Journal articles on the topic 'Calothrixin'
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Owen, Elisabeth A., and Max A. Keniry. "Exploring the Binding of Calothrixin A to the G-Quadruplex from the c-myc Oncogene Promotor." Australian Journal of Chemistry 62, no. 11 (2009): 1544. http://dx.doi.org/10.1071/ch09169.
Full textGuingant, André, Drissa Sissouma, and Sylvain Collet. "A Synthesis of Calothrixin B." Synlett 2004, no. 14 (October 20, 2004): 2612–14. http://dx.doi.org/10.1055/s-2004-834831.
Full textKaliyaperumal, Srinivasan A., Shyamapada Banerjee, and Syam Kumar U. K. "Palladium mediated intramolecular multiple C–X/C–H cross coupling and C–H activation: synthesis of carbazole alkaloids calothrixin B and murrayaquinone A." Org. Biomol. Chem. 12, no. 32 (2014): 6105–13. http://dx.doi.org/10.1039/c4ob00493k.
Full textRamkumar, Nagarajan, and Rajagopal Nagarajan. "Total synthesis of calothrixin B via sequential Sonogashira coupling/copper-catalyzed oxidative cyclization." Organic & Biomolecular Chemistry 13, no. 45 (2015): 11046–51. http://dx.doi.org/10.1039/c5ob01766a.
Full textSperry, Jonathan, Christopher S. P. McErlean, Alexandra M. Z. Slawin, and Christopher J. Moody. "A biomimetic synthesis of calothrixin B." Tetrahedron Letters 48, no. 2 (January 2007): 231–34. http://dx.doi.org/10.1016/j.tetlet.2006.11.053.
Full textChai, Christina, Paul Bernardo, and Wuri Fitriyanto. "Palladium-Mediated Synthesis of Calothrixin B." Synlett 2007, no. 12 (July 2007): 1935–39. http://dx.doi.org/10.1055/s-2007-984520.
Full textRamkumar, Nagarajan, and Rajagopal Nagarajan. "Formal total synthesis of calothrixin B and its N-benzyl analogues." RSC Advances 5, no. 107 (2015): 87838–40. http://dx.doi.org/10.1039/c5ra18120h.
Full textBhosale, Shrikar M., Rupesh L. Gawade, Vedavati G. Puranik, and Radhika S. Kusurkar. "An efficient total synthesis of calothrixin B." Tetrahedron Letters 53, no. 23 (June 2012): 2894–96. http://dx.doi.org/10.1016/j.tetlet.2012.03.131.
Full textSissouma, Drissa, Lucie Maingot, Sylvain Collet, and André Guingant. "Concise and Efficient Synthesis of Calothrixin B." Journal of Organic Chemistry 71, no. 22 (October 2006): 8384–89. http://dx.doi.org/10.1021/jo061270o.
Full textBernardo, Paul H., Christina L. L. Chai, and John A. Elix. "A simple and concise route to calothrixin B." Tetrahedron Letters 43, no. 16 (April 2002): 2939–40. http://dx.doi.org/10.1016/s0040-4039(02)00434-3.
Full textBennasar, M. Lluïsa, Tomàs Roca, and Francesc Ferrando. "A New Radical-Based Route to Calothrixin B." Organic Letters 8, no. 4 (February 2006): 561–64. http://dx.doi.org/10.1021/ol052600e.
Full textSaravanan, Velu, Bose Muthu Ramalingam, and Arasambattu K. Mohanakrishnan. "Total Synthesis of Calothrixin B and Its Analogs." European Journal of Organic Chemistry 2014, no. 6 (December 12, 2013): 1266–79. http://dx.doi.org/10.1002/ejoc.201301524.
Full textRamkumar, Nagarajan, and Rajagopal Nagarajan. "Total Synthesis of Ellipticine Quinones, Olivacine, and Calothrixin B." Journal of Organic Chemistry 79, no. 2 (January 6, 2014): 736–41. http://dx.doi.org/10.1021/jo402593w.
Full textKelly, T. Ross, Yajun Zhao, Marta Cavero, and Mercedes Torneiro. "Synthesis of the Potent Antimalarials Calothrixin A and B." Organic Letters 2, no. 23 (November 2000): 3735–37. http://dx.doi.org/10.1021/ol006649q.
Full textYingyuad, Peerada, Chomdao Sinthuvanich, Theerachart Leepasert, Panumart Thongyoo, and Suwimon Boonrungsiman. "Preparation, characterization and in vitro evaluation of calothrixin B liposomes." Journal of Drug Delivery Science and Technology 44 (April 2018): 491–97. http://dx.doi.org/10.1016/j.jddst.2018.02.010.
Full textBernardo, Paul H., Christina L. L. Chai, and John A. Elix. "ChemInform Abstract: A Simple and Concise Route to Calothrixin B." ChemInform 33, no. 32 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200232211.
Full textSaravanan, Velu, Bose Muthu Ramalingam, and Arasambattu K. Mohanakrishnan. "ChemInform Abstract: Total Synthesis of Calothrixin B and Its Analogues." ChemInform 45, no. 49 (November 20, 2014): no. http://dx.doi.org/10.1002/chin.201449206.
Full textHibino, Satoshi, Tominari Choshi, Shigeo Tohyama, Kohji Matsumoto, Akira Yamabuki, Yuhzo Hieda, and Junko Nobuhiro. "Total Synthesis of Bioactive Indolo[3,2-j]phenanthridine Alkaloid, Calothrixin B." HETEROCYCLES 82, no. 1 (2010): 397. http://dx.doi.org/10.3987/com-10-s(e)11.
Full textRamkumar, Nagarajan, and Rajagopal Nagarajan. "Total Synthesis of Calothrixin A and B via C–H Activation." Journal of Organic Chemistry 78, no. 6 (February 28, 2013): 2802–7. http://dx.doi.org/10.1021/jo302821v.
Full textRamkumar, Nagarajan, and Rajagopal Nagarajan. "ChemInform Abstract: Total Synthesis of Ellipticine Quinones, Olivacine, and Calothrixin B." ChemInform 45, no. 25 (June 5, 2014): no. http://dx.doi.org/10.1002/chin.201425174.
Full textKelly, T. Ross, Yajun Zhao, Marta Cavero, and Mercedes Torneiro. "ChemInform Abstract: Synthesis of the Potent Antimalarials Calothrixin A and B." ChemInform 32, no. 14 (April 3, 2001): no. http://dx.doi.org/10.1002/chin.200114219.
Full textMori-Quiroz, Luis M., Madeline M. Dekarske, Austin B. Prinkki, and Michael D. Clift. "Exploiting Alkylquinone Tautomerization for the Total Synthesis of Calothrixin A and B." Journal of Organic Chemistry 82, no. 23 (November 17, 2017): 12257–66. http://dx.doi.org/10.1021/acs.joc.7b02101.
Full textYamabuki, Akira, Hikohito Fujinawa, Tominari Choshi, Shigeo Tohyama, Kohji Matsumoto, Kana Ohmura, Junko Nobuhiro, and Satoshi Hibino. "A biomimetic synthesