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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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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… 
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… 
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… 
2008
2008
Formal intramolecular photoredox chemistry of anthraquinones in aqueous solution: photodeprotection for alcohols, aldehydes and ketones.
  • Yunyan Hou, P. Wan
  • Photochemical & photobiological sciences…
  • 2008
  • Corpus ID: 10428138
The formal intramolecular photoredox reaction initially discovered for the parent 2-(hydroxymethyl)anthraquinone (1) in aqueous… 
Highly Cited
2006
Highly Cited
2006
Antibacterial activity of Tabebuia impetiginosa Martius ex DC (Taheebo) against Helicobacter pylori.
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… 
2005
2005
Effect of a cytotoxic analog of LH-RH (T-98) on the growth of estrogendependent MXT mouse mammary cancers: Correlations between growth characteristics and EGF receptor content of tumors
SummaryFemale BDF mice bearing estrogen-dependent MXT mouse mammary cancers were treated for 4 weeks with a cytotoxic analog of… 
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… 
Highly Cited
1992
Highly Cited
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… 
1980
1980
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
Hypoxic cells of solid tumors are an obstacle to effective cancer therapy. Since hypoxic cells remote from the tumor blood supply… 
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