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Volumn 12, Issue 1, 2014, Pages 477-490

Alkaloids from the mangrove-derived actinomycete Jishengella endophytica 161111

Author keywords

Actinomycete; Anti H1N1 virus activity; Jishengella endophytica 161111; Mangrove; Pyrazine derivative

Indexed keywords

1 HYDROXY BETA CARBOLINE; 1H INDOLE 3 CARBOXALDEHYDE; 2 (FURAN 2 YL) 5 (4 TRIHYDROXYBUTYL)PYRAZINE; 2 (FURAN 2 YL) 6 (4 TRIHYDROXYBUTYL)PYRAZINE; 2 HYDROXY 1 (1H INDOL 3 YL)ETHANONE; 4 (2 METHYLBUTYL) 3 OXO 3,4 DIHYDRO 1H PYRROLO[2,1C][1,4]OXAZINE 6 CARBALDEHYDE; 4 BENZYL 3 OXO 3,4 DIHYDRO 1H PYRROLO[2,1C][1,4]OXAZINE 6 CARBALDEHYDE; 4 ISOBUTYL 3 OXO 3,4 DIHYDRO 1H PYRROLO[2,1C][1,4]OXAZINE 6 CARBALDEHYDE; 4 ISOPROPYL 3 OXO 3,4 DIHYDRO 1H PYRROLO[2,1C][1,4]OXAZINE 6 CARBALDEHYDE; 5 METHOXYMETHYL 1H PYRROLE 2 CARBALDEHYDE; ALKALOID DERIVATIVE; FLAZIN; LACTONE; LUMICHROME; PERLOLYRINE; RIBAVIRIN; UNCLASSIFIED DRUG;

EID: 84892868044     PISSN: None     EISSN: 16603397     Source Type: Journal    
DOI: 10.3390/md12010477     Document Type: Article
Times cited : (74)

References (51)
  • 1
    • 0036953611 scopus 로고    scopus 로고
    • Bioactivities, bioactive compounds and chemical constituents of mangrove Plants
    • Bandaranayake, W.M. Bioactivities, bioactive compounds and chemical constituents of mangrove Plants. Wetl. Ecol. Manag. 2002, 10, 421-452.
    • (2002) Wetl. Ecol. Manag. , vol.10 , pp. 421-452
    • Bandaranayake, W.M.1
  • 3
    • 84860607739 scopus 로고    scopus 로고
    • Streptocarbazoles A and B, two novel indolocarbazoles from the marine-derived actinomycete strain Streptomyces sp. F MA
    • Fu, P.; Yang, C.L.; Wang, Y.; Liu, P.P.; Ma, Y.M.; Xu, L.; Su, M.B.; Hong, K.; Zhu, W.M. Streptocarbazoles A and B, two novel indolocarbazoles from the marine-derived actinomycete strain Streptomyces sp. F MA. Org. Lett . 2012, 14, 2422-2425.
    • (2012) Org. Lett. , vol.14 , pp. 2422-2425
    • Fu, P.1    Yang, C.L.2    Wang, Y.3    Liu, P.P.4    Ma, Y.M.5    Xu, L.6    Su, M.B.7    Hong, K.8    Zhu, W.M.9
  • 4
    • 34548862062 scopus 로고    scopus 로고
    • Nonomuraea maheshkhaliensis sp. Nov., a novel actinomycete isolated from mangrove rhizosphere mud
    • Ara, I.; Kudo, T.; Matsumoto, A.; Takahashi, Y.; Omura, S. Nonomuraea maheshkhaliensis sp. nov., a novel actinomycete isolated from mangrove rhizosphere mud. J. Gen. Appl. Microbiol. 2007, 53, 159-166.
