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Apexbio Technology LLC Chloropyramine-HCl
SDP

Catalog No. 5000570192
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Chloropyramine hydrochloride (CAS No 6170-42-9) is a first-generation antihistamine used primarily in biomedical research for its histamine H1 receptor antagonist properties Originating from the ethylenediamine class it inhibits histamine-induced physiological effects by blocking H1 receptors thereby mitigating allergic reactions and inflammation pathways In vitro studies have demonstrated its efficacy in the nanomolar to low micromolar range making it a valuable compound for investigating allergic response mechanisms and histamine-related pathways It is commonly applied in various experimental models including cell cultures and animal studies to explore its pharmacokinetics and pharmacodynamics Chloropyramine hydrochloride is also employed in drug screening processes to evaluate potential antihistaminic activity Experimental concentrations typically depend on the specific research design ensuring accurate representation of its pharmacological properties

Catalog No. 50-005-70192 Supplier Apexbio Technology LLC Supplier No. C640125
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Chloropyramine hydrochloride (CAS No 6170-42-9) is a first-generation antihistamine used primarily in biomedical research for its histamine H1 receptor antagonist properties Originating from the ethylenediamine class it inhibits histamine-induced physiological effects by blocking H1 receptors thereby mitigating allergic reactions and inflammation pathways In vitro studies have demonstrated its efficacy in the nanomolar to low micromolar range making it a valuable compound for investigating allergic response mechanisms and histamine-related pathways It is commonly applied in various experimental models including cell cultures and animal studies to explore its pharmacokinetics and pharmacodynamics Chloropyramine hydrochloride is also employed in drug screening processes to evaluate potential antihistaminic activity Experimental concentrations typically depend on the specific research design ensuring accurate representation of its pharmacological properties

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