Kinase Inhibitors from Marine Sponges
暂无分享,去创建一个
Danielle Skropeta | D. Skropeta | Natalie Pastro | Ana V. Živanović | Natalie Pastro | Ana Zivanovic | A. Živanović
[1] J. Vaquero,et al. Palladium-mediated C–N, C–C, and C–O functionalization of azolopyrimidines: a new total synthesis of variolin B , 2008 .
[2] B. Trost,et al. Total synthesis of (+)-frondosin A. Application of the Ru-catalyzed [5+2] cycloaddition. , 2007, Journal of the American Chemical Society.
[3] J. Kobayashi,et al. Nakijiquinones G-I, new sesquiterpenoid quinones from marine sponge. , 2008, Bioorganic & medicinal chemistry.
[4] M. Hemling,et al. Protein kinase C inhibitors: novel spirosesquiterpene aldehydes from a marine sponge Aka (= Siphonodictyon) coralliphagum. , 1994, Journal of natural products.
[5] David E. Williams,et al. Meroterpenoid MAPKAP (MK2) inhibitors isolated from the indonesian marine sponge Acanthodendrilla sp. , 2004, Journal of natural products.
[6] H. Waldmann,et al. Development of natural product-derived receptor tyrosine kinase inhibitors based on conservation of protein domain fold. , 2003, Journal of medicinal chemistry.
[7] Kris Novak. Conference report--protein kinase inhibitors in cancer treatment: mixing and matching? Highlights of the keystone symposium on protein kinases and cancer; February 24-29, 2004; Lake Tahoe, California. , 2004, MedGenMed : Medscape general medicine.
[8] A. Newton,et al. Protein Kinase C: Structure, Function, and Regulation (*) , 1995, The Journal of Biological Chemistry.
[9] P. Andreasen. PAI-1 - a potential therapeutic target in cancer. , 2007, Current drug targets.
[10] E. Eisenhauer,et al. A Phase II Study of Flavopiridol in Patients With Previously Untreated Advanced Soft Tissue Sarcoma , 2006, Sarcoma.
[11] M. Medina,et al. Antiangiogenic activity of aeroplysinin‐1, a brominated compound isolated from a marine sponge , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[12] M. Sauvain,et al. Antiplasmodial Activities of Homogentisic Acid Derivative Protein Kinase Inhibitors Isolated from a Vanuatu Marine Sponge Pseudoceratina sp. , 2009, Marine drugs.
[13] Jing Lin,et al. Fascaplysin, a selective CDK4 inhibitor, exhibit anti-angiogenic activity in vitro and in vivo , 2007, Cancer Chemotherapy and Pharmacology.
[14] M. Rateb,et al. Dibenzofurans from the marine sponge-derived ascomycete Super1F1-09 , 2010 .
[15] P. Furet,et al. Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product. , 2000, Biochemical and biophysical research communications.
[16] R. Wilhelm,et al. Protein tyrosine kinase inhibitory properties of planar polycyclics obtained from the marine sponge Xestospongia cf. carbonaria and from total synthesis , 1993 .
[17] S. Kohmoto,et al. Isolation and structure elucidation of onnamide A, a new bioactive metabolite of a marine sponge, Theonella sp , 1988 .
[18] R. Tyagi,et al. Inhibitors of cyclin dependent kinases: useful targets for cancer treatment. , 2008, Current cancer drug targets.
[19] P. Zarrinkar,et al. High-throughput kinase profiling as a platform for drug discovery , 2008, Nature Reviews Drug Discovery.
[20] L. Meijer,et al. Antimalarial potential of xestoquinone, a protein kinase inhibitor isolated from a Vanuatu marine sponge Xestospongia sp. , 2006, Bioorganic & medicinal chemistry.
[21] Jonathan C. Morris,et al. Variolins and related alkaloids. , 2009, Chemical reviews.
[22] K. Ang,et al. In Vivo Antimalarial Activity of the Beta-Carboline Alkaloid Manzamine A , 2000, Antimicrobial Agents and Chemotherapy.
