Literature DB >> 20009552

Exploring the structural requirements for jasmonates and related compounds as novel plant growth regulators: a current computational perspective.

Ke-Xian Chen1, Zu-Guang Li.   

Abstract

Jasmonates and related compounds have been highlighted recently in the field of plant physiology and plant molecular biology due to their significant regulatory roles in the signaling pathway for the diverse aspects of plant development and survival. Though a considerable amount of studies concerning their biological effects in different plants have been widely reported, the molecular details of the signaling mechanism are still poorly understood. This review sheds new light on the structural requirements for the bioactivity/property of jasmonic acid derivatives in current computational perspective, which differs from previous research that mainly focus on their biological evaluation, gene and metabolic regulation and the enzymes in their biosynthesis. The computational results may contribute to further understanding the mechanism of drug-receptor interactions in their signaling pathway and designing novel plant growth regulators as high effective ecological pesticides.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 20009552      PMCID: PMC2819504          DOI: 10.4161/psb.4.11.9717

Source DB:  PubMed          Journal:  Plant Signal Behav        ISSN: 1559-2316


  27 in total

Review 1.  Jasmonates: key players in the plant defence.

Authors:  M H Beale; J L Ward
Journal:  Nat Prod Rep       Date:  1998-12       Impact factor: 13.423

2.  Emerging complexity: jasmonate-induced volatiles affect parasitoid choice.

Authors:  Claus Wasternack; Bettina Hause
Journal:  J Exp Bot       Date:  2009-06-04       Impact factor: 6.992

Review 3.  Molecular mechanisms underlying plant memory in JA-mediated defence responses.

Authors:  Ivan Gális; Emmanuel Gaquerel; Shree P Pandey; Ian T Baldwin
Journal:  Plant Cell Environ       Date:  2008-07-24       Impact factor: 7.228

4.  Quantitative structure-activity relationship analysis of aryl alkanol piperazine derivatives with antidepressant activities.

Authors:  Ke-Xian Chen; Zu-Guang Li; Hai-Ying Xie; Jian-Rong Gao; Jian-Wei Zou
Journal:  Eur J Med Chem       Date:  2009-06-06       Impact factor: 6.514

5.  Quantitative structure-activity relationship studies on 1-aryl-tetrahydroisoquinoline analogs as active anti-HIV agents.

Authors:  Ke-xian Chen; Hai-ying Xie; Zu-guang Li; Jian-rong Gao
Journal:  Bioorg Med Chem Lett       Date:  2008-09-18       Impact factor: 2.823

6.  Structure-activity relationships of cyclopentane analogs of jasmonic acid for induced responses of canola seedlings,Brassica napus L.

Authors:  R Bodnaryk; T Yoshihara
Journal:  J Chem Ecol       Date:  1995-11       Impact factor: 2.626

7.  Biological activity of novel progesterone derivatives having a bulky ester side chains at C-3.

Authors:  Marisa Cabeza; Eugene Bratoeff; Elena Ramírez; Ivonne Heuze; Sergio Recillas; Hilda Berrios; Angel Cruz; Olmo Cabrera; Victor Perez
Journal:  Steroids       Date:  2008-04-04       Impact factor: 2.668

8.  Comparisons of LIPOXYGENASE3- and JASMONATE-RESISTANT4/6-silenced plants reveal that jasmonic acid and jasmonic acid-amino acid conjugates play different roles in herbivore resistance of Nicotiana attenuata.

Authors:  Lei Wang; Silke Allmann; Jinsong Wu; Ian T Baldwin
Journal:  Plant Physiol       Date:  2007-12-07       Impact factor: 8.340

9.  Quantitative structure-property relationship studies on amino acid conjugates of jasmonic acid as defense signaling molecules.

Authors:  Zu-Guang Li; Ke-Xian Chen; Hai-Ying Xie; Jian-Rong Gao
Journal:  J Integr Plant Biol       Date:  2009-06       Impact factor: 7.061

10.  Independently silencing two JAR family members impairs levels of trypsin proteinase inhibitors but not nicotine.

Authors:  Lei Wang; Rayko Halitschke; Jin-Ho Kang; Albrecht Berg; Falk Harnisch; Ian T Baldwin
Journal:  Planta       Date:  2007-02-02       Impact factor: 4.540

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.