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Volumn 12, Issue 11, 2011, Pages 1654-1673

Chemodiversity in freshwater and terrestrial cyanobacteria - a source for drug discovery

Author keywords

Antibacterial; Antifungal; Cyanobacteria; Cytotoxic; Protease inhibitor

Indexed keywords

AERUGINOSIN DERIVATIVE; ALKALOID DERIVATIVE; AMBIGUINE DERIVATIVE; ANABAENOPEPTIN DERIVATIVE; ANTIINFECTIVE AGENT; BRUNSVICAMIDE B; COMNOSTIN DERIVATIVE; CRYPTOPHYCIN DERIVATIVE; CYANOPEPTOLIN DERIVATIVE; CYTOTOXIN; FISCHERELLIN A; HAPALINDOLE DERIVATIVE; HASSALLIDIN A; MICROGININ DERIVATIVE; MICROVIRIDIN DERIVATIVE; NOSCOMIN; PEPTIDE DERIVATIVE; PROTEINASE INHIBITOR; SCYTOPHYCIN DERIVATIVE; SCYTOSCALAROL; TERPENOID DERIVATIVE; TJIPANAZOLE DERIVATIVE; TOLYTOXIN; UNCLASSIFIED DRUG;

EID: 80054098160     PISSN: 13894501     EISSN: 18735592     Source Type: Journal    
DOI: 10.2174/138945011798109455     Document Type: Review
Times cited : (114)

References (247)
  • 1
    • 0034623416 scopus 로고    scopus 로고
    • Evolution: When did photosynthesis emerge on earth?
    • Des Marais DJ. Evolution: when did photosynthesis emerge on earth? Science 2000; 289: 1703-5.
    • (2000) Science , vol.289 , pp. 1703-1705
    • des Marais, D.J.1
  • 2
    • 0000642932 scopus 로고    scopus 로고
    • In: Whitton BA, Potts M, Eds. The Ecology of Cyanobacteria. Their Diversity in Time and Space. Dordrecht, The Netherlands: Kluwer Academic Publishers
    • Schopf JW. In: Whitton BA, Potts M, Eds. The Ecology of Cyanobacteria. Their Diversity in Time and Space. Dordrecht, The Netherlands: Kluwer Academic Publishers 2000: 13-35.
    • (2000) , pp. 13-35
    • Schopf, J.W.1
  • 3
    • 0036348369 scopus 로고    scopus 로고
    • Toxins and bioactive compounds from cyanobacteria and their implications on human health
    • Rao PV, Gupta N, Bhaskar AS, Jayaraj R. Toxins and bioactive compounds from cyanobacteria and their implications on human health. J Environ Biol 2002; 23: 215-224.
    • (2002) J Environ Biol , vol.23 , pp. 215-224
    • Rao, P.V.1    Gupta, N.2    Bhaskar, A.S.3    Jayaraj, R.4
  • 4
    • 31544477132 scopus 로고    scopus 로고
    • Cyanobacterial toxins--occurrence, biosynthesis and impact on human affairs
    • Dittmann E, Wiegand C. Cyanobacterial toxins--occurrence, biosynthesis and impact on human affairs. Mol Nutr Food Res 2006; 50: 7-17.
    • (2006) Mol Nutr Food Res , vol.50 , pp. 7-17
    • Dittmann, E.1    Wiegand, C.2
  • 5
    • 34548161851 scopus 로고    scopus 로고
    • Health Aspects of Freshwater Cyanobacterial Toxins
    • Shaw G, Lam PKS. Health aspects of freshwater cyanobacterial toxins. Water Sci. Technol. Water Supply 2007; 7: 193-203
    • (2007) Water Sci. Technol. Water Supply , vol.7 , pp. 193-203
    • Shaw, G.1    Lam, P.K.S.2
  • 7
    • 85006998552 scopus 로고    scopus 로고
    • In: Seafood and Freshwater Toxins; Botana LM, Ed. Boca Raton, FL, USA: CRC Press
    • Welker M. In: Seafood and Freshwater Toxins; Botana LM, Ed. Boca Raton, FL, USA: CRC Press 2008: 825-843.
    • (2008) , pp. 825-843
    • Welker, M.1
  • 8
    • 42049111878 scopus 로고    scopus 로고
    • Secondary metabolites from cyanobacteria: Complex structures and powerful bioactivities
    • Gademann K, Portmann C. Secondary metabolites from cyanobacteria: complex structures and powerful bioactivities. Curr Org Chem 2008; 12: 326-341.
    • (2008) Curr Org Chem , vol.12 , pp. 326-341
    • Gademann, K.1    Portmann, C.2
  • 12
    • 0036314931 scopus 로고    scopus 로고
    • Drugs from the seas: Current status and microbiological implications
    • Proksch P, Edrada RA, Ebel R. Drugs from the seas: current status and microbiological implications. Appl Microbiol Biotechnol 2002; 59: 125-134.
    • (2002) Appl Microbiol Biotechnol , vol.59 , pp. 125-134
    • Proksch, P.1    Edrada, R.A.2    Ebel, R.3
  • 13
    • 0035225541 scopus 로고    scopus 로고
    • In: The Alkaloids;, Cordell GA, Ed. San Diego: Academic Press
    • Gerwick WH, Tan LT, Sitachitta N. In: The Alkaloids; Cordell GA, Ed. San Diego: Academic Press 2001; 57: 75-184.
    • (2001) , vol.57 , pp. 75-184
    • Gerwick, W.H.1    Tan, L.T.2    Sitachitta, N.3
  • 14
    • 26444539868 scopus 로고    scopus 로고
    • Bioactive compounds from cyanobacteria and microalgae: An overview
    • Singh S, Kate BN, Banerjee UC. Bioactive compounds from cyanobacteria and microalgae: an overview. Crit Rev Biotechnol 2005; 25: 73-95.
    • (2005) Crit Rev Biotechnol , vol.25 , pp. 73-95
    • Singh, S.1    Kate, B.N.2    Banerjee, U.C.3
  • 15
    • 32544440913 scopus 로고    scopus 로고
    • Natrual products from cyanobacteria: Exploiting a new source for drug discovery
    • Sielaff H, Christiansen G, Schwecke T. Natrual products from cyanobacteria: exploiting a new source for drug discovery. IDrugs 2006; 9: 119-127.
    • (2006) IDrugs , vol.9 , pp. 119-127
    • Sielaff, H.1    Christiansen, G.2    Schwecke, T.3
  • 16
    • 33744965454 scopus 로고    scopus 로고
    • Cyanobacterial peptides - nature's own combinatorial biosynthesis
    • Welker M, von Dohren H. Cyanobacterial peptides - nature's own combinatorial biosynthesis. FEMS Microbiol Rev 2006; 30: 530- 563.
    • (2006) FEMS Microbiol Rev , vol.30 , pp. 530-563
    • Welker, M.1    von Dohren, H.2
  • 17
    • 33947104489 scopus 로고    scopus 로고
    • Bioactive natural products from marine cyanobacteria for drug discovery
    • Tan LT. Bioactive natural products from marine cyanobacteria for drug discovery. Phytochemistry 2007; 68: 954-979.
    • (2007) Phytochemistry , vol.68 , pp. 954-979
    • Tan, L.T.1
  • 19
    • 0028141462 scopus 로고
    • Cryptophycin -a new antimicrotubule agent active against drug- resistant cells
    • Smith CD, Zhang X, Mooberry SL, Patterson GML, Moore RE. Cryptophycin - a new antimicrotubule agent active against drug- resistant cells. Cancer Res 1994; 54: 3779-3784.
    • (1994) Cancer Res , vol.54 , pp. 3779-3784
    • Smith, C.D.1    Zhang, X.2    Mooberry, S.L.3    Patterson, G.M.L.4    Moore, R.E.5
  • 20
    • 0029874514 scopus 로고    scopus 로고
    • Mechanism of action cryptophycin. interaction with the vinca alkaloid domain of tubulin
    • Smith CD, Zhang X. Mechanism of action cryptophycin. interaction with the vinca alkaloid domain of tubulin. J Biol Chem 1996; 271: 6192-6198.
    • (1996) J Biol Chem , vol.271 , pp. 6192-6198
    • Smith, C.D.1    Zhang, X.2
  • 21
    • 4344572608 scopus 로고    scopus 로고
    • Isolation and structure determination of cryptophycins 38, 326, and 327 from the terrestrial cyanobacterium Nostoc sp. GSV 224
    • Chaganty S, Golakoti T, Heltzel C, Moore RE, Yoshida WY. Isolation and structure determination of cryptophycins 38, 326, and 327 from the terrestrial cyanobacterium Nostoc sp. GSV 224. J Nat Prod 2004; 67: 1403-1406.
    • (2004) J Nat Prod , vol.67 , pp. 1403-1406
    • Chaganty, S.1    Golakoti, T.2    Heltzel, C.3    Moore, R.E.4    Yoshida, W.Y.5
  • 22
    • 0028017485 scopus 로고
    • Total structures of cryptophycins, potent antitumor depsipeptides from the blue-green- alga Nostoc sp. Strain GSV-224
    • Golakoti T, Ohtani I, Patterson GML, et al. Total structures of cryptophycins, potent antitumor depsipeptides from the blue-green- alga Nostoc sp. Strain GSV-224. J Am Chem Soc 1994; 116: 4729- 4737.
    • (1994) J Am Chem Soc , vol.116 , pp. 4729-4737
    • Golakoti, T.1    Ohtani, I.2    Patterson, G.M.L.3    Et al.4
  • 23
    • 0041537280 scopus 로고
    • Structure determination, conformational-analysis, chemical-stability studies, and antitumor evaluation of the cryptophycins - isolation of 18 new analogs from Nostoc sp. Strain GSV-224
    • Golakoti T, Ogino J, Heltzel CE, et al. Structure determination, conformational-analysis, chemical-stability studies, and antitumor evaluation of the cryptophycins - isolation of 18 new analogs from Nostoc sp. Strain GSV-224. J Am Chem Soc. 1995; 117: 12030-1249
    • (1995) J Am Chem Soc , vol.117 , pp. 12030-1249
    • Golakoti, T.1    Ogino, J.2    Heltzel, C.E.3
  • 25
    • 0037316411 scopus 로고    scopus 로고
    • Phase 2 study of cryptophycin 52 (LY355703) in patients previously treated with platinum based chemotherapy for advanced non-small cell lung cancer
    • Edelman MJ, Gandara DR, Hausner P, Israel V, Thornton D, DeSanto J, Doyle LA. Phase 2 study of cryptophycin 52 (LY355703) in patients previously treated with platinum based chemotherapy for advanced non-small cell lung cancer. Lung Cancer 2003; 39: 197-199.
    • (2003) Lung Cancer , vol.39 , pp. 197-199
    • Edelman, M.J.1    Gandara, D.R.2    Hausner, P.3    Israel, V.4    Thornton, D.5    Desanto, J.6    Doyle, L.A.7
  • 26
    • 33645352797 scopus 로고    scopus 로고
    • A Multicenter phase ii study of the cryptophycin analog LY355703 in patients with platinum-resistant ovarian cancer
    • D'Agostino G, Del Campo J, Mellado B, et al. A Multicenter phase ii study of the cryptophycin analog LY355703 in patients with platinum-resistant ovarian cancer. Int J Gynecol Cancer 2006; 16: 71-76.
    • (2006) Int J Gynecol Cancer , vol.16 , pp. 71-76
    • D'Agostino, G.1    del Campo, J.2    Mellado, B.3
  • 27
    • 21044434617 scopus 로고    scopus 로고
    • Cryptophycins-309, 249 and Other Cryptophycin Analogs: Preclinical Efficacy Studies With Mouse and Human Tumors
    • Liang J, Moore RE, Moher ED, et al. Cryptophycins-309, 249 and other cryptophycin analogs: preclinical efficacy studies with mouse and human tumors.Invest New Drugs 2005; 23: 213-224.
    • (2005) Invest New Drugs , vol.23 , pp. 213-224
    • Liang, J.1    Moore, R.E.2    Moher, E.D.3
  • 28
    • 33947491846 scopus 로고    scopus 로고
    • Biosynthetic characterization and chemoenzymatic assembly of the cryptophycins. potent anticancer agents from cyanobionts
    • Magarvey NA, Beck ZQ, Golakoti T, et al. Biosynthetic characterization and chemoenzymatic assembly of the cryptophycins. potent anticancer agents from cyanobionts. ACS Chem Biol 2006; 1: 766-779.
    • (2006) ACS Chem Biol , vol.1 , pp. 766-779
    • Magarvey, N.A.1    Beck, Z.Q.2    Golakoti, T.3    Et al.4
  • 30
    • 42949115597 scopus 로고    scopus 로고
    • Analysis of the cryptophycin P450 epoxidase reveals substrate tolerance and cooperativity
    • Ding Y, Seufert WH, Beck ZQ, Sherman DH. Analysis of the cryptophycin P450 epoxidase reveals substrate tolerance and cooperativity. J Am Chem Soc. 2008; 130: 5492-5498.
    • (2008) J Am Chem Soc , vol.130 , pp. 5492-5498
    • Ding, Y.1    Seufert, W.H.2    Beck, Z.Q.3    Sherman, D.H.4
  • 31
    • 0025685426 scopus 로고
    • Tolytoxin and new scytophycins from three species of Scytonema
    • Carmeli S, Moore RE, Patterson GML. Tolytoxin and new scytophycins from three species of Scytonema. J Nat Prod 1990; 53: 1533-1542.
    • (1990) J Nat Prod , vol.53 , pp. 1533-1542
    • Carmeli, S.1    Moore, R.E.2    Patterson, G.M.L.3
  • 32
    • 0142100446 scopus 로고
    • Scytophycins from a blue- green alga belonging to the Nostocaceae
    • Jung JH, Moore RE, Patterson GML. Scytophycins from a blue- green alga belonging to the Nostocaceae. Phytochemistry 1991; 30: 3615-3616.
    • (1991) Phytochemistry , vol.30 , pp. 3615-3616
    • Jung, J.H.1    Moore, R.E.2    Patterson, G.M.L.3
  • 33
    • 0027461737 scopus 로고
    • Scytophycins, novel microfilament-depolymerizing agents which circumvent p- glycoprotein-mediated multidrug resistance
    • Smith CD, Carmeli S, Moore RE, Patterson GML. Scytophycins, novel microfilament-depolymerizing agents which circumvent p- glycoprotein-mediated multidrug resistance. Cancer Res 1993; 53: 1343-1347
    • (1993) Cancer Res , vol.53 , pp. 1343-1347
    • Smith, C.D.1    Carmeli, S.2    Moore, R.E.3    Patterson, G.M.L.4
  • 34
    • 0037122039 scopus 로고    scopus 로고
    • Actin-binding marine macrolides: Total synthesis and biological importance
    • Yeung K, Paterson I. Actin-binding marine macrolides: total synthesis and biological importance. Angew Chem Int Ed Engl 2002; 41: 4632-4653.
