Comparative molecular field analysis (CoMFA) of herbicidal protoporphyrinogen oxidase inhibitors using standard steric and electrostatic fields and an alternative LUMO field

被引:0
|
作者
Durst, GL [1 ]
机构
[1] Dow AgroSci, Indianapolis, IN 46268 USA
来源
关键词
CoMFA; LUMO field; herbicides; protoporphyrinogen oxidase (PPO) inhibitors; protoporphyrin IX;
D O I
10.1002/(SICI)1521-3838(199810)17:05<419::AID-QSAR419>3.0.CO;2-K
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A set of diphenyl ether herbicides [1] was examined with Comparative Molecular Field Analysis (CoMFA) using standard steric and electrostatic fields and alternative frontier orbitals as 3-D fields to explain observed Protoporphyrinogen oxidase (PPO) enzyme inhibition. Significant CoMFA models were obtained utilizing standard CoMFA and the LUMO field both together and separately. These findings support previous QSAR work that identified several electronic properties as important for PPO inhibition. The resulting CoMFA models identify specific 3-D steric and electronic interactions affecting PPO enzyme binding most significantly.
引用
收藏
页码:419 / 426
页数:8
相关论文
共 50 条
  • [21] Comparative molecular field analysis (COMFA) QSAR study of conformationally restricted cinnamyl HIV integrase inhibitors.
    Buolamwini, JK
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 218 : U530 - U531
  • [22] Comparative molecular field analysis (CoMFA) and comparative molecular similarity index analysis (CoMSIA) study of mutagen X
    Bang, SJ
    Cho, SJ
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2004, 25 (10): : 1525 - 1530
  • [23] Comparison of estrogen receptor α and β subtypes based on comparative molecular field analysis (CoMFA)
    Xing, L
    Welsh, WJ
    Tong, W
    Perkins, R
    Sheehan, DM
    SAR AND QSAR IN ENVIRONMENTAL RESEARCH, 1999, 10 (2-3) : 215 - +
  • [24] On the use of comparative-molecular field analysis (COMFA) to define receptor topology
    Compadre, CM
    Compadre, RL
    Bhuvaneswaran, C
    Sanchez, RI
    Sumpter, JA
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1996, 212 : 235 - COMP
  • [25] Inhibition of bilirubin UDP-glucuronosyltransferase: A comparative molecular field analysis (CoMFA)
    Said, M
    Ziegler, JC
    Magdalou, J
    Elass, A
    Vergoten, G
    QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS, 1996, 15 (05): : 382 - 388
  • [26] 3D-QSAR studies on 4-hydroxyphenylpyruvate dioxygenase inhibitors by comparative molecular field analysis (CoMFA)
    Huang, ML
    Yang, DY
    Shang, ZC
    Zou, JW
    Yu, QS
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (17) : 2271 - 2275
  • [27] 3D-QSAR studies on natural acetylcholinesterase inhibitors of Sarcococca saligna by comparative molecular field analysis (CoMFA)
    ul-Haq, Z
    Wellenzohn, B
    Tonmunphean, S
    Khalid, A
    Choudhary, MI
    Rode, BM
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (24) : 4375 - 4380
  • [28] COMPARATIVE MOLECULAR-FIELD ANALYSIS (COMFA) OF CAMPTOTHECIN ANALOGS AS TOPOISOMERASE-I (T-I) INHIBITORS
    FOX, PC
    CARRIGAN, SW
    WANI, MC
    WALL, ME
    BOWEN, JP
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1993, 206 : 124 - MEDI
  • [29] Synthesis and comparative molecular field analysis (CoMFA) of symmetric and nonsymmetric cyclic sulfamide HIV-1 protease inhibitors
    Schaal, W
    Karlsson, A
    Ahlsén, G
    Lindberg, J
    Andersson, HO
    Danielson, UH
    Classon, B
    Unge, T
    Samuelsson, B
    Hultén, J
    Hallberg, A
    Karlén, A
    JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (02) : 155 - 169
  • [30] Synthesis and comparative molecular field analysis (CoMFA) of argentatin B derivatives as growth inhibitors of human cancer cell lines
    Parra-Delgado, H
    Compadre, CM
    Ramírez-Apan, T
    Muñoz-Fambuena, MJ
    Compadre, RL
    Ostrosky-Wegman, P
    Martínez-Vázquez, M
    BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (06) : 1889 - 1901