메뉴 건너뛰기




Volumn 11, Issue 1, 2020, Pages

Synthetic biology based construction of biological activity-related library of fungal decalin-containing diterpenoid pyrones

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; DECALIN; DITERPENOID; GENOMIC DNA; PYRONE DERIVATIVE; AMYLOID BETA PROTEIN; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; NAPHTHALENE DERIVATIVE; PROTEIN AGGREGATE;

EID: 85083503179     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/s41467-020-15664-4     Document Type: Article
Times cited : (61)

References (69)
  • 1
    • 14944383798 scopus 로고    scopus 로고
    • The evolving role of natural products in drug discovery
    • COI: 1:CAS:528:DC%2BD2MXhslSnsrg%3D, PID: 15729362
    • Koehn, F. E. & Carter, G. T. The evolving role of natural products in drug discovery. Nat. Rev. Drug Discov. 4, 206–220 (2005).
    • (2005) Nat. Rev. Drug Discov. , vol.4 , pp. 206-220
    • Koehn, F.E.1    Carter, G.T.2
  • 2
    • 84962367258 scopus 로고    scopus 로고
    • Natural products as source of new drugs from 1981 to 2014
    • COI: 1:CAS:528:DC%2BC28Xit1Kqu7k%3D, PID: 26852623
    • Newman, D. J. & Cragg, G. M. Natural products as source of new drugs from 1981 to 2014. J. Nat. Prod. 79, 629–661 (2016).
    • (2016) J. Nat. Prod. , vol.79 , pp. 629-661
    • Newman, D.J.1    Cragg, G.M.2
  • 3
    • 84952650492 scopus 로고    scopus 로고
    • Biosynthesis of fungal meroterpenoids
    • COI: 1:CAS:528:DC%2BC2MXhslWrtr7N, PID: 26497360
    • Matsuda, Y. & Abe, I. Biosynthesis of fungal meroterpenoids. Nat. Prod. Rep. 33, 26–53 (2016).
    • (2016) Nat. Prod. Rep. , vol.33 , pp. 26-53
    • Matsuda, Y.1    Abe, I.2
  • 4
    • 85022211520 scopus 로고    scopus 로고
    • Antibiotics from Gram-negative bacteria: a comprehensive overview and selected biosynthetic highlights
    • COI: 1:CAS:528:DC%2BC2sXhtVKht73P, PID: 28650032
    • Masschelein, J., Jenner, M. & Challis, G. L. Antibiotics from Gram-negative bacteria: a comprehensive overview and selected biosynthetic highlights. Nat. Prod. Rep. 34, 712–783 (2017).
    • (2017) Nat. Prod. Rep. , vol.34 , pp. 712-783
    • Masschelein, J.1    Jenner, M.2    Challis, G.L.3
  • 5
    • 80052090244 scopus 로고    scopus 로고
    • Similar interactions of natural products with biosynthetic enzymes and therapeutic targets could explain why nature produces such a large proportion of existing drugs
    • COI: 1:CAS:528:DC%2BC3MXht1SiurnF, PID: 21779594
    • Kellenberger, E., Hofmann, A. & Quinn, R. J. Similar interactions of natural products with biosynthetic enzymes and therapeutic targets could explain why nature produces such a large proportion of existing drugs. Nat. Prod. Rep. 28, 1483–1492 (2011).
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 1483-1492
    • Kellenberger, E.1    Hofmann, A.2    Quinn, R.J.3
  • 6
    • 64549160613 scopus 로고    scopus 로고
    • Novel chemical space exploration via natural products
    • PID: 19265440, COI: 1:CAS:528:DC%2BD1MXislKqu78%3D
    • Rosén, J., Gottfries, J., Muresan, S., Backlund, A. & Oprea, T. I. Novel chemical space exploration via natural products. J. Med. Chem. 52, 1953–1962 (2009).
    • (2009) J. Med. Chem. , vol.52 , pp. 1953-1962
    • Rosén, J.1    Gottfries, J.2    Muresan, S.3    Backlund, A.4    Oprea, T.I.5
  • 7
    • 11144311139 scopus 로고    scopus 로고
    • Lessons from natural molecules
    • COI: 1:CAS:528:DC%2BD2cXhtVOht7jP, PID: 15602548
    • Clardy, J. & Walsh, C. Lessons from natural molecules. Nature 432, 829–837 (2004).
    • (2004) Nature , vol.432 , pp. 829-837
    • Clardy, J.1    Walsh, C.2
  • 8
    • 84871599677 scopus 로고    scopus 로고
    • Natural-product-derived fragments for fragment-based ligand discovery
    • COI: 1:CAS:528:DC%2BC38XhslGktbnO, PID: 23247173
    • Over, B. et al. Natural-product-derived fragments for fragment-based ligand discovery. Nat. Chem. 5, 21–28 (2013).
    • (2013) Nat. Chem. , vol.5 , pp. 21-28
    • Over, B.1
  • 9
    • 84929103526 scopus 로고    scopus 로고
    • Design and synthesis of analogues of natural products
    • COI: 1:CAS:528:DC%2BC2MXltFWgsbk%3D, PID: 25829247
    • Maier, M. E. Design and synthesis of analogues of natural products. Org. Biomol. Chem. 13, 5302–5343 (2015).
