Research graph
References from Novel Coumarin Derivatives Containing Oxazole/Isoxazole/Pyrazole Groups as Antifungal Agents: Design, Synthesis, Quantitative Structure–Activity Relationships, and Preliminary Mechanistic Insights. Local targets link to admitted publications; unresolved targets remain external evidence.
Exponential population growth and global food security: challenges and alternatives
10.1016/b978-0-443-13993-2.00001-3 · 2024 · External reference
Exploring the reality of global food insecurity and policy gaps
10.1057/s41599-025-05315-8 · 2025 · External reference
Selected emerging and reemerging plant pathogens affecting the food basket: A threat to food security
10.1016/j.jafr.2023.100827 · 2023 · External reference
The global burden of pathogens and pests on major food crops
10.1038/s41559-018-0793-y · 2019 · External reference
Research and development of green pesticides in China
10.1016/b978-0-12-821035-2.00005-x · 2021 · External reference
Design and synthesis of camphor-thiazole derivatives as potent antifungal agents: structure–activity relationship and preliminary mechanistic study
10.1002/ps.8563 · 2025 · External reference
Rational design and discovery of novel hydrazide derivatives as potent succinate dehydrogenase inhibitors inspired by natural D/L-camphor
10.1002/ps.8481 · 2025 · External reference
Discovery of novel D/L-camphor derivatives containing oxime ester as fungicide candidates: antifungal activity, structure–activity relationship and preliminary mechanistic study
10.1016/j.aac.2024.11.007 · 2025 · External reference
3D-QSAR-directed synthesis of halogenated coumarin-3-hydrazide derivatives: unveiling their potential as SDHI antifungal agents
10.1021/acs.jafc.4c00200 · 2024 · External reference
Design, synthesis, antifungal activity, and 3D-QSAR of novel oxime ether-containing coumarin derivatives as potential fungicides
10.1021/acs.jafc.3c06032 · 2024 · External reference
Discovery of novel 3-phenylhydrazone coumarin derivatives as potential antifungal agents against phytopathogenic fungi
10.1016/j.foodchem.2025.144655 · 2025 · External reference
Xanthoxyletin blocks the RANK/RANKL signaling pathway to suppress the growth of human pancreatic cancer cells
10.2478/acph-2023-0024 · 2023 · External reference
Osthole: A coumarin with dual roles in biology and chemistry
10.3390/biology14060588 · 2025 · External reference
Structural elucidation of flavonoids from Shatianyu (Citrus grandis L. Osbeck) pulp and screening of key antioxidant components
10.1016/j.foodchem.2021.130605 · 2022 · External reference
Microwave-assisted synthesis and antifungal activity of novel coumarin derivatives: pyrano[3,2-c]chromene-2,5-diones
10.1016/j.ejmech.2016.03.069 · 2016 · External reference
New arylpyrazoline-coumarins: synthesis and anti-inflammatory activity
10.1016/j.ejmech.2017.06.044 · 2017 · External reference
Coumarins as anticancer agents: a review on synthetic strategies, mechanism of action and SAR studies
10.1016/j.ejmech.2015.07.010 · 2015 · External reference
Therapeutic potential of coumarins as antiviral agents
10.1016/j.ejmech.2016.07.056 · 2016 · External reference
Recent advancements in the synthetic chemistry of oxazole derivatives and their significant medicinal applications
10.2174/0115734064361520250115090651 · 2025 · External reference
Discovery and characterization of oxazolismycin, an oxazole-containing natural product with an atypical loading mechanism
10.1021/jacsau.5c00326 · 2025 · External reference
Isoxazole/isoxazoline skeleton in the structural modification of natural products: a review
10.3390/ph16020228 · 2023 · External reference
Isoxazole compounds: unveiling the synthetic strategy, in-silico SAR and toxicity studies and future perspective as PARP inhibitor in cancer therapy
10.1016/j.ejmech.2024.116898 · 2024 · External reference
Natural products–isoxazole hybrids: a review of developments in medicinal chemistry
10.1016/j.arabjc.2024.105794 · 2024 · External reference
Pyrazole-containing natural products: synthetic preview and biological significance
10.1016/j.ejmech.2013.08.053 · 2013 · External reference
Discovery of oxazosulfyl: a novel broad-spectrum insecticide
