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DB13687InvestigationalSmall molecule
Niaprazine is a selective brain catecholamine depletor.
- Mechanism
- Curator reviewed
Pharmacologically active on Histamine H1 receptor, Alpha-1 adrenergic receptors, and 5-hydroxytryptamine 2 receptor
- Formula / weight
- C20H25FN4O · 356.445 g/mol (avg)
- Code names
- 1709 CERM
Resolves to
Clinical / RWD
Structure
InChIKey
RSKQGBFMNPDPLR-UHFFFAOYSA-NSMILESCC(CCN1CCN(CC1)C1=CC=C(F)C=C1)NC(=O)C1=CN=CC=C1Targets
What you can answer from here — as of July 07, 2026
3Protein targetsEach mapped to UniProt, with action and pharmacological action
Listed above
Which drugs share a target with Niaprazine, and which of those have an active Phase 3 trial?