Fluorescence and phosphorescence of harmol and harmalol at 77 K
Author:
Publisher
Elsevier BV
Subject
General Physics and Astronomy,General Chemical Engineering,General Chemistry
Reference12 articles.
1. Acid-base and tautomeric equilibria of harmol in the ground and first excited singlet states
2. Acidity constants of harmaline and harmalol in the ground and excited singlet states
3. Monoamine oxidase inhibition in brain and liver produced by β-carbolines: structure-activity relationships and substrate specificity
4. Inhibition patterns of monoamine oxidase in sub-fractions of rat brain mitochondria in presence of some selective inhibitors
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1. Simple naturally occurring β-carboline alkaloids – role in sustainable theranostics;Physical Sciences Reviews;2022-10-14
2. Efficient Metal‐Free Process: A Facile Synthesis of Biologically Versatile Harmol‐Linked Benzothiazoline Hybrids;ChemistrySelect;2020-01-16
3. Comment on “Binding of alkaloid harmalol to DNA: Photophysical and calorimetric approach”;Journal of Photochemistry and Photobiology B: Biology;2014-07
4. Photochemical reaction of full-aromatic β-carbolines in halomethanes 2. CHCl3: Electronic spectra and kinetics;Journal of Photochemistry and Photobiology A: Chemistry;1994-01
5. Photochemical reaction of harmalol. Part 2. Electronic spectra;Journal of the Chemical Society, Perkin Transactions 2;1993
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