Synthesis of Novel Pyrimidinylselenium Compounds as Acetolactate Synthase‐Inhibiting Herbicides. Issue 1 (5th January 2022)
- Record Type:
- Journal Article
- Title:
- Synthesis of Novel Pyrimidinylselenium Compounds as Acetolactate Synthase‐Inhibiting Herbicides. Issue 1 (5th January 2022)
- Main Title:
- Synthesis of Novel Pyrimidinylselenium Compounds as Acetolactate Synthase‐Inhibiting Herbicides
- Authors:
- Chen, Jinglei
Hu, Hang
Ye, Kai
Wang, Wei
Xu, Defeng - Abstract:
- Abstract: A series of pyrimidinylselenosalicylic acid derivatives (5 a –5 l ) and 4‐selenopyrimidine derivatives (6 a –6 f ) were synthesized and evaluated as potential acetylactate synthase (ALS)‐inhibiting herbicides. All synthesized new compounds were characterized by 1 H NMR, 13 C NMR, and high‐resolution mass spectrometry (HRMS). The compounds were subjected to herbicidal activity, in vitro ALS enzyme inhibitory activity, and crop safety studies. The herbicidal activity study shows that 4‐chloro (5 b), 5‐chloro (5 c), 5‐methoxy (5 e), 4, 5‐dimethoxy (5 f), 5‐fluoro (5 h), and 4, 5‐difluoro (5 i) substituted 2‐[(4, 6‐dimethoxy‐2‐pyrimidinyl)selanyl]benzoic acid exhibit significantly enhanced weed control effect than other new compounds and Pyrithiobac. Most of compounds exhibit enhanced inhibition effect on Cyperus difformis Linn than those on barnyard grass, Portulaca oleracea, Eleusine indica, and Amaranthus retroflexus . Importantly, 5 c, 5 f, and 5 i also exhibit more potent inhibition effect on Escherichia coli ALS enzyme than other new compounds and Pyrithiobac in in vitro ALS enzyme inhibitory activity study. The possible binding modes of 5 c, 5 f, and 5 i with ALS enzyme were studied on Discovery Studio. To test the possibility of 5 c, 5 f, and 5 i as potential herbicides in paddy fields, we performed the crop safety study. The results show that 5 f and 5 i are safer to rice than 5 c . The present work indicates that 5 f and 5 i may serveAbstract: A series of pyrimidinylselenosalicylic acid derivatives (5 a –5 l ) and 4‐selenopyrimidine derivatives (6 a –6 f ) were synthesized and evaluated as potential acetylactate synthase (ALS)‐inhibiting herbicides. All synthesized new compounds were characterized by 1 H NMR, 13 C NMR, and high‐resolution mass spectrometry (HRMS). The compounds were subjected to herbicidal activity, in vitro ALS enzyme inhibitory activity, and crop safety studies. The herbicidal activity study shows that 4‐chloro (5 b), 5‐chloro (5 c), 5‐methoxy (5 e), 4, 5‐dimethoxy (5 f), 5‐fluoro (5 h), and 4, 5‐difluoro (5 i) substituted 2‐[(4, 6‐dimethoxy‐2‐pyrimidinyl)selanyl]benzoic acid exhibit significantly enhanced weed control effect than other new compounds and Pyrithiobac. Most of compounds exhibit enhanced inhibition effect on Cyperus difformis Linn than those on barnyard grass, Portulaca oleracea, Eleusine indica, and Amaranthus retroflexus . Importantly, 5 c, 5 f, and 5 i also exhibit more potent inhibition effect on Escherichia coli ALS enzyme than other new compounds and Pyrithiobac in in vitro ALS enzyme inhibitory activity study. The possible binding modes of 5 c, 5 f, and 5 i with ALS enzyme were studied on Discovery Studio. To test the possibility of 5 c, 5 f, and 5 i as potential herbicides in paddy fields, we performed the crop safety study. The results show that 5 f and 5 i are safer to rice than 5 c . The present work indicates that 5 f and 5 i may serve as new herbicide candidates for weed control in paddy fields. Abstract : A series of pyrimidinylselenosalicylic acid derivatives and 4‐selenopyrimidine derivatives were synthesized and evaluated as potential acetylactate synthase (ALS)‐inhibiting herbicides. Among the synthesized compounds, 5 c, 5 f, and 5 i exhibit enhanced herbicidal activity and ALS enzyme inhibitory activity as compared to other synthesized compounds and Pyrithiobac. Moreover, 5 f and 5 i are safer to rice than 5 c. 5 f and 5 i show significant potential for weed control in paddy fields. … (more)
- Is Part Of:
- ChemistrySelect. Volume 7:Issue 1(2022)
- Journal:
- ChemistrySelect
- Issue:
- Volume 7:Issue 1(2022)
- Issue Display:
- Volume 7, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 7
- Issue:
- 1
- Issue Sort Value:
- 2022-0007-0001-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-01-05
- Subjects:
- Acetolactate synthase -- Herbicidal activity -- Molecular docking simulation -- Pyrimidinylselenosalicylic acid derivatives -- 4-Selenopyrimidine derivatives
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.202103763 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20788.xml