Semisynthesis and quantitative structure-activity relationship (QSAR) study of novel aromatic esters of 4'-demethyl-4-deoxypodophyllotoxin as insecticidal agents. 2009

Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
Laboratory of Pharmaceutical Design and Synthesis, College of Life Sciences, Northwest A&F University, Yangling 712100, Shannxi Province, People's Republic of China. orgxuhui@nwsuaf.edu.cn

By using podophyllotoxin as a phytoinsecticidal lead compound, 15 novel aromatic esters of 4'-demethyl-4-deoxypodophyllotoxin were semisynthesized and preliminarily tested for their insecticidal activity against the pre-third-instar larvae of Mythimna separata Walker in vivo for the first time. Among all of the tested compounds, especially two compounds, 4m and 4o, containing a pyridinyl group, for which final corrected mortality rates against M. separata at 1 mg/mL were 62.9 and 59.2%, respectively, showed the most promising and pronounced insecticidal activity as compared with toosendanin, a commercial insecticide derived from Melia azedarach . The quantitative structure-activity relationships (QSAR) of compounds 4a-4o showed that the relative number of benzene rings and final heat of formation were very important descriptors to their insecticidal activity.

UI MeSH Term Description Entries
D007306 Insecticides Pesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics. Insecticide
D007814 Larva Wormlike or grublike stage, following the egg in the life cycle of insects, worms, and other metamorphosing animals. Maggots,Tadpoles,Larvae,Maggot,Tadpole
D009036 Moths Insects of the suborder Heterocera of the order LEPIDOPTERA. Antheraea,Giant Silkmoths,Giant Silkworms,Silkmoths, Giant,Silkworms, Giant,Antheraeas,Giant Silkmoth,Giant Silkworm,Moth,Silkmoth, Giant,Silkworm, Giant
D011034 Podophyllotoxin A lignan (LIGNANS) found in PODOPHYLLIN resin from the roots of PODOPHYLLUM plants. It is a potent spindle poison, toxic if taken internally, and has been used as a cathartic. It is very irritating to skin and mucous membranes, has keratolytic actions, has been used to treat warts and keratoses, and may have antineoplastic properties, as do some of its congeners and derivatives. Epipodophyllotoxin,CPH86,Condyline,Condylox,Podocon-25,Podofilm,Podofilox,Podophyllotoxin, (5R-(5 alpha,5a alpha,8a alpha,9 alpha))-Isomer,Podophyllotoxin, (5R-(5 alpha,5a alpha,8a alpha,9 beta))-Isomer,Podophyllotoxin, (5R-(5 alpha,5a alpha,8a beta,9 alpha))-Isomer,Podophyllotoxin, (5R-(5 alpha,5a beta,8a alpha,9 beta))-Isomer,Wartec,Warticon
D004952 Esters Compounds derived from organic or inorganic acids in which at least one hydroxyl group is replaced by an –O-alkyl or another organic group. They can be represented by the structure formula RCOOR’ and are usually formed by the reaction between an acid and an alcohol with elimination of water. Ester
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001554 Benzene Toxic, volatile, flammable liquid hydrocarbon byproduct of coal distillation. It is used as an industrial solvent in paints, varnishes, lacquer thinners, gasoline, etc. Benzene causes central nervous system damage acutely and bone marrow damage chronically and is carcinogenic. It was formerly used as parasiticide. Benzol,Benzole,Cyclohexatriene
D021281 Quantitative Structure-Activity Relationship A quantitative prediction of the biological, ecotoxicological or pharmaceutical activity of a molecule. It is based upon structure and activity information gathered from a series of similar compounds. Structure Activity Relationship, Quantitative,3D-QSAR,QSAR,QSPR Modeling,Quantitative Structure Property Relationship,3D QSAR,3D-QSARs,Modeling, QSPR,Quantitative Structure Activity Relationship,Quantitative Structure-Activity Relationships,Relationship, Quantitative Structure-Activity,Relationships, Quantitative Structure-Activity,Structure-Activity Relationship, Quantitative,Structure-Activity Relationships, Quantitative

Related Publications

Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
September 2013, Bioorganic & medicinal chemistry letters,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
February 2016, Bioorganic & medicinal chemistry letters,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
February 2004, European journal of medicinal chemistry,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
June 2023, Journal of receptor and signal transduction research,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
February 2008, Journal of enzyme inhibition and medicinal chemistry,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
September 2009, Bioorganic & medicinal chemistry letters,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
December 2020, Journal of medicinal chemistry,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
April 2010, Bioorganic & medicinal chemistry letters,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
February 1998, Chemical & pharmaceutical bulletin,
Hui Xu, and Juanjuan Wang, and Huijun Sun, and Min Lv, and Xuan Tian, and Xiaojun Yao, and Xing Zhang
June 2013, Journal of agricultural and food chemistry,
Copied contents to your clipboard!