메뉴 건너뛰기




Volumn 103, Issue , 2015, Pages 231-241

Insights into drug discovery from natural products through structural modification

Author keywords

Druggability; Natural products; Structural modification

Indexed keywords

4 PHENYLPIPERIDINE DERIVATIVE; ANALGESIC AGENT; ARTEMISININ DERIVATIVE; BENZOMORPHAN; BOTTROMYCIN A2; CAMPTOTHECIN; COMBRETASTATIN A4; CURCUMIN; CYCLOSPORIN A; EPOTHILONE B; EXATECAN; HALICHONDRIN B; IMMUNOSUPPRESSIVE AGENT; IRINOTECAN; ISP 1; LARGAZOLE; LIPHAGAL; LIPOXIN A; METHADONE; MORPHINANE DERIVATIVE; MORPHINE; NATURAL PRODUCT; OLEANOLIC ACID; ORIDONIN; PACLITAXEL; PHLORIZIN; POLYPEPTIDE ANTIBIOTIC AGENT; TOPOTECAN; UNCLASSIFIED DRUG; UNINDEXED DRUG; VANCOMYCIN; BIOLOGICAL PRODUCT; PRODRUG;

EID: 84928801703     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2015.04.012     Document Type: Review
Times cited : (105)

References (145)
  • 1
    • 36348987143 scopus 로고    scopus 로고
    • The value of natural products to future pharmaceutical discovery
    • D.D. Baker, M. Chu, U. Oza, and V. Rajgarhia The value of natural products to future pharmaceutical discovery Nat Prod Rep 24 2007 1225 1244
    • (2007) Nat Prod Rep , vol.24 , pp. 1225-1244
    • Baker, D.D.1    Chu, M.2    Oza, U.3    Rajgarhia, V.4
  • 2
    • 84876002671 scopus 로고
    • Natural products: a continuing source of novel drug leads
    • G.M. Cragg, and D.J. Newman Natural products: a continuing source of novel drug leads Biochim Biophys Acta 2013 1830 3670 3695
    • (1830) Biochim Biophys Acta , vol.2013 , pp. 3670-3695
    • Cragg, G.M.1    Newman, D.J.2
  • 3
    • 84858308226 scopus 로고    scopus 로고
    • Natural products as sources of new drugs over the 30 years from 1981 to 2010
    • D.J. Newman, and G.M. Cragg Natural products as sources of new drugs over the 30 years from 1981 to 2010 J Nat Prod 75 2012 311 335
    • (2012) J Nat Prod , vol.75 , pp. 311-335
    • Newman, D.J.1    Cragg, G.M.2
  • 4
    • 80053203292 scopus 로고    scopus 로고
    • Natural products: an evolving role in future drug discovery
    • B.B. Mishra, and V.K. Tiwari Natural products: an evolving role in future drug discovery Eur J Med Chem 46 2011 4769 4807
    • (2011) Eur J Med Chem , vol.46 , pp. 4769-4807
    • Mishra, B.B.1    Tiwari, V.K.2
  • 6
    • 11144311139 scopus 로고    scopus 로고
    • Lessons from natural molecules
    • J. Clardy, and C. Walsh Lessons from natural molecules Nature 432 2004 829 837
    • (2004) Nature , vol.432 , pp. 829-837
    • Clardy, J.1    Walsh, C.2
  • 7
    • 0037208308 scopus 로고    scopus 로고
    • Property distributions: differences between drugs, natural products, and molecules from combinatorial chemistry
    • M. Feher, and J.M. Schmidt Property distributions: differences between drugs, natural products, and molecules from combinatorial chemistry J Chem Inf Comput Sci 43 2003 218 227
    • (2003) J Chem Inf Comput Sci , vol.43 , pp. 218-227
    • Feher, M.1    Schmidt, J.M.2
  • 8
    • 0033104653 scopus 로고    scopus 로고
    • Statistical investigation into the structural complementarity of natural products and synthetic compounds
    • T. Henkel, R.M. Brunne, H. Müller, and F. Reichel Statistical investigation into the structural complementarity of natural products and synthetic compounds Angew Chem Int Ed 38 1999 643 647
    • (1999) Angew Chem Int Ed , vol.38 , pp. 643-647
    • Henkel, T.1    Brunne, R.M.2    Müller, H.3    Reichel, F.4
  • 10
    • 80054052511 scopus 로고    scopus 로고
    • Exploring and exploiting biologically relevant chemical space
    • L. Eberhardt, K. Kumar, and H. Waldmann Exploring and exploiting biologically relevant chemical space Curr Drug Targets 12 2011 1531 1546
    • (2011) Curr Drug Targets , vol.12 , pp. 1531-1546
    • Eberhardt, L.1    Kumar, K.2    Waldmann, H.3
  • 11
    • 34547265045 scopus 로고    scopus 로고
    • Properties and architecture of drugs and natural products revisited
    • K. Grabowski, and G. Schneider Properties and architecture of drugs and natural products revisited Curr Chem Biol 1 2007 115 127
    • (2007) Curr Chem Biol , vol.1 , pp. 115-127
    • Grabowski, K.1    Schneider, G.2
  • 13
    • 61649109015 scopus 로고    scopus 로고
    • The influence of lead discovery strategies on the properties of drug candidates
    • G.M. Keseru, and G.M. Makara The influence of lead discovery strategies on the properties of drug candidates Nat Rev Drug Discov 8 2009 203 212
    • (2009) Nat Rev Drug Discov , vol.8 , pp. 203-212
    • Keseru, G.M.1    Makara, G.M.2
  • 14
    • 78649254350 scopus 로고    scopus 로고
    • Grand challenge commentary: accessing new chemical space for 'undruggable' targets
    • S. Dandapani, and L.A. Marcaurelle Grand challenge commentary: accessing new chemical space for 'undruggable' targets Nat Chem Biol 6 2010 861 863
    • (2010) Nat Chem Biol , vol.6 , pp. 861-863
    • Dandapani, S.1    Marcaurelle, L.A.2
  • 17
    • 84890069342 scopus 로고    scopus 로고
    • Natural products as starting points for the synthesis of complex and diverse compounds
    • K.C. Morrison, and P.J. Hergenrother Natural products as starting points for the synthesis of complex and diverse compounds Nat Prod Rep 31 2014 6 14
    • (2014) Nat Prod Rep , vol.31 , pp. 6-14
    • Morrison, K.C.1    Hergenrother, P.J.2
  • 18
    • 77955014467 scopus 로고    scopus 로고
    • Natural products as chemical probes
    • E.E. Carlson Natural products as chemical probes ACS Chem Biol 5 2010 639 653
    • (2010) ACS Chem Biol , vol.5 , pp. 639-653
    • Carlson, E.E.1
  • 19
    • 33746001269 scopus 로고    scopus 로고
    • Antibacterial natural products in medicinal chemistry - exodus or revival ?
