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PWZ-029

Structure via PubChem · Public domain (PubChem)

EntityQ7121197· pop 5· linked from 365 articles

PWZ-029 is a benzodiazepine derivative drug with nootropic effects developed by WiSys, It acts as a subtype-selective, mixed agonist-inverse agonist at the benzodiazepine binding site on the GABAA receptor, acting as a partial inverse agonist at the α5 subtype and a weak partial agonist at the α3 subtype. This gives it a mixed pharmacological profile, producing at low doses memory-enhancing effects but with no convulsant or anxiogenic effects or muscle weakness, although at higher doses it produces some sedative effects.

Chemical data

Formula
C14H14ClN3O2
Molecular weight
291.73 g/mol
IUPAC name
8-chloro-3-(methoxymethyl)-5-methyl-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one
SMILES
CN1CC2=C(N=CN2C3=C(C1=O)C=C(C=C3)Cl)COC
InChIKey
FXIDXTIMKAEBGY-UHFFFAOYSA-N
XLogP
1.1
Polar surface area
47.4 Ų
H-bond donors
0
H-bond acceptors
3
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
291.077454
Show 3 more facts
chemical formula
C₁₄H₁₄ClN₃O₂
canonical SMILES
CN1CC2=C(N=CN2C3=C(C1=O)C=C(C=C3)Cl)COC
subject has role
nootropic
Sources (1)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

PWZ-029 is a benzodiazepine derivative drug with nootropic effects developed by WiSys, It acts as a subtype-selective, mixed agonist-inverse agonist at the benzodiazepine binding site on the GABAA receptor, acting as a partial inverse agonist at the α5 subtype and a weak partial agonist at the α3 subtype. This gives it a mixed pharmacological profile, producing at low doses memory-enhancing effects but with no convulsant or anxiogenic effects or muscle weakness, although at higher doses it produces some sedative effects.

==See also== GABAA receptor negative allosteric modulator GABAA receptor § Ligands GL-II-73

Excerpted from Wikipedia’s “PWZ-029” article, available under the CC BY-SA 4.0 licence.

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