    • (2015) Org. Biomol. Chem. , vol.13 , pp. 5302-5343
    • Maier, M.E.1
  • 10
    • 84893951172 scopus 로고    scopus 로고
    • Chemo- and site-selective derivatizations of natural products enabling biological studies
    • COI: 1:CAS:528:DC%2BC2cXisVagsr0%3D, PID: 24468713
    • Robles, O. & Romo, D. Chemo- and site-selective derivatizations of natural products enabling biological studies. Nat. Prod. Rep. 31, 318–334 (2014).
    • (2014) Nat. Prod. Rep. , vol.31 , pp. 318-334
    • Robles, O.1    Romo, D.2
  • 11
    • 84926205808 scopus 로고    scopus 로고
    • The re-emergence of natural products for drug discovery in the genomics era
    • COI: 1:CAS:528:DC%2BC2MXhsVarsbg%3D, PID: 25614221
    • Harvey, A. L., Edrada-Ebel, R. & Quinn, R. J. The re-emergence of natural products for drug discovery in the genomics era. Nat. Rev. Drug Discov. 14, 111–129 (2015).
    • (2015) Nat. Rev. Drug Discov. , vol.14 , pp. 111-129
    • Harvey, A.L.1    Edrada-Ebel, R.2    Quinn, R.J.3
  • 12
    • 84882907547 scopus 로고    scopus 로고
    • 14-step synthesis of (+)-ingenol from (+)-3-carene
    • PID: 23907534, COI: 1:CAS:528:DC%2BC3sXht12gsL%2FP
    • Jørgensen, L. et al. 14-step synthesis of (+)-ingenol from (+)-3-carene. Science 341, 878–882 (2013).
    • (2013) Science , vol.341 , pp. 878-882
    • Jørgensen, L.1
  • 13
    • 85051207265 scopus 로고    scopus 로고
    • Isolation, synthesis and bioactivity studies of phomactin terpenoids
    • COI: 1:CAS:528:DC%2BC1cXhsVegtbfK, PID: 30061613
    • Kuroda, Y. et al. Isolation, synthesis and bioactivity studies of phomactin terpenoids. Nat. Chem. 10, 938–945 (2018).
    • (2018) Nat. Chem. , vol.10 , pp. 938-945
    • Kuroda, Y.1
  • 14
    • 85065757498 scopus 로고    scopus 로고
    • Diverse compounds from pleuromutilin lead to a thioredoxin inhibitor and inducer of ferroptosis
    • COI: 1:CAS:528:DC%2BC1MXpsVagtLk%3D, PID: 31086302
    • Llabani, E. et al. Diverse compounds from pleuromutilin lead to a thioredoxin inhibitor and inducer of ferroptosis. Nat. Chem. 11, 521–532 (2019).
    • (2019) Nat. Chem. , vol.11 , pp. 521-532
    • Llabani, E.1
  • 15
    • 82055161640 scopus 로고    scopus 로고
    • Remodeling of the natural product fumagillol employing a reaction discovery approach
    • COI: 1:CAS:528:DC%2BC3MXhtlKhtrjO, PID: 22213919
    • Balthaser, B. R., Maloney, M. C., Beeler, A. B., Porco, J. A. & Snyder, J. K. Remodeling of the natural product fumagillol employing a reaction discovery approach. Nat. Chem. 3, 969–973 (2011).
    • (2011) Nat. Chem. , vol.3 , pp. 969-973
    • Balthaser, B.R.1    Maloney, M.C.2    Beeler, A.B.3    Porco, J.A.4    Snyder, J.K.5
  • 16
    • 84875466221 scopus 로고    scopus 로고
    • A ring-distortion strategy to construct stereochemically complex and structurally diverse compounds from natural products
    • COI: 1:CAS:528:DC%2BC3sXhtFSgurg%3D, PID: 23422561
    • Huigens, R. W. et al. A ring-distortion strategy to construct stereochemically complex and structurally diverse compounds from natural products. Nat. Chem. 5, 195–202 (2013).
    • (2013) Nat. Chem. , vol.5 , pp. 195-202
    • Huigens, R.W.1
  • 17
    • 84939811853 scopus 로고    scopus 로고
    • Use of a biosynthetic intermediate to explore the chemical diversity of pseudo-natural fungal polyketides
    • Asai, T. et al. Use of a biosynthetic intermediate to explore the chemical diversity of pseudo-natural fungal polyketides. Nat. Chem. 7, 737–743 (2015).
    • (2015) Nat. Chem. , vol.7 , pp. 737-743
    • Asai, T.1
  • 18
    • 30544434099 scopus 로고    scopus 로고
    • Fungal secondary metabolism from biochemistry to genomics
    • COI: 1:CAS:528:DC%2BD2MXht1OnsLbF, PID: 16322742
    • Keller, N. P., Turner, G. & Bennett, J. W. Fungal secondary metabolism from biochemistry to genomics. Nat. Rev. Microbiol. 3, 937–947 (2005).