10.1016/b978-0-12-821035-2.00013-9 · 2021 · External reference
Isoxaflutole: the background to its discovery and the basis of its herbicidal properties
10.1002/1526-4998(200102)57:2<133::aid-ps276>3.0.co;2-0 · 2001 · External reference
The control effect of fungicide pyraclostrobin against freckle disease of banana and its residue dynamics under field conditions
10.1080/03601234.2018.1473974 · 2018 · External reference
Impact of pyraclostrobin on the growth of Fusarium pseudograminearum and its control efficacy against wheat crown rot
10.1007/s42161-023-01466-2 · 2023 · External reference
Synthesis and evaluation of biologically active compounds from heterocycles class
10.3390/molecules30020394 · 2025 · External reference
Recent advances in the natural products-based lead discovery for new agrochemicals
10.1016/j.aac.2023.09.004 · 2023 · External reference
Design, synthesis, antifungal activity, and 3D-QSAR of coumarin derivatives
10.1584/jpestics.d17-075 · 2018 · External reference
The synthesis of coumarin thiazoles containing a trifluoromethyl group and their antifungal activities
10.1016/j.arabjc.2020.10.027 · 2021 · External reference
Design, synthesis, and antifungal activity of 3-(thiophen-2-yl)-1,5-dihydro-2H-pyrrol-2-one derivatives bearing a carbonic ester group
10.1002/jhet.3391 · 2019 · External reference
Design and synthesis of novel 3-(thiophen-2-yl)-1,5-dihydro-2H-pyrrol-2-one derivatives bearing a hydrazone moiety as potential fungicides
10.1186/s13065-018-0452-z · 2018 · External reference
Novel pyrrolidine-2,4-dione derivatives containing pharmacophores of both hydrazine and diphenyl ether as potential antifungal agents: design, synthesis, biological evaluation, and 3D-QSAR study
10.1039/d0nj04551a · 2020 · External reference
Discovery of novel pyrazole/thiazole derivatives containing cyano/thiocyanato groups as fungicide candidates
10.1021/acs.jafc.4c09156 · 2025 · External reference
Design, synthesis, antifungal evaluation, and three-dimensional quantitative structure–activity relationship of novel 5-sulfonyl-1,3,4-thiadiazole flavonoids
10.1021/acs.jafc.4c03505 · 2024 · External reference
Isoxaflutole: the background to its discovery and the basis of its herbicidal properties
10.1002/1526-4998(200102)57:2<133::aid-ps276>3.0.co;2-0 · ExternalCitation · doi-reference
Design, synthesis, and antifungal activity of 3-(thiophen-2-yl)-1,5-dihydro-2H-pyrrol-2-one derivatives bearing a carbonic ester group
10.1002/jhet.3391 · ExternalCitation · doi-reference
Rational design and discovery of novel hydrazide derivatives as potent succinate dehydrogenase inhibitors inspired by natural D/L-camphor
10.1002/ps.8481 · ExternalCitation · doi-reference
Design and synthesis of camphor-thiazole derivatives as potent antifungal agents: structure–activity relationship and preliminary mechanistic study
10.1002/ps.8563 · ExternalCitation · doi-reference
Impact of pyraclostrobin on the growth of Fusarium pseudograminearum and its control efficacy against wheat crown rot
10.1007/s42161-023-01466-2 · ExternalCitation · doi-reference
Research and development of green pesticides in China
10.1016/b978-0-12-821035-2.00005-x · ExternalCitation · doi-reference
Discovery of oxazosulfyl: a novel broad-spectrum insecticide
10.1016/b978-0-12-821035-2.00013-9 · ExternalCitation · doi-reference
Exponential population growth and global food security: challenges and alternatives
10.1016/b978-0-443-13993-2.00001-3 · ExternalCitation · doi-reference
Recent advances in the natural products-based lead discovery for new agrochemicals
10.1016/j.aac.2023.09.004 · ExternalCitation · doi-reference
Discovery of novel D/L-camphor derivatives containing oxime ester as fungicide candidates: antifungal activity, structure–activity relationship and preliminary mechanistic study
10.1016/j.aac.2024.11.007 · ExternalCitation · doi-reference
The synthesis of coumarin thiazoles containing a trifluoromethyl group and their antifungal activities
10.1016/j.arabjc.2020.10.027 · ExternalCitation · doi-reference
Natural products–isoxazole hybrids: a review of developments in medicinal chemistry
10.1016/j.arabjc.2024.105794 · ExternalCitation · doi-reference
