| DC20093 |
Cinchonine ((8R,9S)-Cinchonine; LA40221)
Featured
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Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells. |
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| DC9896 |
Cinnarizine
Featured
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Cinnarizine is a medication derivative of piperazine, and characterized as an antihistamine and a calcium channel blocker. |
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| DCH-062 |
Cinobufotalin
Featured
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Cinobufotalin is a steroid glycoside originally isolated from the Asiatic toad (B. gargarizans) and has diverse biological activities. |
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| DC22295 |
Cintirorgon sodium
Featured
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Cintirorgon (LYC-55716) is novel oral RAR-related orphan receptor γ (RORγ) agonist. |
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| DC22329 |
Cintirorgon
Featured
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Cintirorgon (LYC-55716) is novel oral RAR-related orphan receptor γ (RORγ) agonist. |
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| DCAPI1372 |
Ciprofloxacin (Cipro)
Featured
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Ciprofloxacin (Bay-09867) is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity. |
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| DC2062 |
Ciproxifan (FUB-359)
Featured
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Ciproxifan is an antagonists of H3-type histamine receptors. |
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| DC9466 |
Ciproxifan (maleate)
Featured
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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.
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| DC8156 |
CIQ
Featured
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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). |
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| DC8187 |
Ciraparantag(PER977)
Featured
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Ciraparantag(PER977) is an intravenously administered anticoagulant Reversal Agent. |
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| DCAPI1600 |
Cisapride
Featured
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Cisapride is a SR-4 agonist also known as Enteropride |
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| DC9517 |
Cisatracurium (besylate)
Featured
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Cisatracurium Besylate is a nondepolarizing neuromuscular blocking agent, antagonizing the action of acetylcholine by inhibiting neuromuscular transmission.
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| DC2099 |
cis-Diaminedichloroplatinum
Featured
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Cisplatin is an inorganic platinum agent (cis-diamminedichloroplatinum) with antineoplastic activity. |
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| DC12668 |
Citarinostat(ACY-241)
Featured
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Citarinostat(ACY-241) is a potent, selective and orally available histone deacetylase (HDAC) inhibitor, with potential antineoplastic activity. |
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| DC20906 |
CJ-13610
Featured
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CJ-13610 is a potent 5-Lipoxygenase (5-LO) inhibitor that suppresses 5-LO product formation with IC50 of 70 nM. |
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| DC20907 |
CK 666
Featured
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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). |
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| DC11673 |
CK-2127107
Featured
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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. |
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| DC7386 |
CK-636
Featured
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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. |
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| DC11475 |
CK-869
Featured
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CK-869 is an inhibitor of human and bovine actin-related protein 2/3 (Arp2/3) complex. |
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| DC12595 |
CL27c
Featured
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CL27c is a cell-permeable, inhaled lipophilic ester prodrug of CL27e, which is a potent, selective pan-class I PI3K inhibitor, CL27c is inactive in PI3K enzymatic assay, once inside the cytoplasm, CL27c is metabolized by unspecific esterases into CL27e. |
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| DC7668 |
CL-387785
Featured
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CL-387785(EKI785; WAY-EKI 785) is an irreversible inhibitor of EGFR with IC50 of 370+/-120 pM; is able to overcome resistance caused by the T790M mutation on a functional level. |
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| DC12292 |
Cl-amidine hydrochloride
Featured
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Cl-amidine (hydrochloride) is a peptidylarginine deminase (PAD) inhibitor, with an IC50 5.9 μM for PAD4. |
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| DC9725 |
Cl-amidine
Featured
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Cl-amidine is a cell-permeable compound that acts as a pan PAD inhibitor (IC50 = 0.8 µM, 6.2 µM and 5.9 µM for PAD1, PAD3, and PAD4, respectively) in enzymatic assays. |
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| DC9868 |
Clanfenur
Featured
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Clanfenur is a substituted benzoylphenylurea and an analogue of the pesticide diflubenzuron with potential antineoplastic activity. |
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| DC7387 |
Clemizole Hydrochloride
Featured
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Clemizole is a H1 histamine receptor antagonist.Recently, researchers have identified that clemizole hydrochloride can inhibit NS4B's RNA binding and hepatitis C virus (HCV) replication. |
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| DC8832 |
Clemizole (free base)
Featured
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Clemizole is a H1 histamine receptor antagonist.Recently, researchers have identified that clemizole hydrochloride can inhibit NS4B's RNA binding and hepatitis C virus (HCV) replication. |
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| DC9380 |
Cleviprex
Featured
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Clevidipine(Clevidipine) is a short-acting dihydropyridine calcium channel antagonist (IC50= 7.1 nM, V(H) = -40 mV ) under development for treatment of perioperative hypertension.
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| DCAPI1085 |
Clevudine (Levovir)
Featured
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Clevudine (Levovir) is an antiviral drug for the treatment of hepatitis B,showed potent activity against COVID-19(SARS-COV-2) . |
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| DC21722 |
CLK-IN-T3
Featured
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CLK inhibitor T3 (T3) is a highly potent, selective, and cell-based stable CDC-like kinase (CLK) inhibitor with 0.67, 15 and 110 nM for CLK1,2 and 3, respectively. |
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| DCAPI1428 |
Clofarabine
Featured
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Clofarabine(Clolar; Clofarex) inhibits the enzymatic activities of ribonucleotide reductase (IC50 = 65 nM) and DNA polymerase. IC50 Value: 65 nM Target: in vitro: Clofarabine is a second generation purine nucleoside analog with antineoplastic activity. It |
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