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atagabalin

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atagabalin

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Atagabalin (, ; developmental code name PD-0200390) is a drug developed by Pfizer and related to gabapentin, which similarly binds to the α2δ calcium channels (1 and 2). It was under development as a treatment for insomnia, but was discontinued following unsatisfactory trial results. The drug reached phase 2 clinical trials for this indication prior to the discontinuation of its development.

Chemical data

Formula
C10H19NO2
Molecular weight
185.26 g/mol
IUPAC name
2-[(3S,4S)-1-(aminomethyl)-3,4-dimethylcyclopentyl]acetic acid
SMILES
C[C@H]1CC(C[C@@H]1C)(CC(=O)O)CN
InChIKey
IUVMAUQEZFTTFB-YUMQZZPRSA-N
XLogP
-1.3
Polar surface area
63.3 Ų
H-bond donors
2
H-bond acceptors
3
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule
Indications
insomnia

via ChEMBL · EBI

Wikidata facts

Mass
185.142
Show 3 more facts
chemical formula
C₁₀H₁₉NO₂
canonical SMILES
CC1CC(CC1C)(CC(=O)O)CN
isomeric SMILES
C[C@H]1CC(C[C@@H]1C)(CC(=O)O)CN
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

Atagabalin (, ; developmental code name PD-0200390) is a drug developed by Pfizer and related to gabapentin, which similarly binds to the α2δ calcium channels (1 and 2). It was under development as a treatment for insomnia, but was discontinued following unsatisfactory trial results. The drug reached phase 2 clinical trials for this indication prior to the discontinuation of its development.

==See also== List of investigational insomnia drugs 4-Methylpregabalin Gabapentin enacarbil PD-217,014 PD-0299685

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

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