Related Experiment Video
Updated: Jan 26, 2026

07:17
Production and Detection of Reactive Oxygen Species ROS in Cancers
Published on: November 21, 2011
71.0K
Photocontrolled endogenous reactive oxygen species (ROS) generation
Ajay Kumar Sharma1, Harshit Singh1, Harinath Chakrapani1
1Department of Chemistry, Indian Institute of Science Education and Research Pune, Pune 411 008, Maharashtra, India. harinath@iiserpune.ac.in.
Abstract:
A cell-permeable small molecule for light-triggered generation of endogenous reactive oxygen species (ROS) is reported.
More Related Videos
Related Concept Videos
What is a Species?
49.5K
Overview
49.5K
Keystone Species
24.2K
Measures of species biodiversity, such as richness (i.e., the number of species present) and evenness (i.e., their relative abundance), describe an ecological community’s structure. Many factors affect community structure, including abiotic factors (e.g., sunlight and nutrients), disturbances (e.g., fire or flood), species interactions (e.g., predation or competition), and chance events (e.g., foreign species invasion). Certain species—such as keystone species—also play a...
24.2K
Formation of Species
44.9K
Speciation describes the formation of one or more new species from one or sometimes multiple original species. The resulting species are discrete from the parent species, and barriers to reproduction will typically exist. There are two primary mechanisms, speciation with and without geographic isolation—allopatric and sympatric speciation, respectively.
44.9K
Cross-reactivity
32.9K
Overview
32.9K
Reactivity of Enols
4.0K
Enols are a class of compounds where a hydroxyl group is attached to a carbon–carbon double bond, which implies that it is a vinyl alcohol. A carbonyl compound with an α hydrogen undergoes keto–enol tautomerism and remains in equilibrium with its tautomer, the enol form. Usually, the keto tautomer is present in a higher concentration than the enol tautomer due to the higher bond energy of C=O compared to C=C. Moreover, the direction of the keto–enol equilibrium is...
4.0K
Reactivity of Enolate Ions
3.3K
Enolate ions are formed by the acid–base reaction of a carbonyl compound with a base. This leads to deprotonation of the α hydrogen atom, leading to a resonance-stabilized enolate ion where one of the contributing structures is an oxyanion, which imparts additional stability. Therefore, the proton on the α carbon is more acidic in nature than that of other sp3-hybridized C–H bonds but less acidic than those in O–H bonds where the negative charge in the conjugate...
3.3K

