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Depside (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Depside" in French language version.

refsWebsite
Global rank French rank
14doi.org
2nd place
3rd place
12nih.gov
4th place
12th place
1issn.org
57th place
4th place

doi.org

dx.doi.org

  • Shoji Shibata et Hsüch-Ching Chiang, « The structures of cryptochlorophaeic acid and merochlorophaeic acid », Phytochemistry, vol. 4,‎ , p. 133–139 (DOI 10.1016/S0031-9422(00)86155-5)
  • Ono M, Masuoka C, Koto M, Tateishi M, Komatsu H, Kobayashi H, Igoshi K, Ito Y, Okawa M, Nohara T, « Antioxidant ortho-benzoyloxyphenyl acetic acid ester, vaccihein A, from the fruit of rabbiteye blueberry (Vaccinium ashei) », Chem. Pharm. Bull., vol. 50, no 10,‎ , p. 1416–7 (PMID 12372879, DOI 10.1248/cpb.50.1416)
  • Zgórka G, Głowniak K, « Variation of free phenolic acids in medicinal plants belonging to the Lamiaceae family », J Pharm Biomed Anal, vol. 26, no 1,‎ , p. 79–87 (PMID 11451645, DOI 10.1016/S0731-7085(01)00354-5)
  • Hillenbrand M, Zapp J, Becker H, « Depsides from the petals of Papaver rhoeas », Planta Med., vol. 70, no 4,‎ , p. 380–2 (PMID 15095160, DOI 10.1055/s-2004-818956)
  • Reynertson KA, Wallace AM, Adachi S, Gil RR, Yang H, Basile MJ, D'Armiento J, Weinstein IB, Kennelly EJ, « Bioactive depsides and anthocyanins from jaboticaba (Myrciaria cauliflora) », J. Nat. Prod., vol. 69, no 8,‎ , p. 1228–30 (PMID 16933884, DOI 10.1021/np0600999)
  • Haslam E, Stangroom JE, « The esterase and depsidase activities of tannase », Biochem. J., vol. 99, no 1,‎ , p. 28–31 (PMID 5965343, PMCID 1264952, DOI 10.1042/bj0990028)
  • Kumar KC, Müller K, « Lichen metabolites. 2. Antiproliferative and cytotoxic activity of gyrophoric, usnic, and diffractaic acid on human keratinocyte growth », J. Nat. Prod., vol. 62, no 6,‎ , p. 821–3 (PMID 10395495, DOI 10.1021/np980378z)
  • Neamati N, Hong H, Mazumder A, Wang S, Sunder S, Nicklaus MC, Milne GW, Proksa B, Pommier Y, « Depsides and depsidones as inhibitors of HIV-1 integrase: discovery of novel inhibitors through 3D database searching », J. Med. Chem., vol. 40, no 6,‎ , p. 942–51 (PMID 9083483, DOI 10.1021/jm960759e)
  • Nielsen J, Nielsen PH, Frisvad JC, « Fungl depside, guisinol, from a marine derived strain of Emericella unguis », Phytochemistry, vol. 50, no 2,‎ , p. 263–265 (DOI 10.1016/s0031-9422(98)00517-2)
  • Gerrard JM, Peterson DA, « Structure of the active site of prostaglandin synthase from studies of depsides: an alternate view », Prostaglandins Leukot Med, vol. 13, no 2,‎ , p. 139–42 (PMID 6425861, DOI 10.1016/0262-1746(84)90003-9)
  • Sankawa U, Shibuya M, Ebizuka Y, Noguchi H, Kinoshita T, Iitaka Y, Endo A, Kitahara N, « Depside as potent inhibitor of prostaglandin biosynthesis: a new active site model for fatty acid cyclooxygenase », Prostaglandins, vol. 24, no 1,‎ , p. 21–34 (PMID 6812170, DOI 10.1016/0090-6980(82)90174-5)
  • Kumar KC, Müller K, « Lichen metabolites. 1. Inhibitory action against leukotriene B4 biosynthesis by a non-redox mechanism », J. Nat. Prod., vol. 62, no 6,‎ , p. 817–20 (PMID 10395494, DOI 10.1021/np9803777)
  • ((Kumar KCS)), Müller K, « Depsides as non-redox inhibitors of leukotriene B4 biosynthesis and HaCaT cell growth, 2. Novel analogues of obtusatic acid », Eur J Med Chem, vol. 35, no 4,‎ , p. 405–11 (PMID 10858601, DOI 10.1016/S0223-5234(00)00132-X)
  • Nouri Neamati, Huixiao Hong, Abhijit Mazumder, Shaomeng Wang, Sanjay Sunder, Marc C. Nicklaus, George W. A. Milne, Bohumil Proksa et Yves Pommier, « Depsides and Depsidones as Inhibitors of HIV-1 Integrase: Discovery of Novel Inhibitors through 3D Database Searching† », Journal of Medicinal Chemistry, vol. 40, no 6,‎ , p. 942–951 (ISSN 0022-2623, PMID 9083483, DOI 10.1021/jm960759e)

