메뉴 건너뛰기




Volumn 21, Issue 12, 2014, Pages 1559-1581

Naturally occurring bioactive Cyclobutane-containing (CBC) alkaloids in fungi, fungal endophytes, and plants

Author keywords

Activities; Alkaloids; Cyclobutane; Fungal endophytes; Fungi; Plant

Indexed keywords

ALKALOID DERIVATIVE; AMPULLICIN; BRASILAMIDE A; BRASILAMIDE B; BRASILAMIDE C; BRASILAMIDE D; BROMOPENITREM E; CYCLOBUTANE CONTAINING ALKALOID DERIVATIVE; CYCLOBUTANE DERIVATIVE; DIHYDROAMPULLICIN; HERBACEOUS AGENT; ISOAMPULLICIN; PENITREM A; PENITREM B; PENITREM C; PENITREM D; PENITREM E; PENITREM F; PENITREM G; PENITREMONE A; PENITREMONE B; PENITREMONE C; PENNIGRITREM; PHOMACHALASIN B; PINTHUNAMIDE; SECOPENITREM B; THOMITREM A; THOMITREM E; TRIPARTILACTAM; UNCLASSIFIED DRUG; UNINDEXED DRUG; ALKALOID;

EID: 84907224347     PISSN: 09447113     EISSN: 1618095X     Source Type: Journal    
DOI: 10.1016/j.phymed.2014.07.005     Document Type: Review
Times cited : (144)

References (126)
  • 1
    • 0035046839 scopus 로고    scopus 로고
    • Bioactive sesquiterpenes produced by fungi: Are they useful for humans as well?
    • W.R. Abraham Bioactive sesquiterpenes produced by fungi: are they useful for humans as well? Curr. Med. Chem. 8 2001 583 606
    • (2001) Curr. Med. Chem. , vol.8 , pp. 583-606
    • Abraham, W.R.1
  • 2
    • 21144452500 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of some of new 1,1,3-trisubstituted cyclobutane-containing thiazoles, succinimide and phthalimide derivatives
    • M. Ahmedzade, A. Cukurovali, and M. Koparir Synthesis and antimicrobial activity of some of new 1,1,3-trisubstituted cyclobutane-containing thiazoles, succinimide and phthalimide derivatives J. Chem. Soc. Pak. 25 2003 51 55
    • (2003) J. Chem. Soc. Pak. , vol.25 , pp. 51-55
    • Ahmedzade, M.1    Cukurovali, A.2    Koparir, M.3
  • 8
    • 72149128877 scopus 로고    scopus 로고
    • Tall fescue and associated mutualistic toxic fungal endophytes in agroecosystems
    • D.P. Belesky, and C.W. Bacon Tall fescue and associated mutualistic toxic fungal endophytes in agroecosystems Toxin Rev. 28 2009 102 117
    • (2009) Toxin Rev. , vol.28 , pp. 102-117
    • Belesky, D.P.1    Bacon, C.W.2
  • 9
    • 84885147398 scopus 로고    scopus 로고
    • Anticancer and antifungal compounds from Aspergillus, Penicillium and other filamentous fungi
    • T.T. Bladt, J.C. Frisvad, and P.B. Knudsen Anticancer and antifungal compounds from Aspergillus, Penicillium and other filamentous fungi Molecules 18 2013 11338 11376
    • (2013) Molecules , vol.18 , pp. 11338-11376
    • Bladt, T.T.1    Frisvad, J.C.2    Knudsen, P.B.3
  • 12
    • 84862010656 scopus 로고    scopus 로고
    • Endophytic fungi: Novel sources of anticancer lead molecules
    • S. Chandra Endophytic fungi: novel sources of anticancer lead molecules Appl. Microbiol. Biotechnol. 95 2012 47 59
    • (2012) Appl. Microbiol. Biotechnol. , vol.95 , pp. 47-59
    • Chandra, S.1
  • 14
    • 21744450979 scopus 로고    scopus 로고
    • Butorphanol: Effects of a prototypical agonist-antagonist analgesic on κ-opioid receptors
    • S. Commiskey, L.-W. Fan, I.K. Ho, and R.W. Rockhold Butorphanol: effects of a prototypical agonist-antagonist analgesic on κ-opioid receptors J. Pharmacol. Sci. (Tokyo, Japan) 98 2005 109 116
    • (2005) J. Pharmacol. Sci. (Tokyo, Japan) , vol.98 , pp. 109-116
    • Commiskey, S.1    Fan, L.-W.2    Ho, I.K.3    Rockhold, R.W.4
  • 15
    • 84878935458 scopus 로고    scopus 로고
    • Fifty years of alkaloid biosynthesis in phytochemistry
    • G.A. Cordell Fifty years of alkaloid biosynthesis in phytochemistry Phytochemistry 91 2013 29 51
    • (2013) Phytochemistry , vol.91 , pp. 29-51
    • Cordell, G.A.1
  • 16
    • 84907201711 scopus 로고    scopus 로고
    • Biotechnological applications and potential uses of the mushroom Tramestes versicolor
    • K.A.M. Córdoba, and A.H. Ríos Biotechnological applications and potential uses of the mushroom Tramestes versicolor Mycol. Res. 105 2012 1514 1518
    • (2012) Mycol. Res. , vol.105 , pp. 1514-1518
    • Córdoba, K.A.M.1    Ríos, A.H.2
  • 17
    • 84989052452 scopus 로고
    • Gas chromatographic/mass spectrometric investigation of the volatile main components from roots of Securidaca longipedunculata
    • C. Costa, A. Bertazzo, M. Biasiolo, G. Allegri, O. Curcuruto, and P. Traldi Gas chromatographic/mass spectrometric investigation of the volatile main components from roots of Securidaca longipedunculata Org. Mass Spectrom. 27 1992 255 257
    • (1992) Org. Mass Spectrom. , vol.27 , pp. 255-257
    • Costa, C.1    Bertazzo, A.2    Biasiolo, M.3    Allegri, G.4    Curcuruto, O.5    Traldi, P.6
  • 18
    • 36148955457 scopus 로고    scopus 로고
    • Albert Hofmann: Life and work. Sojourn of a chemist of nature
    • G.W. Craig, and G.B. Kauffman Albert Hofmann: life and work. Sojourn of a chemist of nature Chem. Educator 11 2006 427 437
    • (2006) Chem. Educator , vol.11 , pp. 427-437
    • Craig, G.W.1    Kauffman, G.B.2
  • 20
    • 0346814161 scopus 로고    scopus 로고
    • Ergot alkaloid toxicity
    • D.L. Cross Ergot alkaloid toxicity Mycology Series 19 2003 475 494
    • (2003) Mycology Series , vol.19 , pp. 475-494
    • Cross, D.L.1
  • 21
    • 0036888754 scopus 로고    scopus 로고
    • Carbazole alkaloids as new cell cycle inhibitor and apoptosis inducers from Clausena dunniana Levl
    • C.-B. Cui, S.-Y. Yan, B. Cai, and X.-S. Yao Carbazole alkaloids as new cell cycle inhibitor and apoptosis inducers from Clausena dunniana Levl J. Asian Nat. Prod. Res. 4 2002 233 241
    • (2002) J. Asian Nat. Prod. Res. , vol.4 , pp. 233-241
    • Cui, C.-B.1    Yan, S.-Y.2    Cai, B.3    Yao, X.-S.4
  • 22
    • 0038176459 scopus 로고    scopus 로고
    • Oxidation, epoxidation and sulfoxidation reactions catalyzed by haloperoxidases
    • V.M. Dembitsky Oxidation, epoxidation and sulfoxidation reactions catalyzed by haloperoxidases Tetrahedron 59 2003 4701 4720
    • (2003) Tetrahedron , vol.59 , pp. 4701-4720
    • Dembitsky, V.M.1
  • 23
    • 33745169701 scopus 로고    scopus 로고
    • Natural neo acids and neo alkanes: Their analogues and derivatives
    • V.M. Dembitsky Natural neo acids and neo alkanes: their analogues and derivatives Lipids 41 2006 309 340
    • (2006) Lipids , vol.41 , pp. 309-340
    • Dembitsky, V.M.1
  • 26
    • 0042896552 scopus 로고
    • Chemical constituents of some higher fungi. 2. Fatty acid composition of ascomycetes
    • V.M. Dembitsky, T. Rezanka, and E.E. Shubina Chemical constituents of some higher fungi. 2. Fatty acid composition of ascomycetes Cryptogamic Botany 3 1993 378 381
    • (1993) Cryptogamic Botany , vol.3 , pp. 378-381
    • Dembitsky, V.M.1    Rezanka, T.2    Shubina, E.E.3
  • 28
    • 0010570037 scopus 로고
    • Chemical constituents of some higher fungi. 1. Fatty acid and phospholipid compositions of Basidiomycetes
    • V.M. Dembitsky, T. Rezanka, and E.E. Shubina Chemical constituents of some higher fungi. 1. Fatty acid and phospholipid compositions of Basidiomycetes Cryptogamic Botany 3 1993 373 377
    • (1993) Cryptogamic Botany , vol.3 , pp. 373-377
    • Dembitsky, V.M.1    Rezanka, T.2    Shubina, E.E.3
  • 30
    • 78651380622 scopus 로고    scopus 로고
    • Natural and synthetic small boron-containing molecules as potential inhibitors of bacterial and fungal quorum sensing
    • V.M. Dembitsky, A. Quntar, and M. Srebnik Natural and synthetic small boron-containing molecules as potential inhibitors of bacterial and fungal quorum sensing Chem. Rev. 111 2011 209 237
    • (2011) Chem. Rev. , vol.111 , pp. 209-237
    • Dembitsky, V.M.1    Quntar, A.2    Srebnik, M.3
  • 34
    • 78650011807 scopus 로고    scopus 로고
    • Peroxidase oxidation of lignin and its model compounds
    • M.A. Eisenstadt, and K.G. Bogolitsyn Peroxidase oxidation of lignin and its model compounds Russ. J. Bioorg. Chem. 36 2010 802 815
    • (2010) Russ. J. Bioorg. Chem. , vol.36 , pp. 802-815
    • Eisenstadt, M.A.1    Bogolitsyn, K.G.2
  • 35
    • 0023790090 scopus 로고
    • Production of penitrem A by Penicillium crustosum isolated from foodstuffs
    • A.A. El-Banna, and L. Leistner Production of penitrem A by Penicillium crustosum isolated from foodstuffs Int. J. Food Microbiol. 7 1988 9 17
    • (1988) Int. J. Food Microbiol. , vol.7 , pp. 9-17
    • El-Banna, A.A.1    Leistner, L.2
  • 36
    • 80052808067 scopus 로고    scopus 로고
    • Relationships between the stereochemistry and biological activity of fungal phytotoxins
    • A. Evidente, A. Andolfi, and A. Cimmino Relationships between the stereochemistry and biological activity of fungal phytotoxins Chirality 23 2011 674 693
