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Volumn 8, Issue 11, 2010, Pages 2810-2836

Recent N-atom containing compounds from Indo-Pacific invertebrates

Author keywords

Fascaplysinopsis sp.; Heterocycles; Leukemia cells; Marine invertebrates; Nitrogenous macrolide

Indexed keywords

2 HYDROXYBENZOTHIAZOLE; 2 MERCAPTOBENZOTHIAZOLE; 6 HYDROXY 3 METHYL 2 BENZOTHIAZOLE; AAPTOSINE; ALKALOID; ASMARINE DERIVATIVE; BARRENAZINE A; BARRENAZINE B; BENZOTHIAZOLE DERIVATIVE; CALLYNORMINE A; COMORAMIDE A; COMORAMIDE B; CYCLOSHERMILAMINE D; DIDMOLAMIDE A; DIDMOLAMIDE B; DIDMOLAMIDE C; DIGONAZOLE; EILATIN; ETZIONIN; NAAMIDINE DERIVATIVE; NORSEGOLINE; PHORBAZOLE A; POLYCITONE A; PTILOMYCALIN A; SALARAMIDE A; SALARAMIDE B; SPERMIDINE; TINTAMINE; UNCLASSIFIED DRUG; UNINDEXED DRUG; VIOLATINCTAMINE;

EID: 78649733419     PISSN: None     EISSN: 16603397     Source Type: Journal    
DOI: 10.3390/md8112810     Document Type: Review
Times cited : (9)

References (80)
  • 1
    • 34247642113 scopus 로고    scopus 로고
    • Recent heterocyclic compounds from marine invertebrates: Structure and synthesis
    • Kashman, Y.; Rudi, A.; Pappo, D. Recent heterocyclic compounds from marine invertebrates: Structure and synthesis. Pure Appl. Chem. 2007, 79, 491-505.
    • (2007) Pure Appl. Chem. , vol.79 , pp. 491-505
    • Kashman, Y.1    Rudi, A.2    Pappo, D.3
  • 2
    • 0000768508 scopus 로고
    • N-acyl-2-methylene-β-alanine methy esters from the Sponge Fasciospongia cavernosa
    • Kashman, Y.; Fishelson, L.; Neeman, I. N-acyl-2-methylene-β-alanine methy esters from the Sponge Fasciospongia cavernosa. Tetrahedron 1973, 29, 3655-3657.
    • (1973) Tetrahedron , vol.29 , pp. 3655-3657
    • Kashman, Y.1    Fishelson, L.2    Neeman, I.3
  • 3
    • 78649751134 scopus 로고
    • John Wiley and Sons: New York, NY, USA
    • Pelletier, S.W., Ed.; Alkaloids; John Wiley and Sons: New York, NY, USA, 1983; pp. 25-27.
    • (1983) Alkaloids , pp. 25-27
    • Pelletier, S.W.1
  • 4
    • 78649747591 scopus 로고    scopus 로고
    • note
    • The most "accurate" definition is may be still the following one: "an alkaloid is like my wife, I can recognize her when I see her, but I can not define her".
  • 5
    • 0036007872 scopus 로고    scopus 로고
    • Marine natural products
    • and previous reports in this series
    • Faulkner, D.J. Marine natural products. Nat. Prod. Rep. 2002, 19, 1-48 and previous reports in this series.
    • (2002) Nat. Prod. Rep. , vol.19 , pp. 1-48
    • Faulkner, D.J.1
  • 6
    • 0030003043 scopus 로고    scopus 로고
    • Studies of Australian ascidians. 5. virenamides A-C, new cytotoxic linear peptides from the colonial didemnid ascidian Diplosoma virens
    • Carrole, A.R.; Feng, Y.; Coll, J.C.; Bowden, B.F. Studies of Australian ascidians. 5. virenamides A-C, new cytotoxic linear peptides from the colonial didemnid ascidian Diplosoma virens. J. Nat. Prod. 1996, 61, 4059-4061.
    • (1996) J. Nat. Prod. , vol.61 , pp. 4059-4061
    • Carrole, A.R.1    Feng, Y.2    Coll, J.C.3    Bowden, B.F.4
  • 7
    • 0032558652 scopus 로고    scopus 로고
    • Four new cytotoxic cyclic hexa- and heptapeptides from the marine ascidian Didemnum molle
    • Rudi, A.; Aknin, M.; Gaydou, E.M.; Kashman, Y. Four new cytotoxic cyclic hexa- and heptapeptides from the marine ascidian Didemnum molle. Tetrahedron 1998, 54, 13203-13210.
    • (1998) Tetrahedron , vol.54 , pp. 13203-13210
    • Rudi, A.1    Aknin, M.2    Gaydou, E.M.3    Kashman, Y.4
  • 9
    • 0001030876 scopus 로고
    • Eilatin, a novel alkaloid from the marine tunicate Eudistoma sp.
