Synthesis, in vitro protoporphyrinogen oxidase inhibition, and herbicidal activity of N-(benzothiazol-5-yl)hexahydro-1H-isoindole-1,3-diones and N-(benzothiazol-5-yl)hexahydro-1H-isoindol-1-ones

Chemical Biology and Drug Design

Volumn 84, Issue 4, 2014, Pages 431-442

  Wu, Qiong You ^a   Jiang, Li Li ^a   Zuo, Yang ^a   Wang, Zhi Fang ^a   Xi, Zhen ^b   Yang, Guang Fu ^a,b  

^a CENTRAL CHINA NORMAL UNIVERSITY   (China)

^b SynBio Research Platform   (China)

Author keywords

benzothiazole hexahydro 1H isoindole 1 3(2H) dione; herbicidal activity; hexahydro 1H isoindol 1 one; protoporphyrinogen oxidase

Indexed keywords

BENZOTHIAZOLE DERIVATIVE; ETHYL 2 ((6 FLUORO 5 (4,5,6,7 TETRAHYDRO 1 OXO 1H ISOINDOL 2(3H) YL)BENZO[D]THIAZOL 2 YL) SULFANYLACETATE; HERBICIDE; HEXAHYDRO 1H ISOINDOL 1 ONE; HEXAHYDRO 1H ISOINDOLE 1,3(2H)DIONE; N (BENZOTHIAZOL 5 YL)HEXAHYDRO 1H ISOINDOL 1 ONE; N (BENZOTHIAZOL 5 YL)HEXAHYDRO 1H ISOINDOLE 1,3 DIONE; N (BENZOTHIAZOL 5 YL)TETRAHYDROISOINDOLE 1,3 DIONE; PROTOPORPHYRINOGEN OXIDASE; UNCLASSIFIED DRUG; ENZYME INHIBITOR; ISOINDOLE DERIVATIVE; RECOMBINANT PROTEIN;

ARTICLE; BIOASSAY; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CHENOPODIUM ALBUM; CONTROLLED STUDY; ELECTROSPRAY MASS SPECTROMETRY; ENZYME INHIBITION; GROWTH INHIBITION; HERBICIDAL ACTIVITY; IN VITRO STUDY; NONHUMAN; PLANT ROOT; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SHOOT; SYNTHESIS; X RAY DIFFRACTION; ANTAGONISTS AND INHIBITORS; BINDING SITE; BIOSYNTHESIS; CHEMISTRY; CONFORMATION; DRUG EFFECTS; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; MOLECULAR DOCKING; PLANT; PROTEIN TERTIARY STRUCTURE; TOBACCO; X RAY CRYSTALLOGRAPHY;

CHENOPODIUM ALBUM; PUFFINUS AURICULARIS;

BINDING SITES; CRYSTALLOGRAPHY, X-RAY; ENZYME INHIBITORS; HERBICIDES; ISOINDOLES; MOLECULAR CONFORMATION; MOLECULAR DOCKING SIMULATION; PLANT ROOTS; PLANT SHOOTS; PROTEIN STRUCTURE, TERTIARY; PROTOPORPHYRINOGEN OXIDASE; RECOMBINANT PROTEINS; TOBACCO;

EID: 84925953968     PISSN: 17470277     EISSN: 17470285     Source Type: Journal    
DOI: 10.1111/cbdd.12331     Document Type: Article

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