    • (2011) Chirality , vol.23 , pp. 674-693
    • Evidente, A.1    Andolfi, A.2    Cimmino, A.3
  • 37
    • 0030624683 scopus 로고    scopus 로고
    • Ergot alkaloids-sources, structures and analytical methods
    • M. Flieger, M. Wurst, and R. Shelby Ergot alkaloids-sources, structures and analytical methods Folia Microbiol. 42 1997 3 30
    • (1997) Folia Microbiol. , vol.42 , pp. 3-30
    • Flieger, M.1    Wurst, M.2    Shelby, R.3
  • 38
    • 10644227919 scopus 로고    scopus 로고
    • Mycotoxins, drugs and other extrolites produced by species in Penicillium subgenus Penicillium
    • J.C. Frisvad, J. Smedsgaard, T.O. Larsen, and R.A. Samson Mycotoxins, drugs and other extrolites produced by species in Penicillium subgenus Penicillium Studies Mycol. 49 2004 201 241
    • (2004) Studies Mycol. , vol.49 , pp. 201-241
    • Frisvad, J.C.1    Smedsgaard, J.2    Larsen, T.O.3    Samson, R.A.4
  • 41
    • 0020118644 scopus 로고
    • 14-Alkoxy dihydrocodeinones, dihydromorphinones, and morphinanones - A new class of narcotic analgesics
    • A.C. Ghosh, R.L. Lavoie, P. Herlihy, J.F. Howes, and R.K. Razdan 14-Alkoxy dihydrocodeinones, dihydromorphinones, and morphinanones - a new class of narcotic analgesics NIDA Res. Monogr. 41 1982 105 111
    • (1982) NIDA Res. Monogr. , vol.41 , pp. 105-111
    • Ghosh, A.C.1    Lavoie, R.L.2    Herlihy, P.3    Howes, J.F.4    Razdan, R.K.5
  • 42
    • 0037427227 scopus 로고    scopus 로고
    • Insecticidal activity of penitrems, including penitrem G, a new member of the family isolated from Penicillium crustosum
    • M.C. González, C. Lull, P. Moya, I. Ayala, J. Primo, and E. Primo Yúfera Insecticidal activity of penitrems, including penitrem G, a new member of the family isolated from Penicillium crustosum J. Agric. Food Chem. 51 2003 2156 2160
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 2156-2160
    • González, M.C.1    Lull, C.2    Moya, P.3    Ayala, I.4    Primo, J.5    Primo Yúfera, E.6
  • 43
    • 52049106424 scopus 로고    scopus 로고
    • Tropane alkaloids as medicinally useful natural products and their synthetic derivatives as new drugs
    • G. Grynkiewicz, and M. Gadzikowska Tropane alkaloids as medicinally useful natural products and their synthetic derivatives as new drugs Pharmacol. Rep. 60 2008 439 463
    • (2008) Pharmacol. Rep. , vol.60 , pp. 439-463
    • Grynkiewicz, G.1    Gadzikowska, M.2
  • 44
    • 2342577496 scopus 로고    scopus 로고
    • Use of the mixed agonist-antagonist nalbuphine in opioid based analgesia
    • M.W. Gunion, A.M. Marchionne, and C.T.M. Anderson Use of the mixed agonist-antagonist nalbuphine in opioid based analgesia Acute Pain 6 2004 29 39
    • (2004) Acute Pain , vol.6 , pp. 29-39
    • Gunion, M.W.1    Marchionne, A.M.2    Anderson, C.T.M.3
  • 45
    • 48249111333 scopus 로고    scopus 로고
    • Lipids and fatty acids of wild edible mushrooms of the genus Boletus
    • L.O. Hanuš, I. Shkrob, and V.M. Dembitsky Lipids and fatty acids of wild edible mushrooms of the genus Boletus J. Food Lipids 15 2008 370 383
    • (2008) J. Food Lipids , vol.15 , pp. 370-383
    • Hanuš, L.O.1    Shkrob, I.2    Dembitsky, V.M.3
  • 46
    • 0030733491 scopus 로고    scopus 로고
    • Mitindomide is a catalytic inhibitor of DNA Topoisomerase II that acts at the bisdioxopiperazine binding site
    • B.B. Hasinoff, A.M. Creighton, H. Kozlowska, P. Thampatty, W.P. Allan, and J.C. Yalowich Mitindomide is a catalytic inhibitor of DNA Topoisomerase II that acts at the bisdioxopiperazine binding site Mol. Pharmacol. 52 1997 839 845
    • (1997) Mol. Pharmacol. , vol.52 , pp. 839-845
    • Hasinoff, B.B.1    Creighton, A.M.2    Kozlowska, H.3    Thampatty, P.4    Allan, W.P.5    Yalowich, J.C.6
  • 48
    • 38749142535 scopus 로고
    • The effect of ergot alkaloids, their partial synthetic derivatives and serotonin on blood clotting
    • J. Hladovec, and Z. Votava The effect of ergot alkaloids, their partial synthetic derivatives and serotonin on blood clotting Chekhoslov Fiziologia 7 1958 553 558
    • (1958) Chekhoslov Fiziologia , vol.7 , pp. 553-558
    • Hladovec, J.1    Votava, Z.2
  • 49
    • 0025677679 scopus 로고
    • Structures of new indoloditerpenes, possible biosynthetic precursors of the tremorgenic mycotoxins, penitrems, from Penicillium crustosum
