cp-2

CP-28888 (CP 28888-27) is an interferon inducer, a lipoamine with antitumor activity.

5-AAM-2-CP is one of the major metabolites of Acetamiprid. Acetamiprid, a nAChR agonist, is a neonicotinoid insecticide used worldwide.

CP-226269 is a potent dopamine D4 receptor agonist that regulates calcium flux and has an EC50 value of 32.0 nM. CP 226269 can be used to study neurological disorders such as schizophrenia.

5-AMAM-2-CP, a significant metabolite of Acetamiprid, serves as a global insecticide within the neonicotinoid class and acts as an nAChR agonist [1] [2].

[Rh(Cp-)Cl2]2 is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.

[Ir(Cp-)Cl2]2 serves as a precursor for catalysts used in the asymmetric transfer hydrogenation of ketones. It is also employed as a catalyst in more environmentally friendly amine synthesis.

CP-20961 is a synthetic non-immunogenic adjuvant. It induces arthritis.

CP-24879 hydrochloride (CP-24879 HCl), a Δ5D Δ6D dual-inhibitor, can significantly reduce intracellular lipid accumulation and inflammatory injury in hepatocytes. CP-24879 hydrochloride exhibits superior antisteatotic and anti-inflammatory actions in fat-1 and ω-3-treated hepatocytes.

CP-281384 is a potent, p38alpha-selective inhibitor.

CP-293019 is a potent, selective antagonist of dopamine D4 receptor.

JCP-265 is an ABHD6 inhibitor.

CP 220629 is a potent inhibitor of phosphodiesterase IV (PDE4).

CP-22185 is a bio-active chemical.

CP-283097 is an N-methyl-D-aspartic acid (NMDA) receptor antagonist with NR2B subunit.

CP-294838 is a bioactive chemical.

CP-289 is a potent C5a receptor antagonist with IC50 of 1 μM.

CP2 is a useful organic compound for research related to life sciences and the catalog number is T35338.

CP-547632 is an orally available and potent, ATP-competitive dual inhibitor of VEGFR-2 and FGF kinase F with IC50s of 11 nM and 9 nM, respectively. CP-547632 is selective, with higher selectivity for VEGFR2 and bFGF than for EGFR, PDGFRβ and related tyrosine kinases (TKs). PDGFRβ and related tyrosine kinases (TKs) CP-547632 has antitumour activity.

Tenidap (CP-66248) is a selective COX-1 and SLC26A3 inhibitor with anti-inflammatory, analgesic, and anti-rheumatic activities.

BrBzGCp2 (p BrBzGSH(Cp)2) is an inhibitor of glyoxalase 1 (GLO1) with antitumor and neuroprotective activity. It can alleviate anxiety and be used in neurodegenerative disease research.

CP 461 (UNII-68OJX9I7DT), a specific PDE2A inhibitor, is a novel pro-apoptotic compound that inhibits cyclic GMP phosphodiesterase but not cyclooxygenase-1 or -2. CP 461 inhibits the growth of a variety of human tumor cell lines in vitro and selectively induces apoptosis in cancer cell lines, but not in normal cells.

Piroxicam (CP-16171) is a non-specific COX inhibitor.

Cefoperazone sodium salt (CP 52640-2) is a broad-spectrum cephalosporin with a tetrazolyl moiety, utilized for the treatment of Pseudomonas infections.

Glipizide (CP 28720) is a short-acting, second-generation sulfonylurea with hypoglycemic activity.