Uprosertib (GSK2141795) HCl
This product is for research use only, not for human use. We do not sell to patients.
For small sizes, please check our retail website as below: www.invivochem.com
Size | Price | Stock |
---|---|---|
250mg | $1290 | Check With Us |
500mg | $1850 | Check With Us |
1g | $2775 | Check With Us |
Cat #: V3839 CAS #: 1047635-80-2 Purity ≥ 98%
Description: Uprosertib (formerly known as GSK2141795 and GSK795), an analog of GSK2110183, is a potent, orally bioavailable and ATP-competitive Akt inhibitor with IC50 values of 180 nM, 328 nM, and 38 nM for Akt1/Akt2/Akt3, respectively.
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- Physicochemical and Storage Information
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- Related Biological Data
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Molecular Weight (MW) | 465.71 |
---|---|
Molecular Formula | C18H17Cl3F2N4O2 |
CAS No. | 1047635-80-2 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: ≥ 150 mg/mLr |
Water: N/Ar | |
Ethanol: N/A | |
SMILES Code | O=C(C1=CC(C2=C(Cl)C=NN2C)=C(Cl)O1)NC(CN)CC3=CC=C(F)C(F)=C3.[H]Cl |
Synonyms | Uprosertib HCl; GSK2141795 HCl; GSK2141795 Hydrochloride; GSK 2141795; GSK795; GSK795; GSK 795 |
Protocol | In Vitro | (In Vitro) Uprosertib inhibits Akt1/2/3 with the Kd values of 16/49/5 nM, respectively. Uprosertib potently inhibits only the PKC family members PRKACA and PRKACB as well as the cGMP-dependent protein kinase PRKG1 aqpart from the Akts. Protein targets that bind Uprosertib in the lysate show a dose-dependent reduction in binding to the kinobeads, while proteins unaffected by the drug show no reduction in binding. |
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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 | 2.1473 mL | 10.7363 mL | 21.4726 mL | 42.9452 mL |
5mM | 0.4295 mL | 2.1473 mL | 4.2945 mL | 8.5890 mL |
10mM | 0.2147 mL | 1.0736 mL | 2.1473 mL | 4.2945 mL |
20mM | 0.1074 mL | 0.5368 mL | 1.0736 mL | 2.1473 mL |
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Step One: Enter information below
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Step Two: Enter the in vivo formulation
%DMSO
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%Tween 80
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%ddH2O
Calculation Results:
Working concentration:
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Method for preparing DMSO master liquid:
mg
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,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.