    • T. Hosoe, K. Nozawa, S. Udagawa, S. Nakajima, and K. Kawai Structures of new indoloditerpenes, possible biosynthetic precursors of the tremorgenic mycotoxins, penitrems, from Penicillium crustosum Chem. Pharm. Bull. 38 1990 3473 3475
    • (1990) Chem. Pharm. Bull. , vol.38 , pp. 3473-3475
    • Hosoe, T.1    Nozawa, K.2    Udagawa, S.3    Nakajima, S.4    Kawai, K.5
  • 50
    • 0015073879 scopus 로고
    • Tremorgenic toxins from Penicillia. III. Tremortin production by Penicillium species on various agricultural commodities
    • C.T. Hou, A. Ciegler, and C.W. Hesseltine Tremorgenic toxins from Penicillia. III. Tremortin production by Penicillium species on various agricultural commodities Appl. Microbiol. 21 1971 1101 1103
    • (1971) Appl. Microbiol. , vol.21 , pp. 1101-1103
    • Hou, C.T.1    Ciegler, A.2    Hesseltine, C.W.3
  • 51
    • 84871932944 scopus 로고    scopus 로고
    • Parasitic fungus Claviceps as a source for biotechnological production of ergot alkaloids
    • H. Hulvova, P. Galuszka, J. Frebortova, and I. Frebort Parasitic fungus Claviceps as a source for biotechnological production of ergot alkaloids Biotechnol. Adv. 31 2013 79 89
    • (2013) Biotechnol. Adv. , vol.31 , pp. 79-89
    • Hulvova, H.1    Galuszka, P.2    Frebortova, J.3    Frebort, I.4
  • 53
    • 84878153455 scopus 로고    scopus 로고
    • Drug discovery: Synthesized dreams
    • M. Jay Drug discovery: synthesized dreams Nature (London, UK) 497 2013 435 436
    • (2013) Nature (London, UK) , vol.497 , pp. 435-436
    • Jay, M.1
  • 55
    • 0342427773 scopus 로고
    • Grahamine, an unusual tropane alkaloid from Schizanthus grahamii
    • R. Hartmann, A. San-Martin, O. Munoz, and E. Breitmaier Grahamine, an unusual tropane alkaloid from Schizanthus grahamii Angew. Chem. 102 1990 441 443
    • (1990) Angew. Chem. , vol.102 , pp. 441-443
    • Hartmann, R.1    San-Martin, A.2    Munoz, O.3    Breitmaier, E.4
  • 56
    • 27144513748 scopus 로고    scopus 로고
    • 200 years of morphine. New developments from research
    • U. Holzgrabe 200 years of morphine. New developments from research Pharmaz Z (Germany) 150 2005 32 38
    • (2005) Pharmaz Z (Germany) , vol.150 , pp. 32-38
    • Holzgrabe, U.1
  • 58
    • 80052070698 scopus 로고    scopus 로고
    • Anticancer compounds derived from fungal endophytes: Their importance and future challenges
    • R.N. Kharwar, A. Mishra, and S.K. Gond Anticancer compounds derived from fungal endophytes: their importance and future challenges Nat. Prod. Rep. 28 2011 1208 1228
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 1208-1228
    • Kharwar, R.N.1    Mishra, A.2    Gond, S.K.3
  • 59
    • 0014575185 scopus 로고
    • Terpenoid alkaloids from Murraya koenigii Spreng. II. The constitution of cyclomahanimbine, bicyclomahanibine, and mahanimbidine
    • 1969
    • S.P. Kureel, R.S. Kapil, and S.P. Popli Terpenoid alkaloids from Murraya koenigii Spreng. II. The constitution of cyclomahanimbine, bicyclomahanibine, and mahanimbidine Tetrahedron Lett. 44 1969 3857 3862 1969
    • (1969) Tetrahedron Lett. , vol.44 , pp. 3857-3862
    • Kureel, S.P.1    Kapil, R.S.2    Popli, S.P.3
  • 60
    • 0024519567 scopus 로고
    • Pinthunamide, a new tricyclic sesquiterpene amide produced by a fungus, Ampullifernia sp
    • Y. Kimura, M. Hiromitsu, and H. Takashi Pinthunamide, a new tricyclic sesquiterpene amide produced by a fungus, Ampullifernia sp Tetrahedron Lett. 30 1989 1267 1270
    • (1989) Tetrahedron Lett. , vol.30 , pp. 1267-1270
    • Kimura, Y.1    Hiromitsu, M.2    Takashi, H.3
  • 61
    • 0000417575 scopus 로고
    • Ampullicin and isoampullicin, a new metabolites from Ampullifera - Like fungus sp. No 27
    • Y. Kimura, H. Nakajima, T. Hamasaki, Y. Matsumoto, and A. Tseunda Ampullicin and isoampullicin, a new metabolites from Ampullifera - like fungus sp. No 27 Agric. Biol. Chem. 54 1990 813 814
    • (1990) Agric. Biol. Chem. , vol.54 , pp. 813-814
    • Kimura, Y.1    Nakajima, H.2    Hamasaki, T.3    Matsumoto, Y.4    Tseunda, A.5
  • 62
    • 0000577980 scopus 로고
    • Dihydroampullicin, a new plant growth regulators produced by the Ampulliferina-like fungus sp No 27
    • Y. Kimura, T. Matsumoto, H. Nakajima, T. Hamasaki, and Y. Matsuda Dihydroampullicin, a new plant growth regulators produced by the Ampulliferina-like fungus sp No 27 Biosci. Biotechnol. Biochem. 57 1993 687 688