    • (2007) J. Gen. Appl. Microbiol. , vol.53 , pp. 159-166
    • Ara, I.1    Kudo, T.2    Matsumoto, A.3    Takahashi, Y.4    Omura, S.5
  • 6
    • 38449091944 scopus 로고    scopus 로고
    • A novel analgesic pyrazine derivative from the leaves of Croton tiglium L
    • Wu, X.A.; Zhao, Y.M.; Yu, N.J. A novel analgesic pyrazine derivative from the leaves of Croton tiglium L. J. Asian Nat. Prod. Res. 2007, 9, 451-455.
    • (2007) J. Asian Nat. Prod. Res. , vol.9 , pp. 451-455
    • Wu, X.A.1    Zhao, Y.M.2    Yu, N.J.3
  • 8
    • 0001350972 scopus 로고
    • Studies on flavor components of roasted chicory root
    • Sannai, Y.; Fujimori, T.; Kato, K. Studies on flavor components of roasted chicory root. Agric. Biol. Chem. 1982, 46, 429-433.
    • (1982) Agric. Biol. Chem. , vol.46 , pp. 429-433
    • Sannai, Y.1    Fujimori, T.2    Kato, K.3
  • 10
    • 0034465645 scopus 로고    scopus 로고
    • Synthesis and reactivity of the monosaccharide esters of amino acids as models of teichoic acid fragment
    • Jeric, I.; Simicic, L.; Stipetic, M.; Horvat, S. Synthesis and reactivity of the monosaccharide esters of amino acids as models of teichoic acid fragment. Glycoconj. J. 2000, 17, 273-282.
    • (2000) Glycoconj. J. , vol.17 , pp. 273-282
    • Jeric, I.1    Simicic, L.2    Stipetic, M.3    Horvat, S.4
  • 12
    • 79955808773 scopus 로고    scopus 로고
    • [2+2+2] Cycloadditions of alkynylynamides - A total synthesis of perlolyrine and the first total synthesis of "isoperlolyrine"
    • Dassonneville, B.; Witulski, B.; Detert, H. [2+2+2] Cycloadditions of alkynylynamides - A total synthesis of perlolyrine and the first total synthesis of "isoperlolyrine". Eur. J. Org. Chem. 2011, 2011, 2836-2844.
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 2836-2844
    • Dassonneville, B.1    Witulski, B.2    Detert, H.3
  • 14
    • 36849017493 scopus 로고    scopus 로고
    • Indole alkaloid from the red sea sponge Hyrtios erectus
    • Ashour, M.A.; Elkhayat, E.S.; Ebel, R.; Edrada, R.; Proksch, P. Indole alkaloid from the red sea sponge Hyrtios erectus. Arkivoc 2007, 2007, 225-231.
    • (2007) Arkivoc , vol.2007 , pp. 225-231
    • Ashour, M.A.1    Elkhayat, E.S.2    Ebel, R.3    Edrada, R.4    Proksch, P.5
  • 15
    • 0031024036 scopus 로고    scopus 로고
    • Metabolism studies of indole derivatives using a staurosporine producer, Streptomyces staurosporeus
    • Yang, S.W.; Cordell, G.A. Metabolism studies of indole derivatives using a staurosporine producer, Streptomyces staurosporeus. J. Nat. Prod. 1997, 60, 44-48.
    • (1997) J. Nat. Prod. , vol.60 , pp. 44-48
    • Yang, S.W.1    Cordell, G.A.2
  • 17
    • 0033550204 scopus 로고    scopus 로고
    • Novel alkaloids from the red ascidian Botryllus leachi
    • Duran, R.; Zubia, E.; Ortega, M.J.; Naranjo, S.; Salva, J. Novel alkaloids from the red ascidian Botryllus leachi. Tetrahedron 1999, 55, 13225-13232.
    • (1999) Tetrahedron , vol.55 , pp. 13225-13232
    • Duran, R.1    Zubia, E.2    Ortega, M.J.3    Naranjo, S.4    Salva, J.5
  • 20
    • 0031927985 scopus 로고    scopus 로고
    • Antineoplastic agents. 398. Isolation and structure elucidation of cephalostatins 18 and 19
    • Pettit, G.R.; Tan, R.; Xu, J.P.; Ichihara, Y.; Williams, M.D.; Boyd, M.R. Antineoplastic agents. 398. Isolation and structure elucidation of cephalostatins 18 and 19. J. Nat. Prod. 1998, 61, 955-958.
