| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCAPI1372 | Ciprofloxacin (Cipro) Featured | Ciprofloxacin (Bay-09867) is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity. |
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| 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. |
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| DC12100 | Cirsimaritin | Cirsimaritin binds weakly to the benzodiazepine site on GABAA receptors, with antidepressant, anxiolytic and antinociceptive activities. |
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| 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. |
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| DC9517 | Cisatracurium (besylate) Featured | Cisatracurium Besylate is a nondepolarizing neuromuscular blocking agent, antagonizing the action of acetylcholine by inhibiting neuromuscular transmission. |
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| 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. |
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| 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). |
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| DC20343 | CK1-IN-3c | CK1-IN-3c is a novel casein kinase 1δ/ε (CK1δ/ε) inhibitor with IC50 of 1.6 uM. |
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| 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.. |
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| 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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| DC11098 | CKD-519 | CKD-519 (Rocacetrapib, CKD519) is a potent, selective cholesteryl ester transfer protein (CETP) inhibitor, inhibits the CETP-mediated transfer of cholesteryl ester in human serum with IC50 of 2.3 nM. |
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| DC20847 | CL 316243 | CL 316243 (BTA 243) is a potent, highly selective, orally active β3-adrenoceptor agonist with EC50 of 3 nM. |
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| DC20909 | CL 316243 disodium | CL 316243 is a potent, highly selective, orally active β3-adrenoceptor agonist with EC50 of 3 nM. |
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| DC20910 | CL-82198 hydrochloride | CL-82198 is a potent, selective inhibitor of MMP-13 (89% inhibition at 10 ug/mL), displays no activity at MMP-1, MMP-9 and TACE, significantly reduces the migration of LS174 cells by 55% at 10 uM.. |
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| DC4205 | Cladribine | Cladribine (Leustatin, Litak, 2CDA) is an adenosine deaminase inhibitor for U266, RPMI8226, and MM1.S cells with IC50 of approximately 2.43 μM, 0.75 μM, and 0.18 μM, respectively. |
|
| DC12292 | Cl-amidine hydrochloride Featured | Cl-amidine (hydrochloride) is a peptidylarginine deminase (PAD) inhibitor, with an IC50 5.9 μM for PAD4. |
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| DC9868 | Clanfenur Featured | Clanfenur is a substituted benzoylphenylurea and an analogue of the pesticide diflubenzuron with potential antineoplastic activity. |
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| DC8937 | Clarithromycin | Clarithromycin is a macrolide antibiotic and a CYP3A4 inhibitor. |
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| DC12407 | Class I and IIB HDAC inhibitor 42 | Class I and IIB HDAC inhibitor 42 is a novel potent, selective class I and IIB inhibitor (HDAC1 Ki=0.27 nM) for topical treatment of cutaneous t-cell lymphoma.. |
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| DC10204 | Clinofibrate | Clinofibrate (S-8527) is a hypelipidemic agent and a HMG-CoA reductase inhibitor. |
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| DC10242 | 5-Chloro-8-hydroxy-7-iodoquinoline | Clioquinol is an orally bioavailable, lipophilic, copper-binding, halogenated 8-hydroxyquinoline with antifungal, antiparasitic and potential antitumor activities. |
|
| DC21722 | CLK-IN-T3 Featured | 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. |
|
| DC11004 | CLK2 inhibitor Indazole1 | CLK2 inhibitor Indazole1 is a novel potent, selective inhibitor of CLK2 with IC50 of 2.7 nM, 60-fold selectivity over PKA and >600-fold selectivity over a panel of 34 kinases. |
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| DC23464 | Clobenpropit | Clobenpropit (VUF-9153) is a highly potent histamine H3 antagonist/inverse agonist with pA2 value of 9.93, also displays partial agonist activity at H4 receptors. |
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| DC23440 | Clobenpropit dihydrobromide | Clobenpropit (VUF-9153) is a highly potent histamine H3 antagonist/inverse agonist with pA2 value of 9.93, also displays partial agonist activity at H4 receptors. |
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| DC12304 | Clocapramine hydrochloride hydrate (3-Chlorocarpipramine hydrochloride hydrate) | Clocapramine hydrochloride hydrate is an antagonist of the D2 and 5-HT2A receptors. |
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| DC8681 | Clofentezine | Clofentezine, a growth inhibitor, has sublethal effects on life-table parameters of Tetranychus urticae Koch females. |
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| DC3147 | Clopidogrel hydrogensulfate | Clopidogrel (Plavix) is an oral, thienopyridine class antiplatelet agent. |
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| DC8672 | Cloquintocet-mexyl | Cloquintocet-mexyl is a herbicide, used to control coarse annual grass of the family poaceae (gramineae). |
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| DC7991 | 8-Chloro-11-(4-methyl-1-piperazinyl)-5H-dibenzo[b,e](1,4)diazepine N-oxide Featured | Clozapine N-oxide is a major metabolite of Clozapine noted to decrease SR-2A (5-HT2 serotonin receptor) density in vitro. |
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