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Roggero Chad M.,
Giulietti Jennifer M., Mulcahy Seann P.
Bioorganic & Medicinal Chemistry Letters. 2014 24(15). p.3549
Handbook of Marine Natural Products (2012)
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Yamagishi Hiroaki,
Matsumoto Koji,
Iwasaki Kotaro,
Miyazaki Tohru,
Yokoshima Satoshi,
Tokuyama Hidetoshi, Fukuyama Tohru
Organic Letters. 2008 10(12). p.2369
Crystal structure determination of (1S,13bR)-1-amino-10-methoxy-1,2,7,8,13,13b-hexahydro-[1,6,2]oxathiazepino[2?,3??1,2]pyrido[3,4-b]indole monohydrate, C15H19N3O2S�H2O
Hermkens Pedro H. H.,
Maarseveen J. H. v.,
Bosman W. P.,
Smits J. M. M., Beurskens Paul T.
Journal of Crystallographic and Spectroscopic Research. 1990 20(3). p.313
Synthesis of didemnolines A-D, N9-substituted β-carboline alkaloids from the marine ascidian Didemnum sp.
Schumacher Robert W, Davidson Bradley S
Tetrahedron. 1999 55(4). p.935
Current Applications of Suzuki–Miyaura Coupling Reaction in The Total Synthesis of Natural Products: An update
Taheri Kal Koshvandi Afsaneh,
Heravi Majid M., Momeni Tayebeh
Applied Organometallic Chemistry. 2018 32(3).
Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases
Gul Waseem, Hamann Mark T.
Life Sciences. 2005 78(5). p.442
Stereocontrolled Total Synthesis of (−)-Eudistomin C
Yamashita Tohru,
Kawai Nobutaka,
Tokuyama Hidetoshi, Fukuyama Tohru
Journal of the American Chemical Society. 2005 127(43). p.15038
The Yeast Role in Medical Applications (2018)
Interactions between Metals and Eudistomins of Ascidian Origin: A Computational Study
Parimi Ashutosh, Schreckenbach Georg
Inorganic Chemistry. 2023 62(47). p.19178
Diastereoselective Pictet–Spengler reactions ofL-(Boc)phenylalaninal andL-(Boc)prolinal: biomimetic syntheses of eudistomin T and (–)-woodinine
McNulty James, Still Ian W. J.
J. Chem. Soc., Perkin Trans. 1. 1994 (10). p.1329
Synthesis of Some New Indole-1,3,4-Oxadiazole Hybrids as Tubulin Polymerization Inhibitors
Sunitha Boda ,
Nukala Satheesh Kumar, Manchal Ravinder
Russian Journal of Bioorganic Chemistry. 2022 48(S1). p.S136
A comprehensive overview of β-carbolines and its derivatives as anticancer agents
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Natural products as drugs and tools for influencing core processes of eukaryotic mRNA translation
Burgers Luisa D., Fürst Robert
Pharmacological Research. 2021 170 p.105535
Computer-aided discovery of bis-indole derivatives as multi-target drugs against cancer and bacterial infections: DFT, docking, virtual screening, and molecular dynamics studies
Gupta Parth Sarthi Sen,
Bhat Haamid Rasool,
Biswal Satyaranjan, Rana Malay Kumar
Journal of Molecular Liquids. 2020 320 p.114375
Diastereoselective pictet-spengler reactions of L-(boc)prolinal: a biomimetic synthesis of eudistomins H and I, and woodinine
McNulty James, Still Ian W.J
Tetrahedron Letters. 1991 32(37). p.4875
Progress in Heterocyclic Chemistry - A critical review of the 1989 literature preceded by one chapter on a current heterocyclic topic (1990)
Asymmetric Synthesis of 1‐(2‐Pyrrolyl)alkylamines by the Addition of Organometallic Reagents to Chiral 2‐Pyrroleimines
Alvaro Giuseppe,
Di Fabio Romano,
Gualandi Andrea, Savoia Diego
European Journal of Organic Chemistry. 2007 2007(33). p.5573
A REVIEW ON INDOLE DERIVATIVES WITH DIVERSE MECHANISM IN THE TARGET-BASED DESIGN OF ANTICANCER DRUGS
Koksal Akkoc Meric, Dedeoğlu Elif Ayça
Ankara Universitesi Eczacilik Fakultesi Dergisi. 2019 p.334
Didemnolines A-D, new N9-substituted β-carbolines from the marine ascidian Didemnum sp.
Schumacher Robert W., Davidson Bradley S.