    • F. von Nussbaum, M. Brands, B. Hinzen, S. Weigand, and D. Hbich Antibacterial natural products in medicinal chemistry - exodus or revival ? Angew Chem Int Ed 45 2006 5072 5129
    • (2006) Angew Chem Int Ed , vol.45 , pp. 5072-5129
    • Von Nussbaum, F.1    Brands, M.2    Hinzen, B.3    Weigand, S.4    Hbich, D.5
  • 20
    • 84870249445 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • C.A. Lipinski, F. Lombardo, B.W. Dominy, and P.J. Feeney Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv Drug Deliv Rev 64 2012 4 17
    • (2012) Adv Drug Deliv Rev , vol.64 , pp. 4-17
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 21
    • 84864339209 scopus 로고    scopus 로고
    • Biosynthetic medicinal chemistry of natural product drugs
    • F.E. Koehn Biosynthetic medicinal chemistry of natural product drugs Med Chem Commun 3 2012 854 865
    • (2012) Med Chem Commun , vol.3 , pp. 854-865
    • Koehn, F.E.1
  • 22
    • 0031741846 scopus 로고    scopus 로고
    • Physical chemical properties of oral drug candidates in the discovery and exploratory development settings
    • W. Curatolo Physical chemical properties of oral drug candidates in the discovery and exploratory development settings Pharm Sci Technol Today 1 1998 387 393
    • (1998) Pharm Sci Technol Today , vol.1 , pp. 387-393
    • Curatolo, W.1
  • 24
    • 84923068538 scopus 로고    scopus 로고
    • Artemisinin reduces cell proliferation and induces apoptosis in neuroblastom
    • S.Q. Zhu, W.H. Liu, X.X. Ke, J.F. Li, R.J. Hu, and H.J. Cui et al. Artemisinin reduces cell proliferation and induces apoptosis in neuroblastom Oncol Rep 32 2014 1094 1100
    • (2014) Oncol Rep , vol.32 , pp. 1094-1100
    • Zhu, S.Q.1    Liu, W.H.2    Ke, X.X.3    Li, J.F.4    Hu, R.J.5    Cui, H.J.6
  • 25
    • 80052337277 scopus 로고    scopus 로고
    • An artemisinin-derived dimer has highly potent anti-cytomegalovirus (CMV) and anti-cancer activities
    • R. He, B.T. Mott, A.S. Rosenthal, D.T. Genna, G.H. Posner, and R. Arav-Boger An artemisinin-derived dimer has highly potent anti-cytomegalovirus (CMV) and anti-cancer activities PLoS One 6 2011 e24334
    • (2011) PLoS One , vol.6
    • He, R.1    Mott, B.T.2    Rosenthal, A.S.3    Genna, D.T.4    Posner, G.H.5    Arav-Boger, R.6
  • 26
    • 0023555532 scopus 로고
    • Antimalarial activity of new water-soluble dihydroartemisinin derivatives
    • A.J. Lin, D.L. Klayman, and W.K. Milhous Antimalarial activity of new water-soluble dihydroartemisinin derivatives J Med Chem 30 1987 2147 2150
    • (1987) J Med Chem , vol.30 , pp. 2147-2150
    • Lin, A.J.1    Klayman, D.L.2    Milhous, W.K.3
  • 27
    • 0034692160 scopus 로고    scopus 로고
    • Synthesis and antimalarial activity of artemisinin derivatives containing an amino group
    • Ying Li, Y.M. Zhu, H.J. Jiang, J.P. Pan, G.S. Wu, and J.M. Wu Synthesis and antimalarial activity of artemisinin derivatives containing an amino group J Med Chem 43 2000 1635 1640
    • (2000) J Med Chem , vol.43 , pp. 1635-1640
    • Li, Y.1    Zhu, Y.M.2    Jiang, H.J.3    Pan, J.P.4    Wu, G.S.5    Wu, J.M.6
  • 29
    • 0017172723 scopus 로고
    • The antitumor and antibacterial activity of the Isodon diterpenoids
    • E. Fujita, Y. Nagao, K. Kaneko, S. Nakazawa, and H. Kuroda The antitumor and antibacterial activity of the Isodon diterpenoids Chem Pharm Bull 24 1976 2118 2127
    • (1976) Chem Pharm Bull , vol.24 , pp. 2118-2127
    • Fujita, E.1    Nagao, Y.2    Kaneko, K.3    Nakazawa, S.4    Kuroda, H.5
  • 30
    • 79953029230 scopus 로고    scopus 로고
    • Oridonin: an active diterpenoid targeting cell cycle arrest, apoptotic and autophagic pathways for cancer therapeutics
    • C.Y. Li, E.Q. Wang, Y. Cheng, and J.K. Bao Oridonin: an active diterpenoid targeting cell cycle arrest, apoptotic and autophagic pathways for cancer therapeutics Int J Biochem Cell Biol 43 2011 701 704
    • (2011) Int J Biochem Cell Biol , vol.43 , pp. 701-704
    • Li, C.Y.1    Wang, E.Q.2    Cheng, Y.3    Bao, J.K.4
  • 31
    • 34147131374 scopus 로고    scopus 로고
    • Oridonin, a diterpenoid extracted from medicinal herbs, targets AML1-ETO fusion protein and shows potent antitumor activity with low adverse effects on t(8;21) leukemia in vitro and in vivo
    • G. Zhou, H. Kang, L. Wang, L. Gao, P. Liu, and J. Xie et al. Oridonin, a diterpenoid extracted from medicinal herbs, targets AML1-ETO fusion protein and shows potent antitumor activity with low adverse effects on t(8;21) leukemia in vitro and in vivo Blood 109 2007 3441 3450
    • (2007) Blood , vol.109 , pp. 3441-3450
    • Zhou, G.1    Kang, H.2    Wang, L.3    Gao, L.4    Liu, P.5    Xie, J.6
  • 33
    • 84901793595 scopus 로고    scopus 로고
    • Design, synthesis and antimycobacterial activity evaluation of natural oridonin derivatives
    • S.T. Xu, D.H. Li, L.L. Pei, H. Yao, C.Q. Wang, and H. Can et al. Design, synthesis and antimycobacterial activity evaluation of natural oridonin derivatives Bioorg Med Chem Lett 24 2014 2811 2814
    • (2014) Bioorg Med Chem Lett , vol.24 , pp. 2811-2814
    • Xu, S.T.1    Li, D.H.2    Pei, L.L.3    Yao, H.4    Wang, C.Q.5    Can, H.6
  • 34
    • 48649094535 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of novel 1-O- and 14-O-derivatives of oridonin as potential anticancer drug candidates
    • J.Y. Xu, J.Y. Yang, Q. Ran, L. Wang, J. Liu, and Z.X. Wang et al. Synthesis and biological evaluation of novel 1-O- and 14-O-derivatives of oridonin as potential anticancer drug candidates Bioorg Med Chem Lett 18 2008 4741 4744
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 4741-4744
    • Xu, J.Y.1    Yang, J.Y.2    Ran, Q.3    Wang, L.4    Liu, J.5    Wang, Z.X.6
  • 35
    • 84879588528 scopus 로고    scopus 로고
    • Novel nitrogen-enriched oridonin analogues with thiazole-fused A-ring: protecting group-free synthesis, enhanced anticancer profile, and improved aqueous solubility
    • C.Y. Ding, Y.S. Zhang, H.J. Chen, Z.D. Yang, C. Wild, and L.L. Chu et al. Novel nitrogen-enriched oridonin analogues with thiazole-fused A-ring: protecting group-free synthesis, enhanced anticancer profile, and improved aqueous solubility J Med Chem 56 2013 5048 5058
    • (2013) J Med Chem , vol.56 , pp. 5048-5058
    • Ding, C.Y.1    Zhang, Y.S.2    Chen, H.J.3    Yang, Z.D.4    Wild, C.5    Chu, L.L.6