    • Rudi, A.; Benayahu, Y.; Goldberg, I.; Kashman, Y. Eilatin, a novel alkaloid from the marine tunicate Eudistoma sp. Tetrahedron Lett. 1988, 29, 6655-6656.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 6655-6656
    • Rudi, A.1    Benayahu, Y.2    Goldberg, I.3    Kashman, Y.4
  • 10
    • 0027461338 scopus 로고
    • A two step biomimetic total synthesis of eilatin
    • Gellerman, G.; Babad, M.; Kashman, Y. A two step biomimetic total synthesis of eilatin. Tetrahedron Lett. 1993, 34, 1827-1830.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 1827-1830
    • Gellerman, G.1    Babad, M.2    Kashman, Y.3
  • 11
    • 4644338678 scopus 로고    scopus 로고
    • Violatinctamine, a new heterocyclic compound from the marine tunicate Cystodytes cf. violatinctus
    • Chill, L.; Rudi, A.; Benayahu, Y.; Kashman, Y. Violatinctamine, a new heterocyclic compound from the marine tunicate Cystodytes cf. violatinctus. Tetrahedron Lett. 2004, 45, 7925-7928.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 7925-7928
    • Chill, L.1    Rudi, A.2    Benayahu, Y.3    Kashman, Y.4
  • 12
    • 4043119201 scopus 로고    scopus 로고
    • Callynormine A, a new marine cyclic peptide of a novel class
    • Berrer, N.; Rudi, A.; Goldberg, I.; Benayahu, Y.; Kashman, Y. Callynormine A, a new marine cyclic peptide of a novel class. Org. Lett. 2004, 6, 2543-2545.
    • (2004) Org. Lett. , vol.6 , pp. 2543-2545
    • Berrer, N.1    Rudi, A.2    Goldberg, I.3    Benayahu, Y.4    Kashman, Y.5
  • 13
    • 0037030763 scopus 로고    scopus 로고
    • Metal ions as potential regulatory factors in the biosynthesis of red hair pigments: A new benzothiazole intermediate in the iron or copper assisted oxidation of 5-S-cysteinyldopa
    • Di Donato, P.; Napolitano, A.; Prota, G. Metal ions as potential regulatory factors in the biosynthesis of red hair pigments: a new benzothiazole intermediate in the iron or copper assisted oxidation of 5-S-cysteinyldopa. Biochim. Biophys. Acta 2002, 1571, 157-166.
    • (2002) Biochim. Biophys. Acta , vol.1571 , pp. 157-166
    • Di Donato, P.1    Napolitano, A.2    Prota, G.3
  • 14
    • 0025781915 scopus 로고
    • Benzothiazoles from a putative bacterial symbiont of the marine sponge Tedania ignis
    • Stierle, A.C.; Cardellina, J.H., II; Singelton, F.L. Benzothiazoles from a putative bacterial symbiont of the marine sponge Tedania ignis. Tetrahedron Lett. 1991, 32, 4847-4848.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 4847-4848
    • Stierle, A.C.1    Cardellina II, J.H.2    Singelton, F.L.3
  • 16
    • 0032475864 scopus 로고    scopus 로고
    • Posttranslational formation of formylglycine in prokaryotic sulfatases by modification of either cysteine or serine
    • Dierks, T.; Miech, C.; Hummerjohann, J.; Schmidt, B.; Kertesz, M.A.; von Figura, K. Posttranslational formation of formylglycine in prokaryotic sulfatases by modification of either cysteine or serine. J. Biol. Chem. 1998, 273, 25560-25564.
    • (1998) J. Biol. Chem. , vol.273 , pp. 25560-25564
    • Dierks, T.1    Miech, C.2    Hummerjohann, J.3    Schmidt, B.4    Kertesz, M.A.5    Von Figura, K.6
  • 19
    • 0030785251 scopus 로고    scopus 로고
    • Synthesis and characterization of β-O-tosyldehydroserine as a precursor of dehydroamino acids
    • Nakazawa, T.; Suzuki, T.; Ishii, M. Synthesis and characterization of β-O-tosyldehydroserine as a precursor of dehydroamino acids. Tetrahedron Lett. 1997, 38, 8951-8954.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 8951-8954
    • Nakazawa, T.1    Suzuki, T.2    Ishii, M.3
  • 20
    • 58149515937 scopus 로고    scopus 로고
    • Acyclic and cyclic thioenamino cyclic peptides; Solution and solid phase synthesis
    • Goren, L.; Pappo, D.; Goldberg, I.; Kashman, Y. Acyclic and cyclic thioenamino cyclic peptides; Solution and solid phase synthesis. Tetrahedron Lett. 2009, 50, 1048-1050.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1048-1050
    • Goren, L.1    Pappo, D.2    Goldberg, I.3    Kashman, Y.4
  • 21
    • 77951883439 scopus 로고    scopus 로고
    • Salaramides A and B; Two α-oxoamides isolated from the marine sponge Hippospongia sp.(Porifera, Dictyoceratida)
    • Bensemhoun, J.; Rudi, A.; Kashman, Y.; Gaydou, E.M.; Vacelet, J.; Aknin, M. Salaramides A and B; Two α-oxoamides isolated from the marine sponge Hippospongia sp.(Porifera, Dictyoceratida). Nat. Prod. Commun. 2010, 5, 259-260.
