98 Results for "

Immune Checkpoints

" in MedChemExpress (MCE) Product Catalog:
Products (98)

98 Results for "Immune Checkpoints" in MCE Product Catalog:

Cat. No.: HY-163844
Target:  

PD-1/PD-L1

Research Areas:  

Inflammation/Immunology Cancer

PD-1/PD-L1-IN-49 (compound 1c) is a potent inhibitor of PD-1/PD-L1, with the IC50 of 77 nM. PD-1/PD-L1-IN-49 activates Jurkat T cells, reflecting successful blockade of the PD-1/PD-L1 immune checkpoint .
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Cat. No.: HY-149520
Target:  

MAP4K

Research Areas:  

Cancer

HPK1-IN-39 (Compound 10n) is a selective HPK1 Inhibitor (IC50: 29 nM). HPK1-IN-39 inhibits the phosphorylation of SLP76. HPK1-IN-39 can be used for research of cancer immunotherapy .
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Cat. No.: HY-P990041
CAS No.: 2750031-14-0
Synonyms: ADG-116

Target:  

CTLA-4

Research Areas:  

Inflammation/Immunology Cancer

Firastotug is an IgG1κ antibody targeting CTLA4. CTLA4 is a cytotoxic T lymphocyte-associated protein and a key immune checkpoint in the fields of autoimmunity and cancer .
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Cat. No.: HY-P990740
CAS No.: 2761795-00-8
Synonyms: EMB-02

Target:  

PD-1/PD-L1 LAG-3

Research Areas:  

Inflammation/Immunology Cancer

Fanastomig (EMB-02) is a bispecific antibody against PD-1/LAG3. Fanastomig exhibits potential immune checkpoint inhibitory activity and antineoplastic activity .
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Cat. No.: HY-13735H
CAS No.: 78901-94-7
Synonyms: Acriquine acetate
Research Areas:  

Cancer

Quinacrine (Acriquine) acetate is a small molecule modulator of the cGAS-STING-TBK1 signaling pathway, possessing immune stimulatory activity. Quinacrine acetate has been explored for its potential therapeutic applications in enhancing anti-tumor immunity. Quinacrine acetate can improve the effectiveness of cancer immunotherapies by addressing the poor immunogenicity of various tumors. Quinacrine acetate also presents a promising strategy for overcoming the limitations associated with immune checkpoint inhibitors in cancer treatment.
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Cat. No.: HY-132288
CAS No.: 2488761-03-9
Purity:  95.09%
Research Areas:  

Cancer

Pom-8PEG, an E3 ligase ligand-linker conjugate, incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase and an 8-unit PEG linker. Pom-8PEG can be used in the synthesis of PROTAC, such as IDO1 PROTAC degrader .
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Cat. No.: HY-151559
CAS No.: 3034629-04-1
Research Areas:  

Cancer

Zn-DPA-maytansinoid conjugate 1 is a small molecule-based maytansinoid conjugate targeting immune checkpoint. Zn-DPA-maytansinoid conjugate 1 induces lasting regression of tumor growth and rejuvenates tumor microenvironment (TME) to an "inflamed hot tumor" .
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Cat. No.: HY-P11061
CAS No.: 2036056-69-4
Target:  

Inhibitory Antibodies

Research Areas:  

Cancer

M27 peptide is an MHC class I epitope antigen that can be used in cancer nanovaccine research .
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Cat. No.: HY-P11062
CAS No.: 1415031-10-5
Synonyms: MUT30
Target:  

Inhibitory Antibodies

Research Areas:  

Cancer

M30 peptide is an MHC class II epitope antigen that can be used in cancer nanovaccine research .
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Cat. No.: HY-117161
CAS No.: 189057-68-9
Purity:  99.8%
Target:  

Cytochrome P450

Research Areas:  

Cancer

ZINC05626394 is a cytochrome b5 reductase 3 inhibitor with activity by increasing nitric oxide bioavailability. ZINC05626394 may have potential applications in anti-cancer suppression, especially in combination with antibody drug conjugates (ADCs) and immune checkpoint inhibitors. The efficacy of ZINC05626394 may be limited by different mechanisms, including antigen-related resistance and failure of endocytosis .
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Cat. No.: HY-P990986
CAS No.: 2922216-49-5

Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology Cancer

Efdelikofusp alfa is a bispecific Fc fusion protein. Efdelikofusp alfa is formed by fusing the N-terminal extracellular domain of human CD80 (B7.1) with the Fc fragment of human immunoglobulin G4 (IgG4), and is linked to an interleukin-2 variant (IL-2v) as the C-terminal part. Efdelikofusp alfa exhibits potential immunostimulatory, immune checkpoint inhibitory, and antitumor activities.
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Cat. No.: HY-P990992
CAS No.: 2922216-50-8
Synonyms: GI-102

Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology Cancer

Efzilonkofusp alfa is a bispecific Fc fusion protein. Efzilonkofusp alfa is formed by fusing the N-terminal extracellular domain of human CD80 (B7.1) with the Fc fragment of human immunoglobulin G4 (IgG4), and is linked to an interleukin-2 variant (IL-2v) as the C-terminal part. Efzilonkofusp alfa exhibits potential immunostimulatory, immune checkpoint inhibitory, and antitumor activities.
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Cat. No.: HY-N12041
Axl-IN-16 is a dual inhibitor of Axl/HIF. Axl-IN-16 induces fruiting body formation of Flammulina velutipes. Axl-IN-16 inhibits hypoxia-inducible factor activity and receptor tyrosine kinase expression .
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Cat. No.: HY-120646
CAS No.: 1675204-51-9
Target:  

PD-1/PD-L1

Research Areas:  

Others

BMS-242 is a small molecule PD-1/PD-L1 inhibitor with the activity of inhibiting the PD-1/PD-L1 interaction. BMS-242 can bind to the hydrophobic channel pocket between PD-L1 molecules, inhibit the PD-1/PD-L1 immune checkpoint pathway, and provide a new way for cancer inhibition.
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Cat. No.: HY-155675
Target:  

Drug Intermediate

Research Areas:  

Cancer

TPPC, a porphyrin cholesterol conjugate, can render cancer cells more sensitive to ICIs. TPPC can enhance photodynamic immunotherapy toward lung cancer .
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Cat. No.: HY-102011R
CAS No.: 1818314-88-3
BMS-1166 (Standard) is the analytical standard of BMS-1166 (HY-102011). This product is intended for research and analytical applications. BMS-1166 is a potent PD-1/PD-L1 immune checkpoint inhibitor. BMS-1166 induces dimerization of PD-L1 and blocks its interaction with PD-1, with an IC50 of 1.4 nM. BMS-1166 antagonizes the inhibitory effect of PD-1/PD-L1 immune checkpoint on T cell activation .
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Cat. No.: HY-101093R
CAS No.: 1673534-76-3
CA-170 (Standard) is the analytical standard of CA-170 (HY-101093). This product is intended for research and analytical applications. CA-170 is an orally delivered dual inhibitor of VISTA and PD-L1. CA-170 exhibits potent rescue of proliferation and effector functions of T cells inhibited by PD-L1/L2 and VISTA with selectivity over other immune checkpoint proteins as well as a broad panel of receptors and enzymes .
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Cat. No.: HY-150879A
CAS No.: 2108101-94-4
Target:  

PD-1/PD-L1

Research Areas:  

Cancer

BMS-37 hydrochloride is a PD-1/PD-L1 immune checkpoint inhibitor with an IC50 towards the PD-L1/PD-1 complex in the range of 18 to 200 nM. BMS-37 hydrochloride shows unspecific toxicity against modified Jurkat T cells with an EC50 between 3 and 6 µM. BMS-37 hydrochloride can be used for the study of the PD-L1-induced exhaustion of T-cells or as PD-L1 ligand to synthesize PROTAC molecules .
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Cat. No.: HY-P992377

Research Areas:  

Cancer

HY-0102 is a humanized IgG anti-NKG2A monoclonal antibody and immune checkpoint inhibitor targeting the NKG2A/HLA-E axis. HY-0102 is applicable for the research of advanced solid tumors .
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Cat. No.: HY-184295
Target:  

PD-1/PD-L1

Research Areas:  

Cancer

PD-1/PD-L1-IN-66 is a PD-1/PD-L1 immune checkpoint inhibitor with an IC50 of 3 nM for blocking the PD-1/PD-L1 interaction. PD-1/PD-L1-IN-66 shows good affinity for PD-L1 dimers with a Kd value of 0.75 nM. PD-1/PD-L1-IN-66 can reactivate the proliferation of cytotoxic T cells. PD-L1 ligand-2 is applicable for cancer research .
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