
PIK-93
CAS No. 593960-11-3
PIK-93( PIK 93 | PIK93 )
Catalog No. M15202 CAS No. 593960-11-3
PIK-93 is a potent, synthetic PI4K inhibitor with IC50 of 19 nM (PI4KIIIβ).
Purity : >98% (HPLC)






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Biological Information
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Product NamePIK-93
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NoteResearch use only, not for human use.
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Brief DescriptionPIK-93 is a potent, synthetic PI4K inhibitor with IC50 of 19 nM (PI4KIIIβ).
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DescriptionPIK-93 is a potent, synthetic PI4K inhibitor with IC50 of 19 nM (PI4KIIIβ), also inhibits PI3Kγ and PI3Kα with IC50 of 16 nM and 39 nM, respectively; also inhibits other PI3Ks, including PI3Kα, β, and δ, with IC50 values of 39 nM, 0.59 uM, and 0.12 uM, shows no inhibitory effect against a panel of other kinases; significantly inhibits the conversion of [3H]serine-labeled endogenous ceramide to sphingomyelin, reduces carbachol-induced translocation of TRPC6 to the plasma membrane and net Ca2+ entry in T6.11 cells at 300 nM; also demonstrates anti-enterovirus effects by inhibition of both poliovirus and HCV replication with EC50 of 0.14 uM and 1.9 uM, respectively.
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In VitroPIK-93 inhibits PI3Kγ and PI4KIIIβ, with IC50 values of 16 nM and 19 nM, respectively. PIK-93 also inhibits other members of PI3Ks, including PI3Kα, β, and δ, with IC50 values of 39 nM, 0.59 μM, and 0.12 μM, respectively. PIK-93 shows no obvious inhibitory effect against a panel of other kinases, even at a concentration of 10 μM. In differentiated HL60 (dHL60) cells, PIK-93 (0.5 μM-1 μM) impairs consolidation and stability of the leading edge formed after treatment with uniform f-Met-Leu-Phe (fMLP). PIK-93 alters the localization, but not the amount, of the fMLP-dependent accumulation of total F-actin. In fMLP gradients, PIK-93 reduces the chemotactic index and triples the cells' turning frequency. In COS-7 cells, PIK-93 (250 nM) effectively abrogates the accumulation of CERT-PH domain and FL-Cer in Golgi. PIK-93 of the same concentration also significantly inhibits the conversion of [3H]serine-labeled endogenous ceramide to sphingomyelin. These facts indicate a key role of PI4KIIIβ in ceramide transport between the ER and Golgi, as well as in the regulation of spingomyelin synthesis. In T6.11 cells, PIK-93 (300 nM) reduces carbachol-induced translocation of TRPC6 to the plasma membrane and net Ca2+ entry. A recent report shows that PIK-93 has anti-enterovirus effects, as revealed by its inhibition of both poliovirus (PV) and hepatitis C virus (HCV) replication, with EC50 values of 0.14 μM and 1.9 μM, respectively.
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In Vivo——
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SynonymsPIK 93 | PIK93
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PathwayPI3K/Akt/mTOR signaling
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TargetPI4K
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RecptorATM|C2β|DNA-PK|hsVps34|mTORC1|p110α|p110β|p110γ|p110δ|PI3KIIIβ
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number593960-11-3
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Formula Weight389.8775
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Molecular FormulaC14H16ClN3O4S2
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCC(NC1=NC(C)=C(C2=CC=C(Cl)C(S(=O)(NCCO)=O)=C2)S1)=O
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Chemical NameAcetamide, N-[5-[4-chloro-3-[[(2-hydroxyethyl)amino]sulfonyl]phenyl]-4-methyl-2-thiazolyl]-
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. Knight ZA, et al. Cell. 2006 May 19;125(4):733-47.
2. Monet M, et al. J Biol Chem. 2012 May 18;287(21):17672-81.
3. Tóth B, et al. J Biol Chem. 2006 Nov 24;281(47):36369-77.
4. Arita M, et al. J Virol. 2011 Mar;85(5):2364-72.
molnova catalog



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