issn.org

portal.issn.org

  • Nouri Neamati, Huixiao Hong, Abhijit Mazumder, Shaomeng Wang, Sanjay Sunder, Marc C. Nicklaus, George W. A. Milne, Bohumil Proksa et Yves Pommier, « Depsides and Depsidones as Inhibitors of HIV-1 Integrase: Discovery of Novel Inhibitors through 3D Database Searching† », Journal of Medicinal Chemistry, vol. 40, no 6,‎ , p. 942–951 (ISSN 0022-2623, PMID 9083483, DOI 10.1021/jm960759e)

nih.gov

ncbi.nlm.nih.gov

  • Ono M, Masuoka C, Koto M, Tateishi M, Komatsu H, Kobayashi H, Igoshi K, Ito Y, Okawa M, Nohara T, « Antioxidant ortho-benzoyloxyphenyl acetic acid ester, vaccihein A, from the fruit of rabbiteye blueberry (Vaccinium ashei) », Chem. Pharm. Bull., vol. 50, no 10,‎ , p. 1416–7 (PMID 12372879, DOI 10.1248/cpb.50.1416)
  • Zgórka G, Głowniak K, « Variation of free phenolic acids in medicinal plants belonging to the Lamiaceae family », J Pharm Biomed Anal, vol. 26, no 1,‎ , p. 79–87 (PMID 11451645, DOI 10.1016/S0731-7085(01)00354-5)
  • Hillenbrand M, Zapp J, Becker H, « Depsides from the petals of Papaver rhoeas », Planta Med., vol. 70, no 4,‎ , p. 380–2 (PMID 15095160, DOI 10.1055/s-2004-818956)
  • Reynertson KA, Wallace AM, Adachi S, Gil RR, Yang H, Basile MJ, D'Armiento J, Weinstein IB, Kennelly EJ, « Bioactive depsides and anthocyanins from jaboticaba (Myrciaria cauliflora) », J. Nat. Prod., vol. 69, no 8,‎ , p. 1228–30 (PMID 16933884, DOI 10.1021/np0600999)
  • Haslam E, Stangroom JE, « The esterase and depsidase activities of tannase », Biochem. J., vol. 99, no 1,‎ , p. 28–31 (PMID 5965343, PMCID 1264952, DOI 10.1042/bj0990028)
  • Kumar KC, Müller K, « Lichen metabolites. 2. Antiproliferative and cytotoxic activity of gyrophoric, usnic, and diffractaic acid on human keratinocyte growth », J. Nat. Prod., vol. 62, no 6,‎ , p. 821–3 (PMID 10395495, DOI 10.1021/np980378z)
  • Neamati N, Hong H, Mazumder A, Wang S, Sunder S, Nicklaus MC, Milne GW, Proksa B, Pommier Y, « Depsides and depsidones as inhibitors of HIV-1 integrase: discovery of novel inhibitors through 3D database searching », J. Med. Chem., vol. 40, no 6,‎ , p. 942–51 (PMID 9083483, DOI 10.1021/jm960759e)
  • Gerrard JM, Peterson DA, « Structure of the active site of prostaglandin synthase from studies of depsides: an alternate view », Prostaglandins Leukot Med, vol. 13, no 2,‎ , p. 139–42 (PMID 6425861, DOI 10.1016/0262-1746(84)90003-9)
  • Sankawa U, Shibuya M, Ebizuka Y, Noguchi H, Kinoshita T, Iitaka Y, Endo A, Kitahara N, « Depside as potent inhibitor of prostaglandin biosynthesis: a new active site model for fatty acid cyclooxygenase », Prostaglandins, vol. 24, no 1,‎ , p. 21–34 (PMID 6812170, DOI 10.1016/0090-6980(82)90174-5)
  • Kumar KC, Müller K, « Lichen metabolites. 1. Inhibitory action against leukotriene B4 biosynthesis by a non-redox mechanism », J. Nat. Prod., vol. 62, no 6,‎ , p. 817–20 (PMID 10395494, DOI 10.1021/np9803777)
  • ((Kumar KCS)), Müller K, « Depsides as non-redox inhibitors of leukotriene B4 biosynthesis and HaCaT cell growth, 2. Novel analogues of obtusatic acid », Eur J Med Chem, vol. 35, no 4,‎ , p. 405–11 (PMID 10858601, DOI 10.1016/S0223-5234(00)00132-X)
  • Nouri Neamati, Huixiao Hong, Abhijit Mazumder, Shaomeng Wang, Sanjay Sunder, Marc C. Nicklaus, George W. A. Milne, Bohumil Proksa et Yves Pommier, « Depsides and Depsidones as Inhibitors of HIV-1 Integrase: Discovery of Novel Inhibitors through 3D Database Searching† », Journal of Medicinal Chemistry, vol. 40, no 6,‎ , p. 942–951 (ISSN 0022-2623, PMID 9083483, DOI 10.1021/jm960759e)