Natural product scaffolds as leads to drugs.
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[1] L. Sternbach. The discovery of librium , 1972, Agents and Actions.
[2] W. F. Hoffman,et al. 3-HYDROXY-3-METHYLGLUTARYL-COENZYME A REDUCTASE INHIBITORS. I. STRUCTURAL MODIFICATION OF 5-SUBSTITUTED 3,5-DIHYDROXYPENTANOIC ACIDS AND THEIR LACTONE DERIVATIVES , 1985 .
[3] L. Sternbach,et al. QUINAZOLINES AND 1,4-BENZODIAZEPINES. XVII. SYNTHESIS OF 1,3-DIHYDRO-5-PYRIDYL-2H-1,4-BENZODIAZEPINE DERIVATIVES. , 1964, Journal of pharmaceutical sciences.
[4] B. White,et al. Development, Validation, and Application of PCR Primers for Detection of Tetracycline Efflux Genes of Gram-Negative Bacteria , 2002, Applied and Environmental Microbiology.
[5] Y. Tsujita,et al. ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium. , 1976, The Journal of antibiotics.
[6] A. Endo. Monacolin K, a new hypocholesterolemic agent produced by a Monascus species. , 1979, The Journal of antibiotics.
[7] C. Tsang,et al. Targeting mammalian target of rapamycin (mTOR) for health and diseases. , 2007, Drug discovery today.
[8] B. E. Evans,et al. 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 1. Structural modification of 5-substituted 3,5-dihydroxypentanoic acids and their lactone derivatives. , 1985, Journal of Medicinal Chemistry.
[9] M. Wilson,et al. Inhibitors of cholesterol biosynthesis. 1. trans-6-(2-pyrrol-1-ylethyl)-4-hydroxypyran-2-ones, a novel series of HMG-CoA reductase inhibitors. 1. Effects of structural modifications at the 2- and 5-positions of the pyrrole nucleus. , 1990, Journal of medicinal chemistry.
[10] Karl-Heinz Altmann,et al. Anticancer Drugs from Nature—Natural Products as a Unique Source of New Microtubule‐Stabilizing Agents , 2007 .
[11] Roy D. Welch,et al. Complete genome sequence of the myxobacterium Sorangium cellulosum , 2007, Nature Biotechnology.
[12] K. Altmann,et al. Epothilones as lead structures for the synthesis-based discovery of new chemotypes for microtubule stabilization. , 2008, Accounts of chemical research.
[13] Jy Liu,et al. A novel asymmetric synthesis of cis-3-hydroxy-4-aryl azetidin-2-ones , 1993 .
[14] T. Chou,et al. Therapeutic effect against human xenograft tumors in nude mice by the third generation microtubule stabilizing epothilones , 2008, Proceedings of the National Academy of Sciences.
[15] Scott J. Miller,et al. Catalytic site-selective synthesis and evaluation of a series of erythromycin analogs. , 2008, Bioorganic & medicinal chemistry letters.
[16] Guoqiang Wang,et al. Synthesis of novel 6,11-O-bridged bicyclic ketolides via a palladium-catalyzed bis-allylation. , 2004, Organic letters.
[17] E. Nogales,et al. A common pharmacophore for epothilone and taxanes: molecular basis for drug resistance conferred by tubulin mutations in human cancer cells. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[18] S. Sehgal,et al. Rapamycin (AY-22,989), a new antifungal antibiotic. II. Fermentation, isolation and characterization.:II. FERMENTATION, ISOLATION AND CHARACTERIZATION , 1975 .
[19] Sternbach Lh. The discovery of librium. 1972. , 1994 .
[20] D. A. Foster,et al. Targeting mTOR with rapamycin: One dose does not fit all , 2009, Cell cycle.
[21] C. Heathcock,et al. The synthesis of mevinic acids , 1986 .
[22] A. Ting,et al. Protein-protein interaction detection in vitro and in cells by proximity biotinylation. , 2008, Journal of the American Chemical Society.
[23] Yi Tang,et al. Decoding and engineering tetracycline biosynthesis. , 2009, Metabolic engineering.
[24] J. Clader,et al. Discovery of 1-(4-fluorophenyl)-(3R)-[3-(4-fluorophenyl)-(3S)-hydroxypropyl]-(4S)-(4 -hydroxyphenyl)-2-azetidinone (SCH 58235): a designed, potent, orally active inhibitor of cholesterol absorption. , 1998, Journal of medicinal chemistry.
[25] E. Lazarides,et al. Epothilones, a new class of microtubule-stabilizing agents with a taxol-like mechanism of action. , 1995, Cancer research.
[26] E. Abraham,et al. The structure of cephalosporin C , 1961 .
[27] K. Altmann,et al. Epothilones as lead structures for new anticancer drugs--pharmacology, fermentation, and structure-activity-relationships. , 2008, Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques.