    • (2005) Nat. Rev. Microbiol. , vol.3 , pp. 937-947
    • Keller, N.P.1    Turner, G.2    Bennett, J.W.3
  • 19
    • 84863229860 scopus 로고    scopus 로고
    • Advances in Aspergillus secondary metabolite research in the post-genomic era
    • COI: 1:CAS:528:DC%2BC38Xit1Wju7w%3D, PID: 22228366
    • Sanchez, J. F., Somoza, A. D., Keller, N. P. & Wang, C. C. C. Advances in Aspergillus secondary metabolite research in the post-genomic era. Nat. Prod. Rep. 29, 351–371 (2012).
    • (2012) Nat. Prod. Rep. , vol.29 , pp. 351-371
    • Sanchez, J.F.1    Somoza, A.D.2    Keller, N.P.3    Wang, C.C.C.4
  • 20
    • 67650308266 scopus 로고    scopus 로고
    • Hidden biosynthetic treasures brought to light
    • COI: 1:CAS:528:DC%2BD1MXnsVagu74%3D, PID: 19536102
    • Hertweck, C. Hidden biosynthetic treasures brought to light. Nat. Chem. Biol. 5, 450–452 (2009).
    • (2009) Nat. Chem. Biol. , vol.5 , pp. 450-452
    • Hertweck, C.1
  • 21
    • 85042058614 scopus 로고    scopus 로고
    • Genome mining and assembly-line biosynthesis of the UCS1025A pyrrolizidinone family of fungal alkaloids
    • COI: 1:CAS:528:DC%2BC1cXhslyqurY%3D
    • Li, L. et al. Genome mining and assembly-line biosynthesis of the UCS1025A pyrrolizidinone family of fungal alkaloids. J. Am. Chem. Soc. 140, 2067–2071 (2016).
    • (2016) J. Am. Chem. Soc. , vol.140 , pp. 2067-2071
    • Li, L.1
  • 22
    • 80053166085 scopus 로고    scopus 로고
    • H. Total biosynthesis of diterpene aphidicolin, a specific inhibitor of DNA polymerase α: heterologous expression of four biosynthetic genes in Aspergillus oryzae
    • COI: 1:CAS:528:DC%2BC3MXht12htLjL, PID: 21897020
    • Fujii, R. et al. H. Total biosynthesis of diterpene aphidicolin, a specific inhibitor of DNA polymerase α: heterologous expression of four biosynthetic genes in Aspergillus oryzae. Biosci. Biotechnol. Biochem. 75, 1813–1817 (2011).
    • (2011) Biosci. Biotechnol. Biochem. , vol.75 , pp. 1813-1817
    • Fujii, R.1
  • 23
    • 84873821538 scopus 로고    scopus 로고
    • Reconstitution of biosynthetic machinery for indole-diterpene paxilline in Aspergillus oryzae
    • COI: 1:CAS:528:DC%2BC3sXmvF2mtw%3D%3D, PID: 23311903
    • Tagami, K. et al. Reconstitution of biosynthetic machinery for indole-diterpene paxilline in Aspergillus oryzae. J. Am. Chem. Soc. 135, 1260–1263 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 1260-1263
    • Tagami, K.1
  • 24
    • 84908635350 scopus 로고    scopus 로고
    • Complete biosynthetic pathway of anditomin: nature’s sophisticated synthetic route to a complex fungal meroterpenoid
    • COI: 1:CAS:528:DC%2BC2cXhsFCjsLbJ, PID: 25216349
    • Matsuda, Y., Wakimoto, T., Mori, T., Awakawa, T. & Abe, I. Complete biosynthetic pathway of anditomin: nature’s sophisticated synthetic route to a complex fungal meroterpenoid. J. Am. Chem. Soc. 136, 15326–15336 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 15326-15336
    • Matsuda, Y.1    Wakimoto, T.2    Mori, T.3    Awakawa, T.4    Abe, I.5
  • 25
    • 77957276543 scopus 로고    scopus 로고
    • Reconstitution of a fungal meroterpenoid biosynthesis reveals the involvement of a novel family of terpene cyclases
    • COI: 1:CAS:528:DC%2BC3cXhtF2ms7fJ, PID: 20861902
    • Itoh, T. et al. Reconstitution of a fungal meroterpenoid biosynthesis reveals the involvement of a novel family of terpene cyclases. Nat. Chem. 2, 858–864 (2010).
    • (2010) Nat. Chem. , vol.2 , pp. 858-864
    • Itoh, T.1
  • 26
    • 85067456210 scopus 로고    scopus 로고
    • The discovery of fungal polyene macrolides via a postgenomic approach reveals a polyketide macrocyclization by trans-acting thioesterase in fungi
    • COI: 1:CAS:528:DC%2BC1MXhtFajtrrJ, PID: 31180682
    • Morishita, Y., Zhang, H., Taniguchi, T., Mori, K. & Asai, T. The discovery of fungal polyene macrolides via a postgenomic approach reveals a polyketide macrocyclization by trans-acting thioesterase in fungi. Org. Lett. 21, 4788–4792 (2019).
