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Novel Pyrazole Acyl(thio)urea Derivatives Containing a Biph..:

Na-Bo Sun ; Li-Jing Min ; Xin-Peng Sun...
doi:10.1021/acs.jafc.3c07735.s001. , 2024

Link: https://doi.org/10.1021/acs.jafc.3c07735.s001

RT Journal
T1 <Title>Novel Pyrazole Acyl(thio)urea Derivatives Containing a Biphenyl Scaffold as Potential Succinate Dehydrogenase Inhibitors: Design, Synthesis, Fungicidal Activity, and SAR</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivoxfordfig:oai:figshare.com:article_25107371&Exemplar=1&LAN=DE
				
A1 Na-Bo Sun
A1 Li-Jing Min
A1 Xin-Peng Sun
A1 Zhi-Wen Zhai
A1 Joanna Bajsa-Hirschel
A1 Zhe-Cheng Wei
A1 Xue-Wen Hua
A1 Charles L. Cantrell
A1 Hao Xu
A1 Stephen O. Duke
A1 Xing-Hai Liu
YR 2024
K1 Biochemistry
K1 Microbiology
K1 Cell Biology
K1 Pharmacology
K1 Biotechnology
K1 Ecology
K1 Plant Biology
K1 Chemical Sciences not elsewhere classified
K1 urea derivatives containing
K1 succinate dehydrogenase inhibitors
K1 positive control fluxapyroxad
K1 commercial fungicide bixafen
K1 carboxamide (< b
K1 50 μg ml
K1 41 μg ml
K1 18 μg ml
K1 15 μg ml
K1 11 μg ml
K1 05 μg ml
K1 novel pyrazole acyl
K1 new pyrazole acyl
K1 cercospora arachidicola </
K1 botrytis cinerea </
K1 97 ± 0
K1 71 ± 0
K1 63 ± 0
K1 31 ± 0
K1 15 ± 0
K1 carbamoyl )- 1
K1 sclerotinia sclerotiorum </
K1 alternaria solani </
K1 urea compounds containing
K1 50 </ sub
K1 1 </ sup
K1 sclerotiorum </
K1 n </
K1 h </
K1 >- pyrazole
K1 rhizoctonia solani
K1 substituent effects
K1 single x
K1 significantly phytotoxic
K1 molecular docking
K1 methyl -<
K1 h nmr
K1 fungicidal activity
K1 diphenyl motif
K1 dicotyledonous plants
K1 biphenyl scaffold
JF doi:10.1021/acs.jafc.3c07735.s001
LK http://dx.doi.org/https://doi.org/10.1021/acs.jafc.3c07735.s001
DO https://doi.org/10.1021/acs.jafc.3c07735.s001
SF ELIB - SuUB Bremen

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