Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Within Vinony's link graph, gabapentin enacarbil is referenced by 1,012 other articles, and connects out to valproic acid, drug liberalization and allosteric modulator.
Vinony files it under Analgesics, Anticonvulsants and Carbamates.
Its subject is documented across 9 Wikipedia language editions.
Chemical data
- Formula
- C16H27NO6
- Molecular weight
- 329.39 g/mol
- IUPAC name
- 2-[1-[[1-(2-methylpropanoyloxy)ethoxycarbonylamino]methyl]cyclohexyl]acetic acid
- SMILES
- CC(C)C(=O)OC(C)OC(=O)NCC1(CCCCC1)CC(=O)O
- InChIKey
- TZDUHAJSIBHXDL-UHFFFAOYSA-N
- XLogP
- 3.1
- Polar surface area
- 102 Ų
- H-bond donors
- 2
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 2011
- Admin. routes
- oral
- Indications
- restless legs syndrome, diabetic neuropathy, kidney disease, neuralgia
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 329.183838
- Has use
- medication
Show 3 more facts
- chemical formula
- C₁₆H₂₇NO₆
- canonical SMILES
- CC(C)C(=O)OC(C)OC(=O)NCC1(CCCCC1)CC(=O)O
- World Health Organisation international non-proprietary name
- gabapentin enacarbil
via Wikidata · CC0
Available in 9 languages
via Wikidata sitelinks · CC0
Categories
AnalgesicsAnticonvulsantsCarbamatesChemical pages without DrugBank identifierCyclohexanesDrugboxes which contain changes to verified fieldsDrugboxes which contain changes to watched fieldsDrugs developed by GSK plcDrugs not assigned an ATC codeGABA analoguesGabapentinoidsGamma-Amino acidsIsobutyrate estersProdrugs