  • 36
    • 7144248725 scopus 로고
    • Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminate
    • M.E. Wall, M.C. Wani, C.E. Cook, K.H. Palmer, A.T. McPhail, and G.A. Sim Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminate J Am Chem Soc 88 1966 3888 3890
    • (1966) J Am Chem Soc , vol.88 , pp. 3888-3890
    • Wall, M.E.1    Wani, M.C.2    Cook, C.E.3    Palmer, K.H.4    McPhail, A.T.5    Sim, G.A.6
  • 37
    • 1442334562 scopus 로고    scopus 로고
    • Camptothecin and taxol: historic achievements in natural products research
    • N.H. Oberlies, and D.J. Kroll Camptothecin and taxol: historic achievements in natural products research J Nat Prod 67 2004 129 135
    • (2004) J Nat Prod , vol.67 , pp. 129-135
    • Oberlies, N.H.1    Kroll, D.J.2
  • 38
    • 45549089929 scopus 로고    scopus 로고
    • Design, synthesis and development of novel camptothecin drugs
    • S.T. Liew, and L.X. Yang Design, synthesis and development of novel camptothecin drugs Curr Pharm Des 14 2008 1078 1097
    • (2008) Curr Pharm Des , vol.14 , pp. 1078-1097
    • Liew, S.T.1    Yang, L.X.2
  • 39
    • 65349179115 scopus 로고    scopus 로고
    • Synthesis and biological activities of a pH-dependently activated water-soluble prodrug of a novel hexacyclic camptothecin analog
    • J. Ohwada, S. Ozawa, M. Kohchi, H. Fukuda, C. Murasaki, and H. Suda et al. Synthesis and biological activities of a pH-dependently activated water-soluble prodrug of a novel hexacyclic camptothecin analog Bioorg Med Chem Lett 19 2009 2772 2776
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 2772-2776
    • Ohwada, J.1    Ozawa, S.2    Kohchi, M.3    Fukuda, H.4    Murasaki, C.5    Suda, H.6
  • 40
    • 77954348873 scopus 로고    scopus 로고
    • Cytotoxicity and topo I targeting activity of substituted 10 - nitrogenous heterocyclic aromatic group derivatives of SN-38
    • Q.Y. Li, X.Q. Deng, Y.G. Zu, H.Y. Lv, L. Su, and L.P. Yao et al. Cytotoxicity and topo I targeting activity of substituted 10 - nitrogenous heterocyclic aromatic group derivatives of SN-38 Eur J Med Chem 45 2010 3200 3206
    • (2010) Eur J Med Chem , vol.45 , pp. 3200-3206
    • Li, Q.Y.1    Deng, X.Q.2    Zu, Y.G.3    Lv, H.Y.4    Su, L.5    Yao, L.P.6
  • 41
    • 84863825873 scopus 로고    scopus 로고
    • Charting, navigating, and populating natural product chemical space for drug discovery
    • H. Lachance, S. Wetzel, K. Kumar, and H. Waldmann Charting, navigating, and populating natural product chemical space for drug discovery J Med Chem 55 2012 5989 6001
    • (2012) J Med Chem , vol.55 , pp. 5989-6001
    • Lachance, H.1    Wetzel, S.2    Kumar, K.3    Waldmann, H.4
  • 42
    • 39049135494 scopus 로고    scopus 로고
    • Structure and activity of largazole, a potent antiproliferative agent from the Floridian marine cyanobacterium Symploca sp.
    • K. Taori, V.J. Paul, and H. Luesch Structure and activity of largazole, a potent antiproliferative agent from the Floridian marine cyanobacterium Symploca sp. J Am Chem Soc 130 2008 1806 1807
    • (2008) J Am Chem Soc , vol.130 , pp. 1806-1807
    • Taori, K.1    Paul, V.J.2    Luesch, H.3
  • 43
    • 77953740289 scopus 로고    scopus 로고
    • Synthesis and biological characterization of the histone deacetylase inhibitor largazole and C7-modified analogues
    • J.A. Souto, E. Vaz, I. Lepore, A.C. Poppler, G. Franci, and R. Alvarez et al. Synthesis and biological characterization of the histone deacetylase inhibitor largazole and C7-modified analogues J Med Chem 53 2010 4654 4667
    • (2010) J Med Chem , vol.53 , pp. 4654-4667
    • Souto, J.A.1    Vaz, E.2    Lepore, I.3    Poppler, A.C.4    Franci, G.5    Alvarez, R.6
  • 44
    • 64049106355 scopus 로고    scopus 로고
    • Synthesis and histone deacetylase inhibitory activity of largazole analogs: alteration of the zinc-binding domain and macrocyclic scaffold
    • A.A. Bowers, N. West, T.L. Newkirk, A.E. Troutman-Youngman, S.L. Schreiber, and O. Wiest et al. Synthesis and histone deacetylase inhibitory activity of largazole analogs: alteration of the zinc-binding domain and macrocyclic scaffold Org Lett 11 2009 1301 1304
    • (2009) Org Lett , vol.11 , pp. 1301-1304
    • Bowers, A.A.1    West, N.2    Newkirk, T.L.3    Troutman-Youngman, A.E.4    Schreiber, S.L.5    Wiest, O.6
  • 45
    • 84902457915 scopus 로고    scopus 로고
    • Potent and orally efficacious bisthiazole-based histone deacetylase inhibitors
    • F. Chen, H. Chai, M.B. Su, Y.M. Zhang, J. Li, and X. Xie et al. Potent and orally efficacious bisthiazole-based histone deacetylase inhibitors ACS Med Chem Lett 5 2014 628 633
    • (2014) ACS Med Chem Lett , vol.5 , pp. 628-633
    • Chen, F.1    Chai, H.2    Su, M.B.3    Zhang, Y.M.4    Li, J.5    Xie, X.6
  • 46
    • 0022709534 scopus 로고
    • Halichondrins - antitumor polyether macrolides from a marine sponge
    • Y. Hirata, and D. Uemura Halichondrins - antitumor polyether macrolides from a marine sponge Pure Appl Chem 58 1986 701 710
    • (1986) Pure Appl Chem , vol.58 , pp. 701-710
    • Hirata, Y.1    Uemura, D.2
  • 47
    • 33751102419 scopus 로고    scopus 로고
    • Comparison of the activities of the truncated halichondrin B analog NSC 707389 (E7389) with those of the parent compound and a proposed binding site on tubulin
    • D. Dabydeen, J.C. Burnett, R. Bai, P. Verdier-Pinard, S.J.H. Hickford, and G.R. Pettit et al. Comparison of the activities of the truncated halichondrin B analog NSC 707389 (E7389) with those of the parent compound and a proposed binding site on tubulin Mol Pharmacol 70 2006 1866 1875
    • (2006) Mol Pharmacol , vol.70 , pp. 1866-1875
    • Dabydeen, D.1    Burnett, J.C.2    Bai, R.3    Verdier-Pinard, P.4    Hickford, S.J.H.5    Pettit, G.R.6
  • 48
    • 52449111361 scopus 로고    scopus 로고
    • Options for the treatment of patients with taxane-refractory metastatic breast cancer
    • B. Overmoyer Options for the treatment of patients with taxane-refractory metastatic breast cancer Clin Breast Cancer 8 2008 S61 S70
    • (2008) Clin Breast Cancer , vol.8 , pp. S61-S70
    • Overmoyer, B.1
  • 52
    • 82355191648 scopus 로고    scopus 로고
    • Survival benefit of eribulin mesylate in heavily pretreated metastatic breast cancer: what next?
