XMD16-5
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 | $1485 | Check With Us |
500mg | $2375 | Check With Us |
1g | $3560 | Check With Us |
Cat #: V2594 CAS #: 1345098-78-3 Purity ≥ 98%
Description: XMD16-5 is a novel and potent tyrosine kinase nonreceptor 2(TNK2) inhibitor with IC50s of 16 nmol/L and 77 nmol/L for the D163E and R806Q mutations.
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Molecular Weight (MW) | 416.48 |
---|---|
Molecular Formula | C23H24N6O2 |
CAS No. | 1345098-78-3 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: 83 mg/mL (199.3 mM)r |
Water: <1 mg/mLr | |
Ethanol: 5 mg/mL (12.0 mM) | |
SMILES Code | OC(CC1)CCN1C(C=C2)=CC=C2NC3=NC=C4C(N(C)C(C=CC=C5)=C5C(N4)=O)=N3 |
Synonyms | XMD165; XMD-165; XMD 165; XMD16-5; XMD-16-5; XMD 16-5; |
Protocol | In Vitro | XMD16-5 potently inhibits the growth of the TNK2 mutant expressing cell lines while having little or no effect on the control cells out to the highest tested concentrations (1,000 nM). XMD16-5 has IC50s of 16 nM and 77 nM for the D163E and R806Q mutations. The effects of XMD16-5 on TNK2 cell lines are largely due to on-target effects on TNK2. Auto-phosphorylation of overexpressed TNK2 mutants could be blocked with TNK2 inhibitor XMD16-5. |
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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 | 2.4011 mL | 12.0054 mL | 24.0108 mL | 48.0215 mL |
5mM | 0.4802 mL | 2.4011 mL | 4.8022 mL | 9.6043 mL |
10mM | 0.2401 mL | 1.2005 mL | 2.4011 mL | 4.8022 mL |
20mM | 0.1201 mL | 0.6003 mL | 1.2005 mL | 2.4011 mL |
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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
+
%
+
%Tween 80
+
%ddH2O
Calculation Results:
Working concentration:
mg/ml;
Method for preparing DMSO master liquid:
mg
drug pre-dissolved in
µL
DMSO(Master liquid concentration
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.