    • (1998) J. Nat. Prod. , vol.61 , pp. 955-958
    • Pettit, G.R.1    Tan, R.2    Xu, J.P.3    Ichihara, Y.4    Williams, M.D.5    Boyd, M.R.6
  • 22
    • 36048940753 scopus 로고    scopus 로고
    • Xylogranatinin, a new pyrido[1, 2-a] pyrazine alkaloid from the fruit of a chinese mangrove Xylocarpus granatum
    • Zhou, Y.; Wu, J.; Zou, K. Xylogranatinin, a new pyrido[1, 2-a] pyrazine alkaloid from the fruit of a chinese mangrove Xylocarpus granatum. Chem. Nat. Compd. 2007, 43, 426-428.
    • (2007) Chem. Nat. Compd. , vol.43 , pp. 426-428
    • Zhou, Y.1    Wu, J.2    Zou, K.3
  • 23
    • 84857062616 scopus 로고    scopus 로고
    • Aspergicin, a new antibacterial alkaloid produced by mixed fermentation of two marine-derived mangrove epiphytic fungi
    • Zhu, F.; Chen, G.Y.; Chen, X.; Huang, M.Z.; Wan, X.Q. Aspergicin, a new antibacterial alkaloid produced by mixed fermentation of two marine-derived mangrove epiphytic fungi. Chem. Nat. Compd. 2011, 47, 767-769.
    • (2011) Chem. Nat. Compd. , vol.47 , pp. 767-769
    • Zhu, F.1    Chen, G.Y.2    Chen, X.3    Huang, M.Z.4    Wan, X.Q.5
  • 24
    • 84887542299 scopus 로고    scopus 로고
    • A new isobenzofuranone from the mangrove endophytic fungus Penicillium sp. (ZH58)
    • Yang, J.X.; Huang, R.M.; Qiu, S.X.; She, Z.G.; Lin, Y.C. A new isobenzofuranone from the mangrove endophytic fungus Penicillium sp. (ZH58). Nat. Prod. Res. 2013, 27, 1902-1905.
    • (2013) Nat. Prod. Res. , vol.27 , pp. 1902-1905
    • Yang, J.X.1    Huang, R.M.2    Qiu, S.X.3    She, Z.G.4    Lin, Y.C.5
  • 27
    • 33845470171 scopus 로고
    • Eudistomins C, E, K, and L, potent antiviral compounds containing a novel oxathiazepine ring from the caribbean tunicate Eudistoma olivaceum
    • Rinehart, K.L., Jr.; Kobayashi, J.; Harbour, G.C.; Hughes, R.G., Jr.; Mizsak, S.A.; Scahil, T.A. Eudistomins C, E, K, and L, potent antiviral compounds containing a novel oxathiazepine ring from the caribbean tunicate Eudistoma olivaceum. J. Am. Chem. Soc. 1984, 106, 1524-1526.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 1524-1526
    • Rinehart Jr.1    , K.L.2    Kobayashi, J.3    Harbour, G.C.4    Hughes Jr.5    , R.G.6    Mizsak, S.A.7    Scahil, T.A.8
  • 28
    • 77954292472 scopus 로고    scopus 로고
    • The synergistic antibacterial activity of 1-acetyl-β-carboline and β-lactams against methicillin-resistant Staphylococcus aureus (MRSA)
    • Hee Jae, S.; Lee, H.S.; Lee, D.S. The synergistic antibacterial activity of 1-acetyl-β-carboline and β-lactams against methicillin-resistant Staphylococcus aureus (MRSA). J. Microbiol. Biotechnol. 2010, 20, 501-505.
