7 Results for "

J774-A1 macrophages

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "J774-A1 macrophages" in MCE Product Catalog:

Cat. No.: HY-131521
CAS No.: 89304-26-7
Synonyms: Oxalomalate trisodium
Research Areas:  

Cancer

Oxalomalic acid (Oxalomalate) trisodium is a aconitase and NADP-dependent isocitrate dehydrogenase inhibitor. Oxalomalic acid trisodium inhibits nitrite production and iNOS protein expression in lipopolysaccharide (HY-D1056)-activated J774 macrophages .
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Cat. No.: HY-117432
CAS No.: 2112809-98-8
Purity:  98.41%
Research Areas:  

Inflammation/Immunology

JC-171 is a selective NLRP3 inflammasome inhibitor, with an IC50 of 8.45 μM for inhibiting LPS/ATP-induced interleukin-1β (IL-1β) release from J774A.1 macrophages .
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Cat. No.: HY-N16039
CAS No.: 126221-76-9
TAN-1030A is an indolocarbazole alkaloid with macrophage-activating properties. TAN-1030A induces spreading of a murine macrophage cell line, Mm 1, and augmentes the phagocytic activity, Fc gamma receptor expression and β-glucuronidase activity of murine macrophage cell lines, Mm 1 and J774A.1. TAN-1030A can activate macrophage functions in mice .
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Cat. No.: HY-133133
CAS No.: 4818-19-3
IIIM-1270is a NLRP3 inflammasome inhibitor. IIIM-1270 inhibits IL-1β release in mouse macrophages (J774A.1 cells) (IC50 = 3.5 μM) and significantly reduced the protein expression level of mature IL-1β. IIIM-1270 can be used for the study of inflammation .
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Cat. No.: HY-171905
CAS No.: 3069417-18-8
Target:  

Liposome

Research Areas:  

Others

N-Sterol is a sterol lipid that has been used to generate lipid nanoparticles (LNPs) for delivery of mRNA in vitro and in vivo. N-Sterol LNPs are taken up in J774A.1 macrophages in a lipid composition-dependent manner via clathrin caveolae, caveolin-mediated endocytosis, micropinocytosis, or phagocytosis at different frequencies .
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Cat. No.: HY-133132
CAS No.: 2468202-93-7
IIIM-1266 is a NLRP3 inflammasome inhibitor. IIIM-1266 inhibits IL-1β release in mouse macrophages (J774A.1 cells) (IC50 = 2.3 μM) and significantly reduced the protein expression level of mature IL-1β. IIIM-1266 can be used for the study of inflammation .
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Cat. No.: HY-189461
Target:  

Parasite

Research Areas:  

Infection

Antiparasitic agent-48 is an orally active Schistosoma mansoni cathepsin B1 (SmCB1) modulator that exerts antischistosomal effects by stably binding to the enzyme active site, with an IC50 of 50.74 μM. It induces tegumental disruption, modulates immune responses, inhibits hepatic granuloma formation, and reduces worm burden and tissue egg burden. Antiparasitic agent-48 can be used for research on schistosomiasis .
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