Статті в журналах з теми "Bengamide E"
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Acquah, Kojo Sekyi, Denzil R. Beukes, Ronnett Seldon, Audrey Jordaan, Suthananda N. Sunassee, Digby F. Warner, and David W. Gammon. "Identification of Antimycobacterial Natural Products from a Library of Marine Invertebrate Extracts." Medicines 9, no. 2 (January 28, 2022): 9. http://dx.doi.org/10.3390/medicines9020009.
Повний текст джерелаDao, Phi Thi. "SYNTHESIS OF N-ALKYL AMINO LACTAM DERIVATIVES." Vietnam Journal of Science and Technology 54, no. 2C (March 19, 2018): 291. http://dx.doi.org/10.15625/2525-2518/54/2c/11849.
Повний текст джерелаGarcía-Pinel, Beatriz, Cristina Porras-Alcalá, Laura Cabeza, Raul Ortiz, José Prados, Consolación Melguizo, Iván Cheng-Sánchez, Juan Manuel López-Romero, and Francisco Sarabia. "Bengamide Analogues Show A Potent Antitumor Activity against Colon Cancer Cells: A Preliminary Study." Marine Drugs 18, no. 5 (May 2, 2020): 240. http://dx.doi.org/10.3390/md18050240.
Повний текст джерелаChida, Noritaka, Takahiko Tobe, and Seiichiro Ogawa. "Total synthesis of bengamide E." Tetrahedron Letters 32, no. 8 (February 1991): 1063–66. http://dx.doi.org/10.1016/s0040-4039(00)74488-1.
Повний текст джерелаLiu, Wenming, Joanna M. Szewczyk, Liladhar Waykole, Oljan Repič, and Thomas J. Blacklock. "Total synthesis of bengamide E." Tetrahedron Letters 43, no. 8 (February 2002): 1373–75. http://dx.doi.org/10.1016/s0040-4039(02)00022-9.
Повний текст джерелаKishimoto, Hisakazu, Hiroshi Ohrui, and Hiroshi Meguro. "An enantioselective synthesis of bengamide E." Journal of Organic Chemistry 57, no. 18 (August 1992): 5042–44. http://dx.doi.org/10.1021/jo00044a053.
Повний текст джерелаLiu, Qi Jun, Hong Li, Shao Peng Chen, and Guo Chun Zhou. "Synthesis of (3S,4R)-bengamide E." Chinese Chemical Letters 22, no. 5 (May 2011): 505–7. http://dx.doi.org/10.1016/j.cclet.2010.11.023.
Повний текст джерелаMetri, Prashant K., Raphael Schiess, and Kavirayani R. Prasad. "Enantiospecific Total Synthesis of (−)-Bengamide E." Chemistry - An Asian Journal 8, no. 2 (December 3, 2012): 488–93. http://dx.doi.org/10.1002/asia.201200999.
Повний текст джерелаMukai, Chisato, Sameh M. Moharram, Osamu Kataoka, and Miyoji Hanaoka. "Highly stereocontrolled total synthesis of (+)-bengamide E." Journal of the Chemical Society, Perkin Transactions 1, no. 22 (1995): 2849. http://dx.doi.org/10.1039/p19950002849.
Повний текст джерелаBanwell, Martin G., and Kenneth J. McRae. "A Chemoenzymatic Total Synthesis ofent-Bengamide E." Journal of Organic Chemistry 66, no. 20 (October 2001): 6768–74. http://dx.doi.org/10.1021/jo0159486.
Повний текст джерелаLiu, Wenming, Joanna M. Szewczyk, Liladhar Waykole, Oljan Repic, and Thomas J. Blacklock. "ChemInform Abstract: Total Synthesis of Bengamide E." ChemInform 33, no. 23 (May 21, 2010): no. http://dx.doi.org/10.1002/chin.200223238.
Повний текст джерелаPhi, Thi Dao, Huong Doan Thi Mai, Van Hieu Tran, Bich Ngan Truong, Tuan Anh Tran, Van Loi Vu, Van Minh Chau, and Van Cuong Pham. "Design, synthesis and cytotoxicity of bengamide analogues and their epimers." MedChemComm 8, no. 2 (2017): 445–51. http://dx.doi.org/10.1039/c6md00587j.
Повний текст джерелаChida, Noritaka, Takahiko Tobe, Shinsuke Okada, and Seiichiro Ogawa. "Total synthesis and absolute configuration of bengamide A." Journal of the Chemical Society, Chemical Communications, no. 15 (1992): 1064. http://dx.doi.org/10.1039/c39920001064.
Повний текст джерелаCHIDA, N., T. TOBE, and S. OGAWA. "ChemInform Abstract: Total Synthesis of Bengamide E (I)." ChemInform 22, no. 51 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199151282.