    • (2002) Angew Chem Int Ed Engl , vol.41 , pp. 4632-4653
    • Yeung, K.1    Paterson, I.2
  • 35
    • 84989626340 scopus 로고
    • Antineoplastic activity of cultured blue-green-algae (Cyanophyta)
    • Patterson GML, Baldwin CL, Bolis CM, et al. Antineoplastic activity of cultured blue-green-algae (Cyanophyta). J Phycol 1991; 27: 530-536.
    • (1991) J Phycol , vol.27 , pp. 530-536
    • Patterson, G.M.L.1    Baldwin, C.L.2    Bolis, C.M.3
  • 36
    • 80054093788 scopus 로고
    • Novel scytophycins and their manufacture and use as cytotoxic neoplasm inhibitors. U.S.A Patent 9306825, September 9
    • Patterson GML, Moore RE, Carmeli S, Smith CD, Kimura LH. Novel scytophycins and their manufacture and use as cytotoxic neoplasm inhibitors. U.S.A Patent 9306825, September 9, 1992.
    • (1992)
    • Patterson, G.M.L.1    Moore, R.E.2    Carmeli, S.3    Smith, C.D.4    Kimura, L.H.5
  • 38
    • 0028967310 scopus 로고
    • Korn ED. Swinholide A is a microfilament disrupting marine toxin that stabilizes actin dimers and severs actin filaments
    • Bubb MR, Spector I, Bershadsky AD, Korn ED. Swinholide A is a microfilament disrupting marine toxin that stabilizes actin dimers and severs actin filaments. J Biol Chem 1995; 270: 3463-3466
    • (1995) J Biol Chem , vol.270 , pp. 3463-3466
    • Bubb, M.R.1    Spector, I.2    Bershadsky, A.D.3
  • 39
    • 0030777109 scopus 로고    scopus 로고
    • Microfilament depletion and circumvention of multiple drug resistance by sphinxolides
    • Zhang X, Minale L, Zampella A, Smith CD. Microfilament depletion and circumvention of multiple drug resistance by sphinxolides. Cancer Res 1997; 57: 3751-3758.
    • (1997) Cancer Res , vol.57 , pp. 3751-3758
    • Zhang, X.1    Minale, L.2    Zampella, A.3    Smith, C.D.4
  • 40
    • 17444379382 scopus 로고    scopus 로고
    • Isolation of swinholide A and related glycosylated derivatives from two field collections of marine cyanobacteria
    • Andrianasolo EH, Gross H, Goeger D, et al. Isolation of swinholide A and related glycosylated derivatives from two field collections of marine cyanobacteria. Org Lett 2005; 7: 1375-1378.
    • (2005) Org Lett , vol.7 , pp. 1375-1378
    • Andrianasolo, E.H.1    Gross, H.2    Goeger, D.3
  • 42
    • 0033806562 scopus 로고    scopus 로고
    • Microcyclamide, a cytotoxic cyclic hexapeptide from the cyanobacterium Microcystis aeruginosa
    • Ishida K, Nakagawa H, Murakami M. Microcyclamide, a cytotoxic cyclic hexapeptide from the cyanobacterium Microcystis aeruginosa. J Nat Prod 2000; 63: 1315-1317.
    • (2000) J Nat Prod , vol.63 , pp. 1315-1317
    • Ishida, K.1    Nakagawa, H.2    Murakami, M.3
  • 43
    • 0026593177 scopus 로고
    • Westiellamide, a Bistratamide-related Cyclic Peptide From the Blue- Green Alga Westiellopsis Prolifica
    • Prinsep MR, Moore RE, Levine IA, Patterson GML. Westiellamide, a bistratamide-related cyclic peptide from the blue- green alga Westiellopsis prolifica. J Nat Prod 1992; 55: 140-142
    • (1992) J Nat Prod , vol.55 , pp. 140-142
    • Prinsep, M.R.1    Moore, R.E.2    Levine, I.A.3    Patterson, G.M.L.4
  • 44
    • 0029895437 scopus 로고    scopus 로고
    • Dendroamides, new cyclic hexapeptides from a blue-green alga. multidrug-resistance reversing activity of dendroamide A
    • Ogino J, Moore RE, Patterson GM, Smith CD. Dendroamides, new cyclic hexapeptides from a blue-green alga. multidrug-resistance reversing activity of dendroamide A. J Nat Prod 1996; 59: 581-6.
    • (1996) J Nat Prod , vol.59 , pp. 581-586
    • Ogino, J.1    Moore, R.E.2    Patterson, G.M.3    Smith, C.D.4
  • 45
    • 40849085215 scopus 로고    scopus 로고
    • Microcyclamide biosynthesis in two strains of Microcystis aeruginosa: from structure to genes and vice versa
    • Ziemert N, Ishida K, Quillardet P, et al. Microcyclamide biosynthesis in two strains of Microcystis aeruginosa: from structure to genes and vice versa. Appl Environ Microbiol 2008; 74: 1791-7.
    • (2008) Appl Environ Microbiol , vol.74 , pp. 1791-1797
    • Ziemert, N.1    Ishida, K.2    Quillardet, P.3
  • 46
    • 0033585089 scopus 로고    scopus 로고
    • Calothrixins A and B, novel pentacyclic metabolites from Calothrix cyanobacteria with potent activity against malaria parasites and human cancer cells
    • Rickards RW, Rothschild JM, Willis AC, et al. Calothrixins A and B, novel pentacyclic metabolites from Calothrix cyanobacteria with potent activity against malaria parasites and human cancer cells. Tetrahedron 1999; 55: 13513-13520.
    • (1999) Tetrahedron , vol.55 , pp. 13513-13520
    • Rickards, R.W.1    Rothschild, J.M.2    Willis, A.C.3
  • 47
    • 65249155938 scopus 로고    scopus 로고
    • Calothrixins, a new class of human DNA topoisomerase I poisons
    • Khan QA, Lu J, Hecht SM. Calothrixins, a new class of human DNA topoisomerase I poisons. J Nat Prod 2009; 72: page 442
    • (2009) J Nat Prod , vol.72 , pp. 442
    • Khan, Q.A.1    Lu, J.2    Hecht, S.M.3
  • 49
    • 33644942122 scopus 로고    scopus 로고
    • Identification of peptide metabolites of Microcystis (Cyanobacteria) that inhibit trypsin-like activity in planktonic herbivorous Daphnia (Cladocera)
    • Czarnecki O, Henning M, Lippert I, Welker M. Identification of peptide metabolites of Microcystis (Cyanobacteria) that inhibit trypsin-like activity in planktonic herbivorous Daphnia (Cladocera). Environ Microbiol 2006; 8: 77-87.
    • (2006) Environ Microbiol , vol.8 , pp. 77-87
    • Czarnecki, O.1    Henning, M.2    Lippert, I.3    Welker, M.4
  • 50
    • 25144508725 scopus 로고    scopus 로고
    • Frequency of inhibitors of daphnid trypsin in the widely distributed cyanobacterial genus Planktothrix
    • Rohrlack T, Christoffersen K, Friberg-Jensen U. Frequency of inhibitors of daphnid trypsin in the widely distributed cyanobacterial genus Planktothrix. Environ Microbiol 2005; 7: 1667-1669.
    • (2005) Environ Microbiol , vol.7 , pp. 1667-1669
    • Rohrlack, T.1    Christoffersen, K.2    Friberg-Jensen, U.3
  • 51
    • 21044456863 scopus 로고    scopus 로고
    • Cinanserin is an inhibitor of the 3C- like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro
    • Chen L, Gui C, Luo X, et al. Cinanserin is an inhibitor of the 3C- like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro. J Virol 2005; 79: 7095-7103.
    • (2005) J Virol , vol.79 , pp. 7095-7103
    • Chen, L.1    Gui, C.2    Luo, X.3
  • 52
    • 2342667387 scopus 로고    scopus 로고
    • The development of proteasome inhibitors as anticancer drugs
    • Adams J. The development of proteasome inhibitors as anticancer drugs. Cancer Cell 2004; 5: 417-421.
    • (2004) Cancer Cell , vol.5 , pp. 417-421
    • Adams, J.1
  • 53
    • 0024431034 scopus 로고
    • The refined 1.9 A crystal structure of human alpha-thrombin: Interaction with D-Phe-Pro-Arg chloromethylketone and significance of the Tyr-Pro-Pro-Trp insertion segment
    • Bode W, Mayr I, Baumann U, Huber R, Stone SR, Hofsteenge J. The refined 1.9 A crystal structure of human alpha-thrombin: interaction with D-Phe-Pro-Arg chloromethylketone and significance of the Tyr-Pro-Pro-Trp insertion segment. EMBO J. 1989; 8: 3467-3475.
    • (1989) EMBO J , vol.8 , pp. 3467-3475
    • Bode, W.1    Mayr, I.2    Baumann, U.3    Huber, R.4    Stone, S.R.5    Hofsteenge, J.6
  • 54
    • 3042538418 scopus 로고    scopus 로고
    • The ubiquitin system: From basic mechanisms to the patient bed
    • Ciechanover A, Iwai K. The ubiquitin system: from basic mechanisms to the patient bed. IUBMB Life 2004; 56: 193-201
    • (2004) IUBMB Life , vol.56 , pp. 193-201
    • Ciechanover, A.1    Iwai, K.2
  • 55
    • 0028018268 scopus 로고
    • The ubiquitin-proteasome proteolytic pathway
    • Ciechanover A. The ubiquitin-proteasome proteolytic pathway. Cell 1994; 79: 13-21.
    • (1994) Cell , vol.79 , pp. 13-21
    • Ciechanover, A.1
  • 56
    • 0028236160 scopus 로고
    • Aeruginosin 298-A, a thrombin and trypsin-inhibitor from the blue- green alga Microcystis aeruginosa (NIES-298)
    • Murakami M, Okita Y, Matsuda H, Okino T, Yamaguchi K. Aeruginosin 298-A, a thrombin and trypsin-inhibitor from the blue- green alga Microcystis aeruginosa (NIES-298). Tetrahedron Lett 1994; 35: 3129-3132.
    • (1994) Tetrahedron Lett , vol.35 , pp. 3129-3132
    • Murakami, M.1    Okita, Y.2    Matsuda, H.3    Okino, T.4    Yamaguchi, K.5
  • 57
    • 0033609787 scopus 로고    scopus 로고
    • Carmeli S. Inhibitors of Serine Proteases From a Waterbloom of the Cyanobacterium Microcystis Sp
    • Banker R, Carmeli S. Inhibitors of serine proteases from a waterbloom of the cyanobacterium Microcystis sp. Tetrahedron 1999; 55: 10835-10844.
    • (1999) Tetrahedron , vol.55 , pp. 10835-10844
    • Banker, R.1
  • 58
    • 0037073204 scopus 로고    scopus 로고
    • Dysinosin A: a novel inhibitor of factor VIIa and thrombin from a new genus and species of Australian sponge of the family Dysideidae
    • Carroll AR, Pierens GK, Fechner G, et al. Dysinosin A: a novel inhibitor of factor VIIa and thrombin from a new genus and species of Australian sponge of the family Dysideidae. J Am Chem Soc. 2002; 124: 13340-1.
    • (2002) J Am Chem Soc , vol.124 , pp. 13340-13341
    • Carroll, A.R.1    Pierens, G.K.2    Fechner, G.3
  • 59
    • 4344670607 scopus 로고    scopus 로고
    • Dysinosins B-D, inhibitors of factor VIIa and thrombin from the Australian sponge Lamellodysidea chlorea
    • Carroll AR, Buchanan MS, Edser A, Hyde E, Simpson M, Quinn RJ. Dysinosins B-D, inhibitors of factor VIIa and thrombin from the Australian sponge Lamellodysidea chlorea. J Nat Prod 2004; 67: 1291-1294.
    • (2004) J Nat Prod , vol.67 , pp. 1291-1294
    • Carroll, A.R.1    Buchanan, M.S.2    Edser, A.3    Hyde, E.4    Simpson, M.5    Quinn, R.J.6
  • 60
    • 33747596469 scopus 로고    scopus 로고
    • Total synthesis and structural confirmation of chlorodysinosin A
    • Hanessian S, Del Valle JR, Xue Y, Blomberg N. Total synthesis and structural confirmation of chlorodysinosin A. J Am Chem Soc 2006; 128: 10491-10495.
    • (2006) J Am Chem Soc , vol.128 , pp. 10491-10495
    • Hanessian, S.1    del Valle, J.R.2    Xue, Y.3    Blomberg, N.4
  • 61
    • 34249316869 scopus 로고    scopus 로고
    • Structure-based organic synthesis of unnatural aeruginosin hybrids as potent inhibitors of thrombin
    • Hanessian S, Ersmark K, Wang X, et al. Structure-based organic synthesis of unnatural aeruginosin hybrids as potent inhibitors of thrombin. Bioorg Med Chem Lett 2007; 17: 3480-3485.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 3480-3485
    • Hanessian, S.1    Ersmark, K.2    Wang, X.3
  • 62
    • 41249098707 scopus 로고    scopus 로고
    • Chemistry and biology of the aeruginosin family of serine protease inhibitors
    • Ersmark K, Del Valle JR, Hanessian S. Chemistry and biology of the aeruginosin family of serine protease inhibitors. Angew Chem Int Ed 2008; 47: 1202-1223.
    • (2008) Angew Chem Int Ed , vol.47 , pp. 1202-1223
    • Ersmark, K.1    del Valle, J.R.2    Hanessian, S.3
  • 63
    • 0141762447 scopus 로고    scopus 로고
    • New cyanopeptide-derived low molecular weight thrombin inhibitors
    • Radau G, Gebel J, Rauh D. New cyanopeptide-derived low molecular weight thrombin inhibitors. Arch Pharm (Weinheim) 2003; 336: 372-380.
    • (2003) Arch Pharm (Weinheim) , vol.336 , pp. 372-380
    • Radau, G.1    Gebel, J.2    Rauh, D.3
  • 64
    • 0034860802 scopus 로고    scopus 로고
    • Isolation of new protein phosphatase inhibitors from two cyanobacteria species, Planktothrix spp
    • Sano T, Usui T, Ueda K, Osada H, Kaya K. Isolation of new protein phosphatase inhibitors from two cyanobacteria species, Planktothrix spp. J Nat Prod 2001; 64: 1052-1055.
    • (2001) J Nat Prod , vol.64 , pp. 1052-1055
    • Sano, T.1    Usui, T.2    Ueda, K.3    Osada, H.4    Kaya, K.5
  • 65
    • 59349093212 scopus 로고    scopus 로고
    • New peptolides from the cyanobacterium Nostoc insulare as selective and potent inhibitors of human leukocyte elastase
    • Mehner C, Muller D, Kehraus S, Hautmann S, Gutschow M, Konig GM. New peptolides from the cyanobacterium Nostoc insulare as selective and potent inhibitors of human leukocyte elastase. ChemBioChem 2008; 9: 2692-2703.
    • (2008) ChemBioChem , vol.9 , pp. 2692-2703
    • Mehner, C.1    Muller, D.2    Kehraus, S.3    Hautmann, S.4    Gutschow, M.5    Konig, G.M.6
  • 66
    • 0031027751 scopus 로고    scopus 로고
    • Nostopeptins A and B, elastase inhibitors from the cyanobacterium Nostoc minutum
    • Okino T, Qi S, Matsuda H, Murakami M, Yamaguchi K. Nostopeptins A and B, elastase inhibitors from the cyanobacterium Nostoc minutum. J Nat Prod 1997; 60: 158-161.
