Influence of substituted phenylcarbamoyl group on the fungicidal activites of a new 5,6-dihydro-2-trifluoromethyl-1,4-oxathiincarboxanilide derivatives

새로운 5,6-dihydro-2-trifluoromethyl-1,4-oxathiincarboxanilide 유도체의 항균활성에 미치는 치환-phenylcarbamoyl group의 영향

  • Sung, Nack-Do (Division of Applied Biology & Chemistry, Chung-nam National University) ;
  • Yu, Seong-Jae (Division of Applied Biology & Chemistry, Chung-nam National University) ;
  • Nam, Kee-Dal (Korea Institute of Science & Technology, Division of Applied Science) ;
  • Chang, Kee-Hyuk (Korea Institute of Science & Technology, Division of Applied Science) ;
  • Hahn, Hoh-Gyu (Korea Institute of Science & Technology, Division of Applied Science)
  • 성낙도 (충남대학교 농과대학 응용생물화학부) ;
  • 유성재 (충남대학교 농과대학 응용생물화학부) ;
  • 남기달 (한국 과학기술연구원 응용과학부) ;
  • 장기혁 (한국 과학기술연구원 응용과학부) ;
  • 한호규 (한국 과학기술연구원 응용과학부)
  • Published : 1998.12.30

Abstract

New thirty derivatives of 5,6-dihydro-2-trifluoromethyl-1,4-oxathiin carboxanilide as substrate(S) were synthesized and their fungicidal activities in vivo against rice sheath blight(Rhizoctonia solani) and wheat leaf rust(Puccinia recondita) were examined. The structure activity relationships(SAR) between the activities($pI_{50}$) and a physicochemical parameters of substituents(X) at the phenylcarbamoyl group were analyzed using the adaptive regression analysis method. The 3-methoxy, 11, 3-isopropyloxy, 13 and 3-isopropyl substituent, 25 as X on the phenylcarbamoyl group exhibited the most highest fungicidal activity against the two fungi. The fungicidal potency of the (S) against Puccinia recondita was higher than Rhizoctonia solani. In case of Rhizoctonia solani, the molecular hydrophobicity(${\pi}>0$) and resonance effect(R<0) by meta-alkyl substitutents with electron donating were important factors in determining fungicidal activity. And the HOMO energy(HOMO>0), ABSQ, sum of absolute values of the atomic charges on each atom and specific polarizability(Sp.Pol<0) of (S) were significantly influential towards fungicidal activity against Puccinia recondita.. The interaction between (S) and receptor agonist from the based on SAR studies proceeds through charge-control reaction, and conditions to show higher activity has been also discussed.