Tetrahedron. 1995 51(37). p.10125
Chemical diversity and biological activities of marine-derived sulphur containing alkaloids: A comprehensive update
Zhang Zilong,
Li Yuze,
Sun Yu,
Wang Wei,
Song Xiaomei, Zhang Dongdong
Arabian Journal of Chemistry. 2023 16(9). p.105011
Current Status of Indole-Derived Marine Natural Products: Synthetic Approaches and Therapeutic Applications
Fernández Sergio,
Arnáiz Virginia,
Rufo Daniel, Arroyo Yolanda
Marine Drugs. 2024 22(3). p.126
Synthesis of 4‐Azaindole‐morpholine‐1,3,4‐oxadiazole Conjugates as Epidermal Growth Factor Receptor Inhibitors
Hari Gangadhar Kotni,
Benarjee Velaga, Ratnamala Annapragada
ChemistrySelect. 2022 7(41).
(2015)
Transformations of the tetracyclic skeleton of eudistomins by neighboring‐group participation in the Mitsunobu reaction
van Maarseveen Jan H.,
Oberyé Elna H. H.,
Bolster Marjon B.,
Scheeren Hans W., Kruse Chris G.
Recueil des Travaux Chimiques des Pays-Bas. 1995 114(1). p.27
Bioactive natural Products (Part D) (2000)
Indole in the target-based design of anticancer agents: A versatile scaffold with diverse mechanisms
Dadashpour Sakineh, Emami Saeed
European Journal of Medicinal Chemistry. 2018 150 p.9
Insights of Indole: A Novel Target in Medicinal Chemistry (A Review)
Sarkar N.,
De S.,
Das M.,
Saha T.,
Banerjee S.,
Kumar S. K. Ashok, Kuo Y.-C.
Russian Journal of General Chemistry. 2023 93(7). p.1791
Remarkable examples of double diastereodifferentiation: Application to the Eudistomin and Eudistomidin alkaloids
Polniaszek Richard P., Bell Stephanie J.
Tetrahedron Letters. 1996 37(5). p.575
Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds
M. Heravi Majid,
Zadsirjan Vahideh, Malmir Masumeh
Molecules. 2018 23(4). p.943
Synthesis and Investigation of Tetrahydro-β-carboline Derivatives as Inhibitors of Plant Pathogenic Fungi
Buaban Koonchira,
Phutdhawong Weerachai,
Taechowisan Thongchai, Phutdhawong Waya S.
Molecules. 2021 26(1). p.207
Synthesis of 4-Azaindole-Thiazolidine-2,4-Dione Coupled 1,2,3-Triazoles as EGFR Directing Anticancer Agents
Shreedhar Reddy T.,
Rai Sanjay, Koppula Shiva Kumar
Polycyclic Aromatic Compounds. 2023 p.1
Natural Products with Heteroatom-Rich Ring Systems
Davison Emma K., Sperry Jonathan
Journal of Natural Products. 2017 80(11). p.3060
Iodine-catalyzed chemoselective dehydrogenation and aromatization of tetrahydro-β-carbolines: A short synthesis of Kumujian-C, Eudistomin-U, Norharmane, Harmane Harmalan and Isoeudistomine-M
Gaikwad Sunil,
Kamble Dayanand, Lokhande Pradeep
Tetrahedron Letters. 2018 59(25). p.2387
Synthesis of bioactive nitrogen heterocycles from marine organisms
Hino Tohru, Nakagawa Masako
Journal of Heterocyclic Chemistry. 1994 31(3). p.625
Antiviral and tumor cell antiproliferative SAR studies on tetracyclic eudistomins—II
van Maarseveen Jan H.,
Scheeren Hans W.,
De Clercq Erik,
Balzarini Jan, Kruse Chris G.
Bioorganic & Medicinal Chemistry. 1997 5(5). p.955
Pharmacological Importance of Optically Active Tetrahydro-β-carbolines and Synthetic Approaches to Create the C1 Stereocenter
Laine Aino,
Lood Christopher, Koskinen Ari
Molecules. 2014 19(2). p.1544
Cytotoxic activities of novel hexahydroindolizino[8,7-b]indole derivatives prepared by 1,3-dipolar cycloaddition reactions of 3,4-dihydro-β-carboline ylides
Bertrand Martial,
Poissonnet Guillaume,
Théret-Bettiol Marie-Hélène,
Gaspard Christiane,
Werner Georges H.,
Pfeiffer Bruno,
Renard Pierre,
Léonce Stéphane, Dodd Robert H.
Bioorganic & Medicinal Chemistry. 2001 9(8). p.2155
(1996)
ChemInform Abstract: Eudistomins from the New Zealand Ascidian Ritterella sigillinoides.
LAKE R. J.,
BLUNT J. W., MUNRO M. H. G.
ChemInform. 1989 20(45).