[28] Wolfgang Schwede,et al. Total synthesis and antitumor activity of ZK-EPO: the first fully synthetic epothilone in clinical development. , 2006, Angewandte Chemie.
[29] Robert J. Feeney,et al. THE ISOLATION OF A NEW THYMINE PENTOSIDE FROM SPONGES1 , 1950 .
[30] C. Leamon. Folate-targeted drug strategies for the treatment of cancer. , 2008, Current opinion in investigational drugs.
[31] D. Steinberg,et al. Thematic review series : The Pathogenesis of Atherosclerosis An interpretive history of the cholesterol controversy , part V : The discovery of the statins and the end of the controversy 1 , 2006 .
[32] M. Büchler,et al. Tigecycline for the treatment of patients with severe sepsis or septic shock: a drug use evaluation in a surgical intensive care unit. , 2008, The Journal of antimicrobial chemotherapy.
[33] B. M. Duggar. AUREOMYCIN: A PRODUCT OF THE CONTINUING SEARCH FOR NEW ANTIBIOTICS , 1948, Annals of the New York Academy of Sciences.
[34] D. Illingworth,et al. 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors , 1994 .
[35] Marilyn Roberts,et al. Tetracycline Antibiotics: Mode of Action, Applications, Molecular Biology, and Epidemiology of Bacterial Resistance , 2001, Microbiology and Molecular Biology Reviews.
[36] E. Baulieu,et al. The immunophilin FKBP52 specifically binds to tubulin and prevents microtubule formation , 2007, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[37] A. Mankin,et al. Binding Site of the Bridged Macrolides in the Escherichia coli Ribosome , 2005, Antimicrobial Agents and Chemotherapy.
[38] J. Poehlsgaard,et al. The bacterial ribosome as a target for antibiotics , 2005, Nature Reviews Microbiology.
[39] S. Sehgal,et al. Activity of rapamycin (AY-22,989) against transplanted tumors. , 1984, The Journal of antibiotics.
[40] K. Arima,et al. Studies on tomaymycin, a new antibiotic. I. Isolation and properties of tomaymycin. , 1972, The Journal of antibiotics.
[41] L. Goodman,et al. POTENTIAL ANTICANCER AGENTS.1 XL. SYNTHESIS OF THE β-ANOMER OF 9-(D-ARABINOFURANOSYL)-ADENINE , 1960 .
[42] J. Barrish,et al. (3R,5S,E)-7-(4-(4-fluorophenyl)-6-isopropyl-2-(methyl(1-methyl-1h-1,2,4-triazol-5-yl)amino)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic acid (BMS-644950): a rationally designed orally efficacious 3-hydroxy-3-methylglutaryl coenzyme-a reductase inhibitor with reduced myotoxicity potential. , 2008, Journal of medicinal chemistry.
[43] M. Kuroda,et al. Competitive inhibition of 3‐hydroxy‐3‐methylglutaryl coenzyme a reductase by ML‐236A and ML‐236B fungal metabolites, having hypocholesterolemic activity , 1976, Atherosclerosis. Supplements.
[44] S. Sehgal,et al. Rapamycin (AY-22,989), a new antifungal antibiotic. III. In vitro and in vivo evaluation. , 1978, The Journal of antibiotics.
[45] David J Newman,et al. Natural products as leads to potential drugs: an old process or the new hope for drug discovery? , 2008, Journal of medicinal chemistry.
[46] Suckling Cj,et al. Chemical approaches to the discovery of new drugs. , 1991 .
[47] Christopher D. Reeves,et al. Metagenomic Analysis Reveals Diverse Polyketide Synthase Gene Clusters in Microorganisms Associated with the Marine Sponge Discodermia dissoluta , 2005, Applied and Environmental Microbiology.
[48] O. Kandler,et al. Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[49] M. Falagas,et al. Tigecycline for the treatment of multidrug-resistant Enterobacteriaceae: a systematic review of the evidence from microbiological and clinical studies. , 2008, The Journal of antimicrobial chemotherapy.
[50] D. Siegel,et al. Synthesis of (-)-tetracycline. , 2005, Journal of the American Chemical Society.
[51] A. Uria,et al. Cultivation-independent approaches to investigate the chemistry of marine symbiotic bacteria , 2009, Phytochemistry Reviews.
[52] R. Zarivach,et al. Structural basis for the antibiotic activity of ketolides and azalides. , 2003, Structure.
[53] S. D. Rosa,et al. Antiviral agents from a gorgonian,Eunicella cavolini , 1984, Experientia.
[54] L. Sternbach,et al. Quinazolines and 1,4-Benzodiazepines. VI.1a Halo-, Methyl-, and Methoxy-substituted 1,3-Dihydro-5-phenyl-2H-1,4-benzodiazepin-2-ones1b,c , 1962 .
[55] W. Bergmann,et al. Contributions to the Study of Marine Products. XL. The Nucleosides of Sponges.1 IV. Spongosine2 , 1956 .