[23] V. Kulcițki. A biomimetic approach to some specifically functionalized cyclic terpenoids. , 2009, Acta biochimica Polonica.
[24] D. Faulkner,et al. Marine pharmacology , 2004, Antonie van Leeuwenhoek.
[25] W. Müller,et al. Inhibition of intrinsic protein tyrosine kinase activity of EGF-receptor kinase complex from human breast cancer cells by the marine sponge metabolite (+)-aeroplysinin-1. , 1990, Comparative biochemistry and physiology. B, Comparative biochemistry.
[26] James M. Roberts,et al. CDK inhibitors: positive and negative regulators of G1-phase progression. , 1999, Genes & development.
[27] S. Danishefsky,et al. Toward the synthesis of xestocyclamine A: investigation of double Michael reaction and direct aza Diels–Alder reaction , 2006 .
[28] M. K. Harper,et al. Aldisine alkaloids from the Philippine sponge Stylissa massa are potent inhibitors of mitogen-activated protein kinase kinase-1 (MEK-1). , 2002, Journal of medicinal chemistry.
[29] M. K. Harper,et al. Carteriosulfonic acids A-C, GSK-3beta inhibitors from a Carteriospongia sp. , 2009, Journal of natural products.
[30] M. Tsuda,et al. Ma'edamines A and B, cytotoxic bromotyrosine alkaloids with a unique 2(1H)pyrazinone ring from sponge Suberea sp , 2000 .
[31] B. Strulovici,et al. Penazetidine A, an alkaloid inhibitor of protein kinase C , 1994 .
[32] Wael E Houssen,et al. Bioactive diterpene derivatives from the marine sponge Spongionella sp. , 2009, Journal of natural products.
[33] G. Bifulco,et al. Bioactive Prenylhydroquinone Sulfates and a Novel C31 Furanoterpene Alcohol Sulfate from the Marine Sponge, Ircinia Sp. , 1995 .
[34] S. Horinouchi,et al. Inhibition of protein synthesis and activation of stress‐activated protein kinases by onnamide A and theopederin B, antitumor marine natural products , 2005, Cancer science.
[35] B. Carté,et al. Frondosins, five new sesquiterpene hydroquinone derivatives with novel skeletons from the sponge Dysidea frondosa: Inhibitors of interleukin-8 receptors , 1997 .
[36] N. Toyooka,et al. Model studies toward the total synthesis of halenaquinol and halenaquinone , 2002 .
[37] D. Skropeta,et al. Kinase Inhibitory, Haemolytic and Cytotoxic Activity of Three Deep-water Sponges from North Western Australia and their Fatty Acid Composition , 2011, Natural product communications.
[38] P. Molina,et al. Synthesis of the potent antitumoral marine alkaloid variolin B , 2002 .
[39] P. Furet,et al. Total synthesis and biological evaluation of the nakijiquinones. , 2001, Journal of the American Chemical Society.
[40] J. Neary,et al. Effects of marine sponge extracts on mitogen-activated protein kinase (MAPK/ERK(1,2)) activity in SW-13 human adrenal carcinoma cells. , 2001, Toxicon : official journal of the International Society on Toxinology.
[41] D. Fabbro,et al. New sesquiterpene quinols from a Micronesian sponge, Aka sp. , 2003, Journal of natural products.
[42] T. Tamaoki,et al. Staurosporine, a potent inhibitor of phospholipid/Ca++dependent protein kinase. , 1986, Biochemical and biophysical research communications.
[43] G. Kroemer,et al. Cyclin-dependent kinase-1: linking apoptosis to cell cycle and mitotic catastrophe , 2002, Cell Death and Differentiation.
[44] W. Kolch. Meaningful relationships: the regulation of the Ras/Raf/MEK/ERK pathway by protein interactions. , 2000, The Biochemical journal.
[45] P. Crews,et al. A Madagascar Sponge Batzella sp. as a source of alkylated iminosugars. , 2005, Journal of natural products.