Bioactive Natural Products (Part F) (2001)
N-Bromo-succinimide promoted synthesis of β-carbolines and 3,4-dihydro-β-carbolines from tetrahydro-β-carbolines
Hati Santanu, Sen Subhabrata
Tetrahedron Letters. 2016 57(9). p.1040
Marine Niche: Applications in Pharmaceutical Sciences (2020)
Efficient ‘one-pot’ methodology for the synthesis of novel tetrahydro-β-carboline, tetrahydroisoquinoline and tetrahydrothienopyridine derivatives
Ionescu Alexandra,
Cornut Damien,
Soriano Sébastien,
Guissart Céline,
Van Antwerpen Pierre, Jabin Ivan
Tetrahedron Letters. 2013 54(45). p.6087
Analysis of heterocyclic aromatic amines in wine by high-performance liquid chromatography–electrospray tandem mass spectrometry
Richling Elke,
Decker Claudia,
Häring Dietmar,
Herderich Markus, Schreier Peter
Journal of Chromatography A. 1997 791(1-2). p.71
Bioactive Natural Products (Part I) (2003)
In(OTf)3catalysed an expeditious synthesis of β-carboline–imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrazine conjugates
Devi Nisha,
Singh Dharmender,
Honey Honey,
Mor Satbir,
Chaudhary Sandeep,
Rawal Ravindra K.,
Kumar Vipin,
Chowdhury Asim K., Singh Virender
RSC Advances. 2016 6(50). p.43881
Transition-metal catalyzed C–H activation as a means of synthesizing complex natural products
Sinha Soumya Kumar,
Ghosh Pintu,
Jain Shubhanshu,
Maiti Siddhartha,
Al-Thabati Shaeel A.,
Alshehri Abdulmohsen Ali,
Mokhtar Mohamed, Maiti Debabrata
Chemical Society Reviews. 2023 52(21). p.7461
Recent Advances in Natural Products Analysis (2020)
Chemical constituents from the ascidian Aplidium constellatum
Han Qing-Hua,
Fan Cheng-Qi,
Lu Ya-Nan,
Wu Jin-Ping,
Liu Xin, Yin Sheng
Biochemical Systematics and Ecology. 2013 48 p.6
Synthesis and antitumor activity of tetrahydrocarbazole hybridized with dithioate derivatives
El-Nassan Hala Bakr
Journal of Enzyme Inhibition and Medicinal Chemistry. 2015 30(2). p.308
Ten-Year Research Update Review: Antiviral Activities from Marine Organisms
Riccio Gennaro,
Ruocco Nadia,
Mutalipassi Mirko,
Costantini Maria,
Zupo Valerio,
Coppola Daniela,
de Pascale Donatella, Lauritano Chiara
Biomolecules. 2020 10(7). p.1007
Improvement of the liquid chromatographic separation of the enantiomers of tetracyclic eudistomins by the combination of a β-cyclodextrin stationary phase and camphorsulphonic acid as mobile phase additive
Kuijpers Peter H.,
Gerding Thijs K., de Jong Gerhardus J.
Journal of Chromatography A. 1992 625(2). p.223
Intramolecular Pictet-Spengler reaction of Nb-Alkoxytryptamines. 4. A study towards diastereocontrol in the synthesis of tetracyclic eudistomins
van Maarseveen Jan H.,
Scheeren Hans W., Kruse Chris G.
Tetrahedron. 1993 49(11). p.2325
Eudistomin C, an Antitumor and Antiviral Natural Product, Targets 40S Ribosome and Inhibits Protein Translation
Ota Yu,
Chinen Takumi,
Yoshida Keisuke,
Kudo Shun,
Nagumo Yoko,
Shiwa Yuh,
Yamada Ryosuke,
Umihara Hirotatsu,
Iwasaki Kotaro,
Masumoto Hiroshi,
Yokoshima Satoshi,
Yoshikawa Hirofumi,
Fukuyama Tohru,
Kobayashi Junichi, Usui Takeo
ChemBioChem. 2016 17(17). p.1616
Encyclopedia of Marine Natural Products (2014)
Marine products as a source of antiviral drug leads
Che Chun‐Tao
Drug Development Research. 1991 23(3). p.201
Simple naturally occurring β-carboline alkaloids – role in sustainable theranostics
Bhattacharya Piyali, De Swati
Physical Sciences Reviews. 2024 9(1). p.397
(2012)
Alkaloids and Nucleoside Derivatives from a Fungal Endophyte of Huperzia serrata
Ying You-Min,
Shan Wei-Guang,
Liu Wen-Hong, Zhan Zha-Jun
Chemistry of Natural Compounds. 2013 49(1). p.184
Nonsymmetrical β-Carboline Dimers from an Ascidian, Didemnum sp.
Kearns Philip S., Rideout John A.
Journal of Natural Products. 2008 71(7). p.1280
