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Cat.No. Product Name / Introduction Added
CS-3761 (-)-Epicatechin-gallate January 2015
(-)-Epicatechin gallate is a flavan-3-ol, a type of flavonoid, present in green tea.
 
CS-3757 Psoralidin January 2015
Psoralidin, a natural furanocoumarin, is isolated from Psoralea corylifolia L.
 
CS-3750 Bavachalcone January 2015
Bavachalcone is a major bioactive compounds isolated from Psoralea corylifolia L.
 
CS-3762 (-)-Epigallocatechin January 2015
(-)-Epigallocatechin is the most abundant flavonoid in green tea, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils.
 
CS-3730 Peimisine January 2015
Peimisine(Ebeiensine) is a steroidal alkaloid which is the major biologically active component in Bulbus Fritillariae; possess a variety of toxicological and pharmacological effects on humans.
 
CS-3732 Peiminine January 2015
Peiminine(Verticinone; Raddeanine) is a natural compound with anti-inflammatory activity.
 
CS-3731 Peimine January 2015
Peimine(Dihydroisoimperialine; Verticine) is a natural compound with good anti-inflammatory effects in vivo.
 
CS-3709 Aloe-emodin January 2015
Aloe emodin is a hydroxyanthraquinone present in Aloe vera leaves, has a specific in vitro and in vivo antitumor activity.
 
CS-3766 Chlorogenic-acid January 2015
Chlorogenic acid(NSC-407296; 3-O-Caffeoylquinic acid) is one of the most abundant polyphenols in the human diet, has been reported to inhibit cancer cell growth and a major anti-inflammatory constituent of lonicerae flos extract.
 
CS-3760 (-)-Epicatechin January 2015
(-)-Epicatechin is a naturally occurring flavanol; a likely candidate for cocoa-based product reported reductions in cardiometabolic risk.
 
CS-3746 Dalasetron-Mesylate-hydrate January 2015
Dolasetron(MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy.
 
CS-3748 Dalasetron-Mesylate January 2015
Dolasetron Mesylate (MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy.
 
CS-3747 Dolasetron January 2015
Dolasetron(MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy.
 
CS-3783 Brefeldin-A January 2015
Brefeldin A is a fungal metabolite that disrupts the structure and function of the Golgi apparatus; induces the Golgi proteins to redistribute into the ER and blocks the secretion from the Golgi apparatus.
 
CS-3781 Forodesine January 2015
Forodesine(BCX-1777 freebase; Immucillin-H) is an orally bioavailable PNP inhibitor with picomolar potency; induces apoptosis, mainly in T cells.
 
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CS-0757 SB-705498
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Aripiprazole(Abilify) is a human 5-HT1A receptor partial agonist with a Ki of 4.
CS-0765 CYT387 sulfate salt
CYT387 sulfate(momelotinib) is an ATP-competitive inhibitor of JAK1/JAK2 with IC50 of 11 nM/18 nM, ~10-fold selectivity versus JAK3.
CS-0645 Rimonabant
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CS-0494 XAV-939
XAV939 is a small molecule and selective Wnt pathway β-catenin-mediated transcription inhibitor and axin stabilizing agent with IC50 of 11 and 4 nM for the inhibition of TNKS1 and TNKS2, respectively.
CS-0264 DAPT
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CS-0361 Boceprevir
Boceprevir(EBP-520, SCH503034) is an HCV protease inhibitor (Ki=14 nM) for the treatment of hepatitis C virus infection.
CS-0592 YM-201636
YM201636 is a selective PIKfyve inhibitor with IC50 of 33 nM, less potent to p110α.
CS-0613 Tideglusib
Tideglusib(NP-031112) is an irreversible, non ATP-competitive GSK-3β inhibitor with IC50 of 60 nM.
CS-0625 Avosentan
Avosentan(Ro 67-0565; SPP-301) is a potent, selective endothelin receptor(ETA receptor) antagonist.
CS-0609 SCH 527123
SCH-527123 is a potent antagonist of both CXCR1 and CXCR2 with IC50 of 42 nM and 3 nM, respectively.
CS-0612 T 705
T 705 (Favipiravir) is an experimental anti-viral drug with activity against many RNA viruses; RNA-directed RNA polymerase NS5B inhibitor.
CS-0614 Suvorexant
Suvorexant (MK-4305) is a potent dual OX receptor antagonist with Ki of 0.
CS-0627 MEK162
MEK162(ARRY-438162; ARRY-162) is a potent inhibitor of MEK1/2 with IC50 of 12 nM.
CS-0608 BMS-754807
BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR with IC50 of 1.

 
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