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Cat.No. Product Name / Introduction Added
CS-4788 Dipyrocetyl August 2015
Dipyrocetyl is a pharmaceutical drug used as an analgesic and antipyretic.
 
CS-4929 ML346 August 2015
ML346 is a novel activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.
 
CS-4927 LTV-1 August 2015
LTV-1 is a highly potent, cell-permeable and reversible inhibitor of lymphoid tyrosine phosphatase (LYP) (IC50 = 508 nM).
 
CS-4926 D77 August 2015
D77 is anti-HIV-1 inhibitor targeting the interaction between integrase and cellular LEDGF/p75.
 
CS-4920 RQ-00203078 August 2015
RQ-00203078 is a highly selective, potent and orally available TRPM8 antagonist (IC50 values are 5.
 
CS-4870 Hetacillin August 2015
Hetacillin is a beta-lactam antibiotic that is part of the aminopenicillin family.
 
CS-4871 Hetacillin-potassium August 2015
Hetacillin potassium is a broad-spectrum treatment for use against a wide range of common Gram-positive and Gram-negative bacteria.
 
CS-4924 QNZ46 August 2015
QNZ46 is a NR2C/NR2D-selective NMDA receptor non-competitive antagonist (IC50 values are 3, 6, 229, and >300, >300 μM for NR2D, NR2C, NR2A, NR2B, and GluR1, respectively).
 
CS-4887 Mps1-IN-5 August 2015
Mps1-IN-5 inhibits Mps1 kinase activity with IC50 of <1 nM when assay with 10 μM ATP, with IC50 of <1.
 
CS-4922 IMD-0354 August 2015
IMD-0354 is a synthetic selective NF-kB inhibitor.
 
CS-4869 Pardoprunox-hydrochloride August 2015
Pardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.
 
CS-4889 W-54011 August 2015
W-54011 is a potent, specific, and orally active CD88 (C5a receptor) antagonist.
 
CS-4846 Cefotiam-hydrochloride August 2015
Cefotiam hydrochloride is a second-generation cephalosporin antibiotic, has broad-spectrum activity against Gram-positive and Gram-negative bacteria, its bactericidal activity results from the inhibition of cell wall synthesis via affinity for penicillin-binding proteins.
 
CS-4848 Ribostamycin-sulfate August 2015
 
CS-4849 Protoporphyrin-IX August 2015
Protoporphyrin IX, in the metabolism of porphyrin, is created by the enzyme protoporphyrinogen oxidase.
 
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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(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
Rimonabant(SR141716) is a selective central cannabinoid (CB1) receptor inverse agonist with Ki of 1.
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
DAPT(GSI-IX) is an inhibitor of γ-secretase; DAPT causes a reduction in Aβ40 and Aβ42 levels in human primary neuronal cultures (IC50 values are 115 and 200 nM for total Aβ and Aβ42 respectively) and in brain extract, cerebrospinal fluid and plasma in vivo.
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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