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Cat. No. Product Name Field of Application Chemical Structure
DC21345 Contezolid Contezolid (MRX I) is an orally active oxazolidinone agent with antibacterial activity Gram-positive pathogens, including MRSA, penicillin-PRSP, PISP, and vancomycin-resistant enterococci (VRE) with MIC of 0.25-4 ug/mL.
DC11048 Contilisant Contilisant is a neuroprotective, non-toxic, antioxidant, permeable ligand, showing in vitro pharmacological properties on the selected biological targets (hAChE IC50=0.53 uM.
DC10776 Cordycepin Featured Cordycepin is an adenosine analogue, which is readily phosphorylated to its mono-, di-, and triphosphate intracellularly. It has a very potent anti-cancer, anti-oxidant and anti-inflammatory activities.
DC12098 Corin Featured Corin is a dual inhibitor of histone lysine specific demethylase (LSD1) and histone deacetylase (HDAC), with a Ki(inact) of 110 nM for LSD1 and an IC50 of 147 nM for HDAC1.
DC11104 Tildacerfont Featured corticotropin releasing factor (CRF) antagonist.
DC22488 Corticotropin-releasing factor (human) Featured Corticotropin-releasing hormone (CRH) is a peptide hormone involved in the stress response..
DC22479 Cortisone acetate Cortisone acetate (Cortisone 21-acetate) is a synthetic glucocorticoid corticosteroid and corticosteroid ester.
DC23908 Cortisone Featured Cortisone is a pregnane (21-carbon) steroid hormone, one of the main hormones released by the adrenal gland in response to stress.
DC8694 Cortodoxone Cortodoxone is a glucocorticoid steroid hormone that can be oxygenated to cortisol (Hydrocortisone).
DC10686 Cosan-528 Featured Cosan-528 is a bioactive chemical.
DC9554 Cot inhibitor-1 Cot inhibitor-1 is a COT/Tpl2 inhibitor.
DC9555 Cot inhibitor-2 Cot inhibitor-2 is a COT/Tpl2 inhibitor.
DC10657 COTI-2 Featured COTI-2 is a small molecule candidate anti-cancer drug which can convert mutant p53 to wild-type conformation.
DC20933 Cotylimide-VI Cotylimide-VI (CTL-VI) is a small molecule that perturbs plant hormone strigolactone accumulation and inhibits hypocotyl growth..
DC10363 Coumestrol Featured Coumestrol, a phytoestrogen present in soybean products, exhibits activities against cancers, neurological disorders, and autoimmune diseases. It suppresses proliferation of ES2 cells with an IC50 of 50 μM.
DC21413 Cowanin Cowanin is a novel natural product from Garcinia speciosa that inhibits the Notch signaling pathway with IC50 of 2.4 uM.
DC10528 CP 376395 Featured CP 376395 is a potent and selective CRF1 receptor antagonist (Ki values are 12 and >10000 nM for CRF1 and CRF2 receptors respectively).
DC8543 CP465022 HCl CP 465022 hydrochloride is a selective GluR (AMPA) antagonist which is non-competitive.
DC7389 CP-673451 Featured CP 673451 is a selective inhibitor of PDGFRα/β with IC50 of 10 nM/1 nM, exhibits >450-fold selectivity over other angiogenic receptors, has antiangiogenic and antitumor activity.
DC12046 CP 105696 Featured CP-105696 is a potent and selective Leukotriene B4 Receptor antagonist, with an IC50 of 8.42 nM.
DC9726 CP21 (CP21R7) Featured CP21R7 is a potent and selective GSK-3β inhibitor.
DC23320 CP 31398 dihydrochloride Featured CP-31398 is a small molecule p53 reactivator that protects p53 from thermal denaturation, not only reactivates mutant p53 but also induces stabilization of wild type p53.
DC23610 CP-339818 hydrochloride Featured CP-339818 is a potent, selective, non-peptide KV1.3 channel antagonist with IC50 of 200 nM.
DC4112 CP466722 Featured CP-466722 is an potent and reversible ATM inhibitor.
DC23415 CP-481715 CP-481715 is a potent and selective CCR1 antagonist with Ki of 9.2 nM and IC50 of 74 nM, lacks intrinsic agonist activity and .
DC9303 Taprenepag(CP-544326) Featured CP-544326 is a selective prostaglandin EP(2) agonist on intraocular pressure in preclinical models of glaucoma.
DC4132 CP-547632 Featured CP-547632 is as a potent inhibitor of the VEGFR-2 and basic fibroblast growth factor (FGF) kinases (IC50 11 and 9 nM, respectively).
DC9265 CP-640186 hydrochloride Featured CP-640186 Hcl is an isozyme-nonselective acetyl-CoA carboxylase (ACC) inhibitor with IC50s of 53 nM and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2 respectively; with improved metabolic stability vs CP-610431.
DC7975 CP 640186 Featured CP-640186 is an isozyme-nonselective acetyl-CoA carboxylase inhibitor with IC50s of 53 nM and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2 respectively.
DC11410 CP-671305 Featured CP-671305 is a potent and selective inhibitor of phosphodiesterase 4.

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