| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V3676 | (-)-JQ-1 | 1268524-71-5 | JQ-1 is the (R)-Enantiomer of JQ1 or the stereoisomer of (+)-JQ1. |
|
V77385 | (D)-PPA 1 TFA | (D)-PPA 1 TFA is a hydrolytic D-peptide antagonist. | |
|
V88733 | Antitumor agent-169 | Antitumor agent-169 (Compound B3) is a dual inhibitor of PD-1/PD-L1 interaction and PARP7 with IC50 of 0.426 μM and 2.50 nM, respectively. | |
|
V88725 | Antitumor agent-170 | Antitumor agent-170 (Compound C6) exhibits inhibitory activity against PD-1/PD-L1 interaction and PARP7 with IC50 of 0.342 μM and 7.05 nM, respectively. | |
|
V115356 | BMS-142 | 1675203-24-3 | BMS-142 is a PDL1 inhibitor (IC50 = 96.7 nM) (kd = 13.2 nM). |
|
V3256 | BMS-8 | 1675201-90-7 | BMS-8is a novel small molecule inhibitor of the PD-1 (Programmed death-1)/PD-L1 (Programmed death-ligand 1) protein/protein interaction with potential anticancer activities. |
|
V86960 | BMS-986189 | 1629665-96-8 | BMS-986189 is a macrocyclic peptide PD-L1 inhibitor (IC50: 1.03 nM) for cancer research. |
|
V77194 | BMSpep-57 hydrochloride | BMSpep-57 HCl is a potent macrocyclic peptide inhibitor that can suppress PD-1/PD-L1 interaction with IC50 of 7.68 nM. | |
|
V100278 | Cemavafusp | Cemavafusp is an anti-PD-L1 monoclonal antibody composed of a single-chain variable fragment, an antibody heavy chain, and a kappa antibody light chain. | |
|
V78904 | CYP51/PD-L1-IN-2 | 3032386-58-3 | CYP51/PD-L1-IN-2 (compound L20) is a quinazoline compound with antifungal activity. |
|
V78665 | CYP51/PD-L1-IN-3 | 3032386-59-4 | CYP51/PD-L1-IN-3 (compound L21) is a quinazoline compound with antifungal activity. |
|
V135212 | Erfonrilimab | 2367013-69-0 | Erfonrilimab is a monoclonal antibody that targets PD-L1/CTLA-4. |
|
V136646 | GJ19 | 3099808-68-8 | GJ19 is a PD-L1 inhibitor with an IC50 value of 32.06 nM. |
|
V86966 | HBV/HDV-IN-2 | 3034161-76-4 | HBV/HDV-IN-2 (Compd 143) is an inhibitor of HBV, HDV and PD-1/PD-L1 with an EC50 of 35 nM for T cell activation. |
|
V137646 | HX009 | HX009 is a bispecific antibody that targets PD1 and CD47, but its binding ability to CD47 is relatively weak. | |
|
V114480 | IBI-363 | IBI-363 is a PD-1/IL-2 bispecific antibody that blocks the PD-1/PD-L1 pathway and activates the IL-2 pathway. | |
|
V86940 | Lomvastomig | Lomvastomig is a human IgG1 kappa monoclonal antibody against PDCD1/HAVCR2. | |
|
V139160 | LY3415244 | LY3415244 is a human bispecific antibody (bsAb) that targets B7-H1/PD-L1/CD274 and TIM-3/HAVCR2/CD366. | |
|
V3255 | N-deacetylated BMS-202 | 2310135-18-1 | N-deacetylated BMS-202, the deacetylated product of BMS-202 (also known asPD1-PDL1 inhibitor 2,BMS 202, BMS202), is a inhibitor of the PD-1 (Programmed death- 1)/PD-Ll (Programmed death-ligand 1) protein/protein interaction with potential anticancer activities. |
|
V141598 | NPH16 | NPH16 is an orally effective PD-1/PD-L1 inhibitor with an IC50 value of 24.4 nM. |