Lotilaner
This isoxazoline compound kills parasites like fleas and ticks on companion animals by blocking insect-specific chloride channels, causing paralysis and death of the parasites. It is used in oral or ophthalmic formulations for veterinary and some human parasitic infections.
分子量
596.8000 g/mol
LogP
6.60
TPSA
108.00 Ų
Lipinski 五规则
不符合
Pharmacokinetics (PK)
Pharmacodynamics (PD)
二维结构
Cite this structure
Embed this structure
SMILES
Cc1cc(C2=NO[C@@](c3cc(Cl)c(Cl)c(Cl)c3)(C(F)(F)F)C2)sc1C(=O)NCC(=O)NCC(F)(F)F
InChI
InChI=1S/C20H14Cl3F6N3O3S/c1-8-2-13(36-16(8)17(34)30-6-14(33)31-7-19(24,25)26)12-5-18(35-32-12,20(27,28)29)9-3-10(21)15(23)11(22)4-9/h2-4H,5-7H2,1H3,(H,30,34)(H,31,33)/t18-/m0/s1
Molecular Formula
C20H14Cl3F6N3O3S
HBD / HBA
2 / 11
可旋转键数
6
重原子数
36
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
常见问题
This isoxazoline compound kills parasites like fleas and ticks on companion animals by blocking insect-specific chloride channels, causing paralysis and death of the parasites. It is used in oral or ophthalmic formulations for veterinary and some human parasitic infections.
Yes, Lotilaner is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3707310. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 76959255. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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