    • (1993) Biosci. Biotechnol. Biochem. , vol.57 , pp. 687-688
    • Kimura, Y.1    Matsumoto, T.2    Nakajima, H.3    Hamasaki, T.4    Matsuda, Y.5
  • 64
    • 0013182933 scopus 로고
    • Sulpinines A-C and secopenitrem B: New antiinsectan metabolites from the sclerotia of Aspergillus sulphureus
    • J. Laakso, J.B. Gloer, D.T. Wicklow, and P.F. Dowd Sulpinines A-C and secopenitrem B: new antiinsectan metabolites from the sclerotia of Aspergillus sulphureus J. Org. Chem. 57 1992 2066 2071
    • (1992) J. Org. Chem. , vol.57 , pp. 2066-2071
    • Laakso, J.1    Gloer, J.B.2    Wicklow, D.T.3    Dowd, P.F.4
  • 65
    • 0000366412 scopus 로고
    • A new penitrem analog with antiinsectan activity from the sclerotia of Aspergillus sulphureus
    • J.A. Laakso, J.B. Gloer, D.T. Wicklow, and P.F. Dowd A new penitrem analog with antiinsectan activity from the sclerotia of Aspergillus sulphureus J. Agric. Food Chem. 41 1993 973 975
    • (1993) J. Agric. Food Chem. , vol.41 , pp. 973-975
    • Laakso, J.A.1    Gloer, J.B.2    Wicklow, D.T.3    Dowd, P.F.4
  • 67
    • 79959979820 scopus 로고    scopus 로고
    • Pentacyclic polyketides from Endiandra kingiana as inhibitors of the Bcl-xL/Bak interaction
    • A. Leverrier, K. Awang, F. Gueritte, and M. Litaudon Pentacyclic polyketides from Endiandra kingiana as inhibitors of the Bcl-xL/Bak interaction Phytochemistry 72 2011 1443 1452
    • (2011) Phytochemistry , vol.72 , pp. 1443-1452
    • Leverrier, A.1    Awang, K.2    Gueritte, F.3    Litaudon, M.4
  • 70
    • 68349106971 scopus 로고    scopus 로고
    • Nematicidal activity of Paecilomyces spp. and isolation of a novel active compound
    • Y.J. Liu, C.Y. Zhai, Y. Liu, and K.Q. Zhang Nematicidal activity of Paecilomyces spp. and isolation of a novel active compound J. Microbiol. 47 2009 248 252
    • (2009) J. Microbiol. , vol.47 , pp. 248-252
    • Liu, Y.J.1    Zhai, C.Y.2    Liu, Y.3    Zhang, K.Q.4
  • 71
    • 38749087220 scopus 로고
    • Ergot alkaloids. XXIV. Paper chromatography of lysergic acid cycloalkamides and N-methy-lergolinyl-N 0 -cycloalkylureas
    • K. Macek, and S. Vanecek Ergot alkaloids. XXIV. Paper chromatography of lysergic acid cycloalkamides and N-methy-lergolinyl-N 0 -cycloalkylureas Pharmazie 17 1962 442 444
    • (1962) Pharmazie , vol.17 , pp. 442-444
    • Macek, K.1    Vanecek, S.2
  • 72
    • 0021271140 scopus 로고
    • A novel process for the production of Penitrem mycotoxins by submerged fermentation of Penicillium nigricuns
    • P.G. Mantle, I. Laws, M.J. Tan, and M. Tizard A novel process for the production of Penitrem mycotoxins by submerged fermentation of Penicillium nigricuns J. Gen. Microbiol. 130 1984 1293 1298
    • (1984) J. Gen. Microbiol. , vol.130 , pp. 1293-1298
    • Mantle, P.G.1    Laws, I.2    Tan, M.J.3    Tizard, M.4
  • 73
    • 0346664903 scopus 로고
    • A role for paxilline in the biosynthesis of indole-diterpenoid penitrem mycotoxins
    • P.G. Mantle, and J. Penn A role for paxilline in the biosynthesis of indole-diterpenoid penitrem mycotoxins J. Chem. Soc.; Perkin Trans. 1 1989 1539 1540
    • (1989) J. Chem. Soc.; Perkin Trans. , vol.1 , pp. 1539-1540
    • Mantle, P.G.1    Penn, J.2
  • 75
    • 79251618552 scopus 로고    scopus 로고
    • Isolation and structure elucidation of secopenitrem D, an indole alkaloid from Penicillium crustosum Thom
    • A. Moldes-Anaya, T. Rundberget, S. Uhlig, F. Rise, and A.L. Wilkins Isolation and structure elucidation of secopenitrem D, an indole alkaloid from Penicillium crustosum Thom Toxicon 57 2011 259 265
    • (2011) Toxicon , vol.57 , pp. 259-265
    • Moldes-Anaya, A.1    Rundberget, T.2    Uhlig, S.3    Rise, F.4    Wilkins, A.L.5
  • 77
    • 37049072133 scopus 로고
    • Penicillium metabolites containing an oxidized penitrem carbon skeleton giving insight into structure - Tremorgenic relationships
    • J.T. Naik, P.G. Mantle, R.N. Sheppard, E.S. Waight, and A.-C Penitremones Penicillium metabolites containing an oxidized penitrem carbon skeleton giving insight into structure - tremorgenic relationships J. Chem. Soc.; Perkin Trans. 1 9 1995 1121 1125
    • (1995) J. Chem. Soc.; Perkin Trans. , vol.1 , Issue.9 , pp. 1121-1125
