New hybrid type strigolactone mimics derived from plant growth regulator auxin
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
30077756
DOI
10.1016/j.nbt.2018.08.001
PII: S1871-6784(17)30606-4
Knihovny.cz E-resources
- Keywords
- Auxins, O. minor, P. ramose, Parasitic weeds, S. hermonthica, SL mimics, Strigolactones, Suicidal germinations,
- MeSH
- Biomimetic Materials chemical synthesis chemistry pharmacology MeSH
- Germination drug effects MeSH
- Indoleacetic Acids chemical synthesis chemistry pharmacology MeSH
- Lactones chemical synthesis chemistry pharmacology MeSH
- Molecular Structure MeSH
- Plant Weeds drug effects growth & development MeSH
- Drug Design MeSH
- Plant Growth Regulators chemical synthesis chemistry pharmacology MeSH
- Drug Stability MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Indoleacetic Acids MeSH
- Lactones MeSH
- Plant Growth Regulators MeSH
Strigolactones (SLs) constitute a new class of plant hormones of increasing importance in plant science. The structure of natural SLs is too complex for ready access by synthesis. Therefore, much attention is being given to design of SL analogues and mimics with a simpler structure but with retention of bioactivity. Here new hybrid type SL mimics have been designed derived from auxins, the common plant growth regulators. Auxins were simply coupled with the butenolide D-ring using bromo (or chloro) butenolide. D-rings having an extra methyl group at the vicinal C-3' carbon atom, or at the C-2' carbon atom, or at both have also been studied. The new hybrid type SL mimics were bioassayed for germination activity of seeds of the parasitic weeds S. hermonthica, O. minor and P. ramosa using the classical method of counting germinated seeds and a colorimetric method. For comparison SL mimics derived from phenyl acetic acid were also investigated. The bioassays revealed that mimics with a normal D-ring had appreciable to good activity, those with an extra methyl group at C-2' were also appreciably active, whereas those with a methyl group in the vicinal C-3' position were inactive (S. hermonthica) or only slightly active. The new hybrid type mimics may be attractive as potential suicidal germination agents in agronomic applications.
References provided by Crossref.org
Hybrid-type strigolactone analogues derived from auxins