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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T11211 | EP4 receptor antagonist 1 | Prostaglandin Receptor | |
EP4 Receptor Antagonist 1 is a highly potent and selective competitive prostanoid EP4 receptor antagonist, effective for cancer immunotherapy. It inhibits both human and mouse EP4 receptors with IC50 values of 6.1 nM and... | |||
T7860 | SM-324405 | SM 324405 | TLR |
SM-324405 is an agonist of TLR7. | |||
T8961 | GW280264X | Carbamic acid | MMP |
GW280264X (Carbamic acid) is an inhibitor of ADAM17 . | |||
T12516 | Polyinosinic-polycytidylic acid sodium | Poly(I:C) sodium | Apoptosis , Others , TLR |
Polyinosinic-polycytidylic acid sodium (Poly(I:C) sodium) is a synthetic analog of double-stranded RNA and an agonist of toll-like receptor 3 (TLR3) and retinoic acid inducible gene I (RIG-I)-like receptors (RIG-I and MD... | |||
T4349 | Sitravatinib | MG516,MGCD516 | Discoidin Domain Receptor (DDR) , VEGFR , FLT , Trk receptor , TAM Receptor , c-Kit , Ephrin Receptor |
Sitravatinib (MGCD516) (MGCD516) is an inhibitor targeting multiple RTKs involved in driving sarcoma cell growth, including c-Met, c-Kit, PDGFRα/β, PDGFR, and Axl. | |||
TP1493L1 | PSA1 141-150 acetate | PSA1 141-150 acetate(160215-60-1 free base) | Others |
PSA1 141-150 acetate is used in the immunotherapy of cancer experiments that is a prostate specific antigen 1 peptide. | |||
T40350 | HPK1-IN-4 | HPK1-IN-4 | MAPK |
HPK1-IN-4 is an HPK1 (MAPK41) inhibitor with an IC 50 of 0.061 nM. HPK1-IN-4 is often used as a preclinical immunotherapy tool compound. | |||
T77764 | DC-Y13-27 | Others | |
Dc-y13-27, a derivative of DC-Y13, is a potent YTHDF2 inhibitor (KD: 37.9 μM). DC-Y13-27 has antitumor activity that enhances the response of radiotherapy and immunotherapy to tumors. | |||
T69560 | ENPP1 inhibitor 43 | ||
ENPP1 inhibitor 43 is a novel small molecule for cancer immunotherapy. | |||
TP2478 | WT-1 A1 | Tyr-Met-Phe-Pro-agn-Ala-Pro-Tyr-Leu | |
WT-1 A1 is an attractive target for immunotherapy in patients with pancreatic adenocarcinoma. | |||
T61386 | CXCR2 antagonist 2 | ||
CXCR2 antagonist 2 is a potent CXCR2 antagonist for cancer immunotherapy with an IC 50 value of 95 nM. | |||
TP1493 | PSA1 (141-150) | PSA1 141-150 | |
This Prostate Specific Antigen 1 peptide was used in the immunotherapy of cancer experiments. | |||
T83135 | Alrefimotide | hTERT (660–689) | |
Alrefimotide, an immunogenic peptide derived from hTERT, possesses the sequence ALFSVLNYERARRPGLLGASVLGLDDIHRA and has applications in cancer immunotherapy research [1]. | |||
T63948 | PD-1/PD-L1-IN-16 | ||
PD-1/PD-L1-IN-16 is a potent inhibitor of PD-1/PD-L1 (IC50: 53.2 nM) and has shown research potential for tumour immunotherapy. | |||
T63458 | STING agonist-11 | ||
STING agonist-11 is a potent activator of the small molecule cyclic urea class of STING (EC50: 18 nM).STING activation is a highly promising immunotherapy. | |||
T82348 | GAGGVGKSAL | ||
GAGGVGKSAL, a wild-type KRAS G12D 10mer peptide, serves as an immunogenic neoantigen in cancer immunotherapy research [1]. | |||
T82352 | GADGVGKSAL | ||
GADGVGKSAL, a mutant KRAS G12D 10mer peptide, serves as an immunogenic neoantigen in cancer immunotherapy research [1]. | |||
T80961 | TPPC | ||
TPPC, a porphyrin-cholesterol conjugate, sensitizes cancer cells to immune checkpoint inhibitors (ICIs) and augments photodynamic immunotherapy in the treatment of lung cancer [1]. | |||
T63457 | STING agonist-10 | ||
STING agonist-10 is a potent activator of the STING small molecule cyclic urea class (EC50: 2600 nM).STING activation is a highly promising immunotherapy. | |||
T82349 | GAGGVGKSA | ||
GAGGVGKSA, a wild-type KRAS G12D 9mer peptide, serves as an immunogenic neoantigen pivotal for cancer immunotherapy research [1]. |