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Erratum to: Top Med Chem
DOI: 10.1007/7355_2013_29
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On page 316, figure 19 was incorrect. The correct version is below:
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On pages 360, 372, 377, 379, 387, references [42], [247], [343], [368] and [387] had incorrect information. The correct information is given below:
42. Naylor EM, Chakravarty PK, Costello CA, Chang RS, Chen T-B, Faust KA, Lotti VJ, Kivlighn SD, Zingaro GJ, Siegl PKS, Wong PC, Carini DJ, Wexler RR, Patchett AA, Greenlee WJ (1994) Potent imidazole angiotensin II antagonists: acyl sulfonamides and acyl sulfamides as tetrazole replacements. Bioorg Med Chem Lett 4:69–74
247. Morgenthaler M, Schweizer E, Hoffman-Röder A, Benini F, Martin RE, Jaeschke G,Wagner B, Fischer H, Bendels S, Zimmeli D, Scheider J, Diedeich F, Kansy M, Müller K (2007) Predicting and tuning physicochemical properties in lead optimization: amine-basicities. ChemMedChem 2:1100–1115
343. Darnell M,Weidolf L (2013) Metabolism of xenobiotic carboxylic acids: focus on coenzyme A conjugation, reactivity, and interference with lipid metabolism. Chem Res Toxicol 26:1139–1155
368. Atwal KS, Rovnyak GC, Schwartz J, Moreland S, Hedberg A, Gougoutas JZ, Malley MM, Floyd DM (1990) Dihydropyrimidine calcium channel blockers: 2-heterosubstituted 4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines. J Med Chem 33:1510–1515
387. Staben ST, Blaquiere N, Tsui V, Kolesnikov A, Do S, Bradley EK, Dotson J, Goldsmith R, Heffron TP, Lesnick J, Lewis C, Murray J, Nonomiya J, Olivero AG, Pang J, Rouge L, Salphati L, Wei BQ, Wiesmann C, Wu P (2013) cis-Amide isosteric replacement in thienobenzoxepin inhibitors of PI3-kinase. Bioorg Med Chem Lett 23:897–901
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Meanwell, N.A. (2014). Erratum to: The Influence of Bioisosteres in Drug Design: Tactical Applications to Address Developability Problems. In: Meanwell, N. (eds) Tactics in Contemporary Drug Design. Topics in Medicinal Chemistry, vol 9. Springer, Berlin, Heidelberg. https://doi.org/10.1007/7355_2014_74
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DOI: https://doi.org/10.1007/7355_2014_74
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