    • (2019) Org. Lett. , vol.21 , pp. 4788-4792
    • Morishita, Y.1    Zhang, H.2    Taniguchi, T.3    Mori, K.4    Asai, T.5
  • 27
    • 85066433889 scopus 로고    scopus 로고
    • Genome-based discovery of alkylresorcinols from a cricket-associated fungus, Penicillium soppi, that displays an unusual polyketide biosynthetic machinery
    • COI: 1:CAS:528:DC%2BC1MXoslKqsrc%3D, PID: 31086874
    • Kaneko, A., Morishita, Y., Tsukada, K., Taniguchi, T. & Asai, T. Genome-based discovery of alkylresorcinols from a cricket-associated fungus, Penicillium soppi, that displays an unusual polyketide biosynthetic machinery. Org. Biomol. Chem. 17, 5239–5243 (2019).
    • (2019) Org. Biomol. Chem. , vol.17 , pp. 5239-5243
    • Kaneko, A.1    Morishita, Y.2    Tsukada, K.3    Taniguchi, T.4    Asai, T.5
  • 28
    • 85045733334 scopus 로고    scopus 로고
    • HEx: a heterologous expression platform for the discovery of fungal natural products
    • PID: 29651464, COI: 1:CAS:528:DC%2BC1cXisVGlsrzE
    • Harvey, C. J. B. et al. HEx: a heterologous expression platform for the discovery of fungal natural products. Sci. Adv. 4, eaar5459 (2018).
    • (2018) Sci. Adv. , vol.4 , pp. eaar5459
    • Harvey, C.J.B.1
  • 29
    • 80052078373 scopus 로고    scopus 로고
    • Engineering of an “unnatural” natural product by swapping polyketide synthase domains in Aspergillus nidulans
    • COI: 1:CAS:528:DC%2BC3MXhtVSrtLzE, PID: 21815681
    • Liu, T., Chiang, Y. M., Somoza, A. D., Oakley, B. R. & Wang, C. C. C. Engineering of an “unnatural” natural product by swapping polyketide synthase domains in Aspergillus nidulans. J. Am. Chem. Soc. 133, 13314–13316 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 13314-13316
    • Liu, T.1    Chiang, Y.M.2    Somoza, A.D.3    Oakley, B.R.4    Wang, C.C.C.5
  • 30
    • 84906672709 scopus 로고    scopus 로고
    • Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases
    • COI: 1:CAS:528:DC%2BC2cXhtFyqtLjE, PID: 25049383
    • Xu, Y. et al. Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases. Proc. Natl Acad. Sci. USA 111, 12354–12359 (2014).
    • (2014) Proc. Natl Acad. Sci. USA , vol.111 , pp. 12354-12359
    • Xu, Y.1
  • 31
    • 85052671112 scopus 로고    scopus 로고
    • Reprogramming of the antimycin NRPS-PKS assembly lines inspired by gene evolution
    • PID: 30166552, COI: 1:CAS:528:DC%2BC1cXhs1ChurnI
    • Awakawa, T. et al. Reprogramming of the antimycin NRPS-PKS assembly lines inspired by gene evolution. Nat. Commun. 9, 3534 (2018).
    • (2018) Nat. Commun. , vol.9
    • Awakawa, T.1
  • 32
    • 85054875917 scopus 로고    scopus 로고
    • Synthetic biology approaches and combinatorial biosynthesis towards heterologous lipopeptide production
    • COI: 1:CAS:528:DC%2BC1cXhsVKrurzO, PID: 30319751
    • Yan, F. et al. Synthetic biology approaches and combinatorial biosynthesis towards heterologous lipopeptide production. Chem. Sci. 9, 7510–7519 (2018).
    • (2018) Chem. Sci. , vol.9 , pp. 7510-7519
    • Yan, F.1
  • 33
    • 0006108608 scopus 로고
    • Viridoxins A and B: novel toxins from the fungus Metarhizium flavoviride
    • COI: 1:CAS:528:DyaK3sXpslKmsw%3D%3D
    • Gupta, S. et al. Viridoxins A and B: novel toxins from the fungus Metarhizium flavoviride. J. Org. Chem. 58, 1062–1067 (1993).
    • (1993) J. Org. Chem. , vol.58 , pp. 1062-1067
    • Gupta, S.1
  • 34
    • 0031801643 scopus 로고    scopus 로고
    • Sesquicillin, an inhibitor of glucocorticoid mediated signal transduction
    • &
    • Engel, B., Erkel, G., Anke, T. & Sterner, O. Sesquicillin, an inhibitor of glucocorticoid mediated signal transduction. J. Antibiot. 51, 518–521 (1998).
    • (1998) J. Antibiot. , vol.51 , pp. 518-521
    • Engel, B.1    Erkel, G.2    Anke, T.3    Sterner, O.4
  • 35
    • 22444433146 scopus 로고    scopus 로고
    • New sesquicillins, insecticidal antibiotics produced by Albophoma sp. FKI-1778
    • COI: 1:CAS:528:DC%2BD2MXmtVaqs7o%3D, PID: 16156516
    • Uchida, R. et al. New sesquicillins, insecticidal antibiotics produced by Albophoma sp. FKI-1778. J. Antibiot. 58, 397–404 (2005).
