BAMB-4(ITPKA-IN-C14)

This product is for research use only, not for human use. We do not sell to patients.

BAMB-4(ITPKA-IN-C14)
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
100mg$2150Check With Us
200mg$3225Check With Us
500mg$5440Check With Us

Cat #: V2933 CAS #: 891025-25-5 Purity ≥ 98%

Description: BAMB-4 (formerly known as ITPKA-IN-C14) is a novel and highly potent membrane-permeable inhibitor of inositol-1,4,5-trisphosphate-3-kinase A (ITPKA) with IC50 of 37 uM in ADP-Glo Assay.

References: Dominik Schröder, et al. Identification of a new membrane-permeable inhibitor against inositol-1,4,5-trisphosphate-3-kinase A. Biochem Biophys Res Commun

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Molecular Weight (MW)252.27
Molecular FormulaC15H12N2O2
CAS No.891025-25-5
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: ≥ 40 mg/mLr
Water: <1 mg/mLr
Ethanol: <1 mg/mL
SMILES CodeO=C(NC1=NOC2=CC=CC=C12)C3=CC=C(C)C=C3
SynonymsBamb-4; Bamb 4; Bamb4; ITPKA-IN C14; ITPKA-INC14; ITPKA-IN-C14
ProtocolIn VitroBAMP-4 (0-30 μM) is a mixed type inhibitor with respect to ATP and InsP3 and does not only affect binding of ATP but also binding of InsP3,which affects turnover of two substrate exhibit a higher inhibition specifcity. BAMP-4 (0, 10, 20 and 40 μM) shows increased Km and decreased Vmax. BAMB-4 (100 μM, overnight) has high specificity and the high cellular uptake. BAMB-4 (40 μM) inhibits InsP3 kinase activity with an IC50 value of 20 μM. BAMB-4 (0.3-40 μM) has ITPKA inhibiton effect with an IC50 value of 37 μM.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM3.9640 mL19.8200 mL39.6401 mL79.2801 mL
5mM0.7928 mL3.9640 mL7.9280 mL15.8560 mL
10mM0.3964 mL1.9820 mL3.9640 mL7.9280 mL
20mM0.1982 mL0.9910 mL1.9820 mL3.9640 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
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.