    • Naik, J.T.1    Mantle, P.G.2    Sheppard, R.N.3    Waight, E.S.4    Penitremones, A.-C.5
  • 78
  • 81
    • 70349650687 scopus 로고    scopus 로고
    • Function-oriented biosynthesis of β-lactone proteasome inhibitors in Salinispora tropica
    • M. Nett, T.A.M. Gulder, A.J. Kale, C.C. Hughes, and B.S. Moore Function-oriented biosynthesis of β-lactone proteasome inhibitors in Salinispora tropica J. Med. Chem. 52 2009 6163 6167
    • (2009) J. Med. Chem. , vol.52 , pp. 6163-6167
    • Nett, M.1    Gulder, T.A.M.2    Kale, A.J.3    Hughes, C.C.4    Moore, B.S.5
  • 84
  • 85
    • 84863230340 scopus 로고    scopus 로고
    • Tripartilactam, a cyclobutane-bearing tricyclic lactam from a Streptomyces sp. in a dung beetle's brood ball
    • S.H. Park, K. Moon, H.S. Bang, S.H. Kim, D.G. Kim, K.B. Oh, J. Shin, and D.C. Oh Tripartilactam, a cyclobutane-bearing tricyclic lactam from a Streptomyces sp. in a dung beetle's brood ball Org. Lett. 14 2012 1258 1261
    • (2012) Org. Lett. , vol.14 , pp. 1258-1261
    • Park, S.H.1    Moon, K.2    Bang, H.S.3    Kim, S.H.4    Kim, D.G.5    Oh, K.B.6    Shin, J.7    Oh, D.C.8
  • 86
    • 0012004110 scopus 로고
    • Pennigritrem, a naturally-occurring penitrem A analog with novel cyclization in the diterpenoid moiety
    • J. Penn, J.R. Biddle, P.G. Mantle, J.N. Bilton, and R.N. Sheppard Pennigritrem, a naturally-occurring penitrem A analog with novel cyclization in the diterpenoid moiety J. Chem. Soc.; Perkin Trans. 1 1 1992 23 26
    • (1992) J. Chem. Soc.; Perkin Trans. 1 , vol.1 , pp. 23-26
    • Penn, J.1    Biddle, J.R.2    Mantle, P.G.3    Bilton, J.N.4    Sheppard, R.N.5
  • 87
    • 77749315487 scopus 로고    scopus 로고
    • An overview of mycotoxin contamination in foods and its implications for human health
    • K.R.N. Reddy, B. Salleh, B. Saad, H.K. Abbas, C.A. Abel, and W.T. Shier An overview of mycotoxin contamination in foods and its implications for human health Toxin Rev. 29 2010 3 26
    • (2010) Toxin Rev. , vol.29 , pp. 3-26
    • Reddy, K.R.N.1    Salleh, B.2    Saad, B.3    Abbas, H.K.4    Abel, C.A.5    Shier, W.T.6
  • 88
    • 70549091187 scopus 로고    scopus 로고
    • Photochemical dimerization of wasalexins in UV-irradiated Thellungiella halophila and in vitro generates unique cruciferous phytoalexins
    • M.S.C. Pedras, Q.-A. Zheng, G. Schatte, and A.M. Adio Photochemical dimerization of wasalexins in UV-irradiated Thellungiella halophila and in vitro generates unique cruciferous phytoalexins Phytochemistry 70 2009 2010 2016
    • (2009) Phytochemistry , vol.70 , pp. 2010-2016
    • Pedras, M.S.C.1    Zheng, Q.-A.2    Schatte, G.3    Adio, A.M.4
  • 90
    • 0141654021 scopus 로고
    • Antineoplastic agents. 90 the structure of the benzene-maleimide photosynthetic product (mitindomide)
    • G.R. Pettit, K.D. Paull, C.L. Herald, D.L. Herald, and J.R. Riden Antineoplastic agents. 90. The structure of the benzene-maleimide photosynthetic product (mitindomide) Can. J. Chem. 61 1983 2291 2294
    • (1983) Can. J. Chem. , vol.61 , pp. 2291-2294
    • Pettit, G.R.1    Paull, K.D.2    Herald, C.L.3    Herald, D.L.4    Riden, J.R.5
  • 91
    • 0008892388 scopus 로고
    • Penicillium crustosum and P. Simplicissimum, the correct names for two common species producing tremorgenic mycotoxins
    • J.I. Pitt Penicillium crustosum and P. simplicissimum, the correct names for two common species producing tremorgenic mycotoxins Mycologia 71 1979 1166 1177
    • (1979) Mycologia , vol.71 , pp. 1166-1177
    • Pitt, J.I.1
  • 93
    • 0042416797 scopus 로고    scopus 로고
    • Characterization of the hydroxy fatty acid content of Basidiomycotina
    • T. Rezanka, O.A. Rozentsvet, and V.M. Dembitsky Characterization of the hydroxy fatty acid content of Basidiomycotina Folia Microbiolgia 44 1999 635 641
    • (1999) Folia Microbiolgia , vol.44 , pp. 635-641
    • Rezanka, T.1    Rozentsvet, O.A.2    Dembitsky, V.M.3
  • 94
    • 84892984034 scopus 로고    scopus 로고
    • Loline alkaloid production by fungal endophytes of Fescue species select for particular epiphytic bacterial microflora
    • E. Roberts, and S. Lindow Loline alkaloid production by fungal endophytes of Fescue species select for particular epiphytic bacterial microflora ISME J. 8 2014 359 368
    • (2014) ISME J. , vol.8 , pp. 359-368
    • Roberts, E.1    Lindow, S.2
  • 95
    • 0036897670 scopus 로고    scopus 로고
    • Thomitrems A and E, two indole-alkaloid isoprenoids from Penicillium crustosum Thom
    • T. Rundberget, and A.L. Wilkins Thomitrems A and E, two indole-alkaloid isoprenoids from Penicillium crustosum Thom Phytochemistry 61 2002 979 985
    • (2002) Phytochemistry , vol.61 , pp. 979-985
    • Rundberget, T.1    Wilkins, A.L.2
  • 96
    • 0242507750 scopus 로고    scopus 로고
    • Genotoxicity assessment of five tremorgenic mycotoxins (fumitremorgen B, paxilline, penitrem A, verruculogen, and verrucosidin) produced by molds isolated from fermented meats
    • M. Sabater-Vilar, S. Nijmeijer, and J. Fink-Gremmels Genotoxicity assessment of five tremorgenic mycotoxins (fumitremorgen B, paxilline, penitrem A, verruculogen, and verrucosidin) produced by molds isolated from fermented meats J. Food Prot. 66 2003 2123 2129
    • (2003) J. Food Prot. , vol.66 , pp. 2123-2129
    • Sabater-Vilar, M.1    Nijmeijer, S.2    Fink-Gremmels, J.3
  • 97
    • 84884787016 scopus 로고    scopus 로고
    • Bioguided discovery and pharmacophore modeling of the mycotoxic indole diterpene alkaloids penitrems as breast cancer proliferation, migration, and invasion inhibitors
    • A.A. Sallam, W.E. Houssen, C.R. Gissendanner, K.Y. Orabi, A.I. Foudah, and K.A. El-Sayed Bioguided discovery and pharmacophore modeling of the mycotoxic indole diterpene alkaloids penitrems as breast cancer proliferation, migration, and invasion inhibitors Med. Chem. Commun. 10 2013 1360 1369
    • (2013) Med. Chem. Commun. , vol.10 , pp. 1360-1369
    • Sallam, A.A.1    Houssen, W.E.2    Gissendanner, C.R.3    Orabi, K.Y.4    Foudah, A.I.5    El-Sayed, K.A.6
  • 98
    • 0043284563 scopus 로고
    • Lipids in fungal biotechnology
    • Kück Springer Berlin Heidelberg, New York
    • M. Sancholle, and D.M. Lösel Lipids in fungal biotechnology Kück The Mycota II Genetics and Biotechnology 1995 Springer Berlin Heidelberg, New York 339 367
    • (1995) The Mycota II Genetics and Biotechnology , pp. 339-367
    • Sancholle, M.1    Lösel, D.M.2
  • 99
    • 84856380651 scopus 로고    scopus 로고
    • A new carbazole alkaloid from the leaves of Malayan Murraya koenigii
    • K.-M. Sim, and H.-M. Teh A new carbazole alkaloid from the leaves of Malayan Murraya koenigii J. Asian Nat. Prod. Res. 13 2011 972 975
    • (2011) J. Asian Nat. Prod. Res. , vol.13 , pp. 972-975
    • Sim, K.-M.1    Teh, H.-M.2
  • 100
    • 23944438094 scopus 로고    scopus 로고
    • Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii
    • M. Shoeb, S. Celik, M. Jaspars, Y. Kumarasamy, S.M. MacManus, L. Nahar, P.K. Thoo-Lin, and S.D. Sarker Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii Tetrahedron 61 2005 9001 9006
    • (2005) Tetrahedron , vol.61 , pp. 9001-9006
    • Shoeb, M.1    Celik, S.2    Jaspars, M.3    Kumarasamy, Y.4    Macmanus, S.M.5    Nahar, L.6    Thoo-Lin, P.K.7    Sarker, S.D.8
  • 101
    • 85056069234 scopus 로고    scopus 로고
    • Cyclobutane-containing alkaloids: Origin, synthesis, and biological activity
    • A. Sergeiko, V.V. Poroikov, L.O. Hanus, and V.M. Dembitsky Cyclobutane-containing alkaloids: origin, synthesis, and biological activity Open Med. Chem. J. 2 2008 26 37
    • (2008) Open Med. Chem. J. , vol.2 , pp. 26-37
    • Sergeiko, A.1    Poroikov, V.V.2    Hanus, L.O.3    Dembitsky, V.M.4
  • 102
    • 0024841899 scopus 로고
    • Fungal tremorgens: The mechanism of action of single nitrogen containing toxins-a hypothesis
    • M.I. Selala, F. Daelemans, and P.J. Schepens Fungal tremorgens: the mechanism of action of single nitrogen containing toxins-a hypothesis Drug Chem. Toxicol. 12 1989 215 237
    • (1989) Drug Chem. Toxicol. , vol.12 , pp. 215-237
    • Selala, M.I.1    Daelemans, F.2    Schepens, P.J.3
  • 104
    • 77957063372 scopus 로고
    • Morphine alkaloids
    • R.H.F. Manske, Academic London
    • G. Stork Morphine alkaloids R.H.F. Manske, Alkaloids - Chemistry And Physiology vol. 6 1960 Academic London 219 245
    • (1960) Alkaloids - Chemistry and Physiology , vol.6 , pp. 219-245
    • Stork, G.1
  • 105
    • 0027973653 scopus 로고
    • Welwitindolinones, unusual alkaloids from the blue-green algae Hapalosiphon welwitschii and Westiella intricata. Relationship to Fischer indoles and hapalinodoles
    • K. Stratmann, R.E. Moore, R. Bonjouklian, J.B. Deeter, G.M.L. Patterson, S. Shaffer, C.D. Smith, and T.A. Smitka Welwitindolinones, unusual alkaloids from the blue-green algae Hapalosiphon welwitschii and Westiella intricata. Relationship to Fischer indoles and hapalinodoles J. Am. Chem. Soc. 116 1994 9935 9942
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 9935-9942
    • Stratmann, K.1    Moore, R.E.2    Bonjouklian, R.3    Deeter, J.B.4    Patterson, G.M.L.5    Shaffer, S.6    Smith, C.D.7    Smitka, T.A.8
  • 106
    • 33744913556 scopus 로고    scopus 로고
    • Alkamides from Piper nigrum L. and their inhibitory activity against human liver microsomal cytochrome P450 2D6 (CYP2D6)
    • U.T. Subehan, S. Kadota, and Y. Tezuka Alkamides from Piper nigrum L. and their inhibitory activity against human liver microsomal cytochrome P450 2D6 (CYP2D6) Planta Med. 72 2006 527 532
    • (2006) Planta Med. , vol.72 , pp. 527-532
    • Subehan, U.T.1    Kadota, S.2    Tezuka, Y.3
  • 107
    • 62549100395 scopus 로고    scopus 로고
    • Using Roquefortine C as a Biomarker for Penitrem A Intoxication
    • A.K. Tiwaryl, B. Puschner, and R.H. Poppenda Using Roquefortine C as a Biomarker for Penitrem A Intoxication J. Vet. Diagn. Invest. 21 2009 237 239
    • (2009) J. Vet. Diagn. Invest. , vol.21 , pp. 237-239
    • Tiwaryl, A.K.1    Puschner, B.2    Poppenda, R.H.3
  • 108
    • 0037169919 scopus 로고    scopus 로고
    • Dipiperamides A, B, and C: Bisalkaloids from the white pepper Piper nigrum inhibiting CYP3A4 activity
    • S. Tsukamoto, B.-C. Cha, and T. Ohta Dipiperamides A, B, and C: bisalkaloids from the white pepper Piper nigrum inhibiting CYP3A4 activity Tetrahedron 58 2002 1667 1671
    • (2002) Tetrahedron , vol.58 , pp. 1667-1671
    • Tsukamoto, S.1    Cha, B.-C.2    Ohta, T.3
  • 111
    • 79952014752 scopus 로고    scopus 로고
    • Ergot alkaloids: Structure diversity, biosynthetic gene clusters and functional proof of biosynthetic genes
    • C. Wallwey, and S.-M. Li Ergot alkaloids: structure diversity, biosynthetic gene clusters and functional proof of biosynthetic genes Nat. Prod. Rep. 28 2011 496 510
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 496-510
    • Wallwey, C.1    Li, S.-M.2
  • 112
    • 82955250122 scopus 로고    scopus 로고
    • Natural products with antitumor activity from endophytic fungi
    • L.-W. Wang, Y.-L. Zhang, and F.-C. Lin Natural products with antitumor activity from endophytic fungi Mini-Rev. Med. Chem. 11 2011 1056 1074
    • (2011) Mini-Rev. Med. Chem. , vol.11 , pp. 1056-1074
    • Wang, L.-W.1    Zhang, Y.-L.2    Lin, F.-C.3
  • 114
    • 84866494995 scopus 로고    scopus 로고
    • Discovery and characterization of terpenoid biosynthetic pathways of fungi
    • G.T. Wawrzyn, S.E. Bloch, and C. Schmidt-Dannert Discovery and characterization of terpenoid biosynthetic pathways of fungi Methods Enzymol. 515 2012 83 105
    • (2012) Methods Enzymol. , vol.515 , pp. 83-105
    • Wawrzyn, G.T.1    Bloch, S.E.2    Schmidt-Dannert, C.3
  • 115
    • 0141657722 scopus 로고
    • Production of penitrem A and of an unidentified toxin by Penicillium lanoso-coeruleum isolated from weevil-damaged pecans
    • J.M. Wells, and R.J. Cole Production of penitrem A and of an unidentified toxin by Penicillium lanoso-coeruleum isolated from weevil-damaged pecans Phytopathology 67 1977 779 782
    • (1977) Phytopathology , vol.67 , pp. 779-782
    • Wells, J.M.1    Cole, R.J.2
  • 116
    • 0029186703 scopus 로고
    • Two carbazole alkaloids from leaves of Murraya euchrestifolia
    • T.-S. Wu, M.-L. Wang, P.-L. Wu, and T.-T. Jong Two carbazole alkaloids from leaves of Murraya euchrestifolia Phytochemistry 40 1995 1817 1819
    • (1995) Phytochemistry , vol.40 , pp. 1817-1819
    • Wu, T.-S.1    Wang, M.-L.2    Wu, P.-L.3    Jong, T.-T.4
  • 119
    • 0000530364 scopus 로고
    • Indoloditerpenes related to tremorgenic mycotoxins, penitrems, from Penicillium crustosum
    • T. Yamaguchi, K. Nozawa, T. Hosoe, S. Nakajima, and K. Kawai Indoloditerpenes related to tremorgenic mycotoxins, penitrems, from Penicillium crustosum Phytochemistry 32 1993 1177 1181
    • (1993) Phytochemistry , vol.32 , pp. 1177-1181
    • Yamaguchi, T.1    Nozawa, K.2    Hosoe, T.3    Nakajima, S.4    Kawai, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.