    • (2010) Nat. Prod. Commun. , vol.5 , pp. 259-260
    • Bensemhoun, J.1    Rudi, A.2    Kashman, Y.3    Gaydou, E.M.4    Vacelet, J.5    Aknin, M.6
  • 23
    • 0345765138 scopus 로고    scopus 로고
    • New cytotoxic steroidal alkaloids from the Philippine sponge Corticium niger
    • Ridley, C.P.; Faulkner, D.J. New cytotoxic steroidal alkaloids from the Philippine sponge Corticium niger. J. Nat. Prod. 2003, 66, 1536-1539
    • (2003) J. Nat. Prod. , vol.66 , pp. 1536-1539
    • Ridley, C.P.1    Faulkner, D.J.2
  • 24
    • 0028120371 scopus 로고
    • Two steroidal alkaloids from a sponge, Corticium sp.
    • Jurek, J.; Scheuer, P.J.; Kelly-Borges, M. Two steroidal alkaloids from a sponge, Corticium sp. J. Nat. Prod. 1994, 57, 1004-1007.
    • (1994) J. Nat. Prod. , vol.57 , pp. 1004-1007
    • Jurek, J.1    Scheuer, P.J.2    Kelly-Borges, M.3
  • 25
    • 77950463417 scopus 로고    scopus 로고
    • Plakinamine L: A new steroidal alkaloid from the marine sponge Corticium sp.
    • Aknin, M.; Rudi, A.; Kashman, Y.; Vacelet, J.; Gaydou, E.M. Plakinamine L: A new steroidal alkaloid from the marine sponge Corticium sp. Nat. Prod. Commun. 2010, 5, 33-34.
    • (2010) Nat. Prod. Commun. , vol.5 , pp. 33-34
    • Aknin, M.1    Rudi, A.2    Kashman, Y.3    Vacelet, J.4    Gaydou, E.M.5
  • 26
    • 65649117032 scopus 로고    scopus 로고
    • Saldedines A and B, dibromo proaporphine alkaloids from a Madagascan tunicate
    • Sorek, H.; Rudi, A.; Goldberg, I.; Aknin, M.; Kashman, Y. Saldedines A and B, dibromo proaporphine alkaloids from a Madagascan tunicate. J. Nat. Prod. 2009, 72, 784-786.
    • (2009) J. Nat. Prod. , vol.72 , pp. 784-786
    • Sorek, H.1    Rudi, A.2    Goldberg, I.3    Aknin, M.4    Kashman, Y.5
  • 28
    • 33644770079 scopus 로고    scopus 로고
    • Novel and efficient synthetic path to proaporphine alkaloids: Total synthesis of (+/-)-stepharine and (+/-)-pronuciferine
    • and references therein
    • Honda, T.; Shigehisa, H. Novel and efficient synthetic path to proaporphine alkaloids: total synthesis of (+/-)-stepharine and (+/-)-pronuciferine. Org. Lett. 2006, 8, 657-659, and references therein.
    • (2006) Org. Lett. , vol.8 , pp. 657-659
    • Honda, T.1    Shigehisa, H.2
  • 29
    • 0022857162 scopus 로고
    • Imbricatine, an unusual benzyltetrahydroisoquinoline alkaloid isolated from the starfish Dermasterias imbricata
    • Pathirana, C.; Andersen, R.J. Imbricatine, an unusual benzyltetrahydroisoquinoline alkaloid isolated from the starfish Dermasterias imbricata. J. Am. Chem. Soc. 1986, 108, 8288-8289.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 8288-8289
    • Pathirana, C.1    Andersen, R.J.2
  • 30
    • 34548837988 scopus 로고    scopus 로고
    • Njaoamines G and H, two new cytotoxic polycyclic alkaloids from the marine sponge Neopetrosia sp.
    • Sorek, H.; Rudi, A.; Benayahu, Y.; Kashman, Y. Njaoamines G and H, two new cytotoxic polycyclic alkaloids from the marine sponge Neopetrosia sp. Tetrahedron Lett. 2007, 48, 7691-7694.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 7691-7694
    • Sorek, H.1    Rudi, A.2    Benayahu, Y.3    Kashman, Y.4
  • 31
    • 33846877613 scopus 로고    scopus 로고
    • Njaoamines A-F, new cytotoxic polycyclic alkaloids from the haplosclerid sponge Reniera sp.
