Results 71 to 80 of about 5,249 (228)

Pyrrolo‐Fused Phenanthridines as Potential Anticancer Agents: Synthesis, Prediction, and Biological Evaluation

open access: yesJournal of Biochemical and Molecular Toxicology, Volume 39, Issue 9, September 2025.
ABSTRACT We report the synthesis of four novel monoquaternary salts and four fused pyrrolo‐phenanthridine compounds, fully characterized by NMR, FT‐IR, and mass spectrometry. Guided by theoretical predictions, including molecular docking studies, we assessed their cytotoxic activity and biocompatibility.
Ashraf Al‐Matarneh   +6 more
wiley   +1 more source

In vitro Cytotoxic Activity of Four Plants Used in Persian Traditional Medicine [PDF]

open access: yes, 2013
Purpose: The aim of this study was to investigate in vitro cytotoxic activity of four methanolic crude plant extracts against panel cell lines. Methods: Methanolic extracts were tested for their possible antitumor activity and cytotoxicity using the 3-(4,
Behzad Baradaran   +3 more
core   +1 more source

Sanguinarine and Its Salts [PDF]

open access: yesThe Boston Medical and Surgical Journal
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openaire   +1 more source

Programmed Cell Death in Cancer

open access: yesMedComm, Volume 6, Issue 9, September 2025.
Cancer is one of the most common and lethal diseases globally, with programmed cell death (PCD) playing a pivotal role in its pathogenesis and treatment. This comprehensive review covers the origin, developmental trajectory, and mechanisms of various PCDs, as well as their molecular connections with cancers. Latest studies have increasingly highlighted
Yuang Wei   +3 more
wiley   +1 more source

Nonconventional Techniques in Plant Alkaloid Extraction: A Decade of Progress (2014–2023)

open access: yesChemistry &Biodiversity, Volume 22, Issue 8, August 2025.
This figure seeks to represent the evolution of the different unconventional approaches that were adopted for the extraction of plant‐derived alkaloids during the decade from 2014 to 2023. ABSTRACT Plant metabolism encompasses primary and secondary pathways, with secondary metabolism yielding diverse natural products crucial for plant adaptation and ...
Victor Menezes Sipoloni   +5 more
wiley   +1 more source

Molecular isolation of cDNA encoding N-methylstylopine hydroxylase from greater celandine (Chelidonium majus L.) and its expression enhancement in response to salinity abiotic elicitor [PDF]

open access: yesمجله بیوتکنولوژی کشاورزی, 2018
  The greater celandine (Chelidonium majus L.) contains important alkaloids such as Sanguinarine. Sanguinarine is an active alkaloid with potentially antimicrobial, anti-inflammatory and anti-tumor properties that is widely found in plants of ...
Zahra Soleimani   +2 more
doaj   +1 more source

Shape-selective recognition of DNA abasic sites by metallohelices : inhibition of human AP endonuclease 1 [PDF]

open access: yes, 2015
Loss of a base in DNA leading to creation of an abasic (AP) site leaving a deoxyribose residue in the strand, is a frequent lesion that may occur spontaneously or under the action of various physical and chemical agents.
Brabec, V., Malina, J., Scott, Peter
core   +1 more source

Fluorescence switching of sanguinarine in micellar environments

open access: yesPhysical Chemistry Chemical Physics, 2015
Conversion from iminium to alkanolamine form of Sanguinarine, a key member of benzylisoquinoline alkaloid family, is monitored in micellar environments by fluorescence switch.
Sagar, Satpathi   +2 more
openaire   +3 more sources

Analysis of the Aerial Parts of Millettia speciosa Champ. and Mechanistic Study of Its Active Ingredient Formononetin in Improving Metabolic Syndrome

open access: yesFood Science &Nutrition, Volume 13, Issue 7, July 2025.
Millettia speciosa Champ. is a traditional medicinal and edible plant. Its aerial parts are often discarded, leading to resource waste. HPLC‐Q‐TOF‐MS/MS analysis identified a total of 41 chemical compounds in the stems, branches, and leaves of M. speciosa. Network pharmacology screening identified Formononetin (FMN) as a key compound of M.
Wenjing Niu   +4 more
wiley   +1 more source

Charge Transfer-oxy Radical Mechanism for Anti-cancer Agents [PDF]

open access: yes, 1986
The proposal is advanced that anti-cancer drugs generally function by charge transfer resulting in formation of toxic oxy radicals which destroy the neoplasm.
Ames, James R.   +5 more
core   +1 more source

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