Sustainable sonochemistry in medicinal heterocycle design: Advances and anticancer implications.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
Ultrasound enables a variety of complex transformations, including multicomponent reactions, annulation and cyclizations, often under ambient temperature or low-energy conditions.
I · Intervention 중재 / 시술
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C · Comparison 대조 / 비교
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O · Outcome 결과 / 결론
The resulting heterocycles demonstrated cytotoxicity against several cancer cell lines in vitro. This review focuses on sonochemical approaches for heterocycle synthesis from 2021 to 2025, as well as the anticancer properties of the compounds generated by these methods.
ℹ️ 이 논문은 무료 전문이 아직 없습니다. 코퍼스 전체의 43.9%는 무료 가능 (통계 →) · 🏥 기관 EZproxy로 시도
One of the powerful tools for sustainable and efficient synthetic strategies in medicinal chemistry is ultrasound-assisted synthesis of heterocyclic scaffolds.
APA
Das P, Hemamalini V, et al. (2026). Sustainable sonochemistry in medicinal heterocycle design: Advances and anticancer implications.. Bioorganic chemistry, 169, 109412. https://doi.org/10.1016/j.bioorg.2025.109412
MLA
Das P, et al.. "Sustainable sonochemistry in medicinal heterocycle design: Advances and anticancer implications.." Bioorganic chemistry, vol. 169, 2026, pp. 109412.
PMID
41456427 ↗
Abstract 한글 요약
One of the powerful tools for sustainable and efficient synthetic strategies in medicinal chemistry is ultrasound-assisted synthesis of heterocyclic scaffolds. In recent years, considerable attention has been directed toward employing ultrasonic energy to generate nitrogen, sulfur and oxygen-containing heterocycles, some of which exhibit notable anticancer activities. This review comprehensively summarizes recent advances in ultrasound-mediated synthetic methodologies, highlighting their ability to accelerate reaction rates, increase yields, and reduce energy consumption, while minimising the use of hazardous solvents and catalysts compared to conventional methods. Ultrasound enables a variety of complex transformations, including multicomponent reactions, annulation and cyclizations, often under ambient temperature or low-energy conditions. The resulting heterocycles demonstrated cytotoxicity against several cancer cell lines in vitro. This review focuses on sonochemical approaches for heterocycle synthesis from 2021 to 2025, as well as the anticancer properties of the compounds generated by these methods.
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