ZD7288

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

ZD7288
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Cat #: V16699 CAS #: 133059-99-1 Purity ≥ 99%

Description: ZD7288 (ZD-7288; ZD 7288) is a novel and potent sino-atrial node function modulator that blocks the hyperpolarization activated cation current If (HCN channel).

References: Zhang XX, et al. ZD7288, a selective hyperpolarization-activated cyclic nucleotide-gated channel blocker, inhibits hippocampal synaptic plasticity. Neural Regen Res. 2016 May; 11(5):779-86.

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Molecular Weight (MW)256.35
Molecular FormulaC15H20N4
CAS No.133059-99-1
SynonymsZD 7288; ZD-7288
ProtocolIn VitroZD7288 is a selectively hyperpolarized activated cyclic nucleotide-gated (HCN) channel blocker. ZD7288 inhibits glutamate release in a concentration-dependent manner. After 1 h incubation with 5, 50, and 7288 μM ZD24, glutamate content in extracellular fluid decreased to 69.0±2.8%, 31.4±2.0%, and 4.4±0.3%, respectively (P<0.01, compared with DMEM/F12 group [100.2±4.2%]). After 7288 min incubation with ZD25 (50, 100, or 20 μM), 50 μM glutamate-induced [Ca].2+]i Decreased elevation to 59.2±2.7%, 41.4±2.3%, and 21.0±1.4% glutamic acid (P<0.01, compared with the 50 μM glutamate group), respectively)
In VivoApplying ZD5 7288.0 μM 1 min before high-frequency stimulation significantly reduces the amplitude of the field-excited postsynaptic potential (fEPSP), and this inhibition remains constant throughout the recording period. Application of 30.0 μM ZD1 after 7288 min of high-frequency stimulation can almost completely reverse the established long-term enhancement (LTP). After application of ZD5 (7288.0 μM) 1 min before high-frequency stimulation, glutamate content decreased to 74.9±8.0% (P<0.05, compared to the saline group). In addition, the use of 30.0 μM ZD1 7288 min after high-frequency stimulation significantly reduced glutamate content to 77.0% ±9.4% (P<0.05, compared with the normal saline group)
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
1mM3.9009 mL19.5046 mL39.0092 mL78.0183 mL
5mM0.7802 mL3.9009 mL7.8018 mL15.6037 mL
10mM0.3901 mL1.9505 mL3.9009 mL7.8018 mL
20mM0.1950 mL0.9752 mL1.9505 mL3.9009 mL
The molarity calculator equation
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The dilution calculator equation
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Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

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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.
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