    • Reyes, F.; Fernandez, R.; Urda, C.; Francesch, A.; Bueno, S.; de Eguilior, C.; Cuevas, C. Njaoamines A-F, new cytotoxic polycyclic alkaloids from the haplosclerid sponge Reniera sp. Tetrahedron 2007, 63, 2432-2438.
    • (2007) Tetrahedron , vol.63 , pp. 2432-2438
    • Reyes, F.1    Fernandez, R.2    Urda, C.3    Francesch, A.4    Bueno, S.5    De Eguilior, C.6    Cuevas, C.7
  • 32
    • 0028293765 scopus 로고
    • Ingenamine, a novel pentacyclic alkaloid from the marine sponge Xestospongia ingens
    • Kong, F.; Andersen, R.J.; Allen, T.M. Ingenamine, a novel pentacyclic alkaloid from the marine sponge Xestospongia ingens. Tetrahedron Lett. 1994, 35, 1643-1646.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 1643-1646
    • Kong, F.1    Andersen, R.J.2    Allen, T.M.3
  • 33
    • 0028876914 scopus 로고
    • Ingenamine alkaloids isolated from sponge Xestospongia ingens: Structures and absolute configurations
    • Kong, F.; Andersen, R.J. Ingenamine alkaloids isolated from sponge Xestospongia ingens: structures and absolute configurations. Tetrahedron 1995, 51, 2895-2906.
    • (1995) Tetrahedron , vol.51 , pp. 2895-2906
    • Kong, F.1    Andersen, R.J.2
  • 34
    • 7044262248 scopus 로고    scopus 로고
    • Ingenamine G and cyclostellettamines G-I, K, and L from the new Brazilian species of marine sponge Pachychalina sp.
    • de Oliveira, J.H.H.L.; Grube, A.; KoÅNck, M.; Berlinck, R.G.S.; Macedo, M.L.; Ferreira, A.G.; Hadju, E. Ingenamine G and cyclostellettamines G-I, K, and L from the new Brazilian species of marine sponge Pachychalina sp. J. Nat. Prod. 2004, 67, 1685-1689.
    • (2004) J. Nat. Prod. , vol.67 , pp. 1685-1689
    • De Oliveira, J.H.H.L.1    Grube, A.2    KoÅNck, M.3    Berlinck, R.G.S.4    Macedo, M.L.5    Ferreira, A.G.6    Hadju, E.7
  • 36
    • 4043054588 scopus 로고    scopus 로고
    • Department of Chemistry, University of Canterbury, New Zealand
    • Munro, M.H.G.; Blunt, J.W. Marine literature database. Department of Chemistry, University of Canterbury, New Zealand, 2009.
    • (2009) Marine Literature Database
    • Munro, M.H.G.1    Blunt, J.W.2
  • 37
    • 32444434385 scopus 로고    scopus 로고
    • Malonganenones A-C, novel tetraprenylated alkaloids from the Mozambique gorgonian Leptogorgia gilchristi
    • Keyzers, R.A.; Gray, C.A.; Schleyer, M.H.; Whibley, C.E; Hendricks, D.T.; Davies-Coleman, M. Malonganenones A-C, novel tetraprenylated alkaloids from the Mozambique gorgonian Leptogorgia gilchristi. Tetrahedron 2006, 62, 2200-2206.
    • (2006) Tetrahedron , vol.62 , pp. 2200-2206
    • Keyzers, R.A.1    Gray, C.A.2    Schleyer, M.H.3    Whibley, C.E.4    Hendricks, D.T.5    Davies-Coleman, M.6
  • 38
    • 0034055770 scopus 로고    scopus 로고
    • 15N Heteronuclear shift correlation at natural abundance
    • 15N Heteronuclear shift correlation at natural abundance. J. Nat. Prod. 2000, 63, 543-585.
    • (2000) J. Nat. Prod. , vol.63 , pp. 543-585
    • Martin, E.G.1    Hadden, E.C.2
  • 39
    • 84962383426 scopus 로고    scopus 로고
    • 5)-Labeled adenine derivatives: Synthesis and studies of tautomerism by 15N NMR spectroscopy and theoretical calculations
    • 5)-Labeled adenine derivatives: synthesis and studies of tautomerism by 15N NMR spectroscopy and theoretical calculations. J. Org. Chem. 2001, 66, 5463-5481.
    • (2001) J. Org. Chem. , vol.66 , pp. 5463-5481
    • Laxer, A.1    Major, D.T.2    Gottlieb, H.E.3    Fischer, B.4
  • 40
    • 0042703457 scopus 로고    scopus 로고
    • Synthesis of 9-substituted tetrahydrodiazepinones-asmarine A analogues
    • Pappo, D.; Kashman, Y. Synthesis of 9-substituted tetrahydrodiazepinones- asmarine A analogues. Tetrahedron 2003, 59, 6493-6501.