    • (2010) J. Microbiol. Biotechnol. , vol.20 , pp. 501-505
    • Hee Jae, S.1    Lee, H.S.2    Lee, D.S.3
  • 29
    • 0038203630 scopus 로고    scopus 로고
    • New manzamine alkaloids with activity against infectious and tropical parasitic diseases from an indonesian sponge
    • Rao, K.V.; Santarsiero, B.D.; Mesecar, A.D.; Schinazi, R.F.; Tekwani, B.L.; Hamann, M.T. New manzamine alkaloids with activity against infectious and tropical parasitic diseases from an indonesian sponge. J. Nat. Prod. 2003, 66, 823-828.
    • (2003) J. Nat. Prod. , vol.66 , pp. 823-828
    • Rao, K.V.1    Santarsiero, B.D.2    Mesecar, A.D.3    Schinazi, R.F.4    Tekwani, B.L.5    Hamann, M.T.6
  • 30
    • 53849111592 scopus 로고    scopus 로고
    • Assembly of β-cyclodextrin with 3S-tetrahydro-β-carboline-3- carboxylic acid and self-assembly of 6-(3′S-carboline-3′- carboxylamino ethylamino)-6-deoxy-β-cyclodextrin: Approaches to enhance anti-oxidation stability and anti-thrombotic potency
    • Li, L.; Cui, G.H.; Zhao, M.; Wang, Y.J.; Wang, H.; Li, W.; Peng, S.Q. Assembly of β-cyclodextrin with 3S-tetrahydro-β-carboline-3-carboxylic acid and self-assembly of 6-(3′S-carboline-3′-carboxylamino ethylamino)-6-deoxy-β-cyclodextrin: Approaches to enhance anti-oxidation stability and anti-thrombotic potency. J. Phys. Chem. B 2008, 112, 12139-12147.
    • (2008) J. Phys. Chem. B , vol.112 , pp. 12139-12147
    • Li, L.1    Cui, G.H.2    Zhao, M.3    Wang, Y.J.4    Wang, H.5    Li, W.6    Peng, S.Q.7
  • 31
    • 84860341435 scopus 로고    scopus 로고
    • Cytotoxic alkaloids from Fusarium incarnatum associated with the mangrove tree Aegiceras corniculatum
    • Ding, L.; Dahse, H.M.; Hertweck, C. Cytotoxic alkaloids from Fusarium incarnatum associated with the mangrove tree Aegiceras corniculatum. J. Nat. Prod. 2012, 75, 617-621.
    • (2012) J. Nat. Prod. , vol.75 , pp. 617-621
    • Ding, L.1    Dahse, H.M.2    Hertweck, C.3
  • 32
    • 0036741295 scopus 로고    scopus 로고
    • Cytotoxic β-carbolines and cyclic Peroxides from the palauan sponge Plakortis nigra
    • Sandler, J.S.; Colin, P.L.; Hooper, J.N.A.; John Faulkner, D. Cytotoxic β-carbolines and cyclic Peroxides from the palauan sponge Plakortis nigra. J. Nat. Prod. 2002, 65, 1258-1261.
    • (2002) J. Nat. Prod. , vol.65 , pp. 1258-1261
    • Sandler, J.S.1    Colin, P.L.2    Hooper, J.N.A.3    John Faulkner, D.4
  • 33
    • 0037332243 scopus 로고    scopus 로고
    • Eudistomins W and X, two new β-carbolines from the micronesian tunicate Eudistoma sp
    • Schupp, P.; Poehner, T.; Edrada, R.; Ebel, R.; Berg, A.; Wray, V.; Proksch, P. Eudistomins W and X, two new β-carbolines from the micronesian tunicate Eudistoma sp. J. Nat. Prod. 2003, 66, 272-275.
    • (2003) J. Nat. Prod. , vol.66 , pp. 272-275
    • Schupp, P.1    Poehner, T.2    Edrada, R.3    Ebel, R.4    Berg, A.5    Wray, V.6    Proksch, P.7
  • 34
    • 40549100992 scopus 로고    scopus 로고
    • β-carboline alkaloids from a korean tunicate Eudistoma sp.
