Cat. No. | 製品名 | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T0844 | Sulfamethoxypyridazine | 80-35-3 | 98% |
|
Sulfamethoxypyridazine (CL 13494) is a sulfanilamide antibacterial agent. | ||||
T40111L | BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride | 2691796-83-3 | 98% |
|
BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride is a resorcinol di-Ph ether scaffold-based programmed cell death-1 (PD-1)/programmed cell death ligand 1 (P... | ||||
T77635 | LSD1-IN-27 | 2904571-94-2 | 98% |
|
LSD1-IN-27 is a potent LSD1 inhibitor with an IC50 value of 13 nM.LSD1-IN-27 inhibited the stemness and migration of gastric cancer cells.LSD1-IN-27 inhibited th... | ||||
T9616 | PD-1/PD-L1-IN-10 | 2487550-41-2 | 98% |
|
PD-1/PD-L1-IN-10 is an orally active PD-1/PD-L1 inhibitor (IC50 of 2.7 nM) with potent anticancer efficacy. | ||||
T38369 | CAY10678 | 1268709-57-4 | 98% |
|
CAY10678 is an mPGES-1 inhibitor that inhibits PD-1.CAY10678 reduces collagen deposition and T-cell depletion, and may be used to study melanoma.CASHIPS | ||||
T77433 | Feladilimab | 2252518-85-5 | 98% |
Feladilimab
|
Feladilimab (GSK3359609) is an IgG4 monoclonal antibody that is an ICOS agonist. Feladilimab binds to ICOS-expressing T cells, induces IFNγ, and increases PD-1/L... | ||||
T11126 | Durvalumab | 1428935-60-7 | 98% |
|
Durvalumab (MEDI 4736) is a humanized monoclonal antibody targeting PD-L1. It can block the interaction of PD-L1 with PD-1 and CD80, with IC50 values of 0.1 and ... | ||||
T77075 | Spartalizumab | 1935694-88-4 | 98% |
Spartalizumab
|
Spartalizumab (PDR001) is a humanized immunoglobulin 4 monoclonal antibody that selectively binds to PD-1 at low concentrations and shows high activity. Spartali... | ||||
T83970 | IMMH 010 maleate | 2541982-47-0 | 98% |
|
IMMH 010 maleate (YPD-30 maleate) is an orally available programmed cell death ligand 1 inhibitor with potential antitumor activity for the study of neurological... | ||||
T35394 | Sintilimab (anti-PD-1) | 2072873-06-2 | 95% |
Sintilimab (anti-PD-1)
|
Sintilimab (IBI308) is a humanized IgG4 monoclonal antibody with significant anti-tumor activity that restores endogenous anti-tumor T-cell responses by binding ... | ||||
TP1076L | AUNP-12 acetate | 95.07% |
|
|
AUNP-12 acetate is a polypeptide inhibitor of PD-1 that is equivalent to PD-1 and PD-2 in inhibiting lymphocyte proliferation and effector fuction, in addition t... | ||||
T9902 | Atezolizumab | 1380723-44-3 | 95.10% |
|
Atezolizumab anti-PD-L1) is a fully humanized IgG1 monoclonal antibody that blocks the interaction of PD-L1 with both PD-1 and B7.1 but not the interaction of PD... | ||||
T9359 | PDL-1 cpd 10 | 2767424-13-3 | 98% |
|
PDL-1 cpd 10 is a novel small molecule PD-L1 inhititor. | ||||
T9907 | Nivolumab | 946414-94-4 | 98% |
|
Nivolumab (anti-PD-1) is a genetically engineered fully human immunoglobulin Ig) G4 monoclonal antibody directed against the negative immunoregulatory human cell... | ||||
T4696 | BMS202 hydrochloride (1675203-84-5(free base)) | 2089334-95-0 | 98% |
|
BMS202 hydrochloride (1675203-84-5(free base)) (PD-1/PD-L1 inhibitor 2 hydrochloride) is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50: 18 nM). Biophys... | ||||
T78269 | Anti-Mouse PD-1 Antibody (RMP1-14) | 98.01% |
Anti-Mouse PD-1 Antibody (RMP1-14)
|
|
RMP1-14 is an IgG1-like immunoglobulin and anti-Mouse PD-1 antibody that blocks PD-1/PD-L1 signaling. | ||||
T36899 | INCB086550 | 2230911-59-6 | 98.21% |
|
INCB086550 (PD-1/PD-L1-IN-8) (example 24) is a PD-1/PD-L1 inhibitor, with an IC50 <= 10 nM. | ||||
T3146 | BMS-202 | 1675203-84-5 | 98.24% |
|
BMS-202 (PD1-PDL1 inhibitor 2) is an inhibitor of the PD-1 (Programmed death- 1) /PD-Ll (Programmed death-ligand 1) protein/protein interaction. | ||||
T9903 | Avelumab | 1537032-82-8 | 98.30% |
|
Avelumab is a fully human IgG1 anti-PD-L1 monoclonal antibody. Avelumab shows potential antibody-dependent cell-mediated cytotoxicity. | ||||
T12379 | PD-1-IN-22 | 2349372-98-9 | 98.64% |
|
PD-1-IN-22 is a potent programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) interaction inhibitor(IC50 of 92.3 nM). |