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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 241 Get Quote
5MG 410 Get Quote
10MG 605 Get Quote
25MG 954 Get Quote
50MG 1287 Get Quote
100MG 1728 Get Quote
500MG 3465 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    UCT943
  • Note
    Research use only, not for human use.
  • Brief Description
    UCT943 (UCT-943) is a potent, selective, next generation Plasmodium falciparum PI4K inhibitor with IC50 of 23 nM.
  • Description
    UCT943 (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.
  • In Vitro
    UCT943 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.
  • In Vivo
    UCT943 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.
  • Synonyms
    UCT 943 | UCT-943
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    PI4K
  • Recptor
    PI4K
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1450666-80-4
  • Formula Weight
    427.431
  • Molecular Formula
    C22H20F3N5O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 250 mg/mL (584.90 mM)
  • SMILES
    C1CN(CCN1)C(=O)C2=CC=C(C=C2)C3=CN=C(C(=N3)C4=CC=C(C=C4)C(F)(F)F)N
  • Chemical Name
    (4-(5-amino-6-(4-(trifluoromethyl)phenyl)pyrazin-2-yl)phenyl)(piperazin-1-yl)methanone

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Brunschwig C, et al. Antimicrob Agents Chemother. 2018 Jun 25. pii: AAC.00012-18.
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