    • (1997) J Nat Prod , vol.60 , pp. 158-161
    • Okino, T.1    Qi, S.2    Matsuda, H.3    Murakami, M.4    Yamaguchi, K.5
  • 67
    • 33750446641 scopus 로고    scopus 로고
    • Unusual cyclic peptides from the marine cyanobacterium Oscillatoria sp
    • Plaza A, Bewley CA. Largamides A-H, unusual cyclic peptides from the marine cyanobacterium Oscillatoria sp. J Org Chem 2006; 71: 6898-6907.
    • (2006) J Org Chem , vol.71 , pp. 6898-6907
    • Plaza, A.1    Bewley, C.A.2    Largamides, A.-H.3
  • 68
    • 33847063427 scopus 로고    scopus 로고
    • Lyngbyastatin 4, a dolastatin 13 analogue with elastase and chymotrypsin inhibitory activity from the marine cyanobacterium Lyngbya confervoides
    • Matthew S, Ross C, Rocca JR, Paul VJ, Luesch H. Lyngbyastatin 4, a dolastatin 13 analogue with elastase and chymotrypsin inhibitory activity from the marine cyanobacterium Lyngbya confervoides. J Nat Prod 2007; 70: 124-127.
    • (2007) J Nat Prod , vol.70 , pp. 124-127
    • Matthew, S.1    Ross, C.2    Rocca, J.R.3    Paul, V.J.4    Luesch, H.5
  • 69
    • 36348972843 scopus 로고    scopus 로고
    • Lyngbyastatins 5-7, potent elastase inhibitors from floridian marine cyanobacteria, Lyngbya spp
    • Taori K, Matthew S, Rocca JR, Paul VJ, Luesch H. Lyngbyastatins 5-7, potent elastase inhibitors from floridian marine cyanobacteria, Lyngbya spp. J Nat Prod 2007; 70: 1593-1600.
    • (2007) J Nat Prod , vol.70 , pp. 1593-1600
    • Taori, K.1    Matthew, S.2    Rocca, J.R.3    Paul, V.J.4    Luesch, H.5
  • 70
    • 54149108953 scopus 로고    scopus 로고
    • A and B, serine protease inhibitors with different selectivity profiles from a marine cyanobacterium, Lyngbya sp
    • Taori K, Paul VJ, Luesch H. Kempopeptins A and B, serine protease inhibitors with different selectivity profiles from a marine cyanobacterium, Lyngbya sp. J Nat Prod 2008; 71: 1625-1629
    • (2008) J Nat Prod , vol.71 , pp. 1625-1629
    • Taori, K.1    Paul, V.J.2    Kempopeptins Luesch, H.3
  • 71
    • 40849117988 scopus 로고    scopus 로고
    • Pompanopeptins A and B, new cyclic peptides from the marine cyanobacterium Lyngbya confervoides
    • Matthew S, Ross C, Paul VJ, Luesch H. Pompanopeptins A and B, new cyclic peptides from the marine cyanobacterium Lyngbya confervoides. Tetrahedron 2008; 64: 4081-9.
    • (2008) Tetrahedron , vol.64 , pp. 4081-4089
    • Matthew, S.1    Ross, C.2    Paul, V.J.3    Luesch, H.4
  • 72
    • 39049108641 scopus 로고    scopus 로고
    • Symplocamide A, a potent cytotoxin and chymotrypsin inhibitor from the marine cyanobacterium Symploca sp
    • Linington RG, Edwards DJ, Shuman CF, McPhail KL, Matainaho T, Gerwick WH. Symplocamide A, a potent cytotoxin and chymotrypsin inhibitor from the marine cyanobacterium Symploca sp. J Nat Prod 2008; 71: 22-27.
    • (2008) J Nat Prod , vol.71 , pp. 22-27
    • Linington, R.G.1    Edwards, D.J.2    Shuman, C.F.3    McPhail, K.L.4    Matainaho, T.5    Gerwick, W.H.6
  • 73
    • 0028518887 scopus 로고
    • Atomic structure of the trypsin-A90720A complex: A unified approach to structure and function
    • Lee AY, Smitka TA, Bonjouklian R, Clardy J. Atomic structure of the trypsin-A90720A complex: a unified approach to structure and function. Chem Biol 1994; 1: 113-117.
    • (1994) Chem Biol , vol.1 , pp. 113-117
    • Lee, A.Y.1    Smitka, T.A.2    Bonjouklian, R.3    Clardy, J.4
  • 75
    • 0025107820 scopus 로고
    • Microviridin. A novel tricyclic depsipeptide from the toxic cyanobacterium Microcystis viridis
    • Ishitsuka MO, Kusumi T, Kakisawa H, Kaya K, Watanabe MM. Microviridin. A novel tricyclic depsipeptide from the toxic cyanobacterium Microcystis viridis. J Am Chem Soc 1990; 112: 8180-8182.
    • (1990) J Am Chem Soc , vol.112 , pp. 8180-8182
    • Ishitsuka, M.O.1    Kusumi, T.2    Kakisawa, H.3    Kaya, K.4    Watanabe, M.M.5
  • 76
    • 0029091489 scopus 로고
    • New Microviridins, Elastase Inhibitors From the Blue-green Alga Microcystis Aeruginosa
    • Okino T, Matsuda H, Murakami M, Yamaguchi K. New microviridins, elastase inhibitors from the blue-green alga Microcystis aeruginosa. Tetrahedron 1995; 51: 10679-10686
    • (1995) Tetrahedron , vol.51 , pp. 10679-10686
    • Okino, T.1    Matsuda, H.2    Murakami, M.3    Yamaguchi, K.4
  • 77
    • 0034723324 scopus 로고    scopus 로고
    • Non-toxic peptides from toxic cyanobacteria, Oscillatoria agardhii
    • Fujii K, Sivonen K, Naganawa E, Harada K. Non-toxic peptides from toxic cyanobacteria, Oscillatoria agardhii. Tetrahedron 2000; 56: 725-33.
    • (2000) Tetrahedron , vol.56 , pp. 725-733
    • Fujii, K.1    Sivonen, K.2    Naganawa, E.3    Harada, K.4
  • 78
    • 0030913076 scopus 로고    scopus 로고
    • Microviridins, Elastase Inhibitors From the Cyanobacterium Nostoc Minutum (NIES-26)
    • Murakami M, Sun Q, Ishida K, Matsuda H, Okino T, Yamaguchi K. Microviridins, elastase inhibitors from the cyanobacterium Nostoc minutum (NIES-26). Phytochemistry 1997; 45: 1197-1202.
    • (1997) Pytochemistry , vol.45 , pp. 1197-1202
    • Murakami, M.1    Sun, Q.2    Ishida, K.3    Matsuda, H.4    Okino, T.5    Yamaguchi, K.6
  • 79
    • 0001059763 scopus 로고    scopus 로고
    • Microviridins D-F, serine protease inhibitors from the cyanobacterium Oscillatoria agardhii (NIES-204)
    • Shin HJ, Murakami M, Matsuda H, Yamaguchi K. Microviridins D-F, serine protease inhibitors from the cyanobacterium Oscillatoria agardhii (NIES-204). Tetrahedron 1996; 52: 8159-68.
    • (1996) Tetrahedron , vol.52 , pp. 8159-8168
    • Shin, H.J.1    Murakami, M.2    Matsuda, H.3    Yamaguchi, K.4
  • 82
    • 0030768940 scopus 로고    scopus 로고
    • Mozamides A and B, cyclic peptides from a Theonellid sponge from Mozambique
    • Schmidt EW, Harper MK, Faulkner DJ. Mozamides A and B, cyclic peptides from a Theonellid sponge from Mozambique. J Nat Prod 1997; 60: 779-82.
    • (1997) J Nat Prod , vol.60 , pp. 779-782
    • Schmidt, E.W.1    Harper, M.K.2    Faulkner, D.J.3
  • 84
    • 0025733727 scopus 로고
    • Konbamide, a novel peptide with calmodulin antagonistic activity from the Okinawan marine sponge Theonella sp
    • Kobayashi J, Sato M, Murayama T, et al. Konbamide, a novel peptide with calmodulin antagonistic activity from the Okinawan marine sponge Theonella sp. J Chem Soc, Chem Commun 1991: 1050-1052.
    • (1991) J Chem Soc, Chem Commun , pp. 1050-1052
    • Kobayashi, J.1    Sato, M.2    Murayama, T.3
  • 85
    • 0032507906 scopus 로고    scopus 로고
    • Keramamides K and L, new cyclic peptides containing unusual tryptophan residue from Theonella sponge
    • Uemoto H, Yahiro Y, Shigemori H, et al. Keramamides K and L, new cyclic peptides containing unusual tryptophan residue from Theonella sponge. Tetrahedron 1998; 54: 6719-24.
    • (1998) Tetrahedron , vol.54 , pp. 6719-6724
    • Uemoto, H.1    Yahiro, Y.2    Shigemori, H.3
  • 86
    • 84961486590 scopus 로고
    • A new type of carboxypeptidase A inhibitor: Design, synthesis, and mechanistic implication
    • Kim DH, Kim YM, Li ZH, et al. A new type of carboxypeptidase A inhibitor: design, synthesis, and mechanistic implication. Pure Appl Chem 1994; 66: 721-728.
    • (1994) Pure Appl Chem , vol.66 , pp. 721-728
    • Kim, D.H.1    Kim, Y.M.2    Li, Z.H.3
  • 87
    • 80054115233 scopus 로고    scopus 로고
    • Use of cyclic anabaenopeptin-type peptides for the treatment of a condition wherein inhibition of carboxypeptidase U is beneficial, novel anabaenopeptin derivatives and intermediates thereof. U.S.A. Patent 2005039617, October
    • Bjoerquist P, Buchanan M, Campitelli M, et al. Use of cyclic anabaenopeptin-type peptides for the treatment of a condition wherein inhibition of carboxypeptidase U is beneficial, novel anabaenopeptin derivatives and intermediates thereof. U.S.A. Patent 2005039617, October 28, 2004.
    • (2004) , pp. 28
    • Bjoerquist, P.1    Buchanan, M.2    Campitelli, M.3    Et al.4
  • 88
    • 67749145269 scopus 로고    scopus 로고
    • Comparative study of inhibitory antibody derivatives towards thrombin activatable fibrinolysis inhibitor
    • Develter J, Dewilde M, Gils A, Declerck PJ. Comparative study of inhibitory antibody derivatives towards thrombin activatable fibrinolysis inhibitor. Thromb Haemost 2009; 102: 69-75.
    • (2009) Thromb Haemost , vol.102 , pp. 69-75
    • Develter, J.1    Dewilde, M.2    Gils, A.3    Declerck, P.J.4
  • 89
    • 0030742896 scopus 로고    scopus 로고
    • Thrombin, thrombomodulin and TAFI in the molecular link between coagulation and fibrinolysis
    • Nesheim M, Wang W, Boffa M, Nagashima M, Morser J, Bajzar L. Thrombin, thrombomodulin and TAFI in the molecular link between coagulation and fibrinolysis. Thromb Haemost 1997; 78: 386-391.
    • (1997) Thromb Haemost , vol.78 , pp. 386-391
    • Nesheim, M.1    Wang, W.2    Boffa, M.3    Nagashima, M.4    Morser, J.5    Bajzar, L.6
  • 90
    • 67650457881 scopus 로고    scopus 로고
    • Synthesis and structure-activity correlation of a brunsvicamide-inspired cyclopeptide collection
    • Walther T, Renner S, Waldmann H, Arndt H. Synthesis and structure-activity correlation of a brunsvicamide-inspired cyclopeptide collection. ChemBioChem 2009; 10: 1153-62.
    • (2009) ChemBioChem , vol.10 , pp. 1153-1162
    • Walther, T.1    Renner, S.2    Waldmann, H.3    Arndt, H.4
  • 91
    • 0027514449 scopus 로고
    • Microginin, an angiotensin converting enzyme inhibitor from the blue-green alga Microcystis aeruginosa
    • Okino T, Matsuda H, Murakami M, Yamaguchi K. Microginin, an angiotensin converting enzyme inhibitor from the blue-green alga Microcystis aeruginosa. Tetrahedron Lett 1993; 34: 501-4.
    • (1993) Tetrahedron Lett , vol.34 , pp. 501-504
    • Okino, T.1    Matsuda, H.2    Murakami, M.3    Yamaguchi, K.4
  • 92
    • 0030837178 scopus 로고    scopus 로고
    • Microginin FR1, a linear peptide from a water bloom of Microcystis species
    • Neumann U, Forchert A, Flury T, Weckesser J. Microginin FR1, a linear peptide from a water bloom of Microcystis species. FEMS Microbiol Lett 1997; 153: 475-8.
    • (1997) FEMS Microbiol Lett , vol.153 , pp. 475-478
    • Neumann, U.1    Forchert, A.2    Flury, T.3    Weckesser, J.4
  • 93
    • 0032847006 scopus 로고    scopus 로고
    • Five new cyanobacterial peptides from water bloom materials of lake Teganuma (Japan)
    • Kodani S, Suzuki S, Ishida K, Murakami M. Five new cyanobacterial peptides from water bloom materials of lake Teganuma (Japan). FEMS Microbiol Lett 1999; 178: 343-8.
    • (1999) FEMS Microbiol Lett , vol.178 , pp. 343-348
    • Kodani, S.1    Suzuki, S.2    Ishida, K.3    Murakami, M.4
  • 94
    • 0034721686 scopus 로고    scopus 로고
    • Microginins, zinc metalloproteases inhibitors from the cyanobacterium Microcystis aeruginosa
    • Ishida K, Kato T, Murakami M, Watanabe M, Watanabe MF. Microginins, zinc metalloproteases inhibitors from the cyanobacterium Microcystis aeruginosa. Tetrahedron 2000; 56: 8643-56.
    • (2000) Tetrahedron , vol.56 , pp. 8643-8656
    • Ishida, K.1    Kato, T.2    Murakami, M.3    Watanabe, M.4    Watanabe, M.F.5
  • 95
    • 77449137096 scopus 로고    scopus 로고
    • Secondary prevention of coronary artery disease
    • Hall SL, Lorenc T. Secondary prevention of coronary artery disease. Am Fam Physician 2010; 81: 289-96.
    • (2010) Am Fam Physician , vol.81 , pp. 289-296
    • Hall, S.L.1    Lorenc, T.2
  • 96
    • 0019507433 scopus 로고
    • Captopril approved for hypertension
    • Captopril approved for hypertension. FDA Drug Bull 1981; 11: 10- 11.
    • (1981) FDA Drug Bull , vol.11 , pp. 10-11
  • 97
    • 0027008013 scopus 로고
    • Use of ACE inhibitors in the treatment of cardiovascular disease
    • Gums JG. Use of ACE inhibitors in the treatment of cardiovascular disease. Am Pharm 1992; NS32: 62-70.
