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Histamine H
3
R antagonists: From scaffold hopping to clinical candidates
B. Sadek
, D. Łażewska
, S. Hagenow
, K. Kieć-Kononowicz
, H. Stark
Department of Pharmacology and Therapeutics
Research output
:
Chapter in Book/Report/Conference proceeding
›
Chapter
21
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Citations (Scopus)
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3
R antagonists: From scaffold hopping to clinical candidates'. Together they form a unique fingerprint.
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Neuroscience
H3 Receptor Antagonist
100%
Central Nervous System
66%
Neuropathic Pain
66%
Alzheimer's Disease
33%
Parkinson's Disease
33%
Diabetes Mellitus
33%
Aspartic Acid
33%
Norepinephrine
33%
Serotonin
33%
Acetylcholine
33%
G Protein Coupled Receptor
33%
Histamine H3 Receptor
33%
Neurotransmitter Release
33%
Attention Deficit Hyperactivity Disorder
33%
Mood Disorder
33%
Narcolepsy
33%
Central Nervous System Disease
33%
Obstructive Sleep Apnea
33%
Sleep Disorder
33%
Catalepsy
33%
Tourette Syndrome
33%
Dopamine
33%
Epilepsy
33%
Amine
33%
Schizophrenia
33%
Pharmacology, Toxicology and Pharmaceutical Science
Histamine H3 Receptor Antagonist
100%
Neuropathic Pain
66%
Alzheimer's Disease
33%
Diabetes Mellitus
33%
Serotonin
33%
Noradrenalin
33%
Acetylcholine
33%
Aspartic Acid
33%
Neurotransmitter
33%
G Protein Coupled Receptor
33%
Histamine H3 Receptor
33%
Parkinson's Disease
33%
Central Nervous System Disease
33%
Epilepsy
33%
Attention Deficit Disorder
33%
Mood Disorder
33%
Sleep Disorder
33%
Narcolepsy
33%
Sleep Disordered Breathing
33%
Catalepsy
33%
Gilles De La Tourette Syndrome
33%
Dopamine
33%
Amine
33%
Schizophrenia
33%
Keyphrases
Depression/mood Disorder
50%
Construction Pattern
50%