    • P. Aftimos, and A. Awada Survival benefit of eribulin mesylate in heavily pretreated metastatic breast cancer: what next? Adv Ther 28 2011 973 985
    • (2011) Adv Ther , vol.28 , pp. 973-985
    • Aftimos, P.1    Awada, A.2
  • 53
    • 0028372227 scopus 로고
    • S Fungal metabolites. Part 11. A potent immunosuppressive activity found in Isaria sinclairii metabolite
    • T. Fujita, K. Inoue, S. Yamamoto, T. Ikumoto, S. Sasaki, and R. Toyama et al. S Fungal metabolites. Part 11. A potent immunosuppressive activity found in Isaria sinclairii metabolite J Antibiot 47 1994 208 215
    • (1994) J Antibiot , vol.47 , pp. 208-215
    • Fujita, T.1    Inoue, K.2    Yamamoto, S.3    Ikumoto, T.4    Sasaki, S.5    Toyama, R.6
  • 54
    • 79955408396 scopus 로고    scopus 로고
    • Fingolimod (FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite
    • C.R. Strader, C.J. Pearce, and N.H. Oberlies Fingolimod (FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite J Nat Prod 74 2011 900 907
    • (2011) J Nat Prod , vol.74 , pp. 900-907
    • Strader, C.R.1    Pearce, C.J.2    Oberlies, N.H.3
  • 55
    • 0028936902 scopus 로고
    • Simple compounds, 2-alkyl-2-amino-1,3-propanediols have potent immunosuppressive activity
    • T. Fujita, M. Yoneta, R. Hirose, S. Sasaki, K. Inoue, and M. Kiuchi et al. Simple compounds, 2-alkyl-2-amino-1,3-propanediols have potent immunosuppressive activity Bioorg Med Chem Lett 5 1995 847 852
    • (1995) Bioorg Med Chem Lett , vol.5 , pp. 847-852
    • Fujita, T.1    Yoneta, M.2    Hirose, R.3    Sasaki, S.4    Inoue, K.5    Kiuchi, M.6
  • 56
    • 10244265918 scopus 로고    scopus 로고
    • Determination of absolute configuration and biological activity of new immunosuppressants, mycestericins D, E, F and G
    • T. Fujita, N. Hamamichi, M. Kiuchi, T. Matsuzaki, Y. Kitao, and K. Inoue et al. Determination of absolute configuration and biological activity of new immunosuppressants, mycestericins D, E, F and G J Antibiot 49 1996 846 853
    • (1996) J Antibiot , vol.49 , pp. 846-853
    • Fujita, T.1    Hamamichi, N.2    Kiuchi, M.3    Matsuzaki, T.4    Kitao, Y.5    Inoue, K.6
  • 57
    • 33645283403 scopus 로고    scopus 로고
    • FTY720, sphingosine 1-phosphate receptor modulator, ameliorates experimental autoimmune encephalomyelitis by inhibition of T cell infiltration
    • H. Kataoka, K. Sugahara, K. Shimano, K. Teshima, M. Koyama, and A. Fukunari et al. FTY720, sphingosine 1-phosphate receptor modulator, ameliorates experimental autoimmune encephalomyelitis by inhibition of T cell infiltration Cell Mol Immunol 2 2005 439 448
    • (2005) Cell Mol Immunol , vol.2 , pp. 439-448
    • Kataoka, H.1    Sugahara, K.2    Shimano, K.3    Teshima, K.4    Koyama, M.5    Fukunari, A.6
  • 58
    • 84856249964 scopus 로고    scopus 로고
    • Fingolimod for multiple sclerosis
    • D. Pelletier, and D.A. Hafler Fingolimod for multiple sclerosis N Engl J Med 366 2012 339 347
    • (2012) N Engl J Med , vol.366 , pp. 339-347
    • Pelletier, D.1    Hafler, D.A.2
  • 59
    • 31444457132 scopus 로고    scopus 로고
    • Liphagal, a selective inhibitor of PI3 kinaserisolated from the sponge aka coralliphaga: structure elucidation and biomimetic synthesis
    • F. Marion, D.E. Williams, B.O. Patrick, I. Hollander, R. Mallon, and S.C. Kim et al. Liphagal, a selective inhibitor of PI3 kinaserisolated from the sponge aka coralliphaga: structure elucidation and biomimetic synthesis Org Lett 8 2006 321 324
    • (2006) Org Lett , vol.8 , pp. 321-324
    • Marion, F.1    Williams, D.E.2    Patrick, B.O.3    Hollander, I.4    Mallon, R.5    Kim, S.C.6
  • 60
    • 78650393972 scopus 로고    scopus 로고
    • Synthesis of phosphatidylinositol 3-kinase(PI3k)inhibitory analogues of the sponge meroterpenoid liphagal
    • A.R. Pereira, W.K. Strangman, F. Marion, L. Feldberg, D. Roll, and R. Mallon et al. Synthesis of phosphatidylinositol 3-kinase(PI3k)inhibitory analogues of the sponge meroterpenoid liphagal J Med Chem 53 2010 8523 8533
    • (2010) J Med Chem , vol.53 , pp. 8523-8533
    • Pereira, A.R.1    Strangman, W.K.2    Marion, F.3    Feldberg, L.4    Roll, D.5    Mallon, R.6
  • 61
    • 0018816767 scopus 로고
    • Turmeric - chemistry, technology, and quality
    • V.S. Govindarajan Turmeric - chemistry, technology, and quality Crit Rev Food Sci Nutr 12 1980 199 301
    • (1980) Crit Rev Food Sci Nutr , vol.12 , pp. 199-301
    • Govindarajan, V.S.1
  • 62
    • 84894458572 scopus 로고    scopus 로고
    • Curcumin, a promising anti-cancer therapeutic: a review of its chemical properties, bioactivity and approaches to cancer cell delivery
    • M. Salem, S. Rohani, and E.R. Gillies Curcumin, a promising anti-cancer therapeutic: a review of its chemical properties, bioactivity and approaches to cancer cell delivery RSC Adv 4 2014 10815 10829
    • (2014) RSC Adv , vol.4 , pp. 10815-10829
    • Salem, M.1    Rohani, S.2    Gillies, E.R.3
  • 63
    • 34248684129 scopus 로고    scopus 로고
    • Studies on curcumin and curcuminoids XXXI. Symmetric and asymmetric curcuminoids: stability, activity and complexation with cyclodextrin
    • M.A. Tomren, M. Masson, T. Loftsson, and H.H. Tonnesen Studies on curcumin and curcuminoids XXXI. Symmetric and asymmetric curcuminoids: stability, activity and complexation with cyclodextrin Int J Pharm 338 2007 27 34
    • (2007) Int J Pharm , vol.338 , pp. 27-34
    • Tomren, M.A.1    Masson, M.2    Loftsson, T.3    Tonnesen, H.H.4
  • 64
    • 66249083483 scopus 로고    scopus 로고
    • Effective stabilization of curcumin by association to plasma proteins: human serum albumin and fibrinogen
    • M.H. Leung, and T.W. Kee Effective stabilization of curcumin by association to plasma proteins: human serum albumin and fibrinogen Langmuir 25 2009 5773 5777
    • (2009) Langmuir , vol.25 , pp. 5773-5777
    • Leung, M.H.1    Kee, T.W.2
  • 65
    • 0030839940 scopus 로고    scopus 로고
    • Stability of curcumin in buffer solutions and characterization of its degradation products
    • Y.J. Wang, M.H. Pan, A.L. Cheng, L.I. Lin, Y.S. Ho, and C.Y. Hsieh et al. Stability of curcumin in buffer solutions and characterization of its degradation products Pharm Biomed Anal 15 1997 1867 1878
    • (1997) Pharm Biomed Anal , vol.15 , pp. 1867-1878
    • Wang, Y.J.1    Pan, M.H.2    Cheng, A.L.3    Lin, L.I.4    Ho, Y.S.5    Hsieh, C.Y.6
  • 66
