Synthesis and biological evaluation of trifluoromethyl-containing auxin derivatives
This study focused on the chemical synthesis of auxin analogs, wherein a trifluoromethyl group was introduced near the carboxyl group in the side chain of natural and synthetic auxins, including IAA, NAA, IBA, 2,4-D, and 4-Cl-IAA. The effects of these synthetic compounds and natural auxins on plant growth regulation and callus growth were evaluated. In experiments with black gram, CF<sub>3</sub>-IAA and 4-Cl-CF<sub>3</sub>-IAA exhibited comparable effects to the parent compound, IAA. Meanwhile, CF<sub>3</sub>-NAA, CF<sub>3</sub>-2,4-D, CF<sub>3</sub>-IBA-1, and CF<sub>3</sub>-IBA-2 displayed effects that differed considerably from those of their respective parent auxins. In experiments with lettuce, CF<sub>3</sub>-IAA, 4-Cl-CF<sub>3</sub>-IAA, CF<sub>3</sub>-NAA, CF<sub>3</sub>-2,4-D, and CF<sub>3</sub>-IBA-1 showed effects comparable to the corresponding parent auxins. However, at low concentrations, these analogs induced hypocotyl and root elongations, a response distinct from that observed with their parent compounds. Furthermore, CF<sub>3</sub>-IBA-2 considerably promoted hypocotyl and root elongations across all concentrations relative to the control. The addition of synthetic compounds to callus cultures revealed that CF<sub>3</sub>-IAA, 4-Cl-CF<sub>3</sub>-IAA, CF<sub>3</sub>-NAA, and CF<sub>3</sub>-2,4-D promoted callus proliferation, whereas CF<sub>3</sub>-IBA-1 and CF<sub>3</sub>-IBA-2 did not enhance callus growth.
Authors
- Mitsuaki Yamashita (ORCID: https://orcid.org/0000-0002-6866-0983)
- Atsunori Sano
- T. Arakawa
- Akira Iida
- Fuki Saneoka
Institutions
- Kindai University (JP)
Publication Details
- Journal
- Journal of Pesticide Science
- Published
- 2025-07-18
- DOI
- https://doi.org/10.1584/jpestics.d25-026
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00