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Ciproxifan hydrochloride_Molecular_structure_CAS_1049741-81-2)
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Ciproxifan hydrochloride

Catalog No. C6492 Name Sigma Aldrich
CAS Number 1049741-81-2 Website http://www.sigmaaldrich.com
M. F. C16H19ClN2O2 Telephone 1-800-521-8956
M. W. 306.78726 Fax
Purity ≥98% (HPLC) Email
Storage desiccated Chembase ID: 153961

SYNONYMS

IUPAC name
4-[3-(4-cyclopropanecarbonylphenoxy)propyl]-1H-imidazole hydrochloride
IUPAC Traditional name
4-[3-(4-cyclopropanecarbonylphenoxy)propyl]-1H-imidazole hydrochloride
Synonyms
Cyclopropyl[4-[3-(1H-imidazol-4-yl)propoxyl]phenyl]-methanone hydrochloride

DATABASE IDS

PubChem SID 24724449
MDL Number MFCD08705321
CAS Number 1049741-81-2

PROPERTIES

Empirical Formula (Hill Notation) C16H18N2O2 · HCl
Purity ≥98% (HPLC)
Apperance off-white solid
Solubility DMSO: soluble30 mg/mL
Solubility water, high purity: soluble30 mg/mL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
Risk Statements 22
Storage Condition desiccated
Storage Condition under inert gas
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Ciproxifan belongs to a novel chemical series of histamine H3-receptor antagonists. In vitro, it behaved as a competitive antagonist at the H3 autoreceptor controlling 3H histamine release from synaptosomes and displayed similar Ki values (0.5-1.9 nM) at the H3 receptor controlling the electrically-induced contraction of guinea pig ileum or at the brain H3 receptor labeled with 125I-iodoproxyfan. Ciproxifan appears to be an orally bioavailable, extremely potent and selective H3-receptor antagonist whose vigilance- and attention-promoting effects are promising for therapeutic applications in aging disorders.
Description (简体中文)
Biochem/physiol Actions
Ciproxifan belongs to a novel chemical series of histamine H3-receptor antagonists. In vitro, it behaved as a competitive antagonist at the H3 autoreceptor controlling 3H histamine release from synaptosomes and displayed similar Ki values (0.5-1.9 nM) at the H3 receptor controlling the electrically-induced contraction of guinea pig ileum or at the brain H3 receptor labeled with 125I-iodoproxyfan. Ciproxifan appears to be an orally bioavailable, extremely potent and selective H3-receptor antagonist whose vigilance- and attention-promoting effects are promising for therapeutic applications in aging disorders.

REFERENCES