Structure via PubChem · Public domain (PubChem)
LY334370
Sign in to saveAlso known as LY 334370, LY-334,370, LY-334370
LY-334370 is a selective serotonin 5-HT1F receptor agonist of the triptan and piperidinylindole families which was under development by Eli Lilly and Company for the treatment of migraine headaches. The drug showed efficacy in a phase II clinical trial but further development was halted due to toxicity detected in animals. It is closely related to tryptamines like the psychedelic drug dimethyltryptamine (DMT), but is not technically a tryptamine itself and is instead a piperidinylindole similarly to naratriptan.
Chemical data
- Formula
- C21H22FN3O
- Molecular weight
- 351.4 g/mol
- IUPAC name
- 4-fluoro-N-[3-(1-methylpiperidin-4-yl)-1H-indol-5-yl]benzamide
- SMILES
- CN1CCC(CC1)C2=CNC3=C2C=C(C=C3)NC(=O)C4=CC=C(C=C4)F
- InChIKey
- MDMJLMDBRQXOOI-UHFFFAOYSA-N
- XLogP
- 3.6
- Polar surface area
- 48.1 Ų
- H-bond donors
- 2
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 351.174691
Show 3 more facts
- chemical formula
- C₂₁H₂₂FN₃O
- canonical SMILES
- CN1CCC(CC1)C2=CNC3=C2C=C(C=C3)NC(=O)C4=CC=C(C=C4)F
- Commons category
- LY-334370
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- See also
- References
- External links
LY-334370 is a selective serotonin 5-HT1F receptor agonist of the triptan and piperidinylindole families which was under development by Eli Lilly and Company for the treatment of migraine headaches. The drug showed efficacy in a phase II clinical trial but further development was halted due to toxicity detected in animals. It is closely related to tryptamines like the psychedelic drug dimethyltryptamine (DMT), but is not technically a tryptamine itself and is instead a piperidinylindole similarly to naratriptan.
==See also== Triptan Piperidinylindole Substituted tryptamine § Related compounds CP-135807 Lasmiditan SN-22
Excerpted from Wikipedia’s “LY334370” article, available under the CC BY-SA 4.0 licence.