    • (2003) Tetrahedron , vol.59 , pp. 6493-6501
    • Pappo, D.1    Kashman, Y.2
  • 41
    • 11844295368 scopus 로고    scopus 로고
    • Synthesis of 9-Substituted tetrahydrodiazepinopurines: Studies toward the total synthesis of asmarines
    • Pappo, D.; Shimony, S.; Kashman, Y. Synthesis of 9-Substituted tetrahydrodiazepinopurines: Studies toward the total synthesis of asmarines. J. Org. Chem. 2005, 70, 199-206.
    • (2005) J. Org. Chem. , vol.70 , pp. 199-206
    • Pappo, D.1    Shimony, S.2    Kashman, Y.3
  • 42
    • 34548008830 scopus 로고    scopus 로고
    • Nuttingins A-F and Malonganenones D-H, tetraprenylated alkaloids from the Tanzanian gorgonian Euplexaura nuttingi
    • Sorek, H.; Rudi, A.; Benayahu, Y.; Ben-Califa, N.; Neumann, D.; Kashman, Y. Nuttingins A-F and Malonganenones D-H, tetraprenylated alkaloids from the Tanzanian gorgonian Euplexaura nuttingi. J. Nat. Prod. 2008, 70, 1104-1109.
    • (2008) J. Nat. Prod. , vol.70 , pp. 1104-1109
    • Sorek, H.1    Rudi, A.2    Benayahu, Y.3    Ben-Califa, N.4    Neumann, D.5    Kashman, Y.6
  • 43
    • 0016640079 scopus 로고
    • Human chronic myelogenous leukemia cell-line with positive Philadelphia chromosome
    • Lozzio, C.B.; Lozzio, B.B. Human chronic myelogenous leukemia cell-line with positive Philadelphia chromosome. Blood 1975, 45, 321-334.
    • (1975) Blood , vol.45 , pp. 321-334
    • Lozzio, C.B.1    Lozzio, B.B.2
  • 44
    • 0026034133 scopus 로고
    • Establishment and characterization of a human leukemic cell line with megakaryocytic features: Dependency on granulocyte-macrophage colony-stimulating factor, interleukin 3, or erythropoietin for growth and survival
    • Komatsu, N.; Nakauchi, H.; Miwa, A.; Ishihara, T.; Eguchi, M.; Moroi, M.; Okada, M.; Sato, Y.; Wada, H.; Yawata, Y.; Suda, T.; Niura, Y. Establishment and characterization of a human leukemic cell line with megakaryocytic features: dependency on granulocyte-macrophage colony-stimulating factor, interleukin 3, or erythropoietin for growth and survival. Cancer Res. 1991, 51, 341-348.
    • (1991) Cancer Res. , vol.51 , pp. 341-348
    • Komatsu, N.1    Nakauchi, H.2    Miwa, A.3    Ishihara, T.4    Eguchi, M.5    Moroi, M.6    Okada, M.7    Sato, Y.8    Wada, H.9    Yawata, Y.10    Suda, T.11    Niura, Y.12
  • 45
    • 0031906624 scopus 로고    scopus 로고
    • Haliclorensin, a novel diamino alkaloid from the marine sponge Haliclona tulearensis
    • Koren-Goldshlager, G.; Kashman, Y.; Schleyer, M. Haliclorensin, a novel diamino alkaloid from the marine sponge Haliclona tulearensis. J. Nat. Prod. 1998, 61, 282-284.
    • (1998) J. Nat. Prod. , vol.61 , pp. 282-284
    • Koren-Goldshlager, G.1    Kashman, Y.2    Schleyer, M.3
  • 46
    • 0033613698 scopus 로고    scopus 로고
    • Halitulin, a new cytotoxic alkaloid from the marine sponge Haliclona tulearensis
    • Kashman, Y.; Koren-Goldshlager, G.; Gravalos, M.D.G.; Schleyer, M. Halitulin, a new cytotoxic alkaloid from the marine sponge Haliclona tulearensis. Tetrahedron Lett. 1999, 40, 997-1000.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 997-1000
    • Kashman, Y.1    Koren-Goldshlager, G.2    Gravalos, M.D.G.3    Schleyer, M.4
  • 47
    • 0035821263 scopus 로고    scopus 로고
    • Synthesis of (-)-(3S)-1-(3-aminopropyl)-3-methylazacyclodecane, the structure proposed for the marine alkaloid haliclorensin
    • Heinrich, M.R.; Steglich, W. Synthesis of (-)-(3S)-1-(3-aminopropyl)-3- methylazacyclodecane, the structure proposed for the marine alkaloid haliclorensin. Tetrahedron Lett. 2001, 42, 3287-3289.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 3287-3289
    • Heinrich, M.R.1    Steglich, W.2
  • 48
    • 0035842309 scopus 로고    scopus 로고
    • Revision of the structure of haliclorensin to (S)-7-methyl-1,5- diazacyclotetradecane and confirmation of the new structure by synthesis
    • Heinrich, M.R.; Kashman, Y.; Spiteller, P.; Steglich, W. Revision of the structure of haliclorensin to (S)-7-methyl-1,5-diazacyclotetradecane and confirmation of the new structure by synthesis. Tetrahedron 2001, 57, 9973-9978.