    • 0032479574 scopus 로고    scopus 로고
    • Inhibitory effect of curcuminoids on MCF-7 cell proliferation and structure-activity relationships
    • A. Simon, D.P. Allais, J.L. Duroux, J.P. Basly, S. Durand Fontanier, and C. Delage Inhibitory effect of curcuminoids on MCF-7 cell proliferation and structure-activity relationships Cancer Lett 129 1998 111 116
    • (1998) Cancer Lett , vol.129 , pp. 111-116
    • Simon, A.1    Allais, D.P.2    Duroux, J.L.3    Basly, J.P.4    Durand Fontanier, S.5    Delage, C.6
  • 67
    • 0032908758 scopus 로고    scopus 로고
    • Relation of structure of curcumin analogs to their potencies as inducers of Phase 2 detoxification enzymes
    • A.T. Dinkova-Kostova, and P. Talalay Relation of structure of curcumin analogs to their potencies as inducers of Phase 2 detoxification enzymes Carcinogenesis 20 1999 911 914
    • (1999) Carcinogenesis , vol.20 , pp. 911-914
    • Dinkova-Kostova, A.T.1    Talalay, P.2
  • 68
    • 62149086696 scopus 로고    scopus 로고
    • Exploration and synthesis of curcumin analogues with improved structural stability both in vitro and in vivo as cytotoxic agents
    • G. Liang, L.L. Shao, Y. Wang, C.G. Zhao, Y.H. Chu, and J. Xiao et al. Exploration and synthesis of curcumin analogues with improved structural stability both in vitro and in vivo as cytotoxic agents Bioorg Med Chem 17 2009 2623 2631
    • (2009) Bioorg Med Chem , vol.17 , pp. 2623-2631
    • Liang, G.1    Shao, L.L.2    Wang, Y.3    Zhao, C.G.4    Chu, Y.H.5    Xiao, J.6
  • 69
    • 84893673021 scopus 로고    scopus 로고
    • Design and synthesis of novel iminothiazinylbutadienols and divinylpyrimidinethiones as ARE inducers
    • L. Chen, S. Magesh, H. Wang, C.S. Yang, A.N.T. Kong, and L.Q. Hu Design and synthesis of novel iminothiazinylbutadienols and divinylpyrimidinethiones as ARE inducers Bioorg Med Chem 24 2014 940 943
    • (2014) Bioorg Med Chem , vol.24 , pp. 940-943
    • Chen, L.1    Magesh, S.2    Wang, H.3    Yang, C.S.4    Kong, A.N.T.5    Hu, L.Q.6
  • 70
    • 84886773206 scopus 로고    scopus 로고
    • Stable and potent analogues derived from the modification of the dicarbonyl moiety of curcumin
    • S. Chakraborti, G. Dhar, V. Dwivedi, A. Das, A. Poddar, and G. Chakraborti et al. Stable and potent analogues derived from the modification of the dicarbonyl moiety of curcumin Biochemistry 52 2013 7449 7460
    • (2013) Biochemistry , vol.52 , pp. 7449-7460
    • Chakraborti, S.1    Dhar, G.2    Dwivedi, V.3    Das, A.4    Poddar, A.5    Chakraborti, G.6
  • 71
    • 0023801309 scopus 로고
    • Interactions of tubulin with potent natural and synthetic analogs of the antimitotic agent combretastatin: a structure-activity study
    • C.M. Lin, S.B. Singh, P.S. Chu, R.O. Dempcy, J.M. Schmidt, and G.R. Pettit et al. Interactions of tubulin with potent natural and synthetic analogs of the antimitotic agent combretastatin: a structure-activity study Mol Pharmacol 34 1988 200 208
    • (1988) Mol Pharmacol , vol.34 , pp. 200-208
    • Lin, C.M.1    Singh, S.B.2    Chu, P.S.3    Dempcy, R.O.4    Schmidt, J.M.5    Pettit, G.R.6
  • 72
    • 0033594356 scopus 로고    scopus 로고
    • Antineoplastic agents. 410. Asymmetric hydroxylation of trans-combretastatin A-4
    • G.R. Pettit, B.E. Toki, D.L. Herald, M.R. Boyd, E. Hamel, and R.K. Pettit et al. Antineoplastic agents. 410. Asymmetric hydroxylation of trans-combretastatin A-4 J Med Chem 42 1999 1459 1465
    • (1999) J Med Chem , vol.42 , pp. 1459-1465
    • Pettit, G.R.1    Toki, B.E.2    Herald, D.L.3    Boyd, M.R.4    Hamel, E.5    Pettit, R.K.6
  • 73
    • 33747514168 scopus 로고    scopus 로고
    • Synthesis and cytotoxic evaluation of combretafurans, potential scaffolds for dual-action antitumoral agents
    • T. Pirali, S. Busacca, L. Beltrami, D. Imovilli, F. Pagliai, and G. Miglio et al. Synthesis and cytotoxic evaluation of combretafurans, potential scaffolds for dual-action antitumoral agents J Med Chem 49 2006 5372 5376
    • (2006) J Med Chem , vol.49 , pp. 5372-5376
    • Pirali, T.1    Busacca, S.2    Beltrami, L.3    Imovilli, D.4    Pagliai, F.5    Miglio, G.6
  • 75
    • 84872810364 scopus 로고    scopus 로고
    • Novel cis-restricted β-lactam combretastatin A-4 analogues display anti-vascular and anti-metastatic properties in vitro
    • S.M. Nathwani, L. Hughes, L.M. Greene, M. Carr, N.M. O'Boyle, and S. McDonnell et al. Novel cis-restricted β-lactam combretastatin A-4 analogues display anti-vascular and anti-metastatic properties in vitro Oncol Rep 29 2013 585 594
    • (2013) Oncol Rep , vol.29 , pp. 585-594
    • Nathwani, S.M.1    Hughes, L.2    Greene, L.M.3    Carr, M.4    O'boyle, N.M.5    McDonnell, S.6
  • 76
    • 68649105492 scopus 로고    scopus 로고
    • Isocombretastatins A: 1,1-diarylethenes as potent inhibitors of tubulin polymerization and cytotoxic compounds
    • R. Alvarez, C. Alvarez, F. Mollinedo, B.G. Sierra, M. Medarde, and R. Peláez Isocombretastatins A: 1,1-diarylethenes as potent inhibitors of tubulin polymerization and cytotoxic compounds Bioorg Med Chem 17 2009 6422 6431
    • (2009) Bioorg Med Chem , vol.17 , pp. 6422-6431
    • Alvarez, R.1    Alvarez, C.2    Mollinedo, F.3    Sierra, B.G.4    Medarde, M.5    Peláez, R.6
  • 77
    • 2442639013 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of 3-aminobenzophenones as antimitotic agents
    • J.P. Liou, J.Y. Chang, C.W. Chang, C.Y. Chang, N. Mahindroo, and F.M. Kuo et al. Synthesis and structure-activity relationships of 3-aminobenzophenones as antimitotic agents J Med Chem 47 2004 2897 2905
    • (2004) J Med Chem , vol.47 , pp. 2897-2905
    • Liou, J.P.1    Chang, J.Y.2    Chang, C.W.3    Chang, C.Y.4    Mahindroo, N.5    Kuo, F.M.6
  • 78
    • 64549145428 scopus 로고    scopus 로고
    • A diaryl sulfide, sulfoxide, andsulfone bearing structural similarities to combretastatin A-4
    • E.G. Barbosa, L.A. Bega, A. Beatriz, T. Sarkar, E. Hamel, and M.S. do Amaral et al. A diaryl sulfide, sulfoxide, andsulfone bearing structural similarities to combretastatin A-4 Eur J Med Chem 44 2009 2685 2688
    • (2009) Eur J Med Chem , vol.44 , pp. 2685-2688
    • Barbosa, E.G.1    Bega, L.A.2    Beatriz, A.3    Sarkar, T.4    Hamel, E.5    Do Amaral, M.S.6
  • 79
    • 0030018666 scopus 로고    scopus 로고
    • Epothilons A and B: antifungal and cytotoxic compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties
