| Literature DB >> 26508546 |
Yong-Kang Zhang1, Jacob J Plattner1, Eric E Easom1, Yasheen Zhou1, Tsutomu Akama1, Wei Bu1, W Hunter White2, Jean M Defauw2, Joseph R Winkle2, Terry W Balko2, Shenghai Guo3, Jian Xue3, Jianxin Cao4, Wuxin Zou5.
Abstract
A novel series of isoxazoline benzoxaborole small molecules was designed and synthesized for a structure-activity relationship (SAR) investigation to assess the ectoparasiticide activity against ticks and fleas. The study identified an orally bioavailable molecule, (S)-3,3-dimethyl-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzo[c][1,2]oxaborol-1(3H)-ol (38, AN8030), which was long lasting in dogs (t1/2=22 days). Compound 38 demonstrated 97.6% therapeutic effectiveness within 24 h of treatment, with residual efficacy of 95.3% against American dog ticks (Dermacentor variabilis) on day 30% and 100% against cat fleas (Ctenocephalides felis) on day 32 after a single oral dose at 50 mg/kg in dogs.Entities:
Keywords: Benzoxaborole; Ectoparasiticide; Isoxazoline; Structure–activity relationship; Tick and flea
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Year: 2015 PMID: 26508546 DOI: 10.1016/j.bmcl.2015.10.044
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823