    • (1992) Am Pharm , vol.NS32 , pp. 62-70
    • Gums, J.G.1
  • 99
    • 0001598577 scopus 로고
    • Hapalindoles: New alkaloids from the blue-green alga Hapalosiphon fontinalis
    • Moore RE, Cheuk C, Patterson GML. Hapalindoles: new alkaloids from the blue-green alga Hapalosiphon fontinalis. J Am Chem Soc 1984; 106: 6456-7.
    • (1984) J Am Chem Soc , vol.106 , pp. 6456-6457
    • Moore, R.E.1    Cheuk, C.2    Patterson, G.M.L.3
  • 100
    • 66449107185 scopus 로고    scopus 로고
    • Antimicrobial ambiguine isonitriles from the cyanobacterium Fischerella ambigua
    • Mo S, Krunic A, Chlipala G, Orjala J. Antimicrobial ambiguine isonitriles from the cyanobacterium Fischerella ambigua. J Nat Prod 2009; 72: 894-9.
    • (2009) J Nat Prod , vol.72 , pp. 894-899
    • Mo, S.1    Krunic, A.2    Chlipala, G.3    Orjala, J.4
  • 101
    • 58849128316 scopus 로고    scopus 로고
    • Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindo- linones via a redox economic approach
    • Richter JM, Ishihara Y, Masuda T, et al. Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindo- linones via a redox economic approach. J Am Chem Soc 2008; 130: 17938-54.
    • (2008) J Am Chem Soc , vol.130 , pp. 17938-54
    • Richter, J.M.1    Ishihara, Y.2    Masuda, T.3
  • 102
    • 0035868463 scopus 로고    scopus 로고
    • Inhibition of bacterial RNA polymerase by the cyanobacterial metabolites 12-epi-hapalindole E isonitrile and calothrixin
    • Doan NT, Stewart PR, Smith GD. Inhibition of bacterial RNA polymerase by the cyanobacterial metabolites 12-epi-hapalindole E isonitrile and calothrixin A. FEMS Microbiol Lett 2001; 196: 135- 9.
    • (2001) A. FEMS Microbiol Lett , vol.196 , pp. 135-139
    • Doan, N.T.1    Stewart, P.R.2    Smith, G.D.3
  • 103
    • 0031733197 scopus 로고    scopus 로고
    • Isolation of a nitrile- containing indole alkaloid from the terrestrial blue-green alga Hapalosiphon delicatulus
    • Huber U, Moore RE, Patterson GML. Isolation of a nitrile- containing indole alkaloid from the terrestrial blue-green alga Hapalosiphon delicatulus. J Nat Prod 1998; 61: 1304-6.
    • (1998) J Nat Prod , vol.61 , pp. 1304-1306
    • Huber, U.1    Moore, R.E.2    Patterson, G.M.L.3
  • 105
    • 33845282176 scopus 로고
    • Hapalindoles, antibacterial and antimycotic alkaloids from the cyanophyte Hapalosiphon fontinalis
    • Moore RE, Cheuk C, Yang XQG, et al. Hapalindoles, antibacterial and antimycotic alkaloids from the cyanophyte Hapalosiphon fontinalis. J Org Chem 1987; 52: 1036-43.
    • (1987) J Org Chem , vol.52 , pp. 1036-1043
    • Moore, R.E.1    Cheuk, C.2    Yang, X.Q.G.3
  • 107
    • 0026725094 scopus 로고
    • A new isonitrile from the terrestrial blue-green alga Fischerella muscicola
    • Park A, Moore RE, Patterson GML. Fischerindole L, a new isonitrile from the terrestrial blue-green alga Fischerella muscicola. Tetrahedron Lett 1992; 33: 3257-60.
    • (1992) Tetrahedron Lett , vol.33 , pp. 3257-3260
    • Park, A.1    Moore, R.E.2    Patterson, G.M.L.3    Fischerindole, L.4
  • 108
  • 109
    • 0027973653 scopus 로고
    • Welwitindolinones, unusual alkaloids from the blue-green algae Hapalosiphon welwitschii and Westiella intricata. Relationship to fischerindoles and hapalinodoles
    • Stratmann K, Moore RE, Bonjouklian R, et al. Welwitindolinones, unusual alkaloids from the blue-green algae Hapalosiphon welwitschii and Westiella intricata. Relationship to fischerindoles and hapalinodoles. J Am Chem Soc 1994; 116: 9935-42
    • (1994) J Am Chem Soc , vol.116 , pp. 9935-9942
    • Stratmann, K.1    Moore, R.E.2    Bonjouklian, R.3
  • 110
    • 33947363667 scopus 로고    scopus 로고
    • Antimicrobial ambiguines from the cyanobacterium Fischerella sp. collected in Israel
    • Raveh A, Carmeli S. Antimicrobial ambiguines from the cyanobacterium Fischerella sp. collected in Israel. J Nat Prod 2007; 70: 196-201.
    • (2007) J Nat Prod , vol.70 , pp. 196-201
    • Raveh, A.1    Carmeli, S.2
  • 111
    • 0026606140 scopus 로고
    • Ambiguine isonitriles, fungicidal hapalindole-type alkaloids from three genera of blue- green algae belonging to the Stigonemataceae
    • Smitka TA, Bonjouklian R, Doolin L, et al. Ambiguine isonitriles, fungicidal hapalindole-type alkaloids from three genera of blue- green algae belonging to the Stigonemataceae. J Org Chem 1992; 57: 857-61.
    • (1992) J Org Chem , vol.57 , pp. 857-861
    • Smitka, T.A.1    Bonjouklian, R.2    Doolin, L.3
  • 112
    • 80054120836 scopus 로고
    • Preparation of hapalindole-related alkaloids from blue-green algae. U.S.A. Patent 5292650
    • Bonjouklian R, Moore RE, Patterson GML, Smitka TA. Preparation of hapalindole-related alkaloids from blue-green algae. U.S.A. Patent 5292650, September 16, 1992.
    • (1992) September , pp. 16
    • Bonjouklian, R.1    Moore, R.E.2    Patterson, G.M.L.3    Smitka, T.A.4
  • 113
    • 80054107163 scopus 로고
    • A89271 factors Smitka TA, Patent 5457119, October
    • Bonjouklian R, Moore RE, Patterson GML, Smitka TA. A89271 factors and processes for their production. U.S.A. Patent 5457119, October 10, 1995.
    • (1995) , pp. 10
    • Bonjouklian, R.1    Moore, R.E.2    Patterson, G.M.L.3
  • 114
    • 80054112761 scopus 로고
    • Patent 4755610, July, Patterson GML. Hapalindoles. U.S.A
    • Moore RE, Patterson GML. Hapalindoles. U.S.A. Patent 4755610, July 5, 1988.
    • (1988) , pp. 5
    • Moore, R.E.1
  • 115
    • 33746884706 scopus 로고    scopus 로고
    • Identification of an antimicrobial entity from the cyanobacterium Fischerella sp. isolated from bark of Azadirachta indica (Neem) tree
    • Ravi KA, Arunima S, Akhilesh PS, et al. Identification of an antimicrobial entity from the cyanobacterium Fischerella sp. isolated from bark of Azadirachta indica (Neem) tree. J Appl Phycol 2006; 18: 33-9.
    • (2006) J Appl Phycol , vol.18 , pp. 33-39
    • Ravi, K.A.1    Arunima, S.2    Akhilesh, P.S.3
  • 116
    • 0025950423 scopus 로고
    • Tjipanazoles, new antifungal agents from the blue-green alga Tolypothrix tjipanasensis
    • Bonjouklian R, Smitka TA, Doolin LE, et al. Tjipanazoles, new antifungal agents from the blue-green alga Tolypothrix tjipanasensis. Tetrahedron 1991; 47: 7739-50.
    • (1991) Tetrahedron , vol.47 , pp. 7739-7750
    • Bonjouklian, R.1    Smitka, T.A.2    Doolin, L.E.3
  • 117
    • 17444432922 scopus 로고    scopus 로고
    • Ambigol C and 2,4- dichlorobenzoic acid, natural products produced by the terrestrial cyanobacterium Fischerella ambigua
    • Wright AD, Papendorf O, Koig GM. Ambigol C and 2,4- dichlorobenzoic acid, natural products produced by the terrestrial cyanobacterium Fischerella ambigua. J Nat Prod 2005; 68: 459-61.
    • (2005) J Nat Prod , vol.68 , pp. 459-461
    • Wright, A.D.1    Papendorf, O.2    Koig, G.M.3
  • 118
    • 71749093116 scopus 로고    scopus 로고
    • Natural product leads for drug discovery: Isolation, synthesis and biological evaluation of 6- cyano-5-methoxyindolo[2,3-a]carbazole based ligands as antibacterial agents
    • Guo S, Tipparaju SK, Pegan SD, et al. Natural product leads for drug discovery: Isolation, synthesis and biological evaluation of 6- cyano-5-methoxyindolo[2,3-a]carbazole based ligands as antibacterial agents. Bioorg Med Chem 2009; 17: 7126-30.
    • (2009) Bioorg Med Chem , vol.17 , pp. 7126-7130
    • Guo, S.1    Tipparaju, S.K.2    Pegan, S.D.3
  • 119
  • 120
    • 30544453948 scopus 로고    scopus 로고
    • Nostocarboline: Isolation and synthesis of a new cholinesterase inhibitor from Nostoc 78-12A
    • Becher PG, Beuchat J, Gademann K, Juttner F. Nostocarboline: Isolation and synthesis of a new cholinesterase inhibitor from Nostoc 78-12A. J Nat Prod 2005; 68: 1793-5.
    • (2005) J Nat Prod , vol.68 , pp. 1793-1795
    • Becher, P.G.1    Beuchat, J.2    Gademann, K.3    Juttner, F.4
  • 121
    • 33644750162 scopus 로고    scopus 로고
    • Potent algicides based on the cyanobacterial alkaloid nostocarboline
    • Blom JF, Brutsch T, Barbaras D, et al. Potent algicides based on the cyanobacterial alkaloid nostocarboline. Org Lett 2006; 8: 737- 40.
    • (2006) Org Lett , vol.8 , pp. 737-740
    • Blom, J.F.1    Brutsch, T.2    Barbaras, D.3    Et al.4
  • 122
    • 47749085441 scopus 로고    scopus 로고
    • Potent and selective antiplasmodial activity of the cyanobacterial alkaloid nostocarbo- line and its dimers
    • Barbaras D, Kaiser M, Brun R, Gademann K. Potent and selective antiplasmodial activity of the cyanobacterial alkaloid nostocarbo- line and its dimers. Bioorg Med Chem Lett 2008; 18: 4413-5.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 4413-4415
    • Barbaras, D.1    Kaiser, M.2    Brun, R.3    Gademann, K.4
  • 123
    • 0032464168 scopus 로고    scopus 로고
    • Antibiotic activity of new cyanobacterial isolates from Australia and Asia against green algae and cyanobacteria
    • Schlegel I, Doan N, de Chazal N, Smith G. Antibiotic activity of new cyanobacterial isolates from Australia and Asia against green algae and cyanobacteria. J Appl Phycol 1998; 10: 471-9.
    • (1998) J Appl Phycol , vol.10 , pp. 471-479
    • Schlegel, I.1    Doan, N.2    de Chazal, N.3    Smith, G.4
  • 124
    • 0030565587 scopus 로고    scopus 로고
    • Fischerellin A, a novel photosystem-II- inhibiting allelochemical of the cyanobacterium Fischerella muscicola with antifungal and herbicidal activity
    • Hagmann L, Jütner F. Fischerellin A, a novel photosystem-II- inhibiting allelochemical of the cyanobacterium Fischerella muscicola with antifungal and herbicidal activity. Tetrahedron Lett 1996; 37: 6539-42.
    • (1996) Tetrahedron Lett , vol.37 , pp. 6539-6542
    • Hagmann, L.1    Jütner, F.2
  • 125
    • 0031013462 scopus 로고    scopus 로고
    • Identification and determination of the absolute configuration of Fischerellin B. A new algicide from the freshwater cyanobacterium Fischerella muscicola (Thuret)
    • Papke U, Gross EM, Francke W. Isolation, identification and determination of the absolute configuration of Fischerellin B. A new algicide from the freshwater cyanobacterium Fischerella muscicola (Thuret). Tetrahedron Lett 1997; 38: 379-82.
    • (1997) Tetrahedron Lett , vol.38 , pp. 379-382
    • Papke, U.1    Gross, E.M.2    Isolation Francke, W.3
  • 126
    • 0032575172 scopus 로고    scopus 로고
    • Nostofungicidine, an antifungal lipopeptide from the field-grown terrestrial blue-green alga Nostoc commune
    • Kajiyama S, Kanzaki H, Kawazu K, Kobayashi A. Nostofungicidine, an antifungal lipopeptide from the field-grown terrestrial blue-green alga Nostoc commune. Tetrahedron Lett 1998; 39: 3737-40.
    • (1998) Tetrahedron Lett , vol.39 , pp. 3737-3740
    • Kajiyama, S.1    Kanzaki, H.2    Kawazu, K.3    Kobayashi, A.4
  • 127
    • 0026587173 scopus 로고
    • Calophycin, a fungicidal cyclic decapeptide from the terrestrial blue-green alga Calothrix fusca
    • Moon SS, Chen J, Moore RE, Patterson GML. Calophycin, a fungicidal cyclic decapeptide from the terrestrial blue-green alga Calothrix fusca. J Org Chem 1992; 57: 1097-103.
    • (1992) J Org Chem , vol.57 , pp. 1097-1103
    • Moon, S.S.1    Chen, J.2    Moore, R.E.3    Patterson, G.M.L.4
  • 128
    • 20444448150 scopus 로고    scopus 로고
    • Hassallidin A, a glycosylated lipopeptide with antifungal activity from the cyanobacterium Hassallia sp
    • Neuhof T, Schmieder P, Preussel K, et al. Hassallidin A, a glycosylated lipopeptide with antifungal activity from the cyanobacterium Hassallia sp. J Nat Prod 2005; 68: 695-700.
    • (2005) J Nat Prod , vol.68 , pp. 695-700
    • Neuhof, T.1    Schmieder, P.2    Preussel, K.3
  • 130
    • 33746918717 scopus 로고    scopus 로고
    • Brunsvicamides A-C: Sponge- related cyanobacterial peptides with Mycobacterium tuberculosis protein tyrosine phosphatase inhibitory activity
    • Muller D, Krick A, Kehraus S, et al. Brunsvicamides A-C: sponge- related cyanobacterial peptides with Mycobacterium tuberculosis protein tyrosine phosphatase inhibitory activity. J Med Chem 2006; 49: 4871-8.
    • (2006) J Med Chem , vol.49 , pp. 4871-4878
    • Muller, D.1    Krick, A.2    Kehraus, S.3
  • 131
    • 0029736945 scopus 로고    scopus 로고
    • Tolypodiol, an antiinflammatory diterpenoid from the cyanobacterium Tolypothrix nodosa
    • Prinsep MR, Thomson RA, West ML, Wylie BL. Tolypodiol, an antiinflammatory diterpenoid from the cyanobacterium Tolypothrix nodosa. J Nat Prod 1996; 59: 786-8.
