| 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. |
|
| DC12134 |
Cimiside B |
Cimiside B, a glycoside alkaloid, isolated from the rhizome of Cimicifuga dahurica. |
|
| 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. |
|
| 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. |
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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). |
|
| 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. |
|
| DC8187 |
Ciraparantag(PER977)
Featured
|
Ciraparantag(PER977) is an intravenously administered anticoagulant Reversal Agent. |
|
| 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.
|
|
| 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.. |
|
| DC20847 |
CL 316243 |
CL 316243 (BTA 243) is a potent, highly selective, orally active β3-adrenoceptor agonist with EC50 of 3 nM. |
|
| DC20909 |
CL 316243 disodium |
CL 316243 is a potent, highly selective, orally active β3-adrenoceptor agonist with EC50 of 3 nM. |
|
| 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. |
|
| 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.. |
|
| 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. |
|
| DC9725 |
Cl-amidine
Featured
|
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. |
|
| DC9868 |
Clanfenur
Featured
|
Clanfenur is a substituted benzoylphenylurea and an analogue of the pesticide diflubenzuron with potential antineoplastic activity. |
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