Umbelliferone

Papers

Synthesis and antiinflammatory activity of coumarin derivatives. Christos A Kontogiorgis et al J. Med. Chem. 48, 6400-8, (2005)

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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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Relationship between quantum-chemical descriptors of proton dissociation and experimental acidity constants of various hydroxylated coumarins. Identification of the biologically active species for xanthine oxidase inhibition. Anna Maria Ferrari et al Eur. J. Med. Chem. 42, 1028-31, (2007)

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Coumarin as attractive casein kinase 2 (CK2) inhibitor scaffold: an integrate approach to elucidate the putative binding motif and explain structure-activity relationships. Adriana Chilin et al J. Med. Chem. 51, 752-9, (2008)

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Synthesis and free radical scavenging activity of some new spiropyranocoumarins. Vassiliki Panteleon et al Bioorg. Med. Chem. Lett. 18, 5781-4, (2008)

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Synthesis of hydroxycoumarins and hydroxybenzo[f]- or [h]coumarins as lipid peroxidation inhibitors. Theodoros Symeonidis et al Bioorg. Med. Chem. Lett. 19, 1139-42, (2009)

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Discovery of novel Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase inhibitors. Renato F Freitas et al Bioorg. Med. Chem. 17, 2476-82, (2009)

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Antiamoebic coumarins from the root bark of Adina cordifolia and their new thiosemicarbazone derivatives. Prince Firdoos Iqbal et al Eur. J. Med. Chem. 44, 2252-9, (2009)

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Coumarins incorporating hydroxy- and chloro-moieties selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II. Alfonso Maresca et al Bioorg. Med. Chem. Lett. 20, 4511-4, (2010)

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6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2. Atsushi Kato et al Bioorg. Med. Chem. Lett. 20, 5630-3, (2010)

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7,8-disubstituted- but not 6,7-disubstituted coumarins selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II in the low nanomolar/subnanomolar range. Alfonso Maresca et al Bioorg. Med. Chem. Lett. 20, 7255-8, (2010)

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Synthesis and biological evaluation of (6- and 7-phenyl) coumarin derivatives as selective nonsteroidal inhibitors of 17?-hydroxysteroid dehydrogenase type 1. Stefan Starcevi? et al J. Med. Chem. 54, 248-61, (2011)

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Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors. Nadia Touisni et al J. Med. Chem. 54, 8271-7, (2011)

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New halogenated phenylcoumarins as tyrosinase inhibitors. Maria João Matos et al Bioorg. Med. Chem. Lett. 21, 3342-5, (2011)

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Growth inhibitory activities of oxyprenylated and non-prenylated naturally occurring phenylpropanoids in cancer cell lines. Céline Bruyère et al Bioorg. Med. Chem. Lett. 21, 4174-9, (2011)

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Pancreatic anticancer activity of a novel geranylgeranylated coumarin derivative. Tehsina Devji et al Bioorg. Med. Chem. Lett. 21, 5770-3, (2011)

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Synthesis and pharmacological activity of O-aminoalkyl derivatives of 7-hydroxycoumarin. Joanna Trykowska Konc et al Eur. J. Med. Chem. 46, 2252-63, (2011)

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Synthesis and anti-inflammatory effects of a series of novel 7-hydroxycoumarin derivatives. Juri M Timonen et al Eur. J. Med. Chem. 46, 3845-50, (2011)

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Structure-activity relationships for naturally occurring coumarins as ?-secretase inhibitor. Shinsuke Marumoto et al Bioorg. Med. Chem. 20, 784-8, (2012)

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Merck 14,9847

Beil. 18,V,1,386

Aldrich MSDS 1, 1057:A / Corp MSDS 1 (1), 1916:A / FT-IR 2 (2), 2910:C / FT-IR 1 (2), 325:B / FT-NMR 1 (2), 1315:C / IR-Spectra (3), 1045:B / IR-Spectra (2), 913:F / NMR-Reference 2 (2), 309:C / RegBook 1 (2), 1945:B / Sigma FT-IR 1 (1), 734:A / Structure Index 1, 313:B:1