Hydroquinone

Papers

Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study. Cynthia D Selassie et al J. Med. Chem. 48, 7234-42, (2005)

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Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase. Suhee Song et al Bioorg. Med. Chem. Lett. 17, 461-4, (2007)

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Synthesis and anti-inflammatory activity of 3-(4'-geranyloxy-3'-methoxyphenyl)-2-trans propenoic acid and its ester derivatives. Francesco Epifano et al Bioorg. Med. Chem. Lett. 17, 5709-14, (2007)

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QSAR study on permeability of hydrophobic compounds with artificial membranes. Masaaki Fujikawa et al Bioorg. Med. Chem. 15, 3756-67, (2007)

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Chemical genetics reveals a complex functional ground state of neural stem cells Diamandis, P., et. al. Nat. Chem. Biol. 3(5), 268-273, (2007)

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Carbonic anhydrase inhibitors: Inhibition of the new membrane-associated isoform XV with phenols. Alessio Innocenti et al Bioorg. Med. Chem. Lett. 18, 3593-6, (2008)

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Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. Marc Criton et al Bioorg. Med. Chem. Lett. 18, 3607-10, (2008)

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Carbonic anhydrase inhibitors: inhibition of mammalian isoforms I-XIV with a series of substituted phenols including paracetamol and salicylic acid. Alessio Innocenti et al Bioorg. Med. Chem. 16, 7424-8, (2008)

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Effects of 3-(4'-geranyloxy-3'-methoxyphenyl)-2-trans propenoic acid and its ester derivatives on biofilm formation by two oral pathogens, Porphyromonas gingivalis and Streptococcus mutans. Charles Bodet et al Eur. J. Med. Chem. 43, 1612-20, (2008)

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Air to lung partition coefficients for volatile organic compounds and blood to lung partition coefficients for volatile organic compounds and drugs. Michael H Abraham et al Eur. J. Med. Chem. 43, 478-85, (2008)

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Pyronane monoterpenoids from the fruit of Gardenia jasminoides. Quan Cheng Chen et al J. Nat. Prod. 71, 995-9, (2008)

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Studies on depigmenting activities of dihydroxyl benzamide derivatives containing adamantane moiety. Ho Sik Rho et al Bioorg. Med. Chem. Lett. 19, 1532-3, (2009)

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Convenient QSAR model for predicting the complexation of structurally diverse compounds with beta-cyclodextrins. Alfonso Pérez-Garrido et al Bioorg. Med. Chem. 17, 896-904, (2009)

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Tyrosinase-inhibitory constituents from the twigs of Cinnamomum cassia. Tran Minh Ngoc et al J. Nat. Prod. 72, 1205-8, (2009)

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Melanin synthesis inhibitors from Lespedeza floribunda. Maya Mori-Hongo et al J. Nat. Prod. 72, 194-203, (2009)

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Melanin synthesis inhibitors from Lespedeza cyrtobotrya. Maya Mori-Hongo et al J. Nat. Prod. 72, 63-71, (2009)

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Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum. Jing Yuan et al Nat. Chem. Biol. 5, 765-71, (2009)

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A newly synthesized, potent tyrosinase inhibitor: 5-(6-hydroxy-2-naphthyl)-1,2,3-benzenetriol. Jehun Choi et al Bioorg. Med. Chem. Lett. 20, 4882-4, (2010)

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Identification of a potent and noncytotoxic inhibitor of melanin production. Soonho Hwang et al Bioorg. Med. Chem. 18, 5602-9, (2010)

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Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species. Denis Fourches et al Chem. Res. Toxicol. 23, 171-83, (2010)

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Evaluation of anti-pigmentary effect of synthetic sulfonylamino chalcone. Woo Duck Seo et al Eur. J. Med. Chem. 45, 2010-7, (2010)

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In vitro inhibition of ?-carbonic anhydrase isozymes by some phenolic compounds. Sevim Beyza Oztürk Sarikaya et al Bioorg. Med. Chem. Lett. 21, 4259-62, (2011)

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Discovery of novel SERCA inhibitors by virtual screening of a large compound library. Christopher Elam et al Eur. J. Med. Chem. 46, 1512-23, (2011)

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Merck 14,4808

Beil. 6,IV,5712

Fieser 5,341

Aldrich MSDS 1, 1050:A / Corp MSDS 1 (1), 1900:B / FT-IR 2 (2), 1892:A / FT-IR 1 (1), 1107:D / FT-NMR 1 (2), 304:C / IR-Spectra (2), 594:F / IR-Spectra (3), 666:C / NMR-Reference 2 (1), 902:B / RegBook 1 (1), 1301:A / Sax 6, 1553 / Sigma FT-IR 1 (2), 618:B / Structure Index 1, 198:B:6 / Vapor Phase 3, 1041:B