E3330 (APX-3330)

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

E3330 (APX-3330)
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Size Price Stock
250mg$1550Check With Us
500mg$2550Check With Us
1g$3825Check With Us

Cat #: V1432 CAS #: 136164-66-4 Purity ≥ 98%

Description: E3330 (E-3330; E 3330; APX-3330; APX 3330; APX3330) is a potent, orally bioactive and selective APE1 (Ref-1, AP endonuclease 1) inhibitor with potential antitumor activity.

References: Zou GM, et al. The Ape-1/Ref-1 redox antagonist E3330 inhibits the growth of tumor endothelium and endothelial progenitor cells: therapeutic implications in tumor angiogenesis. J Cell Physiol. 2009 Apr;219(1):209-18.

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Promise
Molecular Weight (MW)378.46
Molecular FormulaC21H30O6
CAS No.136164-66-4
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 75 mg/mL (198.2 mM)r
Water: 75 mg/mL (198.2 mM)r
Ethanol: <1 mg/mL
SynonymsE3330; E-3330; E 3330.
ProtocolIn VitroE3330 (0-5 μM) reduces secreted and intracellular VEGF (vascular endothelial growth factor) expression by pancreatic cancer cells, while concomitantly downregulating the cognate receptor Flk-1/KDR on PCECs.E3330 (0-1 μM) inhibits the differentiation of bone marrow mesenchymal stem cells (BM-MSCs) into CD31+ cells of endothelial lineage.E3330 (0-50 μM, 48 h) inhibits the growth of HUVECs, PCECs and EPCs
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
1mM2.6423 mL13.2114 mL26.4229 mL52.8457 mL
5mM0.5285 mL2.6423 mL5.2846 mL10.5691 mL
10mM0.2642 mL1.3211 mL2.6423 mL5.2846 mL
20mM0.1321 mL0.6606 mL1.3211 mL2.6423 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.