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2-(hydroxymethyl)anthraquinone

Known as: HMAQ-one 
 
National Institutes of Health

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Anthraquinones

Papers overview

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2015
2015
Conformational stability, spectroscopic and computational studies, HOMO-LUMO, NBO, ESP analysis, thermodynamic parameters of natural bioactive compound with anticancer potential of 2-(hydroxymethyl…
Natural product drugs play a dominant role in pharmaceutical care. Nature is an attractive source of new therapeutic candidate… Expand
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2013
2013
Photoremovable protecting groups as controlled-release device for sex pheromone.
Photoremovable protecting groups (PRPGs) were demonstrated as a delivery device for controlled release of pheromone under both UV… Expand
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2011
2011
Relationships between biochemical attributes (non-structural carbohydrates and phenolics) and natural durability against fungi in dry teak wood (Tectona grandis L. f.)
Abstract• IntroductionNon-structural carbohydrates and phenolic compounds are implicated in the natural durability of wood. In… Expand
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2009
2009
Long-range intramolecular photoredox reaction via coupled charge and proton transfer of triplet excited anthraquinones mediated by water.
The formal intramolecular photoredox reaction initially discovered for the parent 2-(hydroxymethyl)anthraquinone (1) has been… Expand
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2008
2008
Formal intramolecular photoredox chemistry of anthraquinones in aqueous solution: photodeprotection for alcohols, aldehydes and ketones.
The formal intramolecular photoredox reaction initially discovered for the parent 2-(hydroxymethyl)anthraquinone (1) in aqueous… Expand
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Highly Cited
2006
Highly Cited
2006
Antibacterial activity of Tabebuia impetiginosa Martius ex DC (Taheebo) against Helicobacter pylori.
The growth-inhibiting activity of Tabebuia impetiginosa Martius ex DC dried inner bark-derived constituents against Helicobacter… Expand
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2006
2006
A simple and smart oxygen sensor based on the intrazeolite reactions of a substituted anthraquinone.
Inclusion of 2-(hydroxymethyl)anthraquinone in zeolite NaY leads to a solid, photoactivated, reusable oxygen sensor capable of… Expand
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2002
2002
Excited state intramolecular redox reaction of 2-(hydroxymethyl)anthraquinone in aqueous solution.
The title compound undergoes a novel excited state intramolecular redox reaction in which the 'distal' side chain benzylic… Expand
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1992
1992
Analogues of luteinizing hormone-releasing hormone containing cytotoxic groups.
In an attempt to produce better cytotoxic analogues, chemotherapeutic antineoplastic radicals including an alkylating nitrogen… Expand
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1980
1980
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents
 
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