    • (2005) J. Antibiot. , vol.58 , pp. 397-404
    • Uchida, R.1
  • 36
    • 84872521602 scopus 로고    scopus 로고
    • Integrated compound profiling screens identify the mitochondrial electron transport chain as the molecular target of the natural products manassantin, sesquicillin, and arctigenin
    • COI: 1:CAS:528:DC%2BC38Xhs1ekt7nJ, PID: 23138533
    • Lai, K. et al. Integrated compound profiling screens identify the mitochondrial electron transport chain as the molecular target of the natural products manassantin, sesquicillin, and arctigenin. ACS Chem. Biol. 8, 257–267 (2013).
    • (2013) ACS Chem. Biol. , vol.8 , pp. 257-267
    • Lai, K.1
  • 37
    • 56949097895 scopus 로고    scopus 로고
    • New diterpene pyrone-type compounds, metarhizins A and B, isolated from entomopathogenic fungus, Metarhizium flavoviride and their inhibitory effects on cellular proliferation
    • COI: 1:CAS:528:DC%2BD1cXhsVOntLnF
    • Kikuchi, H. et al. New diterpene pyrone-type compounds, metarhizins A and B, isolated from entomopathogenic fungus, Metarhizium flavoviride and their inhibitory effects on cellular proliferation. Tetrahedron 65, 469 (2009).
    • (2009) Tetrahedron , vol.65 , pp. 469
    • Kikuchi, H.1
  • 38
    • 0028845809 scopus 로고
    • Subglutinols A and B: immunosuppressive compounds from the endophytic fungus Fusarium subglutinans
    • COI: 1:CAS:528:DyaK2MXos1Ghsbk%3D
    • Lee, J. C., Lobkovsky, E., Pliam, N. B., Strobel, G. & Clardy, J. Subglutinols A and B: immunosuppressive compounds from the endophytic fungus Fusarium subglutinans. J. Org. Chem. 60, 7076–7077 (1995).
    • (1995) J. Org. Chem. , vol.60 , pp. 7076-7077
    • Lee, J.C.1    Lobkovsky, E.2    Pliam, N.B.3    Strobel, G.4    Clardy, J.5
  • 39
    • 84863082756 scopus 로고    scopus 로고
    • Immunosuppressive effects of subglutinol derivatives
    • COI: 1:CAS:528:DC%2BC3MXhsFaltb%2FO, PID: 22114006
    • Lee, W. G. et al. Immunosuppressive effects of subglutinol derivatives. ChemMedChem 7, 218–222 (2012).
    • (2012) ChemMedChem , vol.7 , pp. 218-222
    • Lee, W.G.1
  • 40
    • 84956791948 scopus 로고    scopus 로고
    • Higginsianins A and B, two diterpenoid α-pyrones produced by Colletotrichum higginsianum, with in vitro cytostatic activity
    • COI: 1:CAS:528:DC%2BC28XnvFahsg%3D%3D, PID: 26697898
    • Cimmino, A. et al. Higginsianins A and B, two diterpenoid α-pyrones produced by Colletotrichum higginsianum, with in vitro cytostatic activity. J. Nat. Prod. 79, 116–125 (2016).
    • (2016) J. Nat. Prod. , vol.79 , pp. 116-125
    • Cimmino, A.1
  • 41
    • 0017844195 scopus 로고
    • Structures of colletotrichin and colletotrichin B, phytotoxic metabolites from Colletotrichum nicotianae
    • COI: 1:CAS:528:DyaE1cXkslWrsLw%3D
    • Gohbara, M. et al. Structures of colletotrichin and colletotrichin B, phytotoxic metabolites from Colletotrichum nicotianae. Agric. Biol. Chem. 42, 1037–1043 (1978).
    • (1978) Agric. Biol. Chem. , vol.42 , pp. 1037-1043
    • Gohbara, M.1
  • 42
    • 0037090967 scopus 로고    scopus 로고
    • An efficient stereoselective total synthesis of DL-sesquicillin, a glucocorticoid antagonist
    • COI: 1:CAS:528:DC%2BD38Xjt1eqs7s%3D
    • Zhang, F. & Danishefsky, S. J. An efficient stereoselective total synthesis of DL-sesquicillin, a glucocorticoid antagonist. Angew. Chem. Int. Ed. 41, 1434–1437 (2002).
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1434-1437
    • Zhang, F.1    Danishefsky, S.J.2
  • 43
    • 67649665886 scopus 로고    scopus 로고
    • Stereoselective synthesis and osteogenic activity of subglutinols A and B
    • COI: 1:CAS:528:DC%2BD1MXhvVChurY%3D, PID: 19216570
    • Kim, H. et al. Stereoselective synthesis and osteogenic activity of subglutinols A and B. J. Am. Chem. Soc. 131, 3192–3194 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3192-3194
    • Kim, H.1
  • 44
    • 62349125019 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (–)‐subglutinols A and B: potential immunosuppressive agents isolated from a microorganism
    • COI: 1:CAS:528:DC%2BD1MXjs1Gis74%3D, PID: 19191240
    • Oguchi, T., Watanabe, K., Ohkubo, K., Abe, H. & Katou, T. Enantioselective total synthesis of (–)‐subglutinols A and B: potential immunosuppressive agents isolated from a microorganism. Chem. Eur. J. 15, 2826–2845 (2009).