[46] Robin B. Kinnel,et al. 11-Hydroxystaurosporine: a highly cytotoxic, powerful protein kinase C inhibitor from a tunicate , 1992 .
[47] J. Lazo,et al. Halenaquinone and xestoquinone derivatives, inhibitors of Cdc25B phosphatase from a Xestospongia sp. , 2005, Bioorganic & medicinal chemistry.
[48] A. Bode,et al. Marine Alkaloid Polycarpine and Its Synthetic Derivative Dimethylpolycarpine Induce Apoptosis in JB6 Cells Through p53- and Caspase 3-Dependent Pathways , 2004, Pharmaceutical Research.
[49] L Meijer,et al. Inhibition of cyclin-dependent kinases, GSK-3beta and CK1 by hymenialdisine, a marine sponge constituent. , 2000, Chemistry & biology.
[50] Brian O Patrick,et al. Liphagal, a Selective inhibitor of PI3 kinase alpha isolated from the sponge akacoralliphaga: structure elucidation and biomimetic synthesis. , 2006, Organic letters.
[51] A. Marston. Natural products as a source of protein kinase activators and inhibitors. , 2011, Current Topics in Medicinal Chemistry.
[52] H. Gali-Muhtasib. Cyclin-dependent kinase inhibitors from natural sources: recent advances and future prospects for cancer treatment , 2006 .
[53] R. Isbrucker,et al. Early Effects of Lasonolide A on Pancreatic Cancer Cells , 2009, Journal of Pharmacology and Experimental Therapeutics.
[54] K. Inaba,et al. Tauroacidins A and B, new bromopyrrole alkaloids possessing a taurine residue from Hymeniacidon sponge , 1997 .
[55] M. Diaz,et al. Evaluation of new sesquiterpene quinones from two Dysidea sponge species as inhibitors of protein tyrosine kinase , 1992 .
[56] G. Jameson,et al. Alkaloids from the antarctic sponge Kirkpatrickia varialosa. Part 2: Variolin A and N(3′)-methyl tetrahydrovariolin B , 1994 .
[57] M. Boyd,et al. (-)-Frondosins A and D, HIV-Inhibitory Sesquiterpene Hydroquinone Derivatives from Euryspongia sp , 1998 .
[58] A. Haidour,et al. Enantioselective total synthesis of the selective PI3 kinase inhibitor liphagal. , 2010, Organic letters.
[59] Isolation and structure of bryostatin 1 , 1982 .
[60] P. Crews,et al. An alkaloid protein kinase C inhibitor, xestocyclamine A, from the marine sponge Xestospongia sp , 1993 .
[61] R. Longley,et al. A rapid colorimetric microassay to detect agonists/antagonists of protein kinase C based on adherence of EL-4.IL-2 cells. , 1991, The Journal of antibiotics.
[62] L. Mazzarella,et al. Isolation and X-ray crystal structure of a novel bromo-compound from two marine sponges , 1982 .
[63] M. Carapancea. Strategies to increase effectiveness of growth factor receptors-targeted therapy in glioblastoma , 2007 .
[64] M. Tsuda,et al. Konbu'acidin A, a new bromopyrrole alkaloid with cdk4 inhibitory activity from Hymeniacidon sponge , 1997 .
[65] G. Hofmann,et al. Z-Axinohydantoin and Debromo-Z-Axinohydantoin from the Sponge Stylotella aurantium: Inhibitors of Protein Kinase C , 1997 .
[66] David O. Morgan,et al. The Cell Cycle: Principles of Control , 2014 .
[67] R. Willis,et al. BRS1, a C30 bis-amino, bis-hydroxy polyunsaturated lipid from an Australian calcareous sponge that inhibits protein kinase C. , 1997, Toxicon : official journal of the International Society on Toxinology.
[68] Kobayashi,et al. Spongiacidins A-D, new bromopyrrole alkaloids from hymeniacidon sponge , 1998, Journal of natural products.
