Structure via PubChem · Public domain (PubChem)
BHFF
Sign in to saveBHFF is a compound used in scientific research which acts as a positive allosteric modulator at the GABAB receptor. It has anxiolytic effects in animal studies, and good oral bioavailability.
In the Vinony graph
Within Vinony's link graph, BHFF is referenced by 193 other articles, and connects out to picrotoxin, tetrahydrodeoxycorticosterone and (RS)-baclofen.
It sits within the topics Benzofurans, Chemical pages without DrugBank identifier and Drugs missing an ATC code.
Its subject is documented across 5 Wikipedia language editions.
Chemical data
- Formula
- C17H21F3O3
- Molecular weight
- 330.34 g/mol
- IUPAC name
- 5,7-ditert-butyl-3-hydroxy-3-(trifluoromethyl)-1-benzofuran-2-one
- SMILES
- CC(C)(C)C1=CC2=C(C(=C1)C(C)(C)C)OC(=O)C2(C(F)(F)F)O
- InChIKey
- RVNOANDLZIIFHB-UHFFFAOYSA-N
- XLogP
- 5.1
- Polar surface area
- 46.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 330.144279
Show 3 more facts
- Commons category
- BHFF
- chemical formula
- C₁₇H₂₁F₃O₃
- canonical SMILES
- CC(C)(C)C1=CC(=C2C(=C1)C(C(=O)O2)(C(F)(F)F)O)C(C)(C)C
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- External links
BHFF is a compound used in scientific research which acts as a positive allosteric modulator at the GABAB receptor. It has anxiolytic effects in animal studies, and good oral bioavailability.
== References ==
Excerpted from Wikipedia’s “BHFF” article, available under the CC BY-SA 4.0 licence.