4-Hydroxybenzaldehyde

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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Antitubercular constituents from the stem wood of Cinnamomum kotoense. Fu-Chi Chen et al J. Nat. Prod. 68, 1318-23, (2005)

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Inhibition of GABA shunt enzymes' activity by 4-hydroxybenzaldehyde derivatives. Yun-Hai Tao et al Bioorg. Med. Chem. Lett. 16, 592-5, (2006)

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Methyl 2-(2-(4-formylphenoxy)acetamido)-2-substituted acetate derivatives: a new class of acetylcholinesterase inhibitors. Huan Wen et al Bioorg. Med. Chem. Lett. 17, 2123-5, (2007)

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3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors. Chao-Bin Xue et al Bioorg. Med. Chem. 15, 2006-15, (2007)

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Antitubercular dihydroagarofuranoid sesquiterpenes from the roots of Microtropis fokienensis. Jih-Jung Chen et al J. Nat. Prod. 70, 202-5, (2007)

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Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors. Wei Yi et al Bioorg. Med. Chem. Lett. 18, 6490-3, (2008)

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Synthesis and biological evaluation of helicid analogues as novel acetylcholinesterase inhibitors. Huan Wen et al Eur. J. Med. Chem. 43, 166-73, (2008)

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Inactivation of GABA transaminase by 3-chloro-1-(4-hydroxyphenyl)propan-1-one. Yun-Hai Tao et al Bioorg. Med. Chem. Lett. 19, 731-4, (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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Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities. Qin Yan et al Eur. J. Med. Chem. 44, 4235-43, (2009)

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Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells. Souichi Nakashima et al Bioorg. Med. Chem. 18, 2337-45, (2010)

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Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors. Wei Yi et al Eur. J. Med. Chem. 45, 639-46, (2010)

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New antitumor compounds from Carya cathayensis. Wei Wu et al Bioorg. Med. Chem. Lett. 22, 1895-8, (2012)

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Merck 14,4811

Beil. 8,IV,251

Aldrich MSDS 1, 1052:A / Arctander, 1726 / Corp MSDS 1 (1), 1906:A / FT-IR 1 (2), 112:A / FT-IR 2 (2), 2531:A / FT-NMR 1 (2), 943:A / IR-Spectra (2), 801:B / IR-Spectra (3), 915:D / NMR-Reference 2 (2), 110:C / RegBook 1 (2), 1717:N / RegBook 26 (2), 1717:N / Sax 6, 1457 / Sigma FT-IR 1 (2), 619:D / Structure Index 1, 272:C:8 / Vapor Phase 3, 1291:C