Повний текст джерелаPhi, Thi Dao, Huong Doan Thi Mai, Van Hieu Tran, Van Loi Vu, Bich Ngan Truong, Tuan Anh Tran, Van Minh Chau, and Van Cuong Pham. "Synthesis of bengamide E analogues and their cytotoxic activity." Tetrahedron Letters 58, no. 19 (May 2017): 1830–33. http://dx.doi.org/10.1016/j.tetlet.2017.03.077.
Повний текст джерелаXu, David D., Liladhar Waykole, John V. Calienni, Lech Ciszewski, George T. Lee, Wenming Liu, Joanna Szewczyk, et al. "An Expedient Synthesis of LAF389, a Bengamide B Analogue." Organic Process Research & Development 7, no. 6 (November 2003): 856–65. http://dx.doi.org/10.1021/op0341162.
Повний текст джерелаMUKAI, C., S. M. MOHARRAM, O. KATAOKA, and M. HANAOKA. "ChemInform Abstract: Highly Stereocontrolled Total Synthesis of (+)-Bengamide E." ChemInform 27, no. 10 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199610321.
Повний текст джерелаKISHIMOTO, H., H. OHRUI, and H. MEGURO. "ChemInform Abstract: An Enantioselective Synthesis of Bengamide E (I)." ChemInform 24, no. 5 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199305296.
Повний текст джерелаLu, Jing-Ping, Xiu-Hua Yuan, Hai Yuan, Wen-Long Wang, Baojie Wan, Scott G. Franzblau, and Qi-Zhuang Ye. "Inhibition of Mycobacterium tuberculosis Methionine Aminopeptidases by Bengamide Derivatives." ChemMedChem 6, no. 6 (April 4, 2011): 1041–48. http://dx.doi.org/10.1002/cmdc.201100003.
Повний текст джерелаXu, Wei, Jing-Ping Lu, and Qi-Zhuang Ye. "Structural Analysis of Bengamide Derivatives as Inhibitors of Methionine Aminopeptidases." Journal of Medicinal Chemistry 55, no. 18 (September 14, 2012): 8021–27. http://dx.doi.org/10.1021/jm3008695.
Повний текст джерелаBanwell, Martin G., and Kenneth J. McRae. "ChemInform Abstract: A Chemoenzymatic Total Synthesis of ent-Bengamide E." ChemInform 33, no. 11 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200211187.
Повний текст джерелаTai, Wan-Yi, Run-Tao Zhang, Yi-Ming Ma, Min Gu, Gang Liu, Jia Li, and Fa-Jun Nan. "Design, Synthesis, and Biological Evaluation of Ring-Opened Bengamide Analogues." ChemMedChem 6, no. 9 (June 15, 2011): 1555–58. http://dx.doi.org/10.1002/cmdc.201100164.
Повний текст джерелаLiu, Gang, Yi-Ming Ma, Wan-Yi Tai, Chuan-Ming Xie, Yu-Lin Li, Jia Li, and Fa-Jun Nan. "Design, Synthesis, and Biological Evaluation of Caprolactam-Modified Bengamide Analogues." ChemMedChem 3, no. 1 (January 11, 2008): 74–78. http://dx.doi.org/10.1002/cmdc.200700214.
Повний текст джерелаSarabia, Francisco, Francisca Martín-Gálvez, Samy Chammaa, Laura Martín-Ortiz, and Antonio Sánchez-Ruiz. "Chiral Sulfur Ylides for the Synthesis of Bengamide E and Analogues." Journal of Organic Chemistry 75, no. 16 (August 20, 2010): 5526–32. http://dx.doi.org/10.1021/jo100696w.
Повний текст джерелаZhang, Wenxuan, Qingzhao Liang, Hui Li, Xiangbao Meng, and Zhongjun Li. "Concise synthesis and antitumor activity of Bengamide E and its analogs." Tetrahedron 69, no. 2 (January 2013): 664–72. http://dx.doi.org/10.1016/j.tet.2012.11.004.
Повний текст джерелаKinder,, Frederick R., Richard W. Versace, Kenneth W. Bair, John M. Bontempo, David Cesarz, Steven Chen, Phillip Crews, et al. "Synthesis and Antitumor Activity of Ester-Modified Analogues of Bengamide B." Journal of Medicinal Chemistry 44, no. 22 (October 2001): 3692–99. http://dx.doi.org/10.1021/jm010188c.
Повний текст джерелаFernández, Rogelio, Michel Dherbomez, Yves Letourneux, Mohamed Nabil, Jean François Verbist, and Jean François Biard. "Antifungal Metabolites from the Marine SpongePachastrissasp.: New Bengamide and Bengazole Derivatives." Journal of Natural Products 62, no. 5 (May 1999): 678–80. http://dx.doi.org/10.1021/np980330l.
