PIK-294
This product is for research use only, not for human use. We do not sell to patients.
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Size | Price | Stock |
---|---|---|
250mg | $830 | Check With Us |
500mg | $1320 | Check With Us |
1g | $1980 | Check With Us |
Cat #: V0133 CAS #: 900185-02-6 Purity ≥ 98%
Description: PIK-294 is a novel, potent and highly selective inhibitor of PI3K (phosphatidylinositol 3-kinase) p110δ (IC50 = 10 nM) with potential anticancer activity, showed 1000-, 49- and 16-fold less potency against PI3Kα/β/γ, respectively.
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Molecular Weight (MW) | 489.53 |
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Molecular Formula | C28H23N7O2 |
CAS No. | 900185-02-6 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: 98 mg/mL (200.2 mM)r |
Water:<1 mg/mLr | |
Ethanol: <1 mg/mL | |
SMILES Code | O=C1N(C2=CC=CC=C2C)C(CN3N=C(C4=CC=CC(O)=C4)C5=C(N)N=CN=C53)=NC6=C1C(C)=CC=C6 |
Synonyms | PIK294; PIK 294; PIK-294 |
Protocol | In Vitro | Analysis of the specific Class I PI3 Kinase catalytic isoforms p110α (IC50=10 μM), p110β (IC50=0.49 μM), p110δ (IC50=0.01 μM) and p110γ (IC50=0.16 μM) using the inhibitor PIK-294 indicates differential roles in CXCL8-induced neutrophil migration. PIK-294 inhibits both chemokinetic and chemotactic CXCL8-induced migration. |
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These protocols are for reference only. InvivoChem does not
independently validate these methods.
Solvent volume to be added | Mass (the weight of a compound) | |||
---|---|---|---|---|
Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 2.0428 mL | 10.2139 mL | 20.4278 mL | 40.8555 mL |
5mM | 0.4086 mL | 2.0428 mL | 4.0856 mL | 8.1711 mL |
10mM | 0.2043 mL | 1.0214 mL | 2.0428 mL | 4.0856 mL |
20mM | 0.1021 mL | 0.5107 mL | 1.0214 mL | 2.0428 mL |
The molarity calculator equation
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The dilution calculator equation
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Step One: Enter information below
Dosage mg/kg
Average weight of animals g
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Step Two: Enter the in vivo formulation
%DMSO
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%
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%Tween 80
+
%ddH2O
Calculation Results:
Working concentration:
mg/ml;
Method for preparing DMSO master liquid:
mg
drug pre-dissolved in
µL
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mg/mL)
,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:
Take
µL
DMSO master liquid, next add
µL
PEG300, mix and clarify, next add
µL
Tween 80,mix and clarify, next add
µL
ddH2O,mix and clarify.
Note:
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.