Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN321643 Chloropyramine hydrochloride 6170-42-9
Chloropyramine hydrochloride is a histamine receptor H1 antagonist and has anti-cholinergic, antispasmodic, and antiallergic effects.
YN321441 Chlorprothixene hydrochloride 6469-93-8
an inhibitor of AmpC Beta-Lactamase
YN321585 Hydroxyzine pamoate 10246-75-0
Hydroxyzine pamoate, a derivative of hydroxyzine, is a histamine H1-receptor antagonist that has been used as anxiolytic and antihistaminic so that it is probably effective in the treatment of insomnia and withdrawal treatment.
YN321344 Decloxizine dihydrochloride 13073-96-6
Decloxizine dihydrochloride(UCB-1402; NSC289116) is a histamine 1 receptor antagonist.
YN321446 Clemastine fumarate 14976-57-9
Clemastine Fumarate (Clemastine) is a selective histamine H1 receptor antagonist with IC50 of 3 nM.
YN321409 Mianserin hydrochloride 21535-47-7
Mianserin is an potent antagonist of H1 histamine receptor and 5-HT serotonin receptors, used for the treatment of depression.
YN321658 Dimaprit dihydrochloride 23256-33-9
Dimaprit is a histamine type 2 receptor agonist.
Mianserin is a H1 receptor inverse agonist and is a psychoactive agent of the tetracyclic antidepressant.
YN320284 Niaprazine 27367-90-4
Niaprazine is ahistamine H1-receptorantagonist with marked sedative properties. Niaprazine has antihistamine and antiserotonin activities and can be used for sleep disorder research.
YN321695 Mequitazine 29216-28-2
Mequitazine is a histamine H1 antagonist which competes with histamine for the normal H1-receptor sites on effector cells of the gastrointestinal tract, blood vessels and respiratory tract.
YN320103 Imetit dihydrobromide 32385-58-3
Imetit dihydrobromide (VUF 8325 dihydrobromide) is a high affinity and potent agonist ofhistamine H3 and H4receptors, with Ki values of 0.3 and 2.7nM, respectively. Imetit mimics histamine effect in triggering a shape change in...
YN321397 Ketotifen fumarate 34580-14-8
Ketotifen Fumarate is a fumaric acid salt of ketotifen which is a H1-antihistamine and mast cell stabilizer.
Metiamide (SK&F 92058) is a histamine H2-receptor antagonist developed from another H2 antagonist, burimamide.
YN321624 Terfenadine 50679-08-8
Terfenadine is an antihistamine, generally completely metabolizes to the active form fexofenadine in the liver by the enzyme cytochrome P450 CYP3A4 isoform.
YN320843 Cimetidine 51481-61-9
Cimetidine, a histamine congener, competitively inhibits histamine binding to histamine H2 receptors.
YN320842 Lodoxamide 53882-12-5
Lodoxamide (U-42585E free acid) is an antiallergic compound acting as a mast-cell stabilizer for the treatment of asthma and allergic conjunctivitis.
YN320772 Cimetidine sulfoxide 54237-72-8
Cimetidine sulfoxide (Cimetidine sulphoxide) is a sulfoxide metabolite of Cimetidine. Cimetidine is ahistamine H2-receptorantagonist. Cimetidine has the potential for peptic ulcer disease and upper gastrointestinal haemorrhage treat...
YN321698 Betahistine mesylate 54856-23-4
Betahistine mesylate is the mesylate salt form of Betahistine, a histamine analog and H3 receptor agonist that serves as a vasodilator.
Pirolate is ahistamine H1receptor.
YN321509 Azelastine 58581-89-8
Azelastine is a potent, second-generation, selective, histamine antagonist.
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