    • K. Gerth, N. Bedorf, G. Höfle, H. Irschik, and H. Reichenbach Epothilons A and B: antifungal and cytotoxic compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties J Antibiot 49 1996 560 563
    • (1996) J Antibiot , vol.49 , pp. 560-563
    • Gerth, K.1    Bedorf, N.2    Höfle, G.3    Irschik, H.4    Reichenbach, H.5
  • 80
    • 0035988631 scopus 로고    scopus 로고
    • Epothilones: a novel class of non-taxane microtubule-stabilizing agents
    • R. Altaha, T. Fojo, E. Reed, and J. Abraham Epothilones: a novel class of non-taxane microtubule-stabilizing agents Curr Pharm Des 8 2002 1707 1712
    • (2002) Curr Pharm Des , vol.8 , pp. 1707-1712
    • Altaha, R.1    Fojo, T.2    Reed, E.3    Abraham, J.4
  • 84
    • 84904357195 scopus 로고    scopus 로고
    • Profile and potential of Ixabepilone in the treatment of pancreatic cancer
    • B.G. Smaglo, and M.J. Pishvaian Profile and potential of Ixabepilone in the treatment of pancreatic cancer Drug Des Devel Ther 8 2014 923 930
    • (2014) Drug Des Devel Ther , vol.8 , pp. 923-930
    • Smaglo, B.G.1    Pishvaian, M.J.2
  • 87
    • 77956922344 scopus 로고    scopus 로고
    • Bottromycin derivatives: efficient chemical modifications of the ester moiety and evaluation of anti-MRSA and anti-VRE activities
    • K. Kobayashi, M. Ichioka, T. Hirose, K. Nagai, A. Matsumoto, and H. Matsui et al. Bottromycin derivatives: efficient chemical modifications of the ester moiety and evaluation of anti-MRSA and anti-VRE activities Bioorg Med Chem Lett 20 2010 6116 6120
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 6116-6120
    • Kobayashi, K.1    Ichioka, M.2    Hirose, T.3    Nagai, K.4    Matsumoto, A.5    Matsui, H.6
  • 88
    • 0027184132 scopus 로고
    • Ethyl substitution at the 7 position extends the half-life of 10-hydroxycamptothecin in the presence of human serum albumin
    • T.G. Burke, and Z. Mi Ethyl substitution at the 7 position extends the half-life of 10-hydroxycamptothecin in the presence of human serum albumin J Med Chem 36 1993 2580 2582
    • (1993) J Med Chem , vol.36 , pp. 2580-2582
    • Burke, T.G.1    Mi, Z.2
  • 89
    • 0028012774 scopus 로고
    • The structural basis of camptothecin interactions with human serum albumin: impact on drug stability
    • T.G. Burke, and Z. Mi The structural basis of camptothecin interactions with human serum albumin: impact on drug stability J Med Chem 37 1994 40 46
    • (1994) J Med Chem , vol.37 , pp. 40-46
    • Burke, T.G.1    Mi, Z.2
  • 90
    • 0037212083 scopus 로고    scopus 로고
    • Homocamptothecins: potent topoisomerase I inhibitors and promising anticancer drugs
    • C. Bailly Homocamptothecins: potent topoisomerase I inhibitors and promising anticancer drugs Crit Rev Oncol Hematol 45 2003 91 108
    • (2003) Crit Rev Oncol Hematol , vol.45 , pp. 91-108
    • Bailly, C.1
  • 92
    • 84886450992 scopus 로고    scopus 로고
    • A new strategy to improve the metabolic stability of lactone: discovery of (20S, 21S) -21-fluorocamptothecins as novel, hydrolytically stable topoisomerase I inhibitors
    • Z.Y. Miao, L.J. Zhu, G.Q. Dong, C.L. Zhuang, Y.L. Wu, and S.Z. Wang et al. A new strategy to improve the metabolic stability of lactone: discovery of (20S, 21S) -21-fluorocamptothecins as novel, hydrolytically stable topoisomerase I inhibitors J Med Chem 56 2013 7902 7910
    • (2013) J Med Chem , vol.56 , pp. 7902-7910
    • Miao, Z.Y.1    Zhu, L.J.2    Dong, G.Q.3    Zhuang, C.L.4    Wu, Y.L.5    Wang, S.Z.6
  • 93
    • 0036669399 scopus 로고    scopus 로고
    • Lipoxins and aspirin-triggered 15-epi-lipoxin biosynthesis: an update and role in anti-inflammation and proresolution
    • C.N. Serhan Lipoxins and aspirin-triggered 15-epi-lipoxin biosynthesis: an update and role in anti-inflammation and proresolution Prostaglandins Other Lipid Mediat 68-69 2002 433 455
    • (2002) Prostaglandins Other Lipid Mediat , vol.68-69 , pp. 433-455
    • Serhan, C.N.1
  • 94
    • 0038037241 scopus 로고    scopus 로고
    • Exploring new approaches to the treatment of asthma: potential roles for lipoxins and aspirintriggered lipid mediators
    • B.D. Levy, and C.N. Serhan Exploring new approaches to the treatment of asthma: potential roles for lipoxins and aspirintriggered lipid mediators Drugs Today (Barc) 39 2003 373 384
    • (2003) Drugs Today (Barc) , vol.39 , pp. 373-384
    • Levy, B.D.1    Serhan, C.N.2
  • 95
    • 24344510350 scopus 로고    scopus 로고
    • Anti-inflammatory circuitry: lipoxin, aspirin-triggered lipoxins and their receptor ALX
    • N. Chiang, M. Arita, and C.N. Serhan Anti-inflammatory circuitry: lipoxin, aspirin-triggered lipoxins and their receptor ALX Prostaglandins Leukot Essent Fatty Acids 73 2005 163 177
    • (2005) Prostaglandins Leukot Essent Fatty Acids , vol.73 , pp. 163-177
    • Chiang, N.1    Arita, M.2    Serhan, C.N.3
  • 96
    • 0034682669 scopus 로고    scopus 로고
    • 4 metabolic inactivation: 15-oxaprostaglandin 13-reductase/leukotriene B4 12-hydroxydehydrogenase is a multifunctional eicosanoid oxidoreductase
    • 4 metabolic inactivation: 15-oxaprostaglandin 13-reductase/leukotriene B4 12-hydroxydehydrogenase is a multifunctional eicosanoid oxidoreductase J Biol Chem 275 2000 25372 25380
    • (2000) J Biol Chem , vol.275 , pp. 25372-25380
    • Clish, C.B.1    Levy, B.D.2    Chiang, N.3    Tai, H.H.4    Serhan, C.N.5
  • 98
    • 0033529195 scopus 로고    scopus 로고
    • Local and systemic delivery of a stable aspirin-triggered lipoxin prevents neutrophil recruitment in vivo
    • C.B. Clish, J.A. O'Brien, K. Gronert, G.L. Stahl, N.A. Petasis, and C.N. Serhan Local and systemic delivery of a stable aspirin-triggered lipoxin prevents neutrophil recruitment in vivo Proc Natl Acad Sci U S A 96 1999 8247 8252
    • (1999) Proc Natl Acad Sci U S A , vol.96 , pp. 8247-8252
    • Clish, C.B.1    O'brien, J.A.2    Gronert, K.3    Stahl, G.L.4    Petasis, N.A.5    Serhan, C.N.6
  • 101
    • 12744265382 scopus 로고
    • Analyse des Phloridzins
    • C. Petersen Analyse des Phloridzins Ann Acad Sci Fr 15 1835 178
    • (1835) Ann Acad Sci Fr , vol.15 , pp. 178
    • Petersen, C.1
  • 103
    • 0033619999 scopus 로고    scopus 로고
    • Na(+)-glucose cotransporter (SGLT) inhibitors as antidiabetic agents. 4. Synthesis and pharmacological properties of 4'-dehydroxyphlorizin derivatives substituted on the B ring