    • (2001) Tetrahedron , vol.57 , pp. 9973-9978
    • Heinrich, M.R.1    Kashman, Y.2    Spiteller, P.3    Steglich, W.4
  • 49
    • 0034762307 scopus 로고    scopus 로고
    • Total synthesis of the putative structure of the marine alkaloid haliclorensin
    • DOI 10.1039/b105045c
    • Banwell, M.G.; Bray, A.M.; Edwards, A.J.; Wong, D.J. Synthesis of the putative structure of the marine alkaloid haliclorensin. New J. Chem. 2001, 25, 1347-1350. (Pubitemid 33044076)
    • (2001) New Journal of Chemistry , vol.25 , Issue.11 , pp. 1347-1350
    • Banwell, M.G.1    Bray, A.M.2    Edwards, A.J.3    Wong, D.J.4
  • 51
    • 77950452902 scopus 로고    scopus 로고
    • Isohalitulin and Haliclorensins B and C, three marine alkaloids from Haliclona tulearensis
    • Sorek, H.; Rudi, A.; Aknin, M.; Gaydou, E.M.; Kashman, Y. Isohalitulin and Haliclorensins B and C, three marine alkaloids from Haliclona tulearensis. J. Nat. Prod. 2010, 73, 456-458.
    • (2010) J. Nat. Prod. , vol.73 , pp. 456-458
    • Sorek, H.1    Rudi, A.2    Aknin, M.3    Gaydou, E.M.4    Kashman, Y.5
  • 52
    • 0035686992 scopus 로고    scopus 로고
    • Four new bioactive pyrrole-derived alkaloids from the marine sponge Axinella brevistyla
    • Tsukamoto, S.; Tane, K.; Ohta, T.; Matsunaga, S.; Fusetani, N.; van Soest, R.W.M. Four new bioactive pyrrole-derived alkaloids from the marine sponge Axinella brevistyla. J. Nat. Prod. 2001, 64, 1576-1578.
    • (2001) J. Nat. Prod. , vol.64 , pp. 1576-1578
    • Tsukamoto, S.1    Tane, K.2    Ohta, T.3    Matsunaga, S.4    Fusetani, N.5    Van Soest, R.W.M.6
  • 54
    • 57549088382 scopus 로고    scopus 로고
    • Facile microwave-assisted synthesis of cyclic amidinium salts
    • Aidouni, A.; Bendahou, S.; Demonceau, A.; Delaude, L. Facile microwave-assisted synthesis of cyclic amidinium salts. J. Comb. Chem. 2008, 10, 886-892.
    • (2008) J. Comb. Chem. , vol.10 , pp. 886-892
    • Aidouni, A.1    Bendahou, S.2    Demonceau, A.3    Delaude, L.4
  • 55
    • 0028319137 scopus 로고
    • Keramaphidin C and keramamine C, plausible biogenetic precursors of manzamine C from an Okinawan marine sponge
    • Tsuda, M.; Kawasaki, N.; Kobayashi, J. Keramaphidin C and keramamine C, plausible biogenetic precursors of manzamine C from an Okinawan marine sponge. Tetrahedron Lett. 1994, 35, 4387-4388.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4387-4388
    • Tsuda, M.1    Kawasaki, N.2    Kobayashi, J.3
  • 56
    • 38749131268 scopus 로고    scopus 로고
    • Salarins A and B and tulearin A: New cytotoxic Sponge-derived macrolides
    • Bishara, A.; Rudi, A.; Aknin, M.; Neumann, D.; Ben-Califa, N.; Kashman, Y. Salarins A and B and tulearin A: new cytotoxic Sponge-derived macrolides. Org. Lett. 2008, 10, 153-156.
    • (2008) Org. Lett. , vol.10 , pp. 153-156
    • Bishara, A.1    Rudi, A.2    Aknin, M.3    Neumann, D.4    Ben-Califa, N.5    Kashman, Y.6
  • 58
    • 55449094954 scopus 로고    scopus 로고
    • Taumycins A and B, Two bioactive lipodepsipeptides from the Madagascar sponge Fascaplysinopsis sp.
    • Bishara, A.; Rudi, A.; Aknin, M.; Neumann, D.; Ben-Califa, N.; Kashman, Y. Taumycins A and B, Two bioactive lipodepsipeptides from the Madagascar sponge Fascaplysinopsis sp. Org. Lett. 2008, 10, 4307-4309.