    • Wang, W.H.; Nam, S.J.; Lee, B.C.; Kang, H. β-carboline alkaloids from a korean tunicate Eudistoma sp. J. Nat. Prod. 2008, 71, 163-166.
    • (2008) J. Nat. Prod. , vol.71 , pp. 163-166
    • Wang, W.H.1    Nam, S.J.2    Lee, B.C.3    Kang, H.4
  • 35
    • 65649110929 scopus 로고    scopus 로고
    • 5-bromo-8-methoxy-1-methyl-β-carboline, an alkaloid from the New Zealand marine bryozoan Pterocella Wesiculosa
    • Marisa, T.; Michele, R.P. 5-bromo-8-methoxy-1-methyl-β-carboline, an alkaloid from the New Zealand marine bryozoan Pterocella Wesiculosa. J. Nat. Prod. 2009, 72, 796-798.
    • (2009) J. Nat. Prod. , vol.72 , pp. 796-798
    • Marisa, T.1    Michele, R.P.2
  • 37
    • 0032996036 scopus 로고    scopus 로고
    • A β-carboline alkaloid from the soft coral Lignopsis spongiosum
    • Cabrera, G.M.; Seldes, A.M. A β-carboline alkaloid from the soft coral Lignopsis spongiosum. J. Nat. Prod. 1999, 62, 759-760.
    • (1999) J. Nat. Prod. , vol.62 , pp. 759-760
    • Cabrera, G.M.1    Seldes, A.M.2
  • 38
    • 80055068024 scopus 로고    scopus 로고
    • Antifouling properties of simple indole and purine alkaloids from the mediterranean gorgonian Paramuricea clavata
    • Penez, N.; Culioli, G.; Perez, T.; Briand, J.F.; Thomas, O.P.; Blache, Y. Antifouling properties of simple indole and purine alkaloids from the mediterranean gorgonian Paramuricea clavata. J. Nat. Prod. 2011, 74, 2304-2308.
    • (2011) J. Nat. Prod. , vol.74 , pp. 2304-2308
    • Penez, N.1    Culioli, G.2    Perez, T.3    Briand, J.F.4    Thomas, O.P.5    Blache, Y.6
  • 39
    • 80055091302 scopus 로고    scopus 로고
    • Antimalarial β-carboline and indolactam alkaloids from Marinactinospora thermotolerans, a deep sea isolate
    • Huang, H.B.; Yao, Y.L.; He, Z.X.; Yang, T.T.; Ma, J.Y.; Tian, X.P.; Li, Y.Y.; Huang, C.G.; Chen, X.P.; Li, W.J.; et al. Antimalarial β-carboline and indolactam alkaloids from Marinactinospora thermotolerans, a deep sea isolate. J. Nat. Prod. 2011, 74, 2122-2127.
    • (2011) J. Nat. Prod. , vol.74 , pp. 2122-2127
    • Huang, H.B.1    Yao, Y.L.2    He, Z.X.3    Yang, T.T.4    Ma, J.Y.5    Tian, X.P.6    Li, Y.Y.7    Huang, C.G.8    Chen, X.P.9    Li, W.J.10
  • 40
    • 12944270295 scopus 로고    scopus 로고
    • Antimicrobial screening and active compound isolation from marine bacterium NJ6-3-1 associated with the sponge Hymeniacidon perleve
    • Zheng, L.; Chen, H.M.; Han, X.T.; Lin, W.; Yan, X.J. Antimicrobial screening and active compound isolation from marine bacterium NJ6-3-1 associated with the sponge Hymeniacidon perleve. World J. Microbol. Biotechnol. 2005, 21, 201-206.
