15
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10335 | Antihistamine-1 | P450 | |
Antihistamine-1 is an H1-antihistamine (Ki: 6.9 nM) with acceptable blood-brain barrier penetration and also an inhibitor of CYP2D6 and hERG channel (IC50s: 5.4 and 0.8 μM). | |||
T0059 | Diphenylpyraline hydrochloride | 4-Diphenylmethoxy-1-methylpiperidine hydrochloride | Histamine Receptor |
Diphenylpyraline hydrochloride (4-Diphenylmethoxy-1-methylpiperidine hydrochloride) is used in the treatment of Parkinsonism.It is a first-generation antihistamine with anticholinergic effects, functions as a dopamine re... | |||
T9353 | OXOMEMAZINE | AChR , Histamine Receptor | |
Oxomemazine is a phenothiazine-based histamine H1-receptor blocker with pronounced antimuscarinic activity. Oxomemazine is a selective antagonist of mycotoxins M1 receptors, showing high (Ki=84 nM, M1 receptors) and low ... | |||
T36949 | Niaprazine | 5-HT Receptor , Adrenergic Receptor , Histamine Receptor | |
Niaprazine is a histamine H1-receptor antagonist with marked sedative properties. Niaprazine has antihistamine and antiserotonin activities and can be used for sleep disorder research[1][2]. Niaprazine exhibits a low aff... | |||
T60864 | Sequifenadine | ||
Sequifenadine has the potential in researching of inflammatory eye disease with allergic symptoms that is a H1-antihistamine [1] [2]. | |||
T61088 | Propiomazine | ||
Propiomazine is an orally active antihistamine agent that possesses sedative properties. It finds utility in insomnia research [1] [2]. | |||
T60391 | Phenyltoloxamine | ||
Phenyltoloxamine (Bistrimin) is an antihistamine agent with sedative and analgesic effects. Phenyltoloxamine also has potent Sigma-1 receptor binding affinity with Ki of 160 nM [1] [2] [3]. | |||
T60424 | Phenindamine | ||
Phenindamine (Nu 1504) is an H1-receptor antagonist which is antihistamine[1]. | |||
T36945 | Cetirizine Impurity C | ||
Cetirizine Impurity C is an impurity of Cetirizine. Cetirizine is a second-generation antihistamine and the carboxylated metabolite of hydroxyzine. It acts as a specific, orally active, and long-acting antagonist of the ... | |||
T61013 | Bromodiphenhydramine | ||
Bromodiphenhydramine (Ambodryl) has antimicrobial activities which can be used in the cutaneous allergies research. Bromodiphenhydramine is an effective antihistamine that can inhibit a large number of Gram-negative and ... | |||
T60366 | Epinastine | ||
Epinastine (WAL801), a potent, selective, and orally-active antihistamine and mast cell stabilizer, functions as a histamine H1 receptor antagonist. It also inhibits IL-8 release from human eosinophils, showcasing antial... | |||
T75276 | Dexbrompheniramine | ||
Dexbrompheniramine, an orally active H1 receptor antagonist (antihistamine), mitigates the impacts of the natural chemical histamine in the body. It is utilized in the study of hay fever and urticaria [1]. | |||
T73933 | Cetirizine methyl ester | ||
Cetirizine methyl ester, an impurity of Cetirizine, serves as a specific, orally active, and long-acting histamine H1-receptor antagonist. As a second-generation antihistamine and the carboxylated metabolite of hydroxyzi... | |||
T73962 | Cetirizine Impurity C dihydrochloride | ||
Cetirizine Impurity C dihydrochloride, a specific impurity of Cetirizine, is associated with a second-generation antihistamine that serves as the carboxylated metabolite of hydroxyzine. This compound acts as a specific, ... | |||
T60843 | Brompheniramine | ||
Brompheniramine ((±)-Brompheniramine) is a potent and orally active alkylamine class antihistamine. Brompheniramine is a selective antagonist of histamine H1 receptor (Kd = 6.06 nM). Brompheniramine can be used in the re... |