[69] A. Wright,et al. Microxine, a new cdc2 kinase inhibitor from the Australian marine sponge Microxina species. , 2001, Journal of natural products.
[70] B. Baker,et al. New cytotoxic sesterterpenes from the marine sponge Spongia sp , 1994 .
[71] Burkhard Haefner,et al. Drugs from the deep: marine natural products as drug candidates. , 2003, Drug discovery today.
[72] A. Gossauer. Monopyrrolic natural compounds including tetramic acid derivatives. , 2003, Fortschritte der Chemie organischer Naturstoffe = Progress in the chemistry of organic natural products. Progres dans la chimie des substances organiques naturelles.
[73] D. Newman,et al. Natural products as sources of new drugs over the last 25 years. , 2007, Journal of natural products.
[74] R. Quinn,et al. Cheilanthane sesterterpenes, protein kinase inhibitors, from a marine sponge of the genus Ircinia. , 2001, Journal of natural products.
[75] J. Kobayashi,et al. Nakijiquinones C and D, new sesquiterpenoid quinones with a hydroxy amino acid residue from a marine sponge inhibiting c-erbB-2 kinase , 1995 .
[76] S. Chassaing,et al. Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition , 2009, Marine drugs.
[77] I. Carletti,et al. Dihydrohymenialdisines, new pyrrole-2-aminoimidazole alkaloids from the marine sponge Cymbastela cantharella , 2011 .
[78] Danielle Skropeta,et al. Deep-sea natural products. , 2008, Natural product reports.
[79] S. Cohen,et al. Epidermal growth factor , 1972, The Journal of investigative dermatology.
[80] C. A. Carter,et al. Therapeutic potential of natural compounds that regulate the activity of protein kinase C. , 2004, Current medicinal chemistry.
[81] A. Levitzki,et al. Tyrphostins and other tyrosine kinase inhibitors. , 2006, Annual review of biochemistry.
[82] Ana Martínez,et al. Glycogen synthase kinase-3 (GSK-3) inhibitory activity and structure-activity relationship (SAR) studies of the manzamine alkaloids. Potential for Alzheimer's disease. , 2007, Journal of natural products.
[83] P. Crews,et al. Marine sponge polyketide inhibitors of protein tyrosine kinase. , 1992, Biochemical and biophysical research communications.
[84] N. Fusetani,et al. Enzyme inhibitors from marine invertebrates. , 2007, Journal of natural products.
[85] Sean Parkin,et al. Alkaloids from the antarctic sponge Kirkpatrickia varialosa. , 1994 .
[86] S. Matsunaga,et al. Theopederins A-E, potent antitumor metabolites from a marine sponge, Theonella sp. , 1992 .
[87] J. Tepe,et al. Preparation of hymenialdisine, analogues and their evaluation as kinase inhibitors. , 2009, Current medicinal chemistry.
[88] F. Albericio,et al. Total syntheses of variolin B and deoxyvariolin B. , 2003, The Journal of organic chemistry.
[89] G. Schwartz,et al. Bryostatin-1: A Novel PKC Inhibitor in Clinical Development , 2003, Cancer investigation.
[90] E. Eisenhauer,et al. ClinicalStudy A Phase II Study of Flavopiridol in Patients With Previously Untreated Advanced Soft Tissue Sarcoma , 2006 .
[91] F. Koehn,et al. Lasonolide A, a New Cytotoxic Macrolide from the Marine Sponge Forcepia sp. , 1994 .
[92] W. McGuire,et al. Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. , 1987, Science.
[93] L. Platanias,et al. Activation of the Mitogen- and Stress-activated Kinase 1 by Arsenic Trioxide* , 2006, Journal of Biological Chemistry.
[94] A. Tward,et al. Inhibition of CDK1 as a potential therapy for tumors over-expressing MYC , 2007, Nature Medicine.
[95] L. Meijer,et al. Synthesis and target identification of hymenialdisine analogs. , 2004, Chemistry & biology.