Inhibition of very-long-chain fatty acid formation by indanofan, 2-[2-(3-chlorophenyl)oxiran-2-ylmethyl]-2-ethylindan-1,3-dione, and its relatives

Zeitschrift fur Naturforschung - Section C Journal of Biosciences

Volumn 57, Issue 1-2, 2002, Pages 72-74

  Takahashi, Hideomi ^a   Schmalfuß, Jochen ^a   Ohki, Aiko ^a   Hosokawa, Akemi ^a   Tanaka, Akira ^a   Sato, Yukiharu ^a   Matthes, Bernd ^a   Böger, Peter ^a   Wakabayashi, Ko ^a  

^a UNIVERSITY OF KONSTANZ   (Germany)

Author keywords

Rice Herbicides; Tridiphane; Very Long Chain Fatty Acids

Indexed keywords

ALLIUM; ALLIUM PORRUM; DIGITARIA CILIARIS; ECHINOCHLOA; ECHINOCHLOA ORYZICOLA;

ACYL CARRIER PROTEIN MALONYLTRANSFERASE; ACYL COENZYME A; ACYLTRANSFERASE; CARBON; CHLOROBENZENE; FATTY ACID; HERBICIDE; INDAN DERIVATIVE; INDANOFAN; MALONYL COENZYME A; STEARIC ACID DERIVATIVE;

ARTICLE; BIOSYNTHESIS; CELL FREE SYSTEM; CHEMISTRY; DRUG ANTAGONISM; GARLIC; METABOLISM; STRUCTURE ACTIVITY RELATION;

ACYL COENZYME A; ACYL-CARRIER PROTEIN S-MALONYLTRANSFERASE; ACYLTRANSFERASES; ALLIUM; CARBON RADIOISOTOPES; CELL-FREE SYSTEM; CHLOROBENZENES; FATTY ACIDS; HERBICIDES; INDANS; MALONYL COENZYME A; STEARIC ACIDS; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0036366050     PISSN: 09395075     EISSN: None     Source Type: Journal    
DOI: 10.1515/znc-2002-1-212     Document Type: Article

References (7)

1. Towards the primary target of chloroacetamides-new findings pave the way
2. Synthesis and herbicidal activity of indanofan and related 2-(2-phenyloxiran-2-ylmethyl)indan-1,3-dione derivatives
3. Tridiphane [2-(3,5-dichlorophenyl)-2-(2,2,2-trichloroethyl)]oxirane, an atrazine synergist: Enzymatic conversion to a potent glutathione S-transferase inhibitor
4. Chloroacetamide mode of action II: Inhibition of very long chain fatty acid synthesis in higher plants
5. Inhibition of acyl-CoA elongation by chloroacetamide herbicides in microsomes from leek seedlings
6. Inhibition of very-long-chain fatty acid biosynthesis by 2-chloro-N-(3-methoxy-2-thenyl)-2′,6′-dimethylacetanilide thenylchlor, and its analogs
7. Physiological mechanism responsible for triazine synergism with pro-epoxides of tridiphane herbicides