    • (1996) J Nat Prod , vol.59 , pp. 786-788
    • Prinsep, M.R.1    Thomson, R.A.2    West, M.L.3    Wylie, B.L.4
  • 132
    • 0032940492 scopus 로고    scopus 로고
    • A novel extracellular diterpenoid with antibacterial activity from the cyanobacterium Nostoc commune
    • Jaki B, Orjala J, Sticher O. A novel extracellular diterpenoid with antibacterial activity from the cyanobacterium Nostoc commune. J Nat Prod 1999; 62: 502-3.
    • (1999) J Nat Prod , vol.62 , pp. 502-503
    • Jaki, B.1    Orjala, J.2    Sticher, O.3
  • 133
    • 0034118384 scopus 로고    scopus 로고
    • Novel extracellular diterpenoids with biological activity from the cyanobacterium Nostoc commune
    • Jaki B, Orjala J, Heilmann J, Linden A, Vogler B, Sticher O. Novel extracellular diterpenoids with biological activity from the cyanobacterium Nostoc commune. J Nat Prod 2000; 63: 339-43.
    • (2000) J Nat Prod , vol.63 , pp. 339-343
    • Jaki, B.1    Orjala, J.2    Heilmann, J.3    Linden, A.4    Vogler, B.5    Sticher, O.6
  • 135
    • 73349143320 scopus 로고    scopus 로고
    • An antimicrobial guanidine-bearing sesterterpene from the cultured cyanobacterium Scytonema sp
    • Mo S, Krunic A, Pegan SD, Franzblau SG, Orjala J. An antimicrobial guanidine-bearing sesterterpene from the cultured cyanobacterium Scytonema sp. J Nat Prod 2009; 72: 2043-5.
    • (2009) J Nat Prod , vol.72 , pp. 2043-2045
    • Mo, S.1    Krunic, A.2    Pegan, S.D.3    Franzblau, S.G.4    Orjala, J.5
  • 136
    • 11144311139 scopus 로고    scopus 로고
    • Lessons from natural molecules
    • Clardy J, Walsh C. Lessons from natural molecules. Nature 2004; 432: 829-37.
    • (2004) Nature , vol.432 , pp. 829-837
    • Clardy, J.1    Walsh, C.2
  • 137
    • 0026651340 scopus 로고
    • Cyanobacteria secondary metabolites - the cyanotoxins
    • Carmichael WW. Cyanobacteria secondary metabolites - the cyanotoxins. J Appl Bacteriol 1992; 72: 445-59.
    • (1992) J Appl Bacteriol , vol.72 , pp. 445-459
    • Carmichael, W.W.1
  • 138
    • 0042066368 scopus 로고    scopus 로고
    • Commercial development of microalgal biotechnology: From the test tube to the marketplace
    • Olaizola M. Commercial development of microalgal biotechnology: from the test tube to the marketplace. Biomol Eng 2003; 20: 459-66.
    • (2003) Biomol Eng , vol.20 , pp. 459-466
    • Olaizola, M.1
  • 139
    • 32044458813 scopus 로고    scopus 로고
    • Distribution and diversity of natural product genes in marine and freshwater cyanobacterial cultures and genomes
    • Ehrenreich IM, Waterbury JB, Webb EA. Distribution and diversity of natural product genes in marine and freshwater cyanobacterial cultures and genomes. Appl Environ Microbiol 2005; 71: 7401-13.
    • (2005) Appl Environ Microbiol , vol.71 , pp. 7401-7413
    • Ehrenreich, I.M.1    Waterbury, J.B.2    Webb, E.A.3
  • 140
    • 34249101623 scopus 로고    scopus 로고
    • Genetic analysis of polyketide synthase and peptide synthetase genes in cyanobacteria as a mining tool for secondary metabolites
    • Barrios-Llerena ME, Burja AM, Wright PC. Genetic analysis of polyketide synthase and peptide synthetase genes in cyanobacteria as a mining tool for secondary metabolites. J Ind Microbiol Biotechnol 2007; 34: 443-56.
    • (2007) J Ind Microbiol Biotechnol , vol.34 , pp. 443-456
    • Barrios-Llerena, M.E.1    Burja, A.M.2    Wright, P.C.3
  • 141
    • 70350236654 scopus 로고    scopus 로고
    • Mining cyanobacterial genomes for genes encoding complex biosynthetic pathways
    • Kalaitzis JA, Lauro FM, Neilan BA. Mining cyanobacterial genomes for genes encoding complex biosynthetic pathways. Nat Prod Rep 2009; 26: 1447-65.
    • (2009) Nat Prod Rep , vol.26 , pp. 1447-1465
    • Kalaitzis, J.A.1    Lauro, F.M.2    Neilan, B.A.3
  • 142
    • 62149100042 scopus 로고    scopus 로고
    • Nanomole-scale natural products discovery
    • Molinski TF. Nanomole-scale natural products discovery. Curr Opin Drug Discov Devel 2009; 12: 197-206.
    • (2009) Curr Opin Drug Discov Devel , vol.12 , pp. 197-206
    • Molinski, T.F.1
  • 143
    • 0033807290 scopus 로고    scopus 로고
    • New antibacterial metabolites from the cyanobacterium Nostoc commune (EAWAG 122b)
    • Jaki B, Heilmann J, Sticher O. New antibacterial metabolites from the cyanobacterium Nostoc commune (EAWAG 122b). J Nat Prod 2000; 63: 1283-5.
    • (2000) J Nat Prod , vol.63 , pp. 1283-1285
    • Jaki, B.1    Heilmann, J.2    Sticher, O.3
  • 144
    • 30944469998 scopus 로고    scopus 로고
    • Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth
    • Volk RB, Furkert FH. Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth. Microbiol Res 2006; 161: 180-6.
    • (2006) Microbiol Res , vol.161 , pp. 180-186
    • Volk, R.B.1    Furkert, F.H.2
  • 145
    • 85022484948 scopus 로고
    • Rinehart KL. 9-deazaadenosine and its 5'-alpha-d- glucopyranoside isolated from the cyanobacterium Anabaena affinis strain VS-1
    • Namikoshi M, Carmichael WW, Sakai R, Jareserijman EA, Kaup AM, Rinehart KL. 9-deazaadenosine and its 5'-alpha-d- glucopyranoside isolated from the cyanobacterium Anabaena affinis strain VS-1. J Am Chem Soc 1993; 115: 2504-5.
    • (1993) J Am Chem Soc , vol.115 , pp. 2504-2505
    • Namikoshi, M.1    Carmichael, W.W.2    Sakai, R.3    Jareserijman, E.A.4    Kaup, A.M.5
  • 146
    • 13344275867 scopus 로고    scopus 로고
    • A90720A, a serine protease inhibitor isolated from a terrestrial blue-green alga Microchaete loktakensis
    • Bonjouklian R, Smitka TA, Hunt AH, et al. A90720A, a serine protease inhibitor isolated from a terrestrial blue-green alga Microchaete loktakensis. Tetrahedron 1996; 52: 395-404.
    • (1996) Tetrahedron , vol.52 , pp. 395-404
    • Bonjouklian, R.1    Smitka, T.A.2    Hunt, A.H.3
  • 147
    • 49049085673 scopus 로고    scopus 로고
    • A and B: Isolation and synthesis of toxic ribosomal heterocyclic peptides from the cyanobacterium Microcystis aeruginosa PCC 7806
    • Portmann C, Blom JF, Gademann K, Juttner F. Aerucyclamides A and B: Isolation and synthesis of toxic ribosomal heterocyclic peptides from the cyanobacterium Microcystis aeruginosa PCC 7806. J Nat Prod 2008; 71: 1193-6.
    • (2008) J Nat Prod , vol.71 , pp. 1193-1196
    • Portmann, C.1    Blom, J.F.2    Gademann, K.3    Aerucyclamides Juttner, F.4
  • 148
    • 0037119762 scopus 로고    scopus 로고
    • Aeruginoguanidines 98-A-98-C: Cytotoxic unusual peptides from the cyanobacterium Microcystis aeruginosa
    • Ishida K, Matsuda H, Okita Y, Murakami M. Aeruginoguanidines 98-A-98-C: cytotoxic unusual peptides from the cyanobacterium Microcystis aeruginosa. Tetrahedron 2002; 58: 7645-52.
    • (2002) Tetrahedron , vol.58 , pp. 7645-7652
    • Ishida, K.1    Matsuda, H.2    Okita, Y.3    Murakami, M.4
  • 149
    • 0034907963 scopus 로고    scopus 로고
    • Co-production of microcystins and aeruginopeptins by natural cyanobacterial bloom
    • Harada K, Mayumi T, Shimada T, et al. Co-production of microcystins and aeruginopeptins by natural cyanobacterial bloom. Environ Toxicol 2001; 16: 298-305.
    • (2001) Environ Toxicol , vol.16 , pp. 298-305
    • Harada, K.1    Mayumi, T.2    Shimada, T.3
  • 150
    • 0027364835 scopus 로고
    • Occurrence of four depsipeptides, aeruginopeptins, together with microcystins from toxic cyanobacteria
    • Harada K, Mayumi T, Shimada T, Suzuki M, Kondo F, Watanabe MF. Occurrence of four depsipeptides, aeruginopeptins, together with microcystins from toxic cyanobacteria. Tetrahedron Lett 1993; 34: 6091-4.
    • (1993) Tetrahedron Lett , vol.34 , pp. 6091-6094
    • Harada, K.1    Mayumi, T.2    Shimada, T.3    Suzuki, M.4    Kondo, F.5    Watanabe, M.F.6
  • 151
    • 0033520230 scopus 로고    scopus 로고
    • Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa
    • Ishida K, Okita Y, Matsuda H, Okino T, Murakami M. Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa. Tetrahedron 1999; 55: 10971-88.
    • (1999) Tetrahedron , vol.55 , pp. 10971-88
    • Ishida, K.1    Okita, Y.2    Matsuda, H.3    Okino, T.4    Murakami, M.5
  • 152
    • 0030580449 scopus 로고    scopus 로고
    • Aeruginosins 102-A and B, new thrombin inhibitors from the cyanobacterium Microcystis viridis (NIES-102)
    • Matsuda H, Okino T, Murakami M, Yamaguchi K. Aeruginosins 102-A and B, new thrombin inhibitors from the cyanobacterium Microcystis viridis (NIES-102). Tetrahedron 1996; 52: 14501-6.
    • (1996) Tetrahedron , vol.52 , pp. 14501-14506
    • Matsuda, H.1    Okino, T.2    Murakami, M.3    Yamaguchi, K.4
  • 153
    • 0031690480 scopus 로고    scopus 로고
    • Aeruginosin 103-A, a thrombin inhibitor from the cyanobacterium Microcystis viridis
    • Kodani S, Ishida K, Murakami M. Aeruginosin 103-A, a thrombin inhibitor from the cyanobacterium Microcystis viridis. J Nat Prod 1998; 61: 1046-8.
    • (1998) J Nat Prod , vol.61 , pp. 1046-1048
    • Kodani, S.1    Ishida, K.2    Murakami, M.3
  • 154
    • 0030894360 scopus 로고    scopus 로고
    • 205A and -B, Serine Protease Inhibitory Glycopeptides from the Cyanobacterium Oscillatoria agardhii (NIES-205)
    • Shin HJ, Matsuda H, Murakami M, Yamaguchi K. Aeruginosins 205A and -B, Serine Protease Inhibitory Glycopeptides from the Cyanobacterium Oscillatoria agardhii (NIES-205). J Org Chem 1997; 62: 1810-3.
    • (1997) J Org Chem , vol.62 , pp. 1810-1813
    • Shin, H.J.1    Matsuda, H.2    Murakami, M.3    Aeruginosins Yamaguchi, K.4
  • 155
    • 0028957349 scopus 로고
    • Aeruginosin 98-A and aeruginosin 98-B, trypsin-inhibitors from the blue-green-alga Microcystis aeruginosa (NIES-98)
    • Murakami M, Ishida K, Okino T, Okita Y, Matsuda H, Yamaguchi K. Aeruginosin 98-A and aeruginosin 98-B, trypsin-inhibitors from the blue-green-alga Microcystis aeruginosa (NIES-98). Tetrahedron Lett 1995; 36: 2785-8.
    • (1995) Tetrahedron Lett , vol.36 , pp. 2785-2788
    • Murakami, M.1    Ishida, K.2    Okino, T.3    Okita, Y.4    Matsuda, H.5    Yamaguchi, K.6
  • 156
    • 0036326182 scopus 로고    scopus 로고
    • Three novel protease inhibitors from a natural bloom of the cyanobacterium Microcystis aeruginosa
    • Ploutno A, Shoshan M, Carmeli S. Three novel protease inhibitors from a natural bloom of the cyanobacterium Microcystis aeruginosa. J Nat Prod 2002; 65: 973-8.
    • (2002) J Nat Prod , vol.65 , pp. 973-978
    • Ploutno, A.1    Shoshan, M.2    Carmeli, S.3
  • 157
    • 60649104635 scopus 로고    scopus 로고
    • Two novel biological active modified peptides from the cyanobacterium Microcystis sp
    • Raveh A, Carmeli S. Two novel biological active modified peptides from the cyanobacterium Microcystis sp. Phytochemistry Lett 2009; 2: 10-4.
    • (2009) Phytochemistry Lett , vol.2 , pp. 10-14
    • Raveh, A.1    Carmeli, S.2
  • 158
    • 0030271964 scopus 로고    scopus 로고
    • Agardhipeptins A and B, two new cyclic hepta- and octapeptide, from the cyanobacterium Oscillatoria agardhii (NIES-204)
    • Shin HJ, Matsuda H, Murakami M, Yamaguchi K. Agardhipeptins A and B, two new cyclic hepta- and octapeptide, from the cyanobacterium Oscillatoria agardhii (NIES-204). Tetrahedron 1996; 52: 13129-36.
    • (1996) Tetrahedron , vol.52 , pp. 13129-36
    • Shin, H.J.1    Matsuda, H.2    Murakami, M.3    Yamaguchi, K.4
  • 159
    • 0027730579 scopus 로고
    • Ambigol A and B: New biologically active polychlorinated aromatic compounds from the terrestrial blue-green alga Fischerella ambigua
    • Falch BS, König GM, Wright AD, Sticher O, Ruegger H, Bernardinelli G. Ambigol A and B: new biologically active polychlorinated aromatic compounds from the terrestrial blue-green alga Fischerella ambigua. J Org Chem 1993; 58: 6570-75.
    • (1993) J Org Chem , vol.58 , pp. 6570-6575
    • Falch, B.S.1    König, G.M.2    Wright, A.D.3    Sticher, O.4    Ruegger, H.5    Bernardinelli, G.6
  • 160
    • 0029142462 scopus 로고
    • Biological-activities of cyanobacteria - evaluation of extracts and pure compounds
    • Falch BS, König GM, Wright AD, et al. Biological-activities of cyanobacteria - evaluation of extracts and pure compounds. Planta Med 1995; 61: 321-8.
