
UCT943
CAS No. 1450666-80-4
UCT943( UCT 943 | UCT-943 )
Catalog No. M11936 CAS No. 1450666-80-4
UCT943 (UCT-943) is a potent, selective, next generation Plasmodium falciparum PI4K inhibitor with IC50 of 23 nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 241 | Get Quote |
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5MG | 410 | Get Quote |
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10MG | 605 | Get Quote |
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25MG | 954 | Get Quote |
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50MG | 1287 | Get Quote |
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100MG | 1728 | Get Quote |
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500MG | 3465 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameUCT943
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NoteResearch use only, not for human use.
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Brief DescriptionUCT943 (UCT-943) is a potent, selective, next generation Plasmodium falciparum PI4K inhibitor with IC50 of 23 nM.
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DescriptionUCT943 (UCT-943) is a potent, selective, next generation Plasmodium falciparum PI4K inhibitor with IC50 of 23 nM; displays higher asexual blood stage, transmission-blocking, and liver stage activity than MMV048 and is more potent against resistant P. falciparum and P. vivax clinical isolates; demonstrates excellent in vitro antiplasmodial activity in P. berghei and humanized P. falciparum mouse models.
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In VitroUCT943 maintains high in vitro selectivity (>200-fold) for the parasite PvPI4K versus the human PI4Kβ isozyme (IC50 of PI4Kβ, 5.4 μM), inhibition of which is linked to immunosuppressive effects. In vitro cytotoxicity of UCT943 is tested against L6 cells, chinese hamster ovarian (CHO), Vero, and HepG2 cells, with 50% cytotoxic concentrations (CC50s) of 12, 17, 113, and 13 μM, respectively.
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In VivoUCT943 shows excellent in vivo efficacy in the Plasmodium berghei (10 mg/kg and 3 mg/kg; oral administration; daily; 4 days) and P. falciparum NSG (NOD-scid IL-2Rγnull) mouse models (0.01, 0.1, 0.3, 1.1 and 10 mg/kg; oral administration; once per day; 4 days). When dosed at 10 mg/kg per os (p.o.), UCT943 reduces parasitemia by >99.9% in the mouse P. berghei infection model and cures all mice, with >30 mean survival days (MSD). At 3 mg/kg p.o., no complete cure is achieved, and MSD is 10 days, albeit parasitemia is reduced by 99%. The resulting 90% effective dose (ED90) is 1.0 mg/kg p.o. in the P. berghei infection model. The ED90 is 0.25 mg/kg in the P. falciparum-infected NSG mouse model. Animal Model:Mice with P. berghei and P. falciparum NOD-scid IL-2Rγnull (NSG) models Dosage:10 mg/kg and 3 mg/kg for P. berghei model; 0.01, 0.1, 0.3, 1.1 and 10 mg/kg for P. falciparum NOD-scid IL-2Rγnull (NSG) model Administration:Oral administration; daily; 4 days for P. berghei modelOral administration; once per day; 4 days for P. falciparum NOD-scid IL-2Rγnull (NSG) model Result:The ED90 is 1.0 mg/kg in the P. berghei infection model. The ED90 is 0.25 mg/kg in the P. falciparum-infected NSG mouse model.
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SynonymsUCT 943 | UCT-943
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PathwayPI3K/Akt/mTOR signaling
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TargetPI4K
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RecptorPI4K
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Research Area——
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Indication——
Chemical Information
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CAS Number1450666-80-4
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Formula Weight427.431
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Molecular FormulaC22H20F3N5O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (584.90 mM)
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SMILESC1CN(CCN1)C(=O)C2=CC=C(C=C2)C3=CN=C(C(=N3)C4=CC=C(C=C4)C(F)(F)F)N
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Chemical Name(4-(5-amino-6-(4-(trifluoromethyl)phenyl)pyrazin-2-yl)phenyl)(piperazin-1-yl)methanone
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Brunschwig C, et al. Antimicrob Agents Chemother. 2018 Jun 25. pii: AAC.00012-18.
molnova catalog



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