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Histamine Receptor

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Histamine Receptor

Chemical Structure Cat. No. Product Name CAS No.
MK-0249 Chemical Structure
BCP30795 MK-0249 1167574-41-5
MK-0249 is a histamine H3 inverse antagonist. Current antipsychotic treatments have little impact on the cognitive deficits associated with schizophrenia. It has been proposed that agents which promote histamine release may enhance cognition and, therefore, the H3 inverse agonist MK-0249 might improve cognitive deficits in patients with schizophrenia.
(R)-Meclizine Chemical Structure
BCP28339 (R)-Meclizine 189298-48-4
Meclizine is a histamine H1 antagonist used in the treatment of motion sickness, vertigo, and nausea during pregnancy and radiation sickness.
Tesmilifene Chemical Structure
BCP09123 Tesmilifene 98774-23-3
Tesmilifene is a novel potentiator of chemotherapy which, when added to doxorubicin, achieved an unexpected and very large survival advantage over doxorubicin alone in a randomized trial in advanced breast cancer.
Betahistine Chemical Structure
BCP16849 Betahistine 5638-76-6
Betahistine is a strong affinity histamine H3 receptor antagonist and weak affinity agonist of histamine H1 receptors.
Emedastine Chemical Structure
BCP20085 Emedastine 87233-61-2
Emedastine is a Histamine-1 Receptor Inhibitor. The mechanism of action of emedastine is as a Histamine H1 Receptor Antagonist.
Repirinast Chemical Structure
BCP16315 Repirinast 73080-51-0
Repinirast is an antihistamine.
Profenamine hydrochloride Chemical Structure
BCP12225 Profenamine hydrochloride 1094-08-2
Profenamine hydrochloride is an inhibitor of butyrylcholinesterase, antiparkinsonian. It reduces extrapyramidal motor effects and used as an antidyskinetic, characteristic of Parkinson′s disease. It also alleviates thermal hyperalgesia in rats.
Iodophenpropit Chemical Structure
BCP27685 Iodophenpropit 143407-29-8
Iodophenpropit is a histamine antagonist which binds selectively to the H3 subtype.
Setastine HCl Chemical Structure
BCP27942 Setastine HCl 59767-13-4
Setastine HCl is a potent antagonist of histamine H1-receptor mediated responses.
Decloxizine dihydrochloride Chemical Structure
BCP29896 Decloxizine dihydrochloride 13073-96-6
Decloxizine dihydrochloride is a histamine 1 receptor antagonist.
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