11 Results for "

Perforin

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "Perforin" in MCE Product Catalog:

7
7 Cited Publications
Cat. No.: HY-16307
CAS No.: 261365-11-1
Target:  

FBPase

Research Areas:  

Metabolic Disease Cancer

MB05032 is a fructose-1,6-bisphosphatase (FBP1/FBPase) inhibitor with an IC50 value of 16 nM. MB05032 blocks FBP1-mediated glycolysis inhibition in NK cells, restores NK cell glucose uptake, lactate production, degranulation, perforin production, and cytotoxicity against gastric cancer cells. MB05032 elevates ATP/ADP ratios, increases glucose utilization, and enhances insulin secretion in pancreatic β-cells. MB05032 increases neutrophil adhesion, phagocytosis, and mRNA abundance of HKII, ITGA9, CD36 in subclinically hypocalcemic dairy cows. MB05032 inhibits gluconeogenesis in hepatocytes, acts as the active metabolite of prodrug Managlinat dialanetil (MB06322) (HY-14955). MB05032 can be used for the research of gastric cancer, type 2 diabetes, subclinical hypocalcemia, and insulin resistance .
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1
1 Cited Publications
Cat. No.: HY-160214
CAS No.: 1567836-70-7
Target:  

Complement System

Research Areas:  

Inflammation/Immunology Cancer

Perforin-IN-2 (Compound 1) is the inhibitor for perforin that inhibits perforin-mediated cell lysis, thereby reducing graft rejection during allogeneic bone marrow/stem cell transplantation .
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Cat. No.: HY-P99759
CAS No.: 1622189-43-8
Synonyms: IL-15N72D

Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology Cancer

Nogapendekin alfa his tag (IL-15N72D) is a blood-brain barrier-permeable IL-2Rβ (CD122) binding enhancer and antitumor agent. Nogapendekin alfa his tag promotes the proliferation and activation of NK cells and CD8 + T cells, enhances cytotoxicity through the expression of granzyme B and perforin, reduces tumor burden, and boosts the activity of bacillus Calmette-Guérin (BCG). Nogapendekin alfa his tag promotes the secretion of proinflammatory cytokines including IL-6, IFN-γ, MCP-1, TNF-α, IL-1α, IL-1β and RANTES, and also stimulates the infiltration of immune cells into lymphoid organs and the tumor microenvironment. Nogapendekin alfa his tag reduces tumor angiogenesis and tumor cell proliferation, and enhances antibody-dependent cell-mediated cytotoxicity of anti-PD-L1 monoclonal antibodies as well as bifunctional fusion proteins targeting PD-L1 and TGF-βR2. Nogapendekin alfa his tag is suitable for research on non-muscle-invasive bladder cancer .
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Cat. No.: HY-162972
CAS No.: 2995357-09-8
Target:  

PROTACs PD-1/PD-L1

Research Areas:  

Inflammation/Immunology Cancer

PROTAC PD-L1 degrader-2 is a PD-L1 PROTAC degrader with an IC50 of 197.4 nM and a Kd of 301 nM. PROTAC PD-L1 degrader-2 induces PD-L1 endocytosis, drives degradation via the proteasomal and lysosomal pathways, and inhibits the PD-1/PD-L1 interaction. As an immune activator, PROTAC PD-L1 degrader-2 increases the levels of CD4 +, CD8 +, granzyme B and perforin. PROTAC PD-L1 degrader-2 can be used in studies related to colon cancer immunology .
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Cat. No.: HY-W989139
CAS No.: 178970-88-2
Target:  

Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Perforin-IN-3 is a specific perforin inhibitor that blocks perforin-mediated lytic pore formation and subsequent cell lysis. Perforin-IN-3 potently inhibits the killing effect of NK cells on target cells such as leukemia cells, without interfering with FasL- or TRAIL-mediated cell death pathways. Perforin-IN-3 has no effect on pneumolysin and can be used to study autoimmune diseases, allograft rejection, graft-versus-host disease, and familial hemophagocytic lymphohistiocytosis .
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Cat. No.: HY-P85946
Synonyms: Cytolysin; FLH2; HPLH2; Lymphocyte pore-forming protein; P1; PERF_HUMAN; Perforin 1; pore forming protein; Perforin 1; Perforin-1; PFP; PGFL; PIGF; PIGF-2; PLGF; Pore forming protein; prf1; SHGC-10760

Host:  

Mouse

Application:  

IHC-P, WB, ICC/IF, ELISA

Reactivity:  

Human

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Cat. No.: HY-184299
Research Areas:  

Cancer

PD-1/PD-L1-IN-65 is a PD-1/PD-L1 checkpoint inhibitor, with an EC50 of 6.06 μM for blocking the PD-1/PD-L1 interaction and a Kd of 1.43 μM for PD-L1. PD-1/PD-L1-IN-65 upregulates pro-inflammatory cytokines IFN-γ, IL-1α, IL-1β and the cytolytic protein perforin, and reverses T cell exhaustion. PD-1/PD-L1-IN-65 enhances T cell-mediated cancer cell lysis. PD-1/PD-L1-IN-65 can be used in the research of breast cancer .
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Cat. No.: HY-P706130
Purity:  ≥ 85%, as determined by Bis-Tris PAGE.
Synonyms: Cytolysin; FLH2; HPLH2; Lymphocyte pore-forming protein; P1; PERF_HUMAN; Perforin 1 (pore forming protein); Perforin 1; Perforin-1; PFP; PGFL; PIGF; PIGF-2; PLGF; Pore forming protein; prf1
Species:  
Source:  
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Cat. No.: HY-P84096
Synonyms: P1; PFP; HPLH2

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human, Mouse

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Cat. No.: HY-P84096A
Synonyms: P1; PFP; HPLH2

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human, Mouse

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Cat. No.: HY-185050
CAS No.: 2978670-53-8
Target:  

IFNAR

Research Areas:  

Cancer

Antitumor agent-210 (Compound 1778) is an NK cell activator. Antitumor agent-210 has a weak proliferative effect on NK92 cells, promoting the activation and degranulation of NK cells, and significantly enhancing the cytotoxicity of NK92 cells against tumor cells. Antitumor agent-210 promotes the release of cytokine granzyme B, perforin, and IFN-γ. Antitumor agent-210 reduces the number of lung metastatic lesions in mice and can be used for the study of melanoma lung metastasis .
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