| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC10839 | CIL56(CA3) Featured | CIL56 is a small molecule that induces cellular ferroptosis through production of iron-dependent reactive oxygen species (ROS). |
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| DC11374 | Cilastatin | Cilastatin is an inhibitor of dipeptidase (dehydropeptidase I), a renal dipeptidase. |
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| DCAPI1569 | Cilostazol | Cilastazol is a 2-oxo-quinoline with vasodilator, antimitogenic, antithrombotic, and cardiotonic properties. This compound has been shown to cause inhibition of adenosine uptake, eventually resulting in changes to cAMP levels. Studies have shown Cilostazo |
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| DC9325 | Cilazapril (monohydrate) Featured | Cilazapril Monohydrate is a angiotensin-converting enzyme (ACE) inhibitor used for the treatment of hypertension and congestive heart failure. |
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| DC7561 | Cilengitide (TFA salt) Featured | Cilengitide is a potent integrin inhibitor for αvβ3 receptor and αvβ5 receptor with IC50 of 4.1 nM and 79 nM, respectively; ~10-fold selectivity against gpIIbIIIa. Phase 2. |
|
| DC9875 | Ciliobrevin A(HPI4) Featured | Ciliobrevin A(HPI-4) is a Hedgehog pathway inhibitor and ciliogenesis inhibitor. |
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| DC20341 | Ciliobrevin D Featured | Ciliobrevin D is a cell-permeable, reversible, specific inhibitor of cytoplasmic dynein, blocks dynein-dependent microtubule gliding and ATPase activity while sparing kinesin dependent cellular trafficking. |
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| DC9160 | Cilnidipine Featured | Cilnidipine(FRC8653) is a dual L- and N-type calcium channel blocker and displays antihypertensive, sympatholytic and neuroprotective activity. |
|
| DC10868 | Cilofexor Featured | Cilofexor (GS-9674, GS9674) is novel specific, non-steroidal farnesoid X receptor (FXR) agonist that reduces liver fibrosis and ameliorates portal hypertension in rat NASH models. |
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| DC9582 | Cilomilast | Cilomilast(SB 207499; Ariflo) is a potent PDE4 inhibitor with IC50 of about 110 nM, has anti-inflammatory activity and low central nervous system activity. |
|
| DC22028 | Ciluprevir | Ciluprevir (BILN2061) is a potent HCV NS3/4A protease inhibitor with Ki of 0.66 and 0.30 nM for NS3-NS4A protease of HCV 1b and HCV 1a, respectively. |
|
| DC9002 | Cimetidine | Cimetidine is a histamine-2 (H2) receptor antagonist. |
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| DC12134 | Cimiside B | Cimiside B, a glycoside alkaloid, isolated from the rhizome of Cimicifuga dahurica. |
|
| DC8801 | Cinacalcet (AMG-073) Featured | Cinacalcet(AMG-073) is an orally active, second-generation calcimimetic compound; AMG 073 represents a new class of compounds for the treatment of hyperparathyroidism. |
|
| 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. |
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| 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. |
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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. |
|
| 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. |
|
| 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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