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Inhibitors & Agonists

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Cat. No. Product Name Field of Application Chemical Structure
DC12369 Cinaciguat (hydrochloride) Featured Cinaciguat is an activator of sGC that binds to a regulatory site, resulting in activation in an NO-independent manner (Kd = 3.2 nM).
DC20093 Cinchonine ((8R,9S)-Cinchonine; LA40221) Featured Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells.
DC9174 Cinepazide maleate Cinepazide Maleate is a vasodilator.
DC9896 Cinnarizine Featured Cinnarizine is a medication derivative of piperazine, and characterized as an antihistamine and a calcium channel blocker.
DCH-062 Cinobufotalin Featured Cinobufotalin is a steroid glycoside originally isolated from the Asiatic toad (B. gargarizans) and has diverse biological activities.
DC22295 Cintirorgon sodium Featured Cintirorgon (LYC-55716) is novel oral RAR-related orphan receptor γ (RORγ) agonist.
DC22329 Cintirorgon Featured Cintirorgon (LYC-55716) is novel oral RAR-related orphan receptor γ (RORγ) agonist.
DC21572 Cipemastat Cipemastat (Ro 32-3555) is a potent, second-generation, orally active MMP inhibitor, preferentially inhibits collagenases (MMP-1, -8, and -13) and gelatinase B (MMP-9).
DC9603 Ciprofibrate Ciprofibrate is a peroxisome proliferator-activated receptor agonist.
DCAPI1372 Ciprofloxacin (Cipro) Featured Ciprofloxacin (Bay-09867) is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity.
DC2062 Ciproxifan (FUB-359) Featured Ciproxifan is an antagonists of H3-type histamine receptors.
DC9466 Ciproxifan (maleate) Featured Ciproxifan maleate(FUB-359 maleate) is a highly potent and selective histamin H3-receptor antagonist with IC50 of 9.2 nM, with low apparent affinity at other receptor subtypes.
DC8156 CIQ Featured CIQ is a positive allosteric modulator selective for NR2C/D containing NMDA receptors (EC50 = 2.7 and 2.8 µM for NR2C and NR2D, respectively).
DC8187 Ciraparantag(PER977) Featured Ciraparantag(PER977) is an intravenously administered anticoagulant Reversal Agent.
DC12100 Cirsimaritin Cirsimaritin binds weakly to the benzodiazepine site on GABAA receptors, with antidepressant, anxiolytic and antinociceptive activities.
DC20342 cis Ned-19 cis Ned-19 is the stereoisomer of trans Ned-19, a chemical probe for the Ca(2+)-releasing second messenger NAADP.
DCAPI1600 Cisapride Featured Cisapride is a SR-4 agonist also known as Enteropride
DC9517 Cisatracurium (besylate) Featured Cisatracurium Besylate is a nondepolarizing neuromuscular blocking agent, antagonizing the action of acetylcholine by inhibiting neuromuscular transmission.
DC2099 cis-Diaminedichloroplatinum Featured Cisplatin is an inorganic platinum agent (cis-diamminedichloroplatinum) with antineoplastic activity.
DC9118 Citalopram HBr Citalopram hydrobromide is an antidepressant drug of the selective serotonin reuptake inhibitor (SSRI) class. It has US FDA approval to treat major depression.
DC12668 Citarinostat(ACY-241) Featured Citarinostat(ACY-241) is a potent, selective and orally available histone deacetylase (HDAC) inhibitor, with potential antineoplastic activity.
DCAPI1527 Citicoline Sodium Citicoline Sodium
DC20906 CJ-13610 Featured CJ-13610 is a potent 5-Lipoxygenase (5-LO) inhibitor that suppresses 5-LO product formation with IC50 of 70 nM.
DC20907 CK 666 Featured CK 666 (CK 0944666) is a small molecule Arp2/3 complex inhibitor with IC50 of 4 uM, inhibits actin polymerization with either BtArp2/3 complex (IC50=17 uM) or SpArp2/3 complex (IC50=5 uM).
DC20343 CK1-IN-3c CK1-IN-3c is a novel casein kinase 1δ/ε (CK1δ/ε) inhibitor with IC50 of 1.6 uM.
DC11673 CK-2127107 Featured CK-2127107(CK-107, Reldesemtiv) is a novel orally active fast skeletal troponin activator, selectively activates fast skeletal myofibrils with EC50 of 3.4 uM.
DC20344 CK2-IN-1 CK2-IN-1 is a potent, competitive inhibitor of ATP binding to Casein kinase 2(CK2) with IC50 of 9 nM, induces differentiation of epidermal progenitor cells to terminally differentiated keratinocytes with EC50 of 0.1 uM..
DC7386 CK-636 Featured CK-636(CK-0944636) is a small molecule inhibitor of Arp2/3 complex; Inhibitor of actin polymerization; Cell permeable inhibitor of human (IC50=4μM), fission yeast (IC50=24μM) and bovine (IC50=32μM) Arp2/3 complex between Arp2 and Arp3.
DC11475 CK-869 Featured CK-869 is an inhibitor of human and bovine actin-related protein 2/3 (Arp2/3) complex.
DC11107 CKD-516 CKD-516 (Valecobulin, CKD516) is a potent beta-tubulin polymerization inhibitor with marked antitumor activity both in vitro and in vivo.

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