Drug development and industrial pharmacy · 2026
Recent advancements and clinical translation of cinnamaldehyde derivatives in therapeutics.
СтатьяОбзорНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Shakir Shakir Ullah, Khan Saeed Ahmad, Ullah Majeed, Khan Amjad, Khan Nauman Rahim, Khan Iftikhar
Аннотация
OBJECTIVE: This review systematically evaluates why CA derivatives have failed to transition from bench to bedside despite superior preclinical performance.
SIGNIFICANCE: Cinnamaldehyde (CA) clinical translation is stymied by a biopharmaceutical paradox: promising in vitro efficacy is negated by poor aqueous solubility (≈1 mg/mL), rapid first-pass metabolism, and a short plasma half-life (≈1.7 h). Also, the reactive α,β-unsaturated aldehyde moiety often triggers Pan-Assay Interference (PAINS) behavior.
KEY FINDINGS: We identify three primary chemical strategies that circumvent native CA's limitations: (1) Aldehyde masking (e.g. N-oxide conversion in PX5-9), which improves aqueous solubility by >2000-fold; (2) α-substitution (e.g. α-bromo-4-chloro CA), which modulates Michael acceptor reactivity to achieve an 87-fold higher selectivity index than the parent compound; and (3) Stimuli-responsive polymer conjugation (e.g. ROS-labile thioacetals), which enables tumor-microenvironment-triggered CA release and reduces cytotoxicity to IC50 ≫ 1600 µM in normal cells. While these derivatives show compelling in vivo efficacy in oncological, antiviral, and anti-inflammatory models, progress is halted by a lack of human pharmacokinetic profiling and 'safety bridging' toxicology.
CONCLUSION: The science of CA derivatives is more mature and future development must shift from broad scaffold exploration to targeted translational consortia focused on four priority leads (Compound 5, HCAG, PX5-9, and Compound 6f). Addressing the 'in vitro-in vivo disconnection' through chemoproteomic target validation and IND-enabling PK studies is the essential next step for advancing this reactive scaffold into clinical trials.
SIGNIFICANCE: Cinnamaldehyde (CA) clinical translation is stymied by a biopharmaceutical paradox: promising in vitro efficacy is negated by poor aqueous solubility (≈1 mg/mL), rapid first-pass metabolism, and a short plasma half-life (≈1.7 h). Also, the reactive α,β-unsaturated aldehyde moiety often triggers Pan-Assay Interference (PAINS) behavior.
KEY FINDINGS: We identify three primary chemical strategies that circumvent native CA's limitations: (1) Aldehyde masking (e.g. N-oxide conversion in PX5-9), which improves aqueous solubility by >2000-fold; (2) α-substitution (e.g. α-bromo-4-chloro CA), which modulates Michael acceptor reactivity to achieve an 87-fold higher selectivity index than the parent compound; and (3) Stimuli-responsive polymer conjugation (e.g. ROS-labile thioacetals), which enables tumor-microenvironment-triggered CA release and reduces cytotoxicity to IC50 ≫ 1600 µM in normal cells. While these derivatives show compelling in vivo efficacy in oncological, antiviral, and anti-inflammatory models, progress is halted by a lack of human pharmacokinetic profiling and 'safety bridging' toxicology.
CONCLUSION: The science of CA derivatives is more mature and future development must shift from broad scaffold exploration to targeted translational consortia focused on four priority leads (Compound 5, HCAG, PX5-9, and Compound 6f). Addressing the 'in vitro-in vivo disconnection' through chemoproteomic target validation and IND-enabling PK studies is the essential next step for advancing this reactive scaffold into clinical trials.