    • (2009) Chem. Eur. J. , vol.15 , pp. 2826-2845
    • Oguchi, T.1    Watanabe, K.2    Ohkubo, K.3    Abe, H.4    Katou, T.5
  • 45
    • 85048843793 scopus 로고    scopus 로고
    • Divergent synthesis of pyrone diterpenes via radical cross coupling
    • COI: 1:CAS:528:DC%2BC1cXhtFSqurvI, PID: 29921130
    • Merchant, R. R. et al. Divergent synthesis of pyrone diterpenes via radical cross coupling. J. Am. Chem. Soc. 140, 7462–7465 (2018).
    • (2018) J. Am. Chem. Soc. , vol.140 , pp. 7462-7465
    • Merchant, R.R.1
  • 46
    • 84979788563 scopus 로고    scopus 로고
    • New natural products isolated from Metarhizium robertsii ARSEF 23 by chemical screening and identification of the gene cluster through engineered biosynthesis in Aspergillus nidulans A1145
    • COI: 1:CAS:528:DC%2BC28Xht1GlsbrM, PID: 27189118
    • Kato, H. et al. New natural products isolated from Metarhizium robertsii ARSEF 23 by chemical screening and identification of the gene cluster through engineered biosynthesis in Aspergillus nidulans A1145. J. Antibiot. 69, 561–566 (2016).
    • (2016) J. Antibiot. , vol.69 , pp. 561-566
    • Kato, H.1
  • 47
    • 4644219707 scopus 로고    scopus 로고
    • Development of a novel quadruple auxotrophic host transformation system by argB gene disruption using adeA gene and exploiting adenine auxotrophy in Aspergillus oryzae
    • COI: 1:CAS:528:DC%2BD2cXnvV2ltLo%3D, PID: 15451104
    • Jin, F. J., Maruyama, J., Juvvadi, P. R., Arioka, M. & Kitamoto, K. Development of a novel quadruple auxotrophic host transformation system by argB gene disruption using adeA gene and exploiting adenine auxotrophy in Aspergillus oryzae. FEMS Microbiol. Lett. 239, 79–85 (2004).
    • (2004) FEMS Microbiol. Lett. , vol.239 , pp. 79-85
    • Jin, F.J.1    Maruyama, J.2    Juvvadi, P.R.3    Arioka, M.4    Kitamoto, K.5
  • 48
    • 84881150453 scopus 로고    scopus 로고
    • Reconstituted biosynthesis of fungal meroterpenoid andrastin A
    • COI: 1:CAS:528:DC%2BC3sXhtFOitLjN
    • Matsuda, Y., Awakawa, T. & Abe, I. Reconstituted biosynthesis of fungal meroterpenoid andrastin A. Tetrahedron 69, 8199–8204 (2013).
    • (2013) Tetrahedron , vol.69 , pp. 8199-8204
    • Matsuda, Y.1    Awakawa, T.2    Abe, I.3
  • 49
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher’s method. The absolute configurations of marine terpenoids
    • COI: 1:CAS:528:DyaK3MXktV2jtL0%3D
    • Ohtani, I., Kusumi, T., Kashman, Y. & Kakisawa, H. High-field FT NMR application of Mosher’s method. The absolute configurations of marine terpenoids. J. Am. Chem. Soc. 113, 4092–4096 (1991).
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 50
    • 0036168343 scopus 로고    scopus 로고
    • An integrated database of chemosensitivity to 55 anticancer drugs and gene expression profiles of 39 human cancer cell lines
    • COI: 1:CAS:528:DC%2BD38XitVSmtrg%3D, PID: 11861395
    • Dan, S. et al. An integrated database of chemosensitivity to 55 anticancer drugs and gene expression profiles of 39 human cancer cell lines. Cancer Res. 62, 1139–1147 (2002).
    • (2002) Cancer Res. , vol.62 , pp. 1139-1147
    • Dan, S.1
  • 51
    • 85053491845 scopus 로고    scopus 로고
    • Target Identification of Yaku’amide B and its two distinct activities against mitochondrial F0F1-ATP synthase
    • COI: 1:CAS:528:DC%2BC1cXhs1alsrvP, PID: 30156840
    • Kitamura, K., Itoh, H., Ssakurai, K., Dan, S. & Inoue, M. Target Identification of Yaku’amide B and its two distinct activities against mitochondrial F0F1-ATP synthase. J. Am. Chem. Soc. 140, 12189–12199 (2018).
    • (2018) J. Am. Chem. Soc. , vol.140 , pp. 12189-12199
    • Kitamura, K.1    Itoh, H.2    Ssakurai, K.3    Dan, S.4    Inoue, M.5
  • 52
    • 85053790127 scopus 로고    scopus 로고
    • Stem cell fate in cancer growth, progression and therapy resistance
    • COI: 1:CAS:528:DC%2BC1cXhslCju77O, PID: 30228301
    • Lytle, N. K., Barber, A. G. & Reya, T. Stem cell fate in cancer growth, progression and therapy resistance. Nat. Rev. Cancer 18, 669–680 (2018).
