CAS 6170-42-9: Chloropyramine hydrochloride
Formula:C16H20ClN3·ClH
InChI:InChI=1S/C16H20ClN3.ClH/c1-19(2)11-12-20(16-5-3-4-10-18-16)13-14-6-8-15(17)9-7-14;/h3-10H,11-13H2,1-2H3;1H
InChI key:InChIKey=VEYWWAGBHABATA-UHFFFAOYSA-N
SMILES:N(CC1=CC=C(Cl)C=C1)(CCN(C)C)C2=CC=CC=N2.Cl
Synonyms:- 1,2-Ethanediamine, N-((4-chlorophenyl)methyl)-N',N'-dimethyl-N-2-pyridinyl-, monohydrochloride (9CI)
- 1,2-Ethanediamine, N-[(4-chlorophenyl)methyl]-N′,N′-dimethyl-N-2-pyridinyl-, monohydrochloride
- 1,2-Ethanediamine, N<sup>1</sup>-[(4-chlorophenyl)methyl]-N<sup>2</sup>,N<sup>2</sup>-dimethyl-N<sup>1</sup>-2-pyridinyl-, hydrochloride (1:1)
- 2-[(4-chlorobenzyl)(pyridin-2-yl)amino]-N,N-dimethylethanaminium chloride
- Alergosan
- Allergan S hydrochloride
- Cfak-C 4
- Chloropyramine HCl
- Chloropyribenzamine hydrochloride
- Chlorpiramin hydrochloride
- Chlorpyramine hydrochloride
- See more synonyms
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Found 13 products.
Chloropyramine hydrochloride
CAS:Formula:C16H20ClN3·HClPurity:≥ 98.0%Color and Shape:White to off-white powderMolecular weight:326.26Chloropyramine Hydrochloride
CAS:Applications Chloropyramine hydrochloride is a neurotransmitter related agent for research of drug analysis. Also, it is designed to disrupt the focal adhesion kinase (FAK) and vascular endothelial growth factor receptor-3 (VEGFR-3) interaction in neuroblastoma. References Stewart, J. E., et al.: Mol. Carcinog., 54, 9-23 (2015)Formula:C16H20ClN3·ClHColor and Shape:NeatMolecular weight:326.26Chloropyramine hydrochloride
CAS:Chloropyramine hydrochloride (Alergosan) is a histamine receptor H1 antagonist.Formula:C16H20ClN3·HClPurity:99.45% - 99.8%Color and Shape:SolidMolecular weight:326.26Chloropyramine HCl
CAS:Chloropyramine is a drug that has been used to treat autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus. It is an antihistamine drug that acts by blocking the histamine receptor. Chloropyramine has been shown to have an effect on diastolic pressure in animal models. The model system used was human serum with locomotor activity as the endpoint. The sample preparation involved calcium pantothenate, which is a precursor of coenzymes A and C. The pharmacological agent chloropyramine binds to the agonist binding site, which is located at the end of the cell membrane and regulates ion channels, including those for calcium ions. Tricyclic antidepressant drugs are known to bind to this same binding site, inhibiting the action of both histamine and chloropyramine. Histamine causes increased blood flow due to vasodilation by stimulating H1 receptors in smooth muscles cells. HistamineFormula:C16H20ClN3·HClPurity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:326.26 g/molN1-(4-Chlorobenzyl)-N2,N2-Dimethyl-N1-(Pyridin-2-Yl)Ethane-1,2-Diamine Hydrochloride
CAS:N1-(4-Chlorobenzyl)-N2,N2-Dimethyl-N1-(Pyridin-2-Yl)Ethane-1,2-Diamine HydrochloridePurity:98%Molecular weight:326.26g/molRef: 4Z-P-089
Discontinued productChloropyramine hydrochloride
CAS:Competitive reversible H-1 receptor antagonist This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C16H20ClN3•HClMolecular weight:326.26N1-(4-Chlorobenzyl)-N2,N2-dimethyl-N1-(pyridin-2-yl)ethane-1,2-diamine hydrochloride
CAS:Formula:C16H21Cl2N3Purity:98%Color and Shape:SolidMolecular weight:326.264
