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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T37196 | 5-AAM-2-CP | AChR | |
5-AAM-2-CP is one of the major metabolites of Acetamiprid. Acetamiprid, a nAChR agonist, is a neonicotinoid insecticide used worldwide. | |||
T6685 | Sulbactam sodium | CP-45899-2 | Antibacterial , Antibiotic |
Sulbactam sodium (CP-45899-2) (Unasyn) is an irreversible β-lactamase inhibitor. | |||
T21648 | CP-31398 dihydrochloride | CP 31398 dihydrochloride | p53 |
CP-31398 dihydrochloride is a p53 stabilizer which stabilizes the active conformation of p53 and promotes p53 activity in cancer cell lines with mutant or wild-type p53. | |||
T1218 | Cefoperazone sodium salt | CP 52640-2,Cefoperazone sodium | Antibacterial , Antibiotic |
Cefoperazone sodium salt (CP 52640-2) is broad-spectrum cephalosporin with a tetrazolyl moiety, used to treat Pseudomonas infections. | |||
T1603 | Glipizide | CP 28720,K 4024 | Potassium Channel , PPAR , ABC |
Glipizide (CP 28720) is a short-acting, second-generation sulfonylurea with hypoglycemic activity. | |||
T15259 | Evatanepag | CP-533536 free acid | Prostaglandin Receptor |
Evatanepag (CP-533536 free acid) is an EP2 receptor selective prostaglandin E2 (PGE2) agonist that induces local bone formation with EC50 of 0.3 nM.CP-533536 demonstrated the ability to heal fractures when administered l... | |||
T9032 | MGH-CP1 | Others | |
MGH-CP1 is a potent and selective inhibitor TEAD palmitoylation. It exhibits dose-dependent and potent inhibition of TEAD2/4 auto-palmitoylation in vitro with IC50 of 710 nM and 672 nM, respectively. | |||
T35338 | CP2 | Histone Demethylase | |
CP2 is a useful organic compound for research related to life sciences and the catalog number is T35338. | |||
T24598 | BrBzGCp2 | p BrBzGSH(Cp)2,BBGC,pBrBzGSH(Cp)2,p-BrBzGSH(Cp)2,BBGD | |
p-BrBzGSH(Cp)2 is a glyoxylase 1 inhibitor. In orthotopic mouse models, it acts by increasing DNA-AGEs, stimulating RAGE expression, and inhibiting brain tumor growth. | |||
T31627 | Englitazone sodium | CP-72,467-2,D03996,CP-72467-2,Englitazone sodium (USAN) | |
Englitazone sodium is an antidiabetic agent and a novel NSCA and KATP channel blocker. | |||
T71262 | AZD-8418 | ||
AZD-8418 is an mGlu2 receptor positive allosteric modulators that attenuates nicotine-taking and nicotine-seeking behavior. Acute treatment with AZD8418 (0.37, 1.12, 3.73, 7.46, and 14.92 mg/kg) and AZD8529 (1.75, 5.83, ... | |||
T74086 | 5-AMAM-2-CP | ||
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]. | |||
T40295 | Carindacillin sodium | Carindacillin sodium,CP-15464-2,Carbenicillin indanyl sodium | |
Carindacillin sodium, also known as Carbenicillin indanyl sodium, is an orally active, broad-spectrum antimicrobial agent. In vivo, it undergoes hydrolysis to Carbenicillin. Carindacillin sodium is specifically utilized ... | |||
T10870L | CP-547632 | VEGFR , FGFR , PDGFR , BTK | |
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... | |||
T6328 | Desmethyl Erlotinib | OSI-420,CP-473420,O-Desmethyl Erlotinib | EGFR , Drug Metabolite |
Desmethyl Erlotinib (CP-473420) is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM). | |||
T31020 | CP 461 | OSI 461,UNII-68OJX9I7DT,CP-461,CP461 | Apoptosis , PDE |
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 ce... | |||
T2398 | Tofacitinib Citrate | CP-690550 citrate,Tasocitinib citrate,Tofacitinib (CP-690550) Citrate | Apoptosis , Influenza Virus , JAK , Antibacterial , Antifungal |
Tofacitinib Citrate (CP-690550 citrate) is a a potent, cell-permeable inhibitor of JAK1/2/3 (IC50s: 1/20/112 nM). | |||
T0758 | Piroxicam | CP-16171 | COX |
Piroxicam (CP-16171) is a non-specific COX inhibitor. | |||
T22689 | CP94253 hydrochloride | CP 94253 hydrochloride | Others , 5-HT Receptor |
CP94253 hydrochloride (CP 94253 hydrochloride) is a potent, selective and centrally active agonist of 5-HT1B receptor with Ki of 2 nM. The Kis are 89, 49, 860, and 1600 nM for 5-HT1A, 5-HT1D, 5-HT1C and 5-HT2 receptors, ... | |||
T37075 | CB2R PAM | Ec2la | Cannabinoid Receptor |
CB2R PAM is an orally active cannabinoid type 2 receptor (CB2Rs) positive mutational modulator that enhances CP 55940 and 2-Arachidonylglycerol-stimulated [35S]GTPγS binding to CB2 receptors, but has no effect in the abs... |