    • (2008) Org. Lett. , vol.10 , pp. 4307-4309
    • Bishara, A.1    Rudi, A.2    Aknin, M.3    Neumann, D.4    Ben-Califa, N.5    Kashman, Y.6
  • 59
  • 61
    • 77953119909 scopus 로고    scopus 로고
    • Salarins D-J, seven new nitrogenous macrolides from the Madagascar sponge Fascaplysinopsis sp.
    • Bishara, A.; Rudi, A.; Aknin, M.; Neumann, D.; Ben-Califa, N.; Kashman, Y. Salarins D-J, seven new nitrogenous macrolides from the Madagascar sponge Fascaplysinopsis sp. Tetrahedron 2010, 66, 4339-4345.
    • (2010) Tetrahedron , vol.66 , pp. 4339-4345
    • Bishara, A.1    Rudi, A.2    Aknin, M.3    Neumann, D.4    Ben-Califa, N.5    Kashman, Y.6
  • 62
    • 84856530231 scopus 로고    scopus 로고
    • Salarin C, a member of the salarin superfamily of marine compounds, is a potent inducer of apoptosis
    • in presss
    • Ben-Califa, N.; Bishara, A.; Kashman, Y.; Neumann, D. Salarin C, a member of the salarin superfamily of marine compounds, is a potent inducer of apoptosis. Investig. New Drugs 2010, in presss.
    • (2010) Investig. New Drugs
    • Ben-Califa, N.1    Bishara, A.2    Kashman, Y.3    Neumann, D.4
  • 63
    • 0032985988 scopus 로고    scopus 로고
    • Madangolide and laingolide A, two novel macrolides from Lyngbya bouillonii (Cyanobacteria)
    • Klein, D.; Braekman, J.C.; Daloze, D.; Hoffmann, L.; Castillo, G.; Demoulin, V. Madangolide and laingolide A, two novel macrolides from Lyngbya bouillonii (Cyanobacteria). J. Nat Prod. 1999, 62, 934-936.
    • (1999) J. Nat Prod. , vol.62 , pp. 934-936
    • Klein, D.1    Braekman, J.C.2    Daloze, D.3    Hoffmann, L.4    Castillo, G.5    Demoulin, V.6
  • 65
    • 0000831802 scopus 로고
    • Synthesis and interconversion of the four isomeric 6-oxo-2,4-heptadienoic acids
    • Feliu, A.; Seltzer, S. Synthesis and interconversion of the four isomeric 6-oxo-2,4-heptadienoic acids. J. Org. Chem. 1985, 50, 447-451.
    • (1985) J. Org. Chem. , vol.50 , pp. 447-451
    • Feliu, A.1    Seltzer, S.2
  • 67
    • 33646930452 scopus 로고    scopus 로고
    • Possibility of a non-amino acid pathway in the biosynthesis of marine-derived oxazoles
    • DOI 10.1039/b517149k
    • Ichino, T.; Arimoto, H.; Uemura, D. Daisuke Possibility of a non-amino acid pathway in the biosynthesis of marine-derived oxazoles. Chem. Commun. 2006, 1742-1744. (Pubitemid 43793257)
    • (2006) Chemical Communications , Issue.16 , pp. 1742-1744
    • Ichino, T.1    Arimoto, H.2    Uemura, D.3
  • 68
    • 0034055770 scopus 로고    scopus 로고
    • 15N Heteronuclear shift correlation at natural abundance
    • 15N Heteronuclear shift correlation at natural abundance. J. Nat. Prod. 2000, 63, 543-585.
    • (2000) J. Nat. Prod. , vol.63 , pp. 543-585
    • Martin, G.E.1    Hadden, C.E.2
  • 69
    • 0037174407 scopus 로고    scopus 로고
    • Utilization of alternate substrates by the first three modules of the epothilone synthetase assembly line
    • Schneider, T.L.; Walsh, C.T.; O'Conner, S.E. Utilization of alternate substrates by the first three modules of the epothilone synthetase assembly line. J. Am. Chem. Soc. 2002, 124, 11272-11273.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11272-11273
    • Schneider, T.L.1    Walsh, C.T.2    O'Conner, S.E.3
  • 70
    • 37049089413 scopus 로고
    • Route of triacylamine formation in the thermal conversion of 2,3,7-trioxa-5-azabicyclo[2.2.1]hept-5-enes investigated by nuclear magnetic resonance experiments
    • Iesce, R.; Graziano, M.L.; Cimminiello, G.; Cermola, F.; Parrilli, M.; Scarpati, R. Route of triacylamine formation in the thermal conversion of 2,3,7-trioxa-5-azabicyclo[2.2.1]hept-5-enes investigated by nuclear magnetic resonance experiments J. Chem. Soc. Perkin Trans. 2 1991, 1085-1089.