    • (1995) Planta Med , vol.61 , pp. 321-328
    • Falch, B.S.1    König, G.M.2    Wright, A.D.3
  • 161
    • 25444505307 scopus 로고
    • Novel cyclic peptides together with microcystins produced by toxic cyanobacteria, Anabaena sp
    • Fujii K, Harada K, Suzuki M, et al. Novel cyclic peptides together with microcystins produced by toxic cyanobacteria, Anabaena sp. Tennen Yuki Kagobutsu Toronkai Koen Yoshishu 1995; 37: 445-50.
    • (1995) Tennen Yuki Kagobutsu Toronkai Koen Yoshishu , vol.37 , pp. 445-450
    • Fujii, K.1    Harada, K.2    Suzuki, M.3    Et al.4
  • 162
    • 0037136374 scopus 로고    scopus 로고
    • Structural elucidation of cyanobacterial peptides encoded by peptide synthetase gene in Anabaena species
    • Fujii K, Sivonen K, Nakano T, Harada K. Structural elucidation of cyanobacterial peptides encoded by peptide synthetase gene in Anabaena species. Tetrahedron 2002; 58: 6863-71.
    • (2002) Tetrahedron , vol.58 , pp. 6863-6871
    • Fujii, K.1    Sivonen, K.2    Nakano, T.3    Harada, K.4
  • 163
    • 60549103398 scopus 로고    scopus 로고
    • Homotyrosine-Containing Cyanopeptolins 880 and 960 and Anabaenopeptins 908 and 915 from Planktothrix agardhii CYA 126/8
    • Okumura HS, Philmus B, Portmann C, Hemscheidt TK. Homotyrosine-Containing Cyanopeptolins 880 and 960 and Anabaenopeptins 908 and 915 from Planktothrix agardhii CYA 126/8. J Nat Prod 2009; 72: 172-6.
    • (2009) J Nat Prod , vol.72 , pp. 172-176
    • Okumura, H.S.1    Philmus, B.2    Portmann, C.3    Hemscheidt, T.K.4
  • 164
    • 0028899799 scopus 로고
    • Two cyclic peptides, anabaenopeptins, a third group of bioactive compounds from the cyanobacterium Anabaena flos-aquae NRC 525-17
    • Harada K, Fujii K, Shimada T, et al. Two cyclic peptides, anabaenopeptins, a third group of bioactive compounds from the cyanobacterium Anabaena flos-aquae NRC 525-17. Tetrahedron Lett 1995; 36: 1511-4.
    • (1995) Tetrahedron Lett , vol.36 , pp. 1511-1514
    • Harada, K.1    Fujii, K.2    Shimada, T.3
  • 165
    • 0343247706 scopus 로고    scopus 로고
    • A cyclic peptide, anabaenopeptin B, from the cyanobacterium Oscillatoria agardhii
    • Murakami M, Shin HJ, Matsuda H, Ishida K, Yamaguchi K. A cyclic peptide, anabaenopeptin B, from the cyanobacterium Oscillatoria agardhii. Phytochemistry 1997; 44: 449-52.
    • (1997) Phytochemistry , vol.44 , pp. 449-452
    • Murakami, M.1    Shin, H.J.2    Matsuda, H.3    Ishida, K.4    Yamaguchi, K.5
  • 166
    • 0002424944 scopus 로고    scopus 로고
    • E and F, two new cyclic peptides from the cyanobacterium Oscillatoria agardhii (NIES-204)
    • Shin HJ, Matsuda H, Murakami M, Yamaguchi K. Anabaenopeptins E and F, two new cyclic peptides from the cyanobacterium Oscillatoria agardhii (NIES-204). J Nat Prod 1997; 60: 139-41.
    • (1997) J Nat Prod , vol.60 , pp. 139-141
    • Shin, H.J.1    Matsuda, H.2    Murakami, M.3    Anabaenopeptins Yamaguchi, K.4
  • 167
    • 0033519245 scopus 로고    scopus 로고
    • Anabaenopeptins G and H, potent carboxypeptidase A inhibitors from the cyanobacterium Oscillatoria agardhii (NIES-595)
    • Itou Y, Suzuki S, Ishida K, Murakami M. Anabaenopeptins G and H, potent carboxypeptidase A inhibitors from the cyanobacterium Oscillatoria agardhii (NIES-595). Bioorg Med Chem Lett 1999; 9: 1243-6.
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 1243-1246
    • Itou, Y.1    Suzuki, S.2    Ishida, K.3    Murakami, M.4
  • 168
    • 69949157338 scopus 로고    scopus 로고
    • Protease inhibitors from a water bloom of the cyanobacterium Microcystis aeruginosa
    • Gesner-Apter S, Carmeli S. Protease inhibitors from a water bloom of the cyanobacterium Microcystis aeruginosa. J Nat Prod 2009; 72: 1429-36.
    • (2009) J Nat Prod , vol.72 , pp. 1429-1436
    • Gesner-Apter, S.1    Carmeli, S.2
  • 169
    • 0002424944 scopus 로고    scopus 로고
    • Anabaenopeptins C and D, two new cyclic peptides from the cyanobacterium Oscillatoria agardhii (NIES-204)
    • Shin HJ, Matsuda H, Murakami M, Yamaguchi K. Anabaenopeptins C and D, two new cyclic peptides from the cyanobacterium Oscillatoria agardhii (NIES-204). J Nat Prod 1997; 60: 139-41.
    • (1997) J Nat Prod , vol.60 , pp. 139-141
    • Shin, H.J.1    Matsuda, H.2    Murakami, M.3    Yamaguchi, K.4
  • 170
    • 51349136552 scopus 로고    scopus 로고
    • Three novel anabaenopeptins from the cyanobacterium Anabaena sp
    • Grach-Pogrebinsky O, Carmeli S. Three novel anabaenopeptins from the cyanobacterium Anabaena sp. Tetrahedron 2008; 64: 10233-38.
    • (2008) Tetrahedron , vol.64 , pp. 10233-38
    • Grach-Pogrebinsky, O.1    Carmeli, S.2
  • 171
    • 0031732492 scopus 로고    scopus 로고
    • Cyclic hexapeptides from the cyanobacterium Nostoc spongiaeforme var. tenue
    • Banker R, Carmeli S. Tenuecyclamides A-D, cyclic hexapeptides from the cyanobacterium Nostoc spongiaeforme var. tenue. J Nat Prod 1998; 61: 1248-51.
    • (1998) J Nat Prod , vol.61 , pp. 1248-1251
    • Banker, R.1    Carmeli, S.2    Tenuecyclamides, A.-D.3
  • 172
    • 0027940068 scopus 로고
    • Structure and biosynthesis of borophycin, a new boeseken complex of boric acid from a marine strain of the blue-green alga Nostoc linckia
    • Hemscheidt T, Puglisi MP, Larsen LK, et al. Structure and biosynthesis of borophycin, a new boeseken complex of boric acid from a marine strain of the blue-green alga Nostoc linckia. J Org Chem 1994; 59: 3467-71.
    • (1994) J Org Chem , vol.59 , pp. 3467-3471
    • Hemscheidt, T.1    Puglisi, M.P.2    Larsen, L.K.3
  • 173
    • 69749085714 scopus 로고    scopus 로고
    • Inhibition of human leukocyte elastase by brunsvicamides A-C: Cyanobacterial cyclic peptides
    • Sisay MT, Hautmann S, Mehner C, Konig GM, Bajorath J, Gutschow M. Inhibition of human leukocyte elastase by brunsvicamides A-C: cyanobacterial cyclic peptides. ChemMedChem 2009; 4: 1425-9.
    • (2009) ChemMedChem , vol.4 , pp. 1425-1429
    • Sisay, M.T.1    Hautmann, S.2    Mehner, C.3    Konig, G.M.4    Bajorath, J.5    Gutschow, M.6
  • 174
    • 34249111585 scopus 로고    scopus 로고
    • Carbamidocyclophanes A-E, chlorinated paracyclophanes with cytotoxic and antibiotic activity from the Vietnamese cyanobacterium Nostoc sp
    • Bui HTN, Jansen R, Pham HTL, Mundt S. Carbamidocyclophanes A-E, chlorinated paracyclophanes with cytotoxic and antibiotic activity from the Vietnamese cyanobacterium Nostoc sp. J Nat Prod 2007; 70: 499-503.
    • (2007) J Nat Prod , vol.70 , pp. 499-503
    • Bui, H.T.N.1    Jansen, R.2    Pham, H.T.L.3    Mundt, S.4
  • 175
    • 0037704210 scopus 로고    scopus 로고
    • Fatty acids with antibacterial activity from the cyanobacterium Oscillatoria redekei HUB 051
    • Mundt S, Kreitlow S, Jansen R. Fatty acids with antibacterial activity from the cyanobacterium Oscillatoria redekei HUB 051. J Appl Phycol 2003; 15: 263-7.
    • (2003) J Appl Phycol , vol.15 , pp. 263-267
    • Mundt, S.1    Kreitlow, S.2    Jansen, R.3
  • 176
    • 0034856849 scopus 로고    scopus 로고
    • Cryptophycins: A novel class of potent antimitotic antitumor depsipeptides
    • Chuan S, Teicher BA. Cryptophycins: a novel class of potent antimitotic antitumor depsipeptides. Curr Pharm Des 2001; 7: 1259-76.
    • (2001) Curr Pharm Des , vol.7 , pp. 1259-1276
    • Chuan, S.1    Teicher, B.A.2
  • 177
    • 0028191001 scopus 로고
    • A second algicidal natural product from the cyanobacterium, Scytonema hofmanni
    • Lee EJ, Gleason FK. A second algicidal natural product from the cyanobacterium, Scytonema hofmanni. Plant Sci 1994; 103: 155-60.
    • (1994) Plant Sci , vol.103 , pp. 155-160
    • Lee, E.J.1    Gleason, F.K.2
  • 178
    • 0021055089 scopus 로고
    • Structure of the antibiotic cyanobacterin, a chlorine-containing γ-lactone from the freshwater cyanobacterium Scytonema hofmanni
    • Pignatello JJ, Porwoll J, Carlson RE, Xavier A, Gleason FK, Wood JM. Structure of the antibiotic cyanobacterin, a chlorine-containing γ-lactone from the freshwater cyanobacterium Scytonema hofmanni. J Org Chem 1983; 48: 4035-8.
    • (1983) J Org Chem , vol.48 , pp. 4035-4038
    • Pignatello, J.J.1    Porwoll, J.2    Carlson, R.E.3    Xavier, A.4    Gleason, F.K.5    Wood, J.M.6
  • 179
    • 27144531769 scopus 로고    scopus 로고
    • Cyanopeptolin 954, a chlorine-containing chymotrypsin inhibitor of Microcystis aeruginosa NIVA CYA 43
    • von Elert E, Oberer L, Merkel P, Huhn T, Blom JF. Cyanopeptolin 954, a chlorine-containing chymotrypsin inhibitor of Microcystis aeruginosa NIVA CYA 43. J Nat Prod 2005; 68: 1324-7.
    • (2005) J Nat Prod , vol.68 , pp. 1324-1327
    • von Elert, E.1    Oberer, L.2    Merkel, P.3    Huhn, T.4    Blom, J.F.5
  • 180
    • 7044233198 scopus 로고    scopus 로고
    • Cyanopeptolin 963A, a chymotrypsin inhibitor of Microcystis PCC 7806
    • Bister B, Keller S, Baumann HI, et al. Cyanopeptolin 963A, a chymotrypsin inhibitor of Microcystis PCC 7806. J Nat Prod 2004; 67: 1755-7.
    • (2004) J Nat Prod , vol.67 , pp. 1755-1757
    • Bister, B.1    Keller, S.2    Baumann, H.I.3
  • 181
    • 3142757234 scopus 로고    scopus 로고
    • Diversity and distribution of Microcystis (Cyanobacteria) oligopeptide chemotypes from natural communities studied by single-colony mass spectrometry
    • Welker M, Brunke M, Preussel K, Lippert I, von Dohren H. Diversity and distribution of Microcystis (Cyanobacteria) oligopeptide chemotypes from natural communities studied by single-colony mass spectrometry. Microbiol 2004; 150: 1785-96.
    • (2004) Microbiol , vol.150 , pp. 1785-1796
    • Welker, M.1    Brunke, M.2    Preussel, K.3    Lippert, I.4    von Dohren, H.5
  • 182
    • 48849083257 scopus 로고    scopus 로고
    • Cyanopeptoline CB071: A cyclic depsipeptide isolated from the freshwater cyanobacterium Aphanocapsa s
    • Choi H, Oh SK, Yih W, Chin J, Kang H, Rho JR. Cyanopeptoline CB071: a cyclic depsipeptide isolated from the freshwater cyanobacterium Aphanocapsa sp. Chem Pharm Bull (Tokyo) 2008; 56: 1191-3.
    • (2008) Chem Pharm Bull (Tokyo) , vol.5 , pp. 1191-1113
    • Choi, H.1    Oh, S.K.2    Yih, W.3    Chin, J.4    Kang, H.5    Rho, J.R.6
  • 184
    • 0027482363 scopus 로고
    • Cyanopeptolins, new depsipeptides from the cyanobacterium Microcystis sp. PCC 7806
    • Martin C, Oberer L, Ino T, Koenig WA, Busch M, Weckesser J. Cyanopeptolins, new depsipeptides from the cyanobacterium Microcystis sp. PCC 7806. J. Antibiot 1993; 46: 1550-6.
    • (1993) J. Antibiot , vol.46 , pp. 1550-1556
    • Martin, C.1    Oberer, L.2    Ino, T.3    Koenig, W.A.4    Busch, M.5    Weckesser, J.6
  • 185
    • 13844297751 scopus 로고    scopus 로고
    • Leucine aminopeptidase M inhibitors, cyanostatin A and B, isolated from cyanobacterial water blooms in Scotland
    • Sano T, Takagi H, Morrison LF, Metcalf JS, Codd GA, Kaya K. Leucine aminopeptidase M inhibitors, cyanostatin A and B, isolated from cyanobacterial water blooms in Scotland. Phytochemistry (Amsterdam) 2005; 66: 543-8.
    • (2005) Phytochemistry (Amsterdam) , vol.66 , pp. 543-548
    • Sano, T.1    Takagi, H.2    Morrison, L.F.3    Metcalf, J.S.4    Codd, G.A.5    Kaya, K.6
  • 186
    • 0001624861 scopus 로고
    • Paracyclophanes from blue-green algae
    • Moore BS, Chen J, Patterson GML, et al.[7.7]paracyclophanes from blue-green algae. J Am Chem Soc. 1990; 112: 4061-3.
    • (1990) J Am Chem Soc , vol.112 , pp. 4061-4063
    • Moore, B.S.1    Chen J.Patterson, G.M.L.2
  • 188
    • 0031868209 scopus 로고    scopus 로고
    • Dehydroradiosumin, a trypsin inhibitor from the cyanobacterium Anabaena cylindrica
    • Kodani S, Ishida K, Murakami M. Dehydroradiosumin, a trypsin inhibitor from the cyanobacterium Anabaena cylindrica. J Nat Prod 1998; 61: 854-6.
