CAS 476181-74-5|CNTO 148

Introduction:Basic information about CAS 476181-74-5|CNTO 148, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameCNTO 148
CAS Number476181-74-5Molecular Weight/
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Names

NameCNTO 148

CNTO 148 BiologicalActivity

DescriptionGolimumab (CNTO-148) is a potent human IgG1 TNFα antagonist monoclonal antibody. Golimumab has anti-inflammation activitity and inhibits IL-6 and IL-1β production. Golimumab acts via targeting and neutralizing TNF to prevent inflammation and destruction of cartilage and bone. Golimumab has the anticancer activity and induces cell apoptosis. Golimumab can be used for rheumatoid arthritis, Crohn's disease and cancer research[1][2][3].
Related CatalogSignaling Pathways >>Apoptosis >>ApoptosisResearch Areas >>CancerSignaling Pathways >>Immunology/Inflammation >>Interleukin RelatedSignaling Pathways >>Apoptosis >>CaspaseResearch Areas >>Inflammation/Immunology
Target

TNFα

In VitroGolimumab (CNTO-148) (0.1-10 μg /mL; 24-72 hours; transmembrane TNFα–transfected Jurkat cells) induces reductions in the viability of transmembrane TNFα–expressing cells[1]. Golimumab (CNTO-148) (10 μg /mL; 48 hours; transmembrane TNFα–transfected Jurkat cells) induces apoptosis, increase the levels of active caspase-3 and induces apoptotic DNA fragmentation[1]. Cell Viability Assay[1] Cell Line: Transmembrane TNFα–transfected Jurkat cells Concentration: 0.1, 1 and 10 μg/mL Incubation Time: 24, 48 and 72 hours Result: Reduced cell viability in a dose- and time-dependent manner. Apoptosis Analysis[1] Cell Line: Transmembrane TNFα–transfected Jurkat cells Concentration: 10 μg /mL Incubation Time: 48 hours Result: Had the percentage of apoptotic cells for 30.29%. Western Blot Analysis[1] Cell Line: Transmembrane TNFα–transfected Jurkat cells Concentration: 10 μg /mL Incubation Time: 48 hours Result: Increased the levels of active caspase-3 and induces apoptotic DNA fragmentation.
In VivoGolimumab (CNTO-148) (24 mg/kg; i.h.; daily, for 7 days; swiss-albino healthy male mice) inhibits oxidative stress, apoptotic cell death inflammatory response, thus improving renal function. Golimumab reduces all markers of kidney injury and attenuates cell death[2]. Golimumab (CNTO-148) (1-10 mg/kg; i.p.;daily; for 4 weeks; Tg197 transgenic mouse model) relieves TNFα-induced arthritis in a mouse model of human[3]. Animal Model: Swiss-albino healthy male mice[2] Dosage: 24 mg/kg Administration: Subcutaneous injection; daily, for 7 days Result: Reduced serum parameters like BUN, NGAL creatinine, cystatin C, and urinary parameters like KIM-1, NAG, albumin clusterin. Animal Model: Swiss-albino healthy male mice[2] Dosage: 24 mg/kg Administration: Subcutaneous injection; daily, for 7 days Result: Inhibited oxidative stress, reduces MDA concentrations and increases the GSH and catalase levels. Animal Model: Swiss-albino healthy male mice[2] Dosage: 24 mg/kg Administration: Subcutaneous injection; daily, for 7 days Result: Inhibitd cisplatin-induced inflammation, decreased TNF-α, including IL-6, IL-1β, MCP-1, ICAM-1, and TGF-β1 levels and increases IL-10 concentrations, reduced caspase 3 in cisplatin injected mice kidneys. Animal Model: Tg197 transgenic mouse model[3] Dosage: 1 and 10 mg/kg Administration: Intraperitoneal injection;for 4 weeks Result: Reduced the arthritic index.
References

[1]. Ueda N, et, al. The cytotoxic effects of certolizumab pegol and golimumab mediated by transmembrane tumor necrosis factor α. Inflamm Bowel Dis. 2013 May;19(6):1224-31.

[2]. Pavitrakar V, et, al. Amelioration of Cisplatin-induced Renal Inflammation by Recombinant Human Golimumab in Mice. Curr Pharm Biotechnol. 2022;23(7):970-977.

[3]. Shealy DJ, et, al. Characterization of golimumab, a human monoclonal antibody specific for human tumor necrosis factor α. MAbs. 2010 Jul-Aug;2(4):428-39.

Chemical & Physical Properties

No Any Chemical & Physical Properties
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