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Cat.No. Product Name / Introduction Added
CS-2731 PF-04449913 April 2014
PF-04449913 is a potent and orally bioavailable inhibitor of smoothened with IC50 of 5 nM(Gli-luciferase reporter reporter in C3H10T1/2); the hedgehog pathway inhibitor.
 
CS-2722 Sulfamethazine April 2014
Sulfamethazine is a sulfonamide antibacterial.
 
CS-2717 DBeQ April 2014
DBeQ(JRF-12) is a selective, potent, reversible, and ATP-competitive p97 inhibitor with IC50 of 1.
 
CS-2716 Staurosporine April 2014
Staurosporine is a prototypical potent ATP-competitive kinase inhibitor with IC50 of 0.
 
CS-2715 RO4987655 April 2014
RO4987655(CH-4987655) is an orally active small molecule, targeting mitogen-activated protein kinase kinase 1 (MAP2K1/MEK1 IC50=5.
 
CS-2714 Vanoxerine April 2014
Vanoxerine (GBR12909) is a potent and selective DRI (Dopamine reuptake inhibitor).
 
CS-2713 Vanoxerine-dihydrochloride April 2014
Vanoxerine 2 Hcl(GBR12909) is a potent and selective DRI (Dopamine reuptake inhibitor).
 
CS-2703 Indacaterol-maleate April 2014
Indacaterol Maleate is an ultra-long-acting β-adrenoceptor agonist.
 
CS-2702 Atovaquone April 2014
Atovaquone is a medication used to treat or prevent for pneumocystis pneumonia, toxoplasmosis, malaria, and babesia.
 
CS-2701 Diclofenac-diethylamine April 2014
Diclofenac Diethylamine is a non-selective COX inhibitor used as a nonsteroidal anti-inflammatory drug (NSAID).
 
CS-2700 Medetomidine-hydrochloride April 2014
Medetomidine Hydrochloride is an agonist of adrenergic alpha-2 receptor, which is used in veterinary medicine for its analgesic and sedative properties.
 
CS-2698 Kif15-IN-2 April 2014
Kif15-IN-2 is a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in tumor cell lines.
 
CS-2697 Kif15-IN-1 April 2014
Kif15-IN-1 is a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in tumor cell lines.
 
CS-2696 Meisoindigo April 2014
Meisoindigo(Natura-α; N-Methylisoindigotin; Dian III), a derivative of Indigo naturalis, might induce apoptosis and myeloid differentiation of acute myeloid leukemia (AML).
 
CS-2692 RJR-2403-hemioxalate April 2014
RJR-2403 hemioxalate(Metanicotine; Rivanicline) is a neuronal nicotinic receptor agonist, showing high selectivity for the α4β2 subtype (Ki=26 nM); > 1,000 fold selectivity than α7 receptors(Ki= 36000 nM).
 
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Recommended Products
CS-0757 SB-705498
SB-705498 is a potent, selective and orally bioavailable transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with a pIC50 of 7.
CS-0766 Aripiprazole
Aripiprazole is an atypical antipsychotic and antidepressant used in the treatment of schizophrenia, bipolar disorder, and clinical depression.
CS-0765 CYT387 sulfate salt
CYT387 is an ATP-competitive small molecule JAK1/JAK2 inhibitor with IC50 of 11 and 18 nM for JAK1 and JAK2, respectively.
CS-0645 Rimonabant
Rimonabant, also known as SR141716, was the first selective central cannabinoid (CB1) receptor inverse agonist (Ki = 1.
CS-0494 XAV-939
XAV939 is a small molecule and selective Wnt pathway transcription factor β-catenin-mediated transcription inhibitor and axin stabilizing agent with IC50 of 11 and 4nM for the inhibition of TNKS1 and TNKS2, respectively.
CS-0264 DAPT
DAPT is inhibitor of γ-secretase.
CS-0361 Boceprevir
Boceprevir(EBP 520; SCH 503034 ) is useful for Anti HCV.
CS-0592 YM-201636
YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC50 = 33 nM).
CS-0613 Tideglusib
Tideglusib is useful for Alzheimer's Disease .
CS-0625 Avosentan
Avosentan(Ro 67-0565; SPP-301) is an Endothelin Antagonist.
CS-0609 SCH 527123
Sch527123 is a potent, selective antagonist of the human CXCR1 and CXCR2 receptors.
CS-0612 T 705
T 705(Favipiravir) is a RNA-directed RNA polymerase NS5B inhibitor.
CS-0614 Suvorexant
Suvorexant (MK-4305) is a potent, selective, and orally bioavailable antagonist of OX1R and OX2R currently under clinical investigation as a novel therapy for insomnia.
CS-0627 MEK162
MEK162(ARRY-162; ARRY-438162) is an oral, highly selective MEK inhibitor.
CS-0608 BMS-754807
BMS-754807 is an orally bioavailable antagonist of human insulin-like growth factor type I receptor (IGF-1R) with potential antineoplastic activity.

 
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