    • (1998) J Nat Prod , vol.61 , pp. 854-856
    • Kodani, S.1    Ishida, K.2    Murakami, M.3
  • 189
    • 0029999125 scopus 로고    scopus 로고
    • Ferintoic acids A and B, new cyclic hexapeptides from the freshwater cyanobacterium Microcystis aeruginosa
    • ] Williams DE, Craig M, Holmes CFB, Andersen RJ. Ferintoic acids A and B, new cyclic hexapeptides from the freshwater cyanobacterium Microcystis aeruginosa. J Nat Prod 1996; 59: 570- 5.
    • (1996) J Nat Prod , vol.59 , pp. 570-575
    • Williams, D.E.1    Craig, M.2    Holmes, C.F.B.3    Andersen, R.J.4
  • 191
    • 34548015425 scopus 로고    scopus 로고
    • Cyclic depsipeptides, ichthyopeptins A and B, from Microcystis ichthyoblabe
    • Zainuddin EN, Mentel R, Wray V, et al. Cyclic depsipeptides, ichthyopeptins A and B, from Microcystis ichthyoblabe. J Nat Prod 2007; 70: 1084-8.
    • (2007) J Nat Prod , vol.70 , pp. 1084-1088
    • Zainuddin, E.N.1    Mentel, R.2    Wray, V.3
  • 192
    • 0030877394 scopus 로고    scopus 로고
    • A antibacterial cyclic undecapeptide from the cyanobacterium Microcystis aeruginosa
    • Ishida K, Matsuda H, Murakami M, Yamaguchi K. Kawaguchipeptin B, A antibacterial cyclic undecapeptide from the cyanobacterium Microcystis aeruginosa. J Nat Prod 1997; 60: 724- 6.
    • (1997) J Nat Prod , vol.60 , pp. 724-726
    • Ishida, K.1    Matsuda, H.2    Murakami, M.3    Kawaguchipeptin Yamaguchi, K.4
  • 193
    • 0001419708 scopus 로고    scopus 로고
    • Total structure and biological properties of laxaphycins A and B, cyclic lipopeptides from the marine cyanobacterium Lyngbya majuscula
    • Bonnard I, Rolland M, Francisco C, Banaigs B. Total structure and biological properties of laxaphycins A and B, cyclic lipopeptides from the marine cyanobacterium Lyngbya majuscula. Lett Peptide Sci 1997; 4: 289-92.
    • (1997) Lett Peptide Sci , vol.4 , pp. 289-292
    • Bonnard, I.1    Rolland, M.2    Francisco, C.3    Banaigs, B.4
  • 194
    • 0026736820 scopus 로고
    • Antifungal cyclic peptides from the terrestrial blue-green alga Anabaena laxa. I. isolation and biological properties
    • Frankmölle WP, Larsen LK, Caplan FR, et al. Antifungal cyclic peptides from the terrestrial blue-green alga Anabaena laxa. I. isolation and biological properties. J Antibiot (Tokyo) 1992; 45: 1451-7.
    • (1992) J Antibiot (Tokyo) , vol.45 , pp. 1451-1457
    • Frankmölle, W.P.1    Larsen, L.K.2    Caplan, F.R.3
  • 195
    • 0026754479 scopus 로고
    • Antifungal cyclic peptides from the terrestrial blue-green alga Anabaena laxa. II. structures of laxaphycins A, B, D and
    • Frankmölle WP, Knübel G, Moore RE, Patterson GM. Antifungal cyclic peptides from the terrestrial blue-green alga Anabaena laxa. II. structures of laxaphycins A, B, D and E. J Antibiot (Tokyo) 1992; 45: 1458-66.
    • (1992) E. J Antibiot (Tokyo) , vol.45 , pp. 1458-1466
    • Frankmölle, W.P.1    Knübel, G.2    Moore, R.E.3    Patterson, G.M.4
  • 196
    • 0000457352 scopus 로고
    • Microcystilide A: A novel cell-differentiation-promoting depsipeptide from Microcystis aeruginosa NO-15-1840
    • Tsukamoto S, Painuly P, Young KA, Yang X, Shimizu Y, Cornell L. Microcystilide A: a novel cell-differentiation-promoting depsipeptide from Microcystis aeruginosa NO-15-1840. J Am Chem Soc 1993; 115: 11046-7.
    • (1993) J Am Chem Soc , vol.115 , pp. 11046-11047
    • Tsukamoto, S.1    Painuly, P.2    Young, K.A.3    Yang, X.4    Shimizu, Y.5    Cornell, L.6
  • 197
    • 33746924528 scopus 로고    scopus 로고
    • Toward an understanding of metabolic diversity
    • Welker M, Marsalek B, Sejnohova L, von Doehren H. Detection and identification of oligopeptides in Microcystis (cyanobacteria) colonies: Toward an understanding of metabolic diversity. Peptides (New York) 2006; 27: 2090-103.
    • (2006) Peptides (New York) , vol.27 , pp. 2090-2103
    • Welker, M.1    Marsalek, B.2    Sejnohova, L.3    Detection von Doehren, H.4
  • 198
    • 45449102438 scopus 로고    scopus 로고
    • Three novel metabolites from a bloom of the cyanobacterium Microcystis sp
    • Gesner-Apter S, Carmeli S. Three novel metabolites from a bloom of the cyanobacterium Microcystis sp. Tetrahedron 2008; 64: 6628- 34.
    • (2008) Tetrahedron , vol.64 , pp. 6628-6634
    • Gesner-Apter, S.1    Carmeli, S.2
  • 199
    • 0035795060 scopus 로고    scopus 로고
    • Protease inhibitors from a water bloom of the cyanobacterium Microcystis aeruginosa
    • Reshef V, Carmeli S. Protease inhibitors from a water bloom of the cyanobacterium Microcystis aeruginosa. Tetrahedron 2001; 57: 2885-94.
    • (2001) Tetrahedron , vol.57 , pp. 2885-2894
    • Reshef, V.1    Carmeli, S.2
  • 200
    • 0030806260 scopus 로고    scopus 로고
    • Microginins 299-A and -B, leucine aminopeptidase inhibitors from the cyanobacterium Microcystis aeruginosa (NIES-299)
    • Ishida K, Matsuda H, Murakami M, Yamaguchi K. Microginins 299-A and -B, leucine aminopeptidase inhibitors from the cyanobacterium Microcystis aeruginosa (NIES-299). Tetrahedron 1997; 53: 10281-8.
    • (1997) Tetrahedron , vol.53 , pp. 10281-10288
    • Ishida, K.1    Matsuda, H.2    Murakami, M.3    Yamaguchi, K.4
  • 201
    • 0032578683 scopus 로고    scopus 로고
    • Four new microginins, linear peptides from the cyanobacterium Microcystis aeruginosa
    • Ishida K, Matsuda H, Murakami M. Four new microginins, linear peptides from the cyanobacterium Microcystis aeruginosa. Tetrahedron 1998; 54: 13475-84.
    • (1998) Tetrahedron , vol.54 , pp. 13475-84
    • Ishida, K.1    Matsuda, H.2    Murakami, M.3
  • 202
    • 0030933127 scopus 로고    scopus 로고
    • Micropeptin 103, a chymotrypsin inhibitor from the cyanobacterium Microcystis viridis (NIES-103)
    • Murakami M, Kodani S, Ishida K, Matsuda H, Yamaguchi K. Micropeptin 103, a chymotrypsin inhibitor from the cyanobacterium Microcystis viridis (NIES-103). Tetrahedron Lett 1997; 38: 3035-8.
    • (1997) Tetrahedron Lett , vol.38 , pp. 3035-3038
    • Murakami, M.1    Kodani, S.2    Ishida, K.3    Matsuda, H.4    Yamaguchi, K.5
  • 203
    • 0031018804 scopus 로고    scopus 로고
    • 478-A and B, Plasmin Inhibitors from the Cyanobacterium Microcystis aeruginosa
    • Ishida K, Matsuda H, Murakami M, Yamaguchi K. Micropeptins 478-A and B, Plasmin Inhibitors from the Cyanobacterium Microcystis aeruginosa. J Nat Prod. 1997; 60: 184-7.
    • (1997) J Nat Prod , vol.60 , pp. 184-187
    • Ishida, K.1    Matsuda, H.2    Murakami, M.3    Micropeptins Yamaguchi, K.4
  • 204
    • 0032554845 scopus 로고    scopus 로고
    • Micropeptins 88-A to 88-F, chymotrypsin inhibitors from the cyanobacterium Microcystis aeruginosa (NIES-88)
    • Ishida K, Matsuda H, Murakami M. Micropeptins 88-A to 88-F, chymotrypsin inhibitors from the cyanobacterium Microcystis aeruginosa (NIES-88). Tetrahedron 1998; 54: 5545-56.
    • (1998) Tetrahedron , vol.54 , pp. 5545-5556
    • Ishida, K.1    Matsuda, H.2    Murakami, M.3
  • 205
    • 12944268320 scopus 로고    scopus 로고
    • Two new chymotrypsin inhibitors isolated from the cyanobacterium Microcystis aeruginosa NIES-88
    • Yamaki H, Sitachitta N, Sano T, Kaya K. Two new chymotrypsin inhibitors isolated from the cyanobacterium Microcystis aeruginosa NIES-88. J Nat Prod 2005; 68: 14-8.
    • (2005) J Nat Prod , vol.68 , pp. 14-18
    • Yamaki, H.1    Sitachitta, N.2    Sano, T.3    Kaya, K.4
  • 206
    • 0029067421 scopus 로고
    • Micropeptin 90, a plasmin and trypsin inhibitor from the blue-green alga Microcystis aeruginosa (NIES-90)
    • Ishida K, Murakami M, Matsuda H, Yamaguchi K. Micropeptin 90, a plasmin and trypsin inhibitor from the blue-green alga Microcystis aeruginosa (NIES-90). Tetrahedron Lett 1995; 36: 3535-8.
    • (1995) Tetrahedron Lett , vol.36 , pp. 3535-3538
    • Ishida, K.1    Murakami, M.2    Matsuda, H.3    Yamaguchi, K.4
  • 207
    • 0027133116 scopus 로고
    • Micropeptins A and B, plasmin and trypsin inhibitors from the blue-green alga Microcystis aeruginosa
    • Okino T, Murakami M, Haraguchi R, Munekata H, Matsuda H, Yamaguchi K. Micropeptins A and B, plasmin and trypsin inhibitors from the blue-green alga Microcystis aeruginosa. Tetrahedron Lett 1993; 34: 8131-4.
    • (1993) Tetrahedron Lett , vol.34 , pp. 8131-8134
    • Okino, T.1    Murakami, M.2    Haraguchi, R.3    Munekata, H.4    Matsuda, H.5    Yamaguchi, K.6
  • 208
    • 65649142925 scopus 로고    scopus 로고
    • Micropeptins from the freshwater cyanobacterium Microcystis aeruginosa (NIES-100)
    • Kisugi T, Okino T. Micropeptins from the freshwater cyanobacterium Microcystis aeruginosa (NIES-100). J Nat Prod 2009; 72: 777-81.
    • (2009) J Nat Prod , vol.72 , pp. 777-781
    • Kisugi, T.1    Okino, T.2
  • 209
    • 77950437963 scopus 로고    scopus 로고
    • Micropeptins from an Israeli fishpond water bloom of the cyanobacterium Microcystis sp
    • Zafrir E, Carmeli S. Micropeptins from an Israeli fishpond water bloom of the cyanobacterium Microcystis sp. J Nat Prod 2010; 73: 352-8.
    • (2010) J Nat Prod , vol.73 , pp. 352-358
    • Zafrir, E.1    Carmeli, S.2
  • 210
    • 0033582989 scopus 로고    scopus 로고
    • Micropeptin T-20, a novel phosphate- containing cyclic depsipeptide from the cyanobacterium Microcystis aeruginosa
    • Okano T, Sano T, Kaya K. Micropeptin T-20, a novel phosphate- containing cyclic depsipeptide from the cyanobacterium Microcystis aeruginosa. Tetrahedron Lett 1999; 40: 2379-82.
    • (1999) Tetrahedron Lett , vol.40 , pp. 2379-2382
    • Okano, T.1    Sano, T.2    Kaya, K.3
  • 211
    • 10744228625 scopus 로고    scopus 로고
    • Isolation, characterization, and quantitative analysis of Microviridin J, a new Microcystis metabolite toxic to Daphnia
    • Rohrlack T, Christoffersen K, Hansen PE, et al. Isolation, characterization, and quantitative analysis of Microviridin J, a new Microcystis metabolite toxic to Daphnia. J.Chem Ecol 2003; 29: 1757-70.
    • (2003) J.Chem Ecol , vol.29 , pp. 1757-1770
    • Rohrlack, T.1    Christoffersen, K.2    Hansen, P.E.3
  • 212
    • 33745183562 scopus 로고    scopus 로고
    • New microviridins from a water bloom of the cyanobacterium Microcystis aeruginosa
    • Reshef V, Carmeli S. New microviridins from a water bloom of the cyanobacterium Microcystis aeruginosa. Tetrahedron 2006; 62: 7361-9.
    • (2006) Tetrahedron , vol.62 , pp. 7361-7369
    • Reshef, V.1    Carmeli, S.2
  • 214
    • 0025972133 scopus 로고
    • Mirabimides A-D, new N- acylpyrrolinones from the blue-green alga Scytonema mirabile
    • Carmeli S, Moore RE, Patterson GML. Mirabimides A-D, new N- acylpyrrolinones from the blue-green alga Scytonema mirabile. Tetrahedron 1991; 47: 2087-96.
    • (1991) Tetrahedron , vol.47 , pp. 2087-2096
    • Carmeli, S.1    Moore, R.E.2    Patterson, G.M.L.3
  • 215
    • 0028077856 scopus 로고
    • Mirabimide-E, an unusual N-acylpyrrolinone from the blue-green alga Scytonema mirabile - structure determination and synthesis
    • Paik SG, Carmeli S, Cullingham J, Moore RE, Patterson GML, Tius MA. Mirabimide-E, an unusual N-acylpyrrolinone from the blue-green alga Scytonema mirabile - structure determination and synthesis. J Am Chem Soc 1994; 116: 8116-25.
    • (1994) J Am Chem Soc , vol.116 , pp. 8116-8125
    • Paik, S.G.1    Carmeli, S.2    Cullingham, J.3    Moore, R.E.4    Patterson, G.M.L.5    Tius, M.A.6
  • 216
    • 0029016680 scopus 로고
    • A new oxazole peptide alkaloid from freshwater cyanobacterium Nostoc muscorum
    • Nagatsu A, Kajitani H, Sakakibara J. Muscoride A: A new oxazole peptide alkaloid from freshwater cyanobacterium Nostoc muscorum. Tetrahedron Lett 1995; 36: 4097-100.
    • (1995) Tetrahedron Lett , vol.36 , pp. 4097-4100
    • Nagatsu, A.1    Kajitani, H.2    Sakakibara, J.3    Muscoride, A.4
  • 217
    • 0030762624 scopus 로고    scopus 로고
    • Comparative study of toxic and non-toxic cyanobacterial products: Novel peptides from toxic Nodularia spumigena AV1
    • Fujii K, Sivonen K, Adachi K, et al. Comparative study of toxic and non-toxic cyanobacterial products: novel peptides from toxic Nodularia spumigena AV1. Tetrahedron Lett 1997; 38: 5525-8.