    • (2018) Nat. Rev. Cancer , vol.18 , pp. 669-680
    • Lytle, N.K.1    Barber, A.G.2    Reya, T.3
  • 53
    • 85049872624 scopus 로고    scopus 로고
    • Cancer stem cell in breast cancer therapeutic resistance
    • COI: 1:CAS:528:DC%2BC1cXhtlCntbrE, PID: 30029203
    • Bai, X., Ni, J., Beretov, J., Graham, P. & Li, Y. Cancer stem cell in breast cancer therapeutic resistance. Cancer Treat. Rev. 69, 152–163 (2018).
    • (2018) Cancer Treat. Rev. , vol.69 , pp. 152-163
    • Bai, X.1    Ni, J.2    Beretov, J.3    Graham, P.4    Li, Y.5
  • 54
    • 85010825666 scopus 로고    scopus 로고
    • Development of small molecular compounds targeting cancer stem cells
    • PID: 30108692, COI: 1:CAS:528:DC%2BC28XhvVCisbfN
    • Park, J. H., Chung, S., Matsuo, Y. & Nakamura, Y. Development of small molecular compounds targeting cancer stem cells. Medchemcomm 8, 73–80 (2016).
    • (2016) Medchemcomm , vol.8 , pp. 73-80
    • Park, J.H.1    Chung, S.2    Matsuo, Y.3    Nakamura, Y.4
  • 55
    • 84923283486 scopus 로고    scopus 로고
    • Sphingosine-1-phosphate promotes expansion of cancer stem cells via S1PR3 by a ligand-independent Notch activation
    • COI: 1:CAS:528:DC%2BC2cXhvF2mu7vM, PID: 25254944
    • Hirata, N. et al. Sphingosine-1-phosphate promotes expansion of cancer stem cells via S1PR3 by a ligand-independent Notch activation. Nat. Commun. 5, 4806 (2014).
    • (2014) Nat. Commun. , vol.5
    • Hirata, N.1
  • 56
    • 85045259047 scopus 로고    scopus 로고
    • Inhibition of cancer stem cell like cells by a synthetic retinoid
    • PID: 29643385, COI: 1:CAS:528:DC%2BC1cXhtFSqu7jJ
    • Chen, J. et al. Inhibition of cancer stem cell like cells by a synthetic retinoid. Nat. Commun. 9, 1406 (2018).
    • (2018) Nat. Commun. , vol.9
    • Chen, J.1
  • 57
    • 34047268684 scopus 로고    scopus 로고
    • The host defense of Drosophila melanogaster
    • COI: 1:CAS:528:DC%2BD2sXltlans7w%3D, PID: 17201680
    • Lemaitre, B. & Hoffmann, J. The host defense of Drosophila melanogaster. Annu. Rev. Immunol. 25, 697–743 (2007).
    • (2007) Annu. Rev. Immunol. , vol.25 , pp. 697-743
    • Lemaitre, B.1    Hoffmann, J.2
  • 58
    • 84945578601 scopus 로고    scopus 로고
    • Genome-wide RNAi screening implicates the E3 ubiquitin ligase Sherpa in mediating innate immune signaling by Toll in Drosophila adults
    • Kanoh, H. et al. Genome-wide RNAi screening implicates the E3 ubiquitin ligase Sherpa in mediating innate immune signaling by Toll in Drosophila adults. Sci. Signal. 8, ra107 (2015).
    • (2015) Sci. Signal. , vol.8 , pp. ra107
    • Kanoh, H.1
  • 59
    • 9144269002 scopus 로고    scopus 로고
    • Draper-mediated and phosphatidylserine-independent phagocytosis of apoptotic cells by Drosophila Hemocytes/Macrophages
    • COI: 1:CAS:528:DC%2BD2cXptl2msLw%3D, PID: 15342648
    • Manaka, J. et al. Draper-mediated and phosphatidylserine-independent phagocytosis of apoptotic cells by Drosophila Hemocytes/Macrophages. J. Biol. Chem. 279, 48466–48476 (2004).
    • (2004) J. Biol. Chem. , vol.279 , pp. 48466-48476
    • Manaka, J.1
  • 60
    • 85056571826 scopus 로고    scopus 로고
    • Characterization of Spz5 as a novel ligand for Drosophila Toll-1 receptor
    • COI: 1:CAS:528:DC%2BC1cXhvFyns77K, PID: 30361090
    • Nonaka, S. et al. Characterization of Spz5 as a novel ligand for Drosophila Toll-1 receptor. Biochem. Biophys. Res. Commun. 506, 510–515 (2018).
