Product overview

Name Dimaprit dihydrochloride
Purity >95%
Description Selective H2 receptor agonist
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Biological Data

Biological description Selective H2 receptor agonist. Also inhibits nNOS (IC50 = 49 µM for rat nNOS). Shows cytoprotective and hypotensive actions.

Solubility & Handling

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

Calculators

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Dilution

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Chemical Data

Purity >95%
Chemical name S-(3-Dimethylaminopropyl)isothioure a dihydrochloride
Molecular Weight 234.19
Chemical structure Dimaprit dihydrochloride [23256-33-9] Chemical Structure
Molecular Formula C6H15N3S.2HCl
CAS Number 23256-33-9
PubChem identifier 90045
SMILES CN(C)CCCSC(=N)N.Cl.Cl
InChi InChI=1S/C6H15N3S.2ClH/c1-9(2)4-3-5-10-6(7)8;;/h3-5H2,1-2H3,(H3,7,8);2*1H
InChiKey DFWCPLGXFMSUCW-UHFFFAOYSA-N
MDL number MFCD00069260

References for Dimaprit dihydrochloride

References are publications that support the biological activity of the product
  • Suppression of ischaemia-induced cytokine release by dimaprit and amelioration of liver injury in rats.

    Motoki A et al (2008) Basic Clin Pharmacol Toxicol 102(4) : 394-8.
  • Nitric oxide synthase inhibition by dimaprit and dimaprit analogues.

    Paquay JB et al (1999) Br J Pharmacol 127(2) : 331-4.
  • Cardiovascular effects of the novel histamine H2 receptor agonist amthamine: interaction with the adrenergic system.

    Coruzzi G et al (1996) Naunyn Schmiedebergs Arch Pharmacol 353(4) : 417-22.
  • Dimaprit -(S-[3-(N,N-dimethylamino)prophyl]isothiourea) - a highly specific histamine H2 -receptor agonist. Part 1. Pharmacology.

    Parsons ME et al (1977) Agents Actions 7(1) : 31-7.

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