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D7571

Sigma-Aldrich

Dimaprit dihydrochloride

≥98% (NMR)

Synonyme(s) :

Carbamimidothioic acid, 3-(dimethylamino)propyl ester, hydrochloride (1:2), Dimaprit-2HCl

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About This Item

Formule empirique (notation de Hill):
C6H15N3S · 2HCl
Numéro CAS:
23256-33-9
Poids moléculaire :
234.19
Numéro MDL:
MFCD00069260
Code UNSPSC :
12352200
ID de substance PubChem :
329798854
Nomenclature NACRES :
NA.77

Niveau de qualité

100

Pureté

≥98% (NMR)

Forme

powder

Couleur

white to off-white

Solubilité

H2O: ≥50 mg/mL

Auteur

Roche

Température de stockage

−20°C

Chaîne SMILES 

Cl.Cl.CN(C)CCCSC(N)=N

InChI

1S/C6H15N3S.2ClH/c1-9(2)4-3-5-10-6(7)8;;/h3-5H2,1-2H3,(H3,7,8);2*1H

Clé InChI

DFWCPLGXFMSUCW-UHFFFAOYSA-N

Actions biochimiques/physiologiques

The histamine H2 receptor influences various cardiovascular responses, including vasodilation and cardiac rhythm, regulates gastric acid secretion, and also plays a role in the immune system by inhibiting antibody production, T cell proliferation and cytokine production. Histamine receptors are members of the GPCR family, and H2 mediates cell signaling via internalization and interaction with the GTPase dynamin.

Caractéristiques et avantages

This compound is featured on the Histamine Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Roche. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Hamid Ghasemi et al.
Pharmacological reports : PR, 69(6), 1393-1401 (2017-11-18)
Histamine and opiate systems contribute to supraspinal processing of pain. In the present study, we investigated the effects of microinjection of histamine and agonists and antagonists of histamine H The thalamic ventral posterolateral nuclei were bilaterally implanted with two guide
J Kitanaka et al.
Neuroscience, 147(3), 765-777 (2007-06-16)
The administration of methamphetamine (METH, 10 mg/kg, i.p.) to male ICR mice induced stereotyped behavior consisting of nail and/or wood chip biting (86.0%), continuous sniffing (12.0%), head bobbing (1.1%), and circling (1.0%) during the observation period of 1 h. Pretreatment
J Sethi et al.
Neuroscience, 217, 84-95 (2012-05-15)
Histamine acts centrally to increase energy expenditure and reduce body weight by mechanisms not fully understood. It has been suggested that in the obese state hypothalamic histamine signaling is altered. Previous studies have also shown that histamine acting in the
Binu Kundukad et al.
Biophysical journal, 99(6), 1906-1915 (2010-09-23)
The flow properties of DNA are important for understanding cell division and, indirectly, cancer therapy. DNA topology controlling enzymes such as topoisomerase II are thought to play an essential role. We report experiments showing how double-strand passage facilitated by topoisomerase II
Xiaowei Chen et al.
Cell stem cell, 21(6), 747-760 (2017-12-05)
Myeloid-biased hematopoietic stem cells (MB-HSCs) play critical roles in recovery from injury, but little is known about how they are regulated within the bone marrow niche. Here we describe an auto-/paracrine physiologic circuit that controls quiescence of MB-HSCs and hematopoietic progenitors
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Histamine Receptors

We offers many products related to histamine receptors for your research needs.

Histamine Receptors

We offers many products related to histamine receptors for your research needs.

Histamine Receptors

We offers many products related to histamine receptors for your research needs.

Histamine Receptors

We offers many products related to histamine receptors for your research needs.

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