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Cat.No. Product Name Information/Activity

BCC7061 (S)-(+)-Dimethindene maleate 136152-65-3 (S)-(+)-Dimethindene maleate chemical structure

BCC4542 Fexofenadine HCl Fexofenadine hydrochloride (MDL-16455 hydrochloride), a H1R antagonist, is an anti-allergic agent used in seasonal allergic rhinitis and chronic idiopathic urticarial (person aged ≥16 years). Fexofenadine HCl chemical structure

BCC1262 Loratadine Loratadine (SCH-29851) is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM. Loratadine has anti-dengue-virus (DENV) activity. Loratadine chemical structure

BCC6740 Mepyramine maleate Mepyramine maleate, a first generation antihistamine, is an antagonist of histamine H1 receptor, with Kds of 0.8 nM, 5200 nM and >3000 nM for H1, H2, and H3 receptor, respectively, and a pKd of 9.4 for H1 receptor. Mepyramine maleate chemical structure

BCC4923 Mirtazapine Mirtazapine is a 5-HT receptor inhibitor. Mirtazapine is a potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent by blocking 5-HT2 and 5-HT3 receptors. Mirtazapine chemical structure

BCC4545 Olopatadine HCl Olopatadine hydrochloride (ALO4943A) is a histamine blocker used to treat allergic conjunctivitis. Olopatadine HCl chemical structure

BCC3866 Terfenadine Terfenadine ((±)-Terfenadine) is a potent open-channel blocker of hERG with an IC50 of 204 nM. Terfenadine, an H1 histamine receptor antagonist, acts as a potent apoptosis inducer in melanoma cells through modulation of Ca2+ homeostasis. Terfenadine induces ROS-dependent apoptosis, simultaneously activates Caspase-4, -2, -9. Terfenadine chemical structure

BCC6742 trans-Triprolidine hydrochloride 550-70-9

trans-Triprolidine hydrochloride chemical structure

BCC7838 Zotepine 26615-21-4 Zotepine chemical structure

BCC6744 Amthamine dihydrobromide 142457-00-9 Amthamine dihydrobromide chemical structure

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