[56] F. Koehn. Therapeutic potential of natural product signal transduction agents. , 2006, Current opinion in biotechnology.
[57] B. Hearn,et al. C-15 thiazol-4-yl analogues of (E)-9,10-didehydroepothilone D: synthesis and cytotoxicity. , 2006, Organic letters.
[58] Magid Abou-Gharbia. Discovery of innovative small molecule therapeutics. , 2009, Journal of medicinal chemistry.
[59] C. Lerner,et al. A robust platform for the synthesis of new tetracycline antibiotics. , 2008, Journal of the American Chemical Society.
[60] P. Petersen,et al. "Glycylcyclines". 3. 9-Aminodoxycyclinecarboxamides. , 1994, Journal of medicinal chemistry.
[61] Epothilone, a Myxobacterial Metabolite with Promising Antitumor Activity , 2005 .
[62] Jörn Piel,et al. Metabolites from symbiotic bacteria. , 2009, Natural product reports.
[63] C. Suckling. Chemical approaches to the discovery of new drugs. , 1991, Science progress.
[64] M. Wilson,et al. Inhibitors of cholesterol biosynthesis. 2. 1,3,5-trisubstituted [2-(tetrahydro-4-hydroxy-2-oxopyran-6-yl)ethyl]pyrazoles. , 1990, Journal of medicinal chemistry.
[65] A. Endo,et al. Monacolin K, a new hypocholesterolemic agent that specifically inhibits 3-hydroxy-3-methylglutaryl coenzyme A reductase. , 1980, The Journal of antibiotics.
[66] C. Hertweck,et al. The biosynthetic logic of polyketide diversity. , 2009, Angewandte Chemie.
[67] T. Chou,et al. Second-generation epothilones : discovery of fludelone and its extraordinary antitumor properties , 2005 .
[68] B. Roth,et al. The discovery and development of atorvastatin, a potent novel hypolipidemic agent. , 2002, Progress in medicinal chemistry.
[69] W. F. Hoffman,et al. 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted [1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives. , 1986, Journal of Medicinal Chemistry.
[70] D. Kingston,et al. A common pharmacophore for Taxol and the epothilones based on the biological activity of a taxane molecule lacking a C-13 side chain. , 2000, Biochemistry.
[71] L. Sternbach,et al. Quinazoline 3-Oxide Structure of Compounds Previously Described in the Literature as 3.1.4-Benzoxadiazepines1 , 1960 .
[72] K. Tatsuta,et al. Total synthesis of selected bioactive natural products: illustration of strategy and design. , 2005, Chemical reviews.
[73] A. Endo,et al. Compactin (ML-236B) and related compounds as potential cholesterol-lowering agents that inhibit HMG-CoA reductase. , 1985, Journal of medicinal chemistry.
[74] S. Brady,et al. An environmental DNA-derived type II polyketide biosynthetic pathway encodes the biosynthesis of the pentacyclic polyketide erdacin. , 2009, Angewandte Chemie.
[75] B. E. Evans,et al. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists. , 1988, Journal of Medicinal Chemistry.
[76] T. C. Smale,et al. CRYSTAL AND MOLECULAR STRUCTURE OF COMPACTIN, A NEW ANTIFUNGAL METABOLITE FROM PENICILLIUM BREVICOMPACTUM , 1976 .
[77] Robert J. Feeney,et al. CONTRIBUTIONS TO THE STUDY OF MARINE PRODUCTS. XXXII. THE NUCLEOSIDES OF SPONGES. I.1 , 1951 .
[78] D. Teachey,et al. Mammalian target of rapamycin inhibitors and their potential role in therapy in leukaemia and other haematological malignancies , 2009, British journal of haematology.
[79] L. Bermudez,et al. EDP-420, a Bicyclolide (Bridged Bicyclic Macrolide), Is Active against Mycobacterium avium , 2007, Antimicrobial Agents and Chemotherapy.
[80] C. Hertweck,et al. Triggering cryptic natural product biosynthesis in microorganisms. , 2009, Organic & biomolecular chemistry.
[81] M. Pangalos,et al. Binding of rapamycin analogs to calcium channels and FKBP52 contributes to their neuroprotective activities , 2008, Proceedings of the National Academy of Sciences.
[82] M. Hashimoto,et al. Letter: Nocardicin A and B, novel monocyclic beta-lactam antibiotics from a Nocardia species. , 1976, Journal of the American Chemical Society.
[83] A. Endo. A gift from nature: the birth of the statins , 2008, Nature Medicine.
[84] D. Newman,et al. Impact of natural products on developing new anti-cancer agents. , 2009, Chemical reviews.
[85] TatsutaKuniaki,et al. The First Total Synthesis of Natural (−)-Tetracycline , 2000 .
[86] P. Vagelos,et al. Are prescription drug prices high? , 1991, Science.
[87] E. Graziani,et al. Recent advances in the chemistry, biosynthesis and pharmacology of rapamycin analogs. , 2009, Natural product reports.