Pyrazole-containing natural products: synthetic preview and biological significance
10.1016/j.ejmech.2013.08.053 · ExternalCitation · doi-reference
Coumarins as anticancer agents: a review on synthetic strategies, mechanism of action and SAR studies
10.1016/j.ejmech.2015.07.010 · ExternalCitation · doi-reference
Microwave-assisted synthesis and antifungal activity of novel coumarin derivatives: pyrano[3,2-c]chromene-2,5-diones
10.1016/j.ejmech.2016.03.069 · ExternalCitation · doi-reference
Therapeutic potential of coumarins as antiviral agents
10.1016/j.ejmech.2016.07.056 · ExternalCitation · doi-reference
New arylpyrazoline-coumarins: synthesis and anti-inflammatory activity
10.1016/j.ejmech.2017.06.044 · ExternalCitation · doi-reference
Isoxazole compounds: unveiling the synthetic strategy, in-silico SAR and toxicity studies and future perspective as PARP inhibitor in cancer therapy
10.1016/j.ejmech.2024.116898 · ExternalCitation · doi-reference
Structural elucidation of flavonoids from Shatianyu (Citrus grandis L. Osbeck) pulp and screening of key antioxidant components
10.1016/j.foodchem.2021.130605 · ExternalCitation · doi-reference
Discovery of novel 3-phenylhydrazone coumarin derivatives as potential antifungal agents against phytopathogenic fungi
10.1016/j.foodchem.2025.144655 · ExternalCitation · doi-reference
Selected emerging and reemerging plant pathogens affecting the food basket: A threat to food security
10.1016/j.jafr.2023.100827 · ExternalCitation · doi-reference
Design, synthesis, antifungal activity, and 3D-QSAR of novel oxime ether-containing coumarin derivatives as potential fungicides
10.1021/acs.jafc.3c06032 · ExternalCitation · doi-reference
3D-QSAR-directed synthesis of halogenated coumarin-3-hydrazide derivatives: unveiling their potential as SDHI antifungal agents
10.1021/acs.jafc.4c00200 · ExternalCitation · doi-reference
Design, synthesis, antifungal evaluation, and three-dimensional quantitative structure–activity relationship of novel 5-sulfonyl-1,3,4-thiadiazole flavonoids
10.1021/acs.jafc.4c03505 · ExternalCitation · doi-reference
Discovery of novel pyrazole/thiazole derivatives containing cyano/thiocyanato groups as fungicide candidates
10.1021/acs.jafc.4c09156 · ExternalCitation · doi-reference
Discovery and characterization of oxazolismycin, an oxazole-containing natural product with an atypical loading mechanism
10.1021/jacsau.5c00326 · ExternalCitation · doi-reference
The global burden of pathogens and pests on major food crops
10.1038/s41559-018-0793-y · ExternalCitation · doi-reference
Novel pyrrolidine-2,4-dione derivatives containing pharmacophores of both hydrazine and diphenyl ether as potential antifungal agents: design, synthesis, biological evaluation, and 3D-QSAR study
10.1039/d0nj04551a · ExternalCitation · doi-reference
Exploring the reality of global food insecurity and policy gaps
10.1057/s41599-025-05315-8 · ExternalCitation · doi-reference
The control effect of fungicide pyraclostrobin against freckle disease of banana and its residue dynamics under field conditions
10.1080/03601234.2018.1473974 · ExternalCitation · doi-reference
Design and synthesis of novel 3-(thiophen-2-yl)-1,5-dihydro-2H-pyrrol-2-one derivatives bearing a hydrazone moiety as potential fungicides
10.1186/s13065-018-0452-z · ExternalCitation · doi-reference
Design, synthesis, antifungal activity, and 3D-QSAR of coumarin derivatives
10.1584/jpestics.d17-075 · ExternalCitation · doi-reference
Recent advancements in the synthetic chemistry of oxazole derivatives and their significant medicinal applications
10.2174/0115734064361520250115090651 · ExternalCitation · doi-reference
Xanthoxyletin blocks the RANK/RANKL signaling pathway to suppress the growth of human pancreatic cancer cells
10.2478/acph-2023-0024 · ExternalCitation · doi-reference
Osthole: A coumarin with dual roles in biology and chemistry
10.3390/biology14060588 · ExternalCitation · doi-reference
Synthesis and evaluation of biologically active compounds from heterocycles class
10.3390/molecules30020394 · ExternalCitation · doi-reference
Isoxazole/isoxazoline skeleton in the structural modification of natural products: a review
10.3390/ph16020228 · ExternalCitation · doi-reference