    • K. Tsujihara, M. Hongu, K. Saito, H. Kawanishi, K. Kuriyama, and M. Matsumotu et al. Na(+)-glucose cotransporter (SGLT) inhibitors as antidiabetic agents. 4. Synthesis and pharmacological properties of 4'-dehydroxyphlorizin derivatives substituted on the B ring J Med Chem 42 1999 5311 5324
    • (1999) J Med Chem , vol.42 , pp. 5311-5324
    • Tsujihara, K.1    Hongu, M.2    Saito, K.3    Kawanishi, H.4    Kuriyama, K.5    Matsumotu, M.6
  • 104
    • 33845873376 scopus 로고    scopus 로고
    • Sergliflozin, a novel selective inhibitor of low-affinity sodium glucose cotransporter (SGLT2), validates the critical role of SGLT2 in renal glucose reabsorption and modulates plasma glucose level
    • K. Katsuno, Y. Fujimori, Y. Takemura, M. Hiratochi, F. Itoh, and Y. Komatsu et al. Sergliflozin, a novel selective inhibitor of low-affinity sodium glucose cotransporter (SGLT2), validates the critical role of SGLT2 in renal glucose reabsorption and modulates plasma glucose level J Pharmacol Exp Ther 320 2007 323 330
    • (2007) J Pharmacol Exp Ther , vol.320 , pp. 323-330
    • Katsuno, K.1    Fujimori, Y.2    Takemura, Y.3    Hiratochi, M.4    Itoh, F.5    Komatsu, Y.6
  • 105
    • 79953267465 scopus 로고    scopus 로고
    • Bone: from a reservoir of minerals to a regulator of energy metabolism
    • M. Isaji Bone: from a reservoir of minerals to a regulator of energy metabolism Kidney Int Suppl 79 2011 S14 S19
    • (2011) Kidney Int Suppl , vol.79 , pp. S14-S19
    • Isaji, M.1
  • 106
    • 41649087328 scopus 로고    scopus 로고
    • Discovery of dapagliflozin: a potent, selective renal sodium-dependent glucose cotransporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes
    • M. Meng, B.A. Ellsworth, A.A. Nirschl, P.J. McCann, M. Patel, and R.N. Girotra et al. Discovery of dapagliflozin: a potent, selective renal sodium-dependent glucose cotransporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes J Med Chem 51 2008 1145 1149
    • (2008) J Med Chem , vol.51 , pp. 1145-1149
    • Meng, M.1    Ellsworth, B.A.2    Nirschl, A.A.3    McCann, P.J.4    Patel, M.5    Girotra, R.N.6
  • 107
    • 77956319973 scopus 로고    scopus 로고
    • Discovery of canagliflozin, a novel Cglucoside with thiophene ring, as sodium-dependent glucose cotransporter 2 inhibitor for the treatment of type 2 diabetes mellitus
    • S. Nomura, S. Sakamaki, M. Hongu, E. Kawanishi, Y. Koga, and T. Sakamoto et al. Discovery of canagliflozin, a novel Cglucoside with thiophene ring, as sodium-dependent glucose cotransporter 2 inhibitor for the treatment of type 2 diabetes mellitus J Med Chem 53 2010 6355 6360
    • (2010) J Med Chem , vol.53 , pp. 6355-6360
    • Nomura, S.1    Sakamaki, S.2    Hongu, M.3    Kawanishi, E.4    Koga, Y.5    Sakamoto, T.6
  • 108
    • 0036083301 scopus 로고    scopus 로고
    • Mechanism of action of antitumor drugs that interact with microtubules and tubulin
    • M.A. Jordan Mechanism of action of antitumor drugs that interact with microtubules and tubulin Curr. Med. Chem. Anticancer Agents 2 2002 1 7
    • (2002) Curr. Med. Chem. Anticancer Agents , vol.2 , pp. 1-7
    • Jordan, M.A.1
  • 110
    • 0031695039 scopus 로고    scopus 로고
    • Blood-brain barrier permeation: molecular parameters governing passive diffusion
    • H. Fischer, R. Gottschlich, and A. Seelig Blood-brain barrier permeation: molecular parameters governing passive diffusion J Membr Biol 165 1998 201 211
    • (1998) J Membr Biol , vol.165 , pp. 201-211
    • Fischer, H.1    Gottschlich, R.2    Seelig, A.3
  • 111
    • 13444269007 scopus 로고    scopus 로고
    • Chemical modification of paclitaxel (Taxol) reduces P-glycoprotein interactions and increases permeation across the blood-brain barrier in vitro and in situ
    • R. Antonie, Y.B. Liu, M.L. Michaelis, R.H. Himes, G.I. Georg, and K.L. Audus Chemical modification of paclitaxel (Taxol) reduces P-glycoprotein interactions and increases permeation across the blood-brain barrier in vitro and in situ J Med Chem 48 2005 832 838
    • (2005) J Med Chem , vol.48 , pp. 832-838
    • Antonie, R.1    Liu, Y.B.2    Michaelis, M.L.3    Himes, R.H.4    Georg, G.I.5    Audus, K.L.6
  • 112
    • 84868690878 scopus 로고    scopus 로고
    • Discovery of a novel pharmacological and structural class of gamma secretase modulators derived from the extract of Actaea racemosa
    • M.A. Findeis, F. Schroeder, T.D. McKee, D. Yager, P.C. Fraering, and S.P. Creaser et al. Discovery of a novel pharmacological and structural class of gamma secretase modulators derived from the extract of Actaea racemosa ACS Chem Neurosci 3 2012 941 951
    • (2012) ACS Chem Neurosci , vol.3 , pp. 941-951
    • Findeis, M.A.1    Schroeder, F.2    McKee, T.D.3    Yager, D.4    Fraering, P.C.5    Creaser, S.P.6
  • 113
    • 84868705749 scopus 로고    scopus 로고
    • Initial optimization of a new series of γ secretase modulators derived from a triterpene glycoside
    • N.O. Fuller, J.L. Hubbs, W.F. Austin, S.F. Creaser, T.D. McKee, and R.M.B. Loureiro et al. Initial optimization of a new series of γ secretase modulators derived from a triterpene glycoside ACS Med Chem Lett 3 2012 908 913
    • (2012) ACS Med Chem Lett , vol.3 , pp. 908-913
    • Fuller, N.O.1    Hubbs, J.L.2    Austin, W.F.3    Creaser, S.F.4    Mckee, T.D.5    Loureiro, R.M.B.6
  • 115
    • 34848925492 scopus 로고    scopus 로고
    • A new isochroman-4-one derivative from the peel of Musa sapientum L. and its total synthesis
    • H. Qian, W.L. Huang, X.M. Wu, H.B. Zhang, J.P. Zhou, and W.C. Ye A new isochroman-4-one derivative from the peel of Musa sapientum L. and its total synthesis Chin Chem Lett 18 2007 1227 1230
    • (2007) Chin Chem Lett , vol.18 , pp. 1227-1230
    • Qian, H.1    Huang, W.L.2    Wu, X.M.3    Zhang, H.B.4    Zhou, J.P.5    Ye, W.C.6
  • 116
    • 61349085601 scopus 로고    scopus 로고
    • Total synthesis and antihypertensive activity of (+/-)7,8-dihydroxy-3-methyl-isochromanone-4
    • J. Liu, H. Ren, J.Y. Xu, R.R. Bai, Q. Yan, and W.L. Huang et al. Total synthesis and antihypertensive activity of (+/-)7,8-dihydroxy-3-methyl-isochromanone-4 Bioorg Med Chem Lett 19 2009 1822 1824
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 1822-1824
    • Liu, J.1    Ren, H.2    Xu, J.Y.3    Bai, R.R.4    Yan, Q.5    Huang, W.L.6
  • 117
    • 84869096407 scopus 로고    scopus 로고
    • Novel nitric oxide-releasing isochroman-4-one derivatives: synthesis and evaluation of antihypertensive activity