    • (1991) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 1085-1089
    • Iesce, R.1    Graziano, M.L.2    Cimminiello, G.3    Cermola, F.4    Parrilli, M.5    Scarpati, R.6
  • 71
    • 44649175953 scopus 로고
    • Synthetic methods. 26. The 4,5- and 2,5-additions to oxazoles
    • Hassner, A.; Fischer, B. Synthetic methods. 26. The 4,5- and 2,5-additions to oxazoles. Tetrahedron 1989, 45, 6249-6262.
    • (1989) Tetrahedron , vol.45 , pp. 6249-6262
    • Hassner, A.1    Fischer, B.2
  • 72
    • 33646554810 scopus 로고    scopus 로고
    • Palmerolide A, a cytotoxic macrolide from the Antarctic tunicate Synoicum adareanum
    • Diyabalanage, T.; Amsler, C.D.; McClintok, J.B.; Baker, B.J. Palmerolide A, a cytotoxic macrolide from the Antarctic tunicate Synoicum adareanum. J. Am. Chem. Soc. 2006, 128, 5630-5633.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 5630-5633
    • Diyabalanage, T.1    Amsler, C.D.2    McClintok, J.B.3    Baker, B.J.4
  • 73
    • 0033502429 scopus 로고    scopus 로고
    • Geldanamycin as a potential anticancer agent: Its molecular target and biochemical activity
    • Neckers, L.; Schulte, T.M.; Mimhaugh, E. Geldanamycin as a potential anticancer agent: Its molecular target and biochemical activity. Investig. New Drugs 1999, 17, 361-373.
    • (1999) Investig. New Drugs , vol.17 , pp. 361-373
    • Neckers, L.1    Schulte, T.M.2    Mimhaugh, E.3
  • 74
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
    • Ohtani, I.; Kusumi, T.; Kashman, Y.; Kakisawa, H. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. J. Am. Chem. Soc. 1991, 113, 4092-4096.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 76
    • 85088544690 scopus 로고
    • Hapalosin, a cyanobacterial cyclic depsipeptide with multidrug-resistance reversing activity
    • Stratmann, K.; Burgoyne, D.L.; Moore, R.E.; Patterson, G.M.L.; Smith, C.D. Hapalosin, a cyanobacterial cyclic depsipeptide with multidrug-resistance reversing activity. J. Org. Chem. 1995, 60, 2950-2953.
    • (1995) J. Org. Chem. , vol.60 , pp. 2950-2953
    • Stratmann, K.1    Burgoyne, D.L.2    Moore, R.E.3    Patterson, G.M.L.4    Smith, C.D.5
  • 77
    • 42249106834 scopus 로고    scopus 로고
    • Acremolides A-D, lipodepsipeptides from an Australian marine-derived fungus, Acremonium sp
    • Ratnayake, R.; Fremlin, L.J.; Lacey, E.; Gill, J.H.; Capon, R.J. Acremolides A-D, lipodepsipeptides from an Australian marine-derived fungus, Acremonium sp. J. Nat. Prod. 2008, 71, 403-408.
    • (2008) J. Nat. Prod. , vol.71 , pp. 403-408
    • Ratnayake, R.1    Fremlin, L.J.2    Lacey, E.3    Gill, J.H.4    Capon, R.J.5
  • 78
    • 36549014040 scopus 로고    scopus 로고
    • Stereocalpin A, a bioactive cyclic depsipeptide from the Antarctic lichen Stereocaulon alpinum
    • Seo, C.; Yim, J.H.; Lee, H.K.; Park, S.M.; Sohn, J.H.; Oh, H. Stereocalpin A, a bioactive cyclic depsipeptide from the Antarctic lichen Stereocaulon alpinum. Tetrahedron Lett. 2008, 49, 29-31.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 29-31
    • Seo, C.1    Yim, J.H.2    Lee, H.K.3    Park, S.M.4    Sohn, J.H.5    Oh, H.6
  • 79
    • 0000363997 scopus 로고
    • Isolation of five-membered cyclitol glycolipids, crasserides: Unique glycerides from the sponge Pseudoceratina crassa
    • Costantino, V.; Fattorusso, E.; Mangoni, A. Isolation of five-membered cyclitol glycolipids, crasserides: unique glycerides from the sponge Pseudoceratina crassa. J. Org. Chem. 1993, 58, 186-191.
    • (1993) J. Org. Chem. , vol.58 , pp. 186-191
    • Costantino, V.1    Fattorusso, E.2    Mangoni, A.3
  • 80
    • 0031038263 scopus 로고    scopus 로고
    • Two new sesterterpenoids and a new 9,11-secosterol from Spongia matamata
    • Lu, Q.; Faulkner D.J. Two new sesterterpenoids and a new 9,11-secosterol from Spongia matamata. J. Nat. Prod. 1997, 60, 195-198.
    • (1997) J. Nat. Prod. , vol.60 , pp. 195-198
    • Lu, Q.1    Faulkner, D.J.2


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