signaling pathway, displays equipotent antagonism toward PD-L1 and PD-L2 in rescue of lymphocyte proliferation and effector functions.
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