    • (2018) Biochem. Biophys. Res. Commun. , vol.506 , pp. 510-515
    • Nonaka, S.1
  • 61
    • 84944398565 scopus 로고    scopus 로고
    • Ex vivo genome-wide RNAi screening of the Drosophila Toll signaling pathway elicited by a larva-derived tissue extract
    • COI: 1:CAS:528:DC%2BC2MXhs1aktLfL, PID: 26427875
    • Kanoh, H. et al. Ex vivo genome-wide RNAi screening of the Drosophila Toll signaling pathway elicited by a larva-derived tissue extract. Biochem. Biophys. Res. Commun. 467, 400–406 (2015).
    • (2015) Biochem. Biophys. Res. Commun. , vol.467 , pp. 400-406
    • Kanoh, H.1
  • 62
    • 33947178879 scopus 로고    scopus 로고
    • A novel colorimetric assay for CXCR4 and CCR5 tropic human immunodeficiency viruses
    • COI: 1:CAS:528:DC%2BD28XhtFCgt77L, PID: 17066899
    • Kajiwara, K., Kodama, E. & Matsuoka, M. A novel colorimetric assay for CXCR4 and CCR5 tropic human immunodeficiency viruses. Antivir. Chem. Chemother. 17, 215–223 (2006).
    • (2006) Antivir. Chem. Chemother. , vol.17 , pp. 215-223
    • Kajiwara, K.1    Kodama, E.2    Matsuoka, M.3
  • 63
    • 33847662852 scopus 로고    scopus 로고
    • Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer’s amyloid beta-peptide
    • COI: 1:CAS:528:DC%2BD2sXotFKmtw%3D%3D, PID: 17245412
    • Haass, C. & Selkoe, D. J. Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer’s amyloid beta-peptide. Nat. Rev. Mol. Cell Biol. 8, 101–112 (2007).
    • (2007) Nat. Rev. Mol. Cell Biol. , vol.8 , pp. 101-112
    • Haass, C.1    Selkoe, D.J.2
  • 64
    • 0033598697 scopus 로고    scopus 로고
    • Interaction between A beta(1-42) and A beta(1-40) in Alzheimer’s beta-amyloid fibril formation in vitro
    • COI: 1:CAS:528:DyaK1MXntValsLY%3D, PID: 10569934
    • Hasegawa, K., Yamaguchi, I., Omata, S., Gejyo, F. & Naiki, H. Interaction between A beta(1-42) and A beta(1-40) in Alzheimer’s beta-amyloid fibril formation in vitro. Biochemistry 38, 15514–15521 (1999).
    • (1999) Biochemistry , vol.38 , pp. 15514-15521
    • Hasegawa, K.1    Yamaguchi, I.2    Omata, S.3    Gejyo, F.4    Naiki, H.5
  • 65
    • 0034714351 scopus 로고    scopus 로고
    • Nucleated conformational conversion and the replication of conformational information by a prion determinant
    • COI: 1:CAS:528:DC%2BD3cXmt1Wltr8%3D, PID: 10958771
    • Serio, T. R. et al. Nucleated conformational conversion and the replication of conformational information by a prion determinant. Science 289, 1317–1321 (2000).
    • (2000) Science , vol.289 , pp. 1317-1321
    • Serio, T.R.1
  • 66
    • 78649474332 scopus 로고    scopus 로고
    • Monoclonal antibody against the turn of the 42-residue amyloid β-protein at positions and 23
    • COI: 1:CAS:528:DC%2BC3cXht1Whs7zE
    • Murakami, K. et al. Monoclonal antibody against the turn of the 42-residue amyloid β-protein at positions and 23. ACS Chem. Neurosci. 17, 747–756 (2010).
    • (2010) ACS Chem. Neurosci. , vol.17 , pp. 747-756
    • Murakami, K.1
  • 67
    • 85041637920 scopus 로고    scopus 로고
    • Mechanistic analyses of the suppression of amyloid β42 aggregation by apomorphine
    • COI: 1:CAS:528:DC%2BC1cXisFKns70%3D, PID: 29429575
    • Hanaki, M. et al. Mechanistic analyses of the suppression of amyloid β42 aggregation by apomorphine. Bioorg. Med. Chem. 26, 1538–1546 (2018).
    • (2018) Bioorg. Med. Chem. , vol.26 , pp. 1538-1546
    • Hanaki, M.1
  • 68
    • 84949267061 scopus 로고    scopus 로고
    • A new golden age of natural products drug discovery
    • COI: 1:CAS:528:DC%2BC2MXhvFKksb%2FM, PID: 26638061
    • Shen, B. A new golden age of natural products drug discovery. Cell 163, 1297–1300 (2015).
    • (2015) Cell , vol.163 , pp. 1297-1300
    • Shen, B.1
  • 69
    • 85060388018 scopus 로고    scopus 로고
    • Use of plant hormones to activate silent polyketide biosynthetic pathways in Arthrinium sacchari, a fungus isolated from a spider
    • COI: 1:CAS:528:DC%2BC1cXisF2hsb3I, PID: 30608107
    • Morishita, Y. et al. Use of plant hormones to activate silent polyketide biosynthetic pathways in Arthrinium sacchari, a fungus isolated from a spider. Org. Biomol. Chem. 17, 780–784 (2019).
    • (2019) Org. Biomol. Chem. , vol.17 , pp. 780-784
    • Morishita, Y.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.