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Histamine Receptor

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Histamine Receptor

Chemical Structure Cat. No. Product Name CAS No.
Immethridine dihydrobromide Chemical Structure
 BCP27655 Immethridine dihydrobromide 87976-03-2
Immethridine is a histamine agonist selective for the H3 subtype.
Dimaprit Dihydrochloride Chemical Structure
 BCP27612 Dimaprit Dihydrochloride 23256-33-9
Dimaprit Dihydrochloride is a histamine H2 receptor agonist that is often used to study the activity of histamine and its receptors.
GSK-189254 hydrochloride Chemical Structure
 BCP23443 GSK-189254 hydrochloride 945493-87-8
GSK 189254A is histamine H3 receptor antagonist for the treatment of narcolepsy. The compound may also be useful in the treatment of dementia and neuropathic pain.
Brompheniramine maleate Chemical Structure
 BCP23378 Brompheniramine maleate 980-71-2
Brompheniramine maleate is a histamine H1 receptors antagonist.
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.
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