Write Your Own Review
You're reviewing:Diazoxide
Rate this item:

Biological Data

Biological description Selective KIR6 (ATP-sensitive K+) channel activator. Increases EPSCs to around 150% of control values. Shows cardioprotective actions during ischaemic injury by activating PKCε. Also shows neuroprotective and antihypertensive actions.

Solubility & Handling

Storage instructions Room temperature
Solubility overview Soluble in DMSO (100mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

Molarity

=
x
x
More Info

Dilution

x
=
x
More Info

Chemical Data

Purity >98%
Chemical name 7-Chloro-3-methyl-2H-1,2,4-benzothiadiazine1,1-dioxide
Molecular Weight 230.67
Chemical structure Diazoxide  [364-98-7] Chemical Structure
Molecular Formula C8H7ClN2O2S
CAS Number 364-98-7
PubChem identifier 3019
SMILES CC1=NC2=C(C=C(Cl)C=C2)S(=O)(=O)N1
InChiKey GDLBFKVLRPITMI-UHFFFAOYSA-N

References for Diazoxide

References are publications that support the biological activity of the product
  • The neuroprotective effect of diazoxide is mediated by mitochondrial ATP-dependent potassium channels in a rat model of acute subdural hematoma.

    Nakagawa I et al (2013) J Clin Neurosci 20(1) : 144-7.
  • Diazoxide acts more as a PKC-epsilon activator, and indirectly activates the mitochondrial K(ATP) channel conferring cardioprotection against hypoxic injury.

    Kim MY et al (2006) Br J Pharmacol 149(8) : 1059-70.
  • Towards selective Kir6.2/SUR1 potassium channel openers, medicinal chemistry and therapeutic perspectives.

    Hansen JB (2006) Curr Med Chem 13(4) : 361-76.
  • Diazoxide blocks glutamate desensitization and prolongs excitatory postsynaptic currents in rat hippocampal neurons.

    Yamada KA et al (1992) J Physiol 458 : 409-23.

4 Item(s)