Повний текст джерелаKong, Xue‐Qing, Bing‐Yan Wei, Chen‐Xi Yu, Xiang‐Na Guan, Wei‐Ping Ma, Gang Liu, Cai‐Guang Yang, and Fa‐Jun Nan. "Design, Synthesis and Biological Evaluation of Bengamide Analogues as ClpP Activators." Chinese Journal of Chemistry 38, no. 10 (July 2020): 1111–15. http://dx.doi.org/10.1002/cjoc.202000133.
Повний текст джерелаLu, Jing-Ping, Xiu-Hua Yuan, and Qi-Zhuang Ye. "Structural analysis of inhibition of Mycobacterium tuberculosis methionine aminopeptidase by bengamide derivatives." European Journal of Medicinal Chemistry 47 (January 2012): 479–84. http://dx.doi.org/10.1016/j.ejmech.2011.11.017.
Повний текст джерелаJamison, Matthew, Xiao Wang, Tina Cheng, and Tadeusz Molinski. "Synergistic Anti-Candida Activity of Bengazole A in the Presence of Bengamide A." Marine Drugs 17, no. 2 (February 7, 2019): 102. http://dx.doi.org/10.3390/md17020102.
Повний текст джерелаKinder, Frederick R. "SYNTHETIC APPROACHES TOWARD THE BENGAMIDE FAMILY OF ANTITUMOR MARINE NATURAL PRODUCTS. A REVIEW." Organic Preparations and Procedures International 34, no. 6 (December 2002): 559–83. http://dx.doi.org/10.1080/00304940209355783.
Повний текст джерелаKinder Jr., Frederick R., Richard W. Versace, and et al et al. "ChemInform Abstract: Synthesis and Antitumor Activity of Ester-Modified Analogues of Bengamide B." ChemInform 33, no. 9 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200209237.
Повний текст джерелаDhimane, Hamid, and Safiul Alam. "A Concise Synthesis of Bengamide E and Analogues via E-Selective Cross-Metathesis Olefination." Synlett 2010, no. 19 (November 3, 2010): 2923–27. http://dx.doi.org/10.1055/s-0030-1259015.
Повний текст джерелаChida, Noritaka, Takahiko Tobe, Katsuyuki Murai, Kaori Yamazaki, and Seiichiro Ogawa. "Stereoselective Conversion of L-Quebrachitol into a Novel Hydroxylated Caprolactam: Total Synthesis of Bengamide B." HETEROCYCLES 38, no. 11 (1994): 2383. http://dx.doi.org/10.3987/com-94-6869.
Повний текст джерелаTietjen, Ian, David E. Williams, Silven Read, Xiaomei T. Kuang, Philip Mwimanzi, Emmanuelle Wilhelm, Tristan Markle та ін. "Inhibition of NF-κB-dependent HIV-1 replication by the marine natural product bengamide A". Antiviral Research 152 (квітень 2018): 94–103. http://dx.doi.org/10.1016/j.antiviral.2018.02.017.
Повний текст джерелаMukai, Chisato, Osamu Kataoka, and Miyoji Hanaoka. "A cobalt-complexed propyanl in organic synthesis: A highly stereoselective total synthesis of bengamide E." Tetrahedron Letters 35, no. 37 (September 1994): 6899–902. http://dx.doi.org/10.1016/0040-4039(94)85036-4.
Повний текст джерелаWenzel, Silke C., Holger Hoffmann, Jidong Zhang, Laurent Debussche, Sabine Haag-Richter, Michael Kurz, Frederico Nardi, et al. "Produktion mariner Naturstoffe aus der Klasse der Bengamide in Myxobakterien: Biosynthese und Struktur-Aktivitäts-Beziehungen." Angewandte Chemie 127, no. 51 (October 30, 2015): 15781–85. http://dx.doi.org/10.1002/ange.201508277.
Повний текст джерелаHu, Xiaoyi, Yongjun Dang, Karen Tenney, Phillip Crews, Chiawei W. Tsai, Katherine M. Sixt, Philip A. Cole, and Jun O. Liu. "Regulation of c-Src Nonreceptor Tyrosine Kinase Activity by Bengamide A through Inhibition of Methionine Aminopeptidases." Chemistry & Biology 14, no. 7 (July 2007): 764–74. http://dx.doi.org/10.1016/j.chembiol.2007.05.010.
Повний текст джерелаMarshall, James A., and George P. Luke. "Stereoselective total synthesis of bengamide E from glyceraldehyde acetonide and a nonracemic .gamma.-alkoxy allylic stannane." Journal of Organic Chemistry 58, no. 23 (November 1993): 6229–34. http://dx.doi.org/10.1021/jo00075a017.
Повний текст джерелаWenzel, Silke C., Holger Hoffmann, Jidong Zhang, Laurent Debussche, Sabine Haag-Richter, Michael Kurz, Frederico Nardi, et al. "Production of the Bengamide Class of Marine Natural Products in Myxobacteria: Biosynthesis and Structure-Activity Relationships." Angewandte Chemie International Edition 54, no. 51 (October 30, 2015): 15560–64. http://dx.doi.org/10.1002/anie.201508277.
Повний текст джерелаMartín-Gálvez, Francisca, Cristina García-Ruiz, Antonio Sánchez-Ruiz, Frederick A. Valeriote, and Francisco Sarabia. "An Array of Bengamide E Analogues Modified at the Terminal Olefinic Position: Synthesis and Antitumor Properties." ChemMedChem 8, no. 5 (March 19, 2013): 819–31. http://dx.doi.org/10.1002/cmdc.201300033.
Повний текст джерелаSarabia, Francisco, and Antonio Sánchez-Ruiz. "Total Synthesis of Bengamide E and Analogues by Modification at C-2 and at Terminal Olefinic Positions." Journal of Organic Chemistry 70, no. 23 (November 2005): 9514–20. http://dx.doi.org/10.1021/jo0516032.
Повний текст джерелаMUKAI, C., O. KATAOKA, and M. HANAOKA. "ChemInform Abstract: A Cobalt-Complexed Propynal in Organic Synthesis: A Highly Stereoselective Total Synthesis of Bengamide E." ChemInform 26, no. 7 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199507220.
Повний текст джерелаCHIDA, N., T. TOBE, K. MURAI, K. YAMAZAKI, and S. OGAWA. "ChemInform Abstract: Stereoselective Conversion of L-Quebrachitol Into a Novel Hydroxylated Caprolactam: Total Synthesis of Bengamide B." ChemInform 26, no. 7 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199507256.
Повний текст джерелаSusilowati, Fitria, Respati Tri Swasono, Tatsufumi Okino, and Winarto Haryadi. "IN VITRO CYTOTOXIC ANTICANCER POTENTIAL OF BIOACTIVE FRACTION ISOLATED FROM INDONESIAN TIDAL SPONGE CALTHROPELLA SP." Asian Journal of Pharmaceutical and Clinical Research 12, no. 1 (January 7, 2019): 380. http://dx.doi.org/10.22159/ajpcr.2018.v12i1.23655.
Повний текст джерелаSusilowati, Fitria, Respati Tri Swasono, Tatsufumi Okino, and Winarto Haryadi. "IN VITRO CYTOTOXIC ANTICANCER POTENTIAL OF BIOACTIVE FRACTION ISOLATED FROM INDONESIAN TIDAL SPONGE CALTHROPELLA SP." Asian Journal of Pharmaceutical and Clinical Research 12, no. 1 (January 7, 2019): 380. http://dx.doi.org/10.22159/ajpcr.2019.v12i1.23655.
Повний текст джерелаMARSHALL, J. A., та G. P. LUKE. "ChemInform Abstract: Stereoselective Total Synthesis of Bengamide E from Glyceraldehyde Acetonide and a Nonracemic γ-Alkoxy Allylic Stannane." ChemInform 25, № 10 (19 серпня 2010): no. http://dx.doi.org/10.1002/chin.199410247.
Повний текст джерелаJohnson, Tyler A., Johann Sohn, Yvette M. Vaske, Kimberly N. White, Tanya L. Cohen, Helene C. Vervoort, Karen Tenney, Frederick A. Valeriote, Leonard F. Bjeldanes, and Phillip Crews. "Myxobacteria versus sponge-derived alkaloids: The bengamide family identified as potent immune modulating agents by scrutiny of LC–MS/ELSD libraries." Bioorganic & Medicinal Chemistry 20, no. 14 (July 2012): 4348–55. http://dx.doi.org/10.1016/j.bmc.2012.05.043.
Повний текст джерелаMukai, Chisato, Osamu Kataoka, and Miyoji Hanaoka. "An efficient method for the optical resolution of 3-hydroxy-2-substituted-4-alkynoates: a highly stereoselective total synthesis of (+)-bengamide E1." Journal of Organic Chemistry 60, no. 18 (September 1995): 5910–18. http://dx.doi.org/10.1021/jo00123a030.
Повний текст джерелаPhilip, Anijamol T., Eerlapally Raju та Ramesh Ramapanicker. "Stereoselective Synthesis of Hydroxy Diamino Acid Derivatives and the Caprolactam Unit of Bengamide A through Organocatalytic α-Hydroxylation and Reductive Amination of Aldehydes". European Journal of Organic Chemistry 2016, № 33 (20 жовтня 2016): 5502–10. http://dx.doi.org/10.1002/ejoc.201600842.
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