KDU691
- Product Name
- KDU691
- CAS No.
- 1513879-19-0
- Chemical Name
- KDU691
- Synonyms
- KDU691;KDU691 >=98% (HPLC);KDU691, 10 mM in DMSO;KDU691;KDU-691;KDU 691;1513879-19-0;N-(4-Chlorophenyl)-N-methyl-3-(4-(methylcarbamoyl)phenyl)imidazo[1,2-a]pyrazine-6-carboxamide;Imidazo[1,2-a]pyrazine-6-carboxamide, N-(4-chlorophenyl)-N-methyl-3-[4-[(methylamino)carbonyl]phenyl]-;PI4 kinases,blood,Inhibitor,liver,Phosphatidylinositol 4 kinases,ring-stage,falciparum,Parasite,plasmodium,schizonts,gametocytes,KDU 691,PI4K,KDU-691,inhibit,KDU691,stage
- CBNumber
- CB33384777
- Molecular Formula
- C22H18ClN5O2
- Formula Weight
- 419.86
- MOL File
- 1513879-19-0.mol
KDU691 Property
- Density
- 1.35±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMSO:PBS (pH 7.2) (1:9):0.1(Max Conc. mg/mL);0.24(Max Conc. mM)
Ethanol:10.0(Max Conc. mg/mL);23.82(Max Conc. mM) - form
- A crystalline solid
- pka
- 14.59±0.46(Predicted)
- color
- White to off-white
N-Bromosuccinimide Price
- Product number
- SML2375
- Product name
- KDU691
- Purity
- ≥98% (HPLC)
- Packaging
- 5 mg
- Price
- $127.98
- Updated
- 2025/07/31
- Product number
- SML2375
- Product name
- KDU691
- Purity
- ≥98% (HPLC)
- Packaging
- 25 mg
- Price
- $254.5
- Updated
- 2025/07/31
- Product number
- 29019
- Product name
- KDU691
- Packaging
- 1mg
- Price
- $59
- Updated
- 2024/03/01
- Product number
- 29019
- Product name
- KDU691
- Packaging
- 25mg
- Price
- $699
- Updated
- 2024/03/01
- Product number
- 29019
- Product name
- KDU691
- Packaging
- 5mg
- Price
- $184
- Updated
- 2024/03/01
KDU691 Chemical Properties,Usage,Production
Description
KDU691 is an antimalarial compound. It inhibits recombinant P. vivax phosphatidylinositol 4-kinase (PI4K) with an IC50 value of 1.5 nM. KDU691 is selective for P. vivax PI4K over recombinant human PI4KβIII and PI3Kα, -β, -γ, and -δ (IC50s = 7.9, 8.8, 2.4, 8, and 3.4 μM, respectively), as well as VPS34 (IC50 = >9.7 μM) and 36 additional kinases in a panel of lipid and protein kinases (IC50s = >10 μM). It is active against P. falciparum and P. yoelii schizonts (IC50s = 0.06 and 0.04 μM, respectively), as well as P. cynomolgi schizonts and hypnozoites (IC50s = 0.11 and 0.2 μM, respectively). KDU691 completely prevents, but does not eradicate established, P. cynomolgi infection in rhesus monkeys when administered at a dose of 20 mg/kg.
Uses
KDU691, is a PI4K inhibitor.
in vivo
During the 5 days of dosing, no major weight changes are observed in the animals that receive KDU691 as prophylactic treatment (group 691-proph). From the fourth day of dosing, the animals that are treated with KDU691 show a transient yellow skin color. The KDU691 radical-cure group (group 691-RC) becomes blood-stage positive again at 31.8 days p.i. (range, 31 to 32 days). Clinical chemistry analysis of the group 691-RC monkeys reveals that bilirubin levels accumulate during the 5-day radical-cure treatment with KDU691[2].
IC 50
Plasmodium
References
[1] CASE W. MCNAMARA. Targeting Plasmodium PI(4)K to eliminate malaria[J]. Nature, 2013, 504 7479: 248-253. DOI: 10.1038/nature12782
[2] BIN ZOU*. Lead Optimization of Imidazopyrazines: A New Class of Antimalarial with Activity on Plasmodium Liver Stages[J]. ACS Medicinal Chemistry Letters, 2014, 5 8: 947-950. DOI: 10.1021/ml500244m
[3] A. ZEEMAN. PI4 Kinase Is a Prophylactic but Not Radical Curative Target in Plasmodium vivax-Type Malaria Parasites[J]. Antimicrobial Agents and Chemotherapy, 2016, 60 1: 2858-2863. DOI: 10.1128/aac.03080-15
KDU691 Preparation Products And Raw materials
Raw materials
Preparation Products
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