    • R.R. Bai, X. Yang, Y. Zhu, Z.W. Zhou, W.J. Xie, and H.Q. Yao et al. Novel nitric oxide-releasing isochroman-4-one derivatives: synthesis and evaluation of antihypertensive activity Bioorg Med Chem 20 2012 6848 6855
    • (2012) Bioorg Med Chem , vol.20 , pp. 6848-6855
    • Bai, R.R.1    Yang, X.2    Zhu, Y.3    Zhou, Z.W.4    Xie, W.J.5    Yao, H.Q.6
  • 118
    • 84876112682 scopus 로고    scopus 로고
    • Novel hybrids of natural isochroman-4-one bearing N-substituted isopropanolamine as potential antihypertensive candidates
    • R.R. Bai, X.J. Huang, X. Yang, W. Hong, Y.Q. Tang, and H.Q. Yao et al. Novel hybrids of natural isochroman-4-one bearing N-substituted isopropanolamine as potential antihypertensive candidates Bioorg Med Chem 21 2013 2495 2502
    • (2013) Bioorg Med Chem , vol.21 , pp. 2495-2502
    • Bai, R.R.1    Huang, X.J.2    Yang, X.3    Hong, W.4    Tang, Y.Q.5    Yao, H.Q.6
  • 119
    • 84904334900 scopus 로고    scopus 로고
    • Novel hybrids of natural oridonin-bearing nitrogen mustards as potential anticancer drug candidates
    • S.T. Xu, L.L. Pei, C.Q. Wang, Y.K. Zhang, D.H. Li, and H.Q. Yao et al. Novel hybrids of natural oridonin-bearing nitrogen mustards as potential anticancer drug candidates ACS Med Chem Lett 5 2014 797 802
    • (2014) ACS Med Chem Lett , vol.5 , pp. 797-802
    • Xu, S.T.1    Pei, L.L.2    Wang, C.Q.3    Zhang, Y.K.4    Li, D.H.5    Yao, H.Q.6
  • 120
    • 84864283334 scopus 로고    scopus 로고
    • Anti-oxidative, anti-glycative and antiapoptotic effects of oleanolic acid in brain of mice treated by dgalactose
    • S.J. Tsai, and M.C. Yin Anti-oxidative, anti-glycative and antiapoptotic effects of oleanolic acid in brain of mice treated by dgalactose Eur J Pharmacol 689 2012 81 88
    • (2012) Eur J Pharmacol , vol.689 , pp. 81-88
    • Tsai, S.J.1    Yin, M.C.2
  • 121
    • 84894085642 scopus 로고    scopus 로고
    • Combination of amino acid/dipeptide with nitric oxide donating oleanolic acid derivatives as Pept1 targeting antitumor prodrugs
    • L. Fang, M. Wang, S.H. Gou, X.Y. Liu, H. Zhang, and F. Cao Combination of amino acid/dipeptide with nitric oxide donating oleanolic acid derivatives as Pept1 targeting antitumor prodrugs J Med Chem 57 2014 1116 1120
    • (2014) J Med Chem , vol.57 , pp. 1116-1120
    • Fang, L.1    Wang, M.2    Gou, S.H.3    Liu, X.Y.4    Zhang, H.5    Cao, F.6
  • 122
    • 84879041449 scopus 로고    scopus 로고
    • 2 (2,4-dinitrophenyl)diazeniumdiolate and oleanolic acid: a glutathione s-transferase π-activated nitric oxide prodrug with selective anti-human hepatocellular carcinoma activity and improved stability
    • 2 (2,4-dinitrophenyl)diazeniumdiolate and oleanolic acid: a glutathione s-transferase π-activated nitric oxide prodrug with selective anti-human hepatocellular carcinoma activity and improved stability J Med Chem 56 2013 4641 4655
    • (2013) J Med Chem , vol.56 , pp. 4641-4655
    • Fu, J.J.1    Liu, L.2    Huang, Z.J.3    Lai, Y.S.4    Ji, H.5    Peng, S.X.6
  • 123
    • 0016724057 scopus 로고
    • Rapamycin (AY-22,989), a new antifungal antibiotic. I. Taxonomy of the producing streptomycete and isolation of the active principle
    • C. Vézina, A. Kudelski, and S.N. Sehgal Rapamycin (AY-22,989), a new antifungal antibiotic. I. Taxonomy of the producing streptomycete and isolation of the active principle J Antibiot 28 1975 721 726
    • (1975) J Antibiot , vol.28 , pp. 721-726
    • Vézina, C.1    Kudelski, A.2    Sehgal, S.N.3
  • 124
    • 77956254341 scopus 로고    scopus 로고
    • Biosynthesis of rapamycin and its regulation: past achievements and recent progress
    • S.R. Park, Y.J. Yoo, Y.H. Ban, and Y.J. Yoon Biosynthesis of rapamycin and its regulation: past achievements and recent progress J Antibiot 63 2010 434 441
    • (2010) J Antibiot , vol.63 , pp. 434-441
    • Park, S.R.1    Yoo, Y.J.2    Ban, Y.H.3    Yoon, Y.J.4
  • 125
    • 72049114956 scopus 로고    scopus 로고
    • Intravenous temsirolimus in cancer patients: clinical pharmacology and dosing considerations
    • J.P. Boni, B. Hug, C. Leister, and D. Sonnichsen Intravenous temsirolimus in cancer patients: clinical pharmacology and dosing considerations Semin Oncol 36 2009 S18 S25
    • (2009) Semin Oncol , vol.36 , pp. S18-S25
    • Boni, J.P.1    Hug, B.2    Leister, C.3    Sonnichsen, D.4
  • 129
    • 50249154389 scopus 로고    scopus 로고
    • Advances in the study of berberine and its derivatives
    • P. Li, W.L. Zhu, and K.X. Chen Advances in the study of berberine and its derivatives Acta Pharm Sin 43 2008 773 787
    • (2008) Acta Pharm Sin , vol.43 , pp. 773-787
    • Li, P.1    Zhu, W.L.2    Chen, K.X.3
  • 130
    • 84890900990 scopus 로고    scopus 로고
    • Berberine metabolites could induce low density lipoprotein receptor up-regulation to exert lipid-lowering effects in human hepatoma cells
    • Y. Zhou, S. Cao, Y. Wang, P. Xu, J. Yan, and W. Bin et al. Berberine metabolites could induce low density lipoprotein receptor up-regulation to exert lipid-lowering effects in human hepatoma cells Fitoterapia 92 2014 230 237
    • (2014) Fitoterapia , vol.92 , pp. 230-237
    • Zhou, Y.1    Cao, S.2    Wang, Y.3    Xu, P.4    Yan, J.5    Bin, W.6
  • 131
    • 77955982036 scopus 로고    scopus 로고
    • Design, synthesis, and cholesterol-lowering efficacy for prodrugs of berberrubine
    • Y.H. Li, Y. Li, P. Yang, W.J. Kong, X.F. You, and G. Ren et al. Design, synthesis, and cholesterol-lowering efficacy for prodrugs of berberrubine Bioorg Med Chem 18 2010 6422 6428
    • (2010) Bioorg Med Chem , vol.18 , pp. 6422-6428
    • Li, Y.H.1    Li, Y.2    Yang, P.3    Kong, W.J.4    You, X.F.5    Ren, G.6
  • 132
    • 0028923815 scopus 로고
    • Determination of berberine in plasma, urine and bile by high-performance liquid chromatography
    • C.M. Chen, and H.C. Chang Determination of berberine in plasma, urine and bile by high-performance liquid chromatography J Chromatogr B 665 1995 117 123
    • (1995) J Chromatogr B , vol.665 , pp. 117-123
    • Chen, C.M.1    Chang, H.C.2
  • 134
    • 84904402633 scopus 로고    scopus 로고
    • Patenting natural products just got harder
    • C. Harrison Patenting natural products just got harder Nat Biotechnol 32 2014 403 404
    • (2014) Nat Biotechnol , vol.32 , pp. 403-404
    • Harrison, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.