| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCH-062 | Cinobufotalin Featured | 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 | Cintirorgon (LYC-55716) is novel oral RAR-related orphan receptor γ (RORγ) agonist. |
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| DC22329 | Cintirorgon Featured | Cintirorgon (LYC-55716) is novel oral RAR-related orphan receptor γ (RORγ) agonist. |
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| 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). |
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| DC9603 | Ciprofibrate | Ciprofibrate is a peroxisome proliferator-activated receptor agonist. |
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| DCAPI1372 | Ciprofloxacin (Cipro) Featured | Ciprofloxacin (Bay-09867) is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity. |
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| DC2062 | Ciproxifan (FUB-359) Featured | Ciproxifan is an antagonists of H3-type histamine receptors. |
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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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| 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). |
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| DC8187 | Ciraparantag(PER977) Featured | Ciraparantag(PER977) is an intravenously administered anticoagulant Reversal Agent. |
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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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| DCAPI1600 | Cisapride Featured | Cisapride is a SR-4 agonist also known as Enteropride |
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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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| DC2099 | cis-Diaminedichloroplatinum Featured | Cisplatin is an inorganic platinum agent (cis-diamminedichloroplatinum) with antineoplastic activity. |
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| 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. |
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| DC12668 | Citarinostat(ACY-241) Featured | Citarinostat(ACY-241) is a potent, selective and orally available histone deacetylase (HDAC) inhibitor, with potential antineoplastic activity. |
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| DCAPI1527 | Citicoline Sodium | Citicoline Sodium |
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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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| 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. |
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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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| 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. |
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| DC11475 | CK-869 Featured | CK-869 is an inhibitor of human and bovine actin-related protein 2/3 (Arp2/3) complex. |
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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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| DC12595 | CL27c Featured | 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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