Skip to content
ciproxifan

Structure via PubChem · Public domain (PubChem)

EntityQ5121322· pop 5· linked from 330 articles

ciproxifan

Sign in to save

Also known as FUB-359, FUB359

Ciproxifan is an extremely potent histamine H3 inverse agonist/antagonist.

Chemical data

Formula
C16H18N2O2
Molecular weight
270.33 g/mol
IUPAC name
cyclopropyl-[4-[3-(1H-imidazol-5-yl)propoxy]phenyl]methanone
SMILES
C1CC1C(=O)C2=CC=C(C=C2)OCCCC3=CN=CN3
InChIKey
ACQBHJXEAYTHCY-UHFFFAOYSA-N
XLogP
2.5
Polar surface area
55 Ų
H-bond donors
1
H-bond acceptors
3
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
270.136828
Show 5 more facts
chemical formula
C₁₆H₁₈N₂O₂
canonical SMILES
C1CC1C(=O)C2=CC=C(C=C2)OCCCC3=CN=CN3
subject has role
nootropic
physically interacts with
Histamine receptor H4
Commons category
Ciproxifan
Sources (3)

via Wikidata · CC0

~1 min read

Encyclopedic overview

1 sections
Contents
  • References

Ciproxifan is an extremely potent histamine H3 inverse agonist/antagonist.

The histamine H3 receptor is an inhibitory autoreceptor located on histaminergic nerve terminals, and is believed to be involved in modulating the release of histamine in the brain. Histamine has an excitatory effect in the brain via H1 receptors in the cerebral cortex, and so drugs such as ciproxifan which block the H3 receptor and consequently allow more histamine to be released have an alertness-promoting effect.

Excerpted from Wikipedia’s “ciproxifan” article, available under the CC BY-SA 4.0 licence.

Available in 4 languages

via Wikidata sitelinks · CC0