    • (1997) Tetrahedron Lett , vol.38 , pp. 5525-5528
    • Fujii, K.1    Sivonen, K.2    Adachi, K.3
  • 218
    • 67349185331 scopus 로고    scopus 로고
    • The cyanobacterial alkaloid nostocarboline: An inhibitor of acetylcholinesterase and trypsin
    • Becher PG, Baumann HI, Gademann K, Juettner F. The cyanobacterial alkaloid nostocarboline: an inhibitor of acetylcholinesterase and trypsin. J Appl Phycol 2009; 21: 103-10.
    • (2009) J Appl Phycol , vol.21 , pp. 103-110
    • Becher, P.G.1    Baumann, H.I.2    Gademann, K.3    Juettner, F.4
  • 219
    • 0038170495 scopus 로고    scopus 로고
    • Bioactivities of nostocine a produced by a freshwater cyanobacterium Nostoc spongiaeforme TISTR 8169
    • Hirata K, Yoshitomi S, Dwi S, et al. Bioactivities of nostocine a produced by a freshwater cyanobacterium Nostoc spongiaeforme TISTR 8169. J Biosci Bioeng 2003; 95: 512-7.
    • (2003) J Biosci Bioeng , vol.95 , pp. 512-517
    • Hirata, K.1    Yoshitomi, S.2    Dwi, S.3
  • 220
    • 0030576963 scopus 로고    scopus 로고
    • Nostocyclin, a novel 3- amino-6-hydroxy-2-piperidone-containing cyclic depsipeptide from the cyanobacterium Nostoc sp
    • Kaya K, Sano T, Beattie KA, Codd GA. Nostocyclin, a novel 3- amino-6-hydroxy-2-piperidone-containing cyclic depsipeptide from the cyanobacterium Nostoc sp. Tetrahedron Lett 1996; 37: 6725-8.
    • (1996) Tetrahedron Lett , vol.37 , pp. 6725-6728
    • Kaya, K.1    Sano, T.2    Beattie, K.A.3    Codd, G.A.4
  • 221
    • 0035144142 scopus 로고    scopus 로고
    • Isolation and structure determination of nostocyclopeptides A1 and A2 from the terrestrial cyanobacterium Nostoc sp. ATCC53789
    • Golakoti T, Yoshida WY, Chaganty S, Moore RE. Isolation and structure determination of nostocyclopeptides A1 and A2 from the terrestrial cyanobacterium Nostoc sp. ATCC53789. J Nat Prod 2001; 64: 54-9
    • (2001) J Nat Prod , vol.64 , pp. 54-59
    • Golakoti, T.1    Yoshida, W.Y.2    Chaganty, S.3    Moore, R.E.4
  • 223
    • 0033723809 scopus 로고    scopus 로고
    • A novel antimicrobial cyclophane from the cyanobacterium Nostoc sp
    • Ploutno A, Carmeli S. Nostocyclyne A, a novel antimicrobial cyclophane from the cyanobacterium Nostoc sp. J Nat Prod 2000; 63: 1524-6.
    • (2000) J Nat Prod , vol.63 , pp. 1524-1526
    • Ploutno, A.1    Carmeli, S.2    Nostocyclyne, A.3
  • 224
    • 0037049297 scopus 로고    scopus 로고
    • Modified peptides from a water bloom of the cyanobacterium Nostoc sp
    • Ploutno A, Carmeli S. Modified peptides from a water bloom of the cyanobacterium Nostoc sp. Tetrahedron 2002; 58: 9949-57.
    • (2002) Tetrahedron , vol.58 , pp. 9949-9957
    • Ploutno, A.1    Carmeli, S.2
  • 225
    • 0031127947 scopus 로고    scopus 로고
    • A 3-amino-10-chloro-2-hydroxydecanoic acid- containing tetrapeptide from Oscillatoria agardhii
    • Sano T, Kaya K. A 3-amino-10-chloro-2-hydroxydecanoic acid- containing tetrapeptide from Oscillatoria agardhii. Phytochemistry 1997; 44: 1503-5.
    • (1997) Phytochemistry , vol.44 , pp. 1503-1505
    • Sano, T.1    Kaya, K.2
  • 226
    • 85047669904 scopus 로고
    • A chymotrypsin inhibitor from toxic Oscillatoria agardhii
    • Sano T, Kaya K. Oscillamide Y, a chymotrypsin inhibitor from toxic Oscillatoria agardhii. Tetrahedron Lett 1995; 36: 5933-6.
    • (1995) Tetrahedron Lett , vol.36 , pp. 5933-5936
    • Sano, T.1    Kaya, K.2    Oscillamide, Y.3
  • 227
    • 85047674402 scopus 로고
    • Oscillapeptin, an elastase and chymotrypsin inhibitor from the cyanobacterium Oscillatoria agardhii (NIES-204)
    • Shin HJ, Murakami M, Matsuda H, Ishida K, Yamaguchi K. Oscillapeptin, an elastase and chymotrypsin inhibitor from the cyanobacterium Oscillatoria agardhii (NIES-204). Tetrahedron Lett 1995; 36: 5235-8.
    • (1995) Tetrahedron Lett , vol.36 , pp. 5235-5238
    • Shin, H.J.1    Murakami, M.2    Matsuda, H.3    Ishida, K.4    Yamaguchi, K.5
  • 228
    • 0033612125 scopus 로고    scopus 로고
    • Oscillapeptins A to F. Serine protease inhibitors from the three strains of Oscillatoria agardhii
    • Itou Y, Ishida K, Shin HJ, Murakami M. Oscillapeptins A to F, serine protease inhibitors from the three strains of Oscillatoria agardhii. Tetrahedron 1999; 55: 6871-82.
    • (1999) Tetrahedron , vol.55 , pp. 6871-6882
    • Itou, Y.1    Ishida, K.2    Shin, H.J.3    Murakami, M.4
  • 229
    • 0031819818 scopus 로고    scopus 로고
    • Isolation of bioactive compounds in cyanobacteria from Chinese fresh water. 1. trypsin inhibitor
    • Sano T, He J, Liu Y, Kaya K. Isolation of bioactive compounds in cyanobacteria from Chinese fresh water. 1. trypsin inhibitor. Phycol Res 1998; 46: 13-17.
    • (1998) Phycol Res , vol.46 , pp. 13-17
    • Sano, T.1    He, J.2    Liu, Y.3    Kaya, K.4
  • 231
    • 34250703208 scopus 로고    scopus 로고
    • Structures of pahayokolides A and B, cyclic peptides from a Lyngbya sp
    • An T, Kumar TKS, Wang M, et al. Structures of pahayokolides A and B, cyclic peptides from a Lyngbya sp. J Nat Prod 2007; 70: 730-5.
    • (2007) J Nat Prod , vol.70 , pp. 730-735
    • An, T.1    Kumar, T.K.S.2    Wang, M.3
  • 232
    • 15944368268 scopus 로고    scopus 로고
    • Pharmacology and toxicology of pahayokolide A, a bioactive metabolite from a freshwater species of Lyngbya isolated from the Florida Everglades
    • Berry JP, Gantar M, Gawley RE, Wang M, Rein KS. Pharmacology and toxicology of pahayokolide A, a bioactive metabolite from a freshwater species of Lyngbya isolated from the Florida Everglades. Comp Biochem and Physiol C Toxicol Pharmacol 2004; 139: 231-8.
    • (2004) Comp Biochem and Physiol C Toxicol Pharmacol , vol.139 , pp. 231-238
    • Berry, J.P.1    Gantar, M.2    Gawley, R.E.3    Wang, M.4    Rein, K.S.5
  • 233
    • 0141643420 scopus 로고    scopus 로고
    • Protease inhibitors from a Slovenian lake Bled toxic waterbloom of the cyanobacterium Planktothrix rubescens
    • Grach-Pogrebinsky O, Sedmak B, Carmeli S. Protease inhibitors from a Slovenian lake Bled toxic waterbloom of the cyanobacterium Planktothrix rubescens. Tetrahedron 2003; 59: 8329-36.
    • (2003) Tetrahedron , vol.59 , pp. 8329-8336
    • Grach-Pogrebinsky, O.1    Sedmak, B.2    Carmeli, S.3
  • 234
    • 36349004105 scopus 로고    scopus 로고
    • Planktocyclin, a cyclooctapeptide protease inhibitor produced by the freshwater cyanobacterium Planktothrix rubescens
    • Baumann HI, Keller S, Wolter FE, et al. Planktocyclin, a cyclooctapeptide protease inhibitor produced by the freshwater cyanobacterium Planktothrix rubescens. J Nat Prod 2007; 70: 1611-5.
    • (2007) J Nat Prod , vol.70 , pp. 1611-1615
    • Baumann, H.I.1    Keller, S.2    Wolter, F.E.3
  • 235
    • 0036688783 scopus 로고    scopus 로고
    • Schizopeptin 791, a new anabeanopeptin-like cyclic peptide from the cyanobacterium Schizothrix sp
    • Reshef V, Carmeli S. Schizopeptin 791, a new anabeanopeptin-like cyclic peptide from the cyanobacterium Schizothrix sp. J Nat Prod 2002; 65: 1187-9.
    • (2002) J Nat Prod , vol.65 , pp. 1187-1189
    • Reshef, V.1    Carmeli, S.2
  • 236
    • 0027973157 scopus 로고
    • Schizotrin A; a novel antimicrobial cyclic peptide from a cyanobacterium
    • Pergament I, Carmeli S. Schizotrin A; a novel antimicrobial cyclic peptide from a cyanobacterium. Tetrahedron Lett 1994; 35: 8473-6.
    • (1994) Tetrahedron Lett , vol.35 , pp. 8473-8476
    • Pergament, I.1    Carmeli, S.2
  • 237
    • 0035818758 scopus 로고    scopus 로고
    • Scyptolin A and B, cyclic depsipeptides from axenic cultures of Scytonema hofmanni PCC 7110
    • Matern U, Oberer L, Falchetto RA, et al. Scyptolin A and B, cyclic depsipeptides from axenic cultures of Scytonema hofmanni PCC 7110. Phytochemistry 2001; 58: 1087-95.
    • (2001) Phytochemistry , vol.58 , pp. 1087-1095
    • Matern, U.1    Oberer, L.2    Falchetto, R.A.3
  • 238
    • 0027420888 scopus 로고
    • The structure of scytonemin, an ultraviolet sunscreen pigment from the sheaths of cyanobacteria
    • Proteau PJ, Gerwick WH, Garcia-Pichel F, Castenholz RW. The structure of scytonemin, an ultraviolet sunscreen pigment from the sheaths of cyanobacteria. Experientia 1993; 49: 825-9.
    • (1993) Experientia , vol.49 , pp. 825-829
    • Proteau, P.J.1    Gerwick, W.H.2    Garcia-Pichel, F.3    Castenholz, R.W.4
  • 240
    • 0036300586 scopus 로고    scopus 로고
    • Spiroidesin, a novel lipopeptide from the cyanobacterium Anabaena spiroides that inhibits cell growth of the cyanobacterium Microcystis aeruginosa
    • Kaya K, Mahakhant A, Keovara L, Sano T, Kubo T, Takagi H. Spiroidesin, a novel lipopeptide from the cyanobacterium Anabaena spiroides that inhibits cell growth of the cyanobacterium Microcystis aeruginosa. J Nat Prod 2002; 65: 920-1.
    • (2002) J Nat Prod , vol.65 , pp. 920-921
    • Kaya, K.1    Mahakhant, A.2    Keovara, L.3    Sano, T.4    Kubo, T.5    Takagi, H.6
  • 241
    • 8344277514 scopus 로고    scopus 로고
    • Antibacterial activity of volatile component and various extracts of Spirulina platensis. Phytother
    • Ozdemir G, Karabay NU, Dalay MC, Pazarbasi B.Antibacterial activity of volatile component and various extracts of Spirulina platensis. Phytother. Res. 2004; 18: 754-7.
    • (2004) Res , vol.18 , pp. 754-757
    • Ozdemir, G.1    Karabay, N.U.2    Dalay, M.C.3    Pazarbasi, B.4
  • 242
    • 0035097105 scopus 로고    scopus 로고
    • Two novel cyclic peptides with antifungal activity from the cyanobacterium Tolypothrix byssoidea (EAWAG 195)
    • Jaki B, Zerbe O, Heilmann J, Sticher O. Two novel cyclic peptides with antifungal activity from the cyanobacterium Tolypothrix byssoidea (EAWAG 195). J Nat Prod 2001; 64: 154-8.
    • (2001) J Nat Prod , vol.64 , pp. 154-158
    • Jaki, B.1    Zerbe, O.2    Heilmann, J.3    Sticher, O.4
  • 243
    • 0026500940 scopus 로고
    • Tolyporphin, a novel multidrug resistance reversing agent from the blue-green alga Tolypothrix nodosa
    • Prinsep MR, Caplan FR, Moore RE, Patterson GML, Smith CD. Tolyporphin, a novel multidrug resistance reversing agent from the blue-green alga Tolypothrix nodosa. J Am Chem Soc 1992; 114: 385-7.
    • (1992) J Am Chem Soc , vol.114 , pp. 385-387
    • Prinsep, M.R.1    Caplan, F.R.2    Moore, R.E.3    Patterson, G.M.L.4    Smith, C.D.5
  • 244
  • 245
    • 0031685025 scopus 로고    scopus 로고
    • Tolyporphins J and K, two further porphinoid metabolites from the cyanobacterium Tolypothrix nodos
    • Prinsep MR, Patterson GM, Larsen LK, Smith CD. Tolyporphins J and K, two further porphinoid metabolites from the cyanobacterium Tolypothrix nodosa. J Nat Prod 1998; 61: 1133-6.
    • (1998) J Nat Pro , vol.6 , pp. 1133-1136
    • Prinsep, M.R.1    Patterson, G.M.2    Larsen, L.K.3
  • 246
    • 0023679177 scopus 로고
    • Cyto-toxic, fungicidal nucleosides from blue-green algae belonging to the Scytonemataceae
    • Stewart JB, Bornemann V, Chen JL, et al. Cyto-toxic, fungicidal nucleosides from blue-green algae belonging to the Scytonemataceae. J.Antibiot. 1988; 41: 1048-56.
    • (1988) J.Antibiot , vol.41 , pp. 1048-1056
    • Stewart, J.B.1    Bornemann, V.2    Chen, J.L.3
  • 247
    • 53749087678 scopus 로고    scopus 로고
    • A novel beta-amino acid in cytotoxic peptides from the cyanobacterium Tychonema sp
    • Mehner C, Muller D, Krick A, et al. A novel beta-amino acid in cytotoxic peptides from the cyanobacterium Tychonema sp. Eur J Org Chem 2008: 1732-9
    • (2008) Eur J Org Chem , pp. 1732-1739
    • Mehner, C.1    Muller, D.2    Krick, A.3


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