YN321057 Lodoxamide tromethamine 63610-09-3

Lodoxamide Tromethamine is the tromethamide salt form of lodoxamide, a synthetic mast cell stabilizing compound with anti-inflammatory activity.

YN321560 Ranitidine 66357-35-5

Ranitidine is a histamine H2-receptor antagonist that inhibits stomach acid production.

YN321442 Ranitidine hydrochloride 66357-59-3

Ranitidine is a histamine H2-receptor antagonist, used to treat stomach or intestinal ulcers.

YN320605 Astemizole 68844-77-9

Astemizole is a histamine H1-receptor antagonist with IC50 of 4.7 nM. Astemizole is also a potent inhibitor of ether à-go-go 1 (Eag1) and Eag-related gene (Erg) potassium channels. Astemizole has antineoplastic and antipruritic e...

YN320115 Tiotidine 69014-14-8

Tiotidine (ICI 125211) is a potent and selective antagonist ofhistamine H2-receptor(pA2=7.3-7.8 for guinea-pig right atrium). Tiotidine has low affinity for both the H1 and the H3 receptors.

YN320736 Nedocromil 69049-73-6

Nedocromil suppresses the action or formation of multiple mediators, includinghistamine,leukotriene C4(LTC4), and prostagl and in D2(PGD2).

YN321059 Nedocromil sodium 69049-74-7

Nedocromil sodium suppresses the action or formation of multiple mediators, includinghistamine,leukotriene C4(LTC4), and prostagl and in D2(PGD2).

YN322036 KP136 76239-32-2

KP136 (AL136) is an orally effective antiallergic agent. TheIC50is 76.1 μg/mL forhistamine release and 63 ug/mL fordegranulation.

YN321471 Famotidine 76824-35-6

Famotidine is a histamine H2–receptor antagonist with IC50 of 0.6 mM, commonly used to treat heartburn, GERD, ulcers, and other digestive conditions.

YN320552 Lavoltidine 76956-02-0

Lavoltidine (Loxtidine) is an an orally active, irreversible and highly potenthistamine H2-receptorantagonist. Lavoltidine strongly inhibits gastric acid secretion and also induces hypergastrinemia.

YN321449 Nizatidine 76963-41-2

Nizatidine is a histamine H2 receptor antagonist with IC50 of 0.9 nM, also inhibits AChE with IC50 of 6.7 μM.

YN320018 BMY-25271 78441-82-4

BMY-25271 is ahistamine H2 receptorantagonist.

YN321508 Azelastine hydrochloride 79307-93-0

Azelastine HCl is a potent, second-generation, selective, histamine receptor antagonist, used in the treatment of rhinitis.

YN322007 (±)-Tazifylline 79712-55-3

(±)-Tazifylline is a potent, selective and long-actinghistamine H1 receptorantagonist.

YN321117 Loratadine 79794-75-5

Loratadine is a histamine H1 receptor antagonist, used to treat allergies. Also acts as a selective inhibitor of B(0)AT2 with IC50 of 4 μM.

YN321548 Epinastine 80012-43-7

Epinastine (WAL801) is an antihistamine and mast cell stabilizer. Epinastine is a potent, selective and orally-activehistamine H1 receptorantagonist. Epinastine also inhibits IL-8 release and has an antiallergic action.

YN321112 Cetirizine 83881-51-0

Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamineH1-receptorantagonist. Cetirizine marks antiallergic properties and inhibits eosino...

YN321113 Cetirizine dihydrochloride 83881-52-1

Cetirizine DiHCl is an antihistamine.

YN320695 Cetirizine Impurity C 83881-59-8

Cetirizine Impurity C is an impurity of Cetirizine. Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-actinghistamine H1-receptorantagonist.

YN321001 Niperotidine 84845-75-0

Niperotidine is ahistamine H2-receptorantagonist.