    • (2005) World J. Microbol. Biotechnol. , vol.21 , pp. 201-206
    • Zheng, L.1    Chen, H.M.2    Han, X.T.3    Lin, W.4    Yan, X.J.5
  • 41
    • 0001089453 scopus 로고
    • Supersonic jet studies of alkyl substituted pyrazines and pyridines. Minimum-energy conformations and torsional motion
    • Seeman, J.I.; Paine, J.B., III; Secor, H.V.; Im, H.S.; Bernstein, E.R. Supersonic jet studies of alkyl substituted pyrazines and pyridines. Minimum-energy conformations and torsional motion. J. Am. Chem. Soc. 1992, 114, 5269-5280.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5269-5280
    • Seeman, J.I.1    Paine III, J.B.2    Secor, H.V.3    Im, H.S.4    Bernstein, E.R.5
  • 42
    • 0033525048 scopus 로고    scopus 로고
    • Stereochemical determination of acyclic structures based on carbon-proton spin-coupling constants. A method of configuration analysis for natural products
    • Matsumori, N.; Kaneno, D.; Murata, M.; Nakamura, H.; Tachibana, K. Stereochemical determination of acyclic structures based on carbon-proton spin-coupling constants. A method of configuration analysis for natural products. J. Org. Chem. 1999, 64, 866-876.
    • (1999) J. Org. Chem. , vol.64 , pp. 866-876
    • Matsumori, N.1    Kaneno, D.2    Murata, M.3    Nakamura, H.4    Tachibana, K.5
  • 43
    • 34848837928 scopus 로고    scopus 로고
    • Determination of the absolute configurations of pharmacological natural products via density functional theory calculations of vibrational circular dichroism: The new cytotoxic iridoid prismatomerin
    • Stephens, P.J.; Pan, J.J. Determination of the absolute configurations of pharmacological natural products via density functional theory calculations of vibrational circular dichroism: The new cytotoxic iridoid prismatomerin. J. Org. Chem. 2007, 72, 7641-7649.
    • (2007) J. Org. Chem. , vol.72 , pp. 7641-7649
    • Stephens, P.J.1    Pan, J.J.2
  • 44
    • 37049062138 scopus 로고
    • Optical rotatory dispersion. Part XXIV. Lactones
    • doi:10.1039/JR9650007211
    • Jexkings, J.P.; Klyne, W.; Scope, P.M. Optical rotatory dispersion. Part XXIV. Lactones. J. Chem. Soc. 1965, 7211-7229; doi:10.1039/JR9650007211.
    • (1965) J. Chem. Soc. , pp. 7211-7229
    • Jexkings, J.P.1    Klyne, W.2    Scope, P.M.3
  • 47
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • Mosmann, T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65, 55-63.
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 48
    • 45549095949 scopus 로고    scopus 로고
    • Synthesis of analogues of flazin, in particular, flazinamide, as promising anti-HIV agents
    • Tang, J.G.; Wang, Y.H.; Wang, R.R.; Dong, Z.J.; Yang, L.M.; Zheng, Y.T.; Liu, J.K. Synthesis of analogues of flazin, in particular, flazinamide, as promising anti-HIV agents. Chem. Biodivers. 2008, 5, 447-460.
    • (2008) Chem. Biodivers. , vol.5 , pp. 447-460
    • Tang, J.G.1    Wang, Y.H.2    Wang, R.R.3    Dong, Z.J.4    Yang, L.M.5    Zheng, Y.T.6    Liu, J.K.7
  • 49
    • 70349774236 scopus 로고    scopus 로고
    • Synthesis and antiviral activity of β-carboline derivatives bearing a substituted carbohydrazide at C-3 against poliovirus and herpes simplex virus (HSV-1)
    • Nazari Formagio, A.S.; Santos, P.R.; Zanoli, K.; Ueda-Nakamura, T.; Dusman Tonin, L.T.; Nakamura, C.V.; Sarragiotto, M.H. Synthesis and antiviral activity of β-carboline derivatives bearing a substituted carbohydrazide at C-3 against poliovirus and herpes simplex virus (HSV-1). Eur. J. Med. Chem. 2009, 44, 4695-4701.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 4695-4701
    • Nazari Formagio, A.S.1    Santos, P.R.2    Zanoli, K.3    Ueda-Nakamura, T.4    Dusman Tonin, L.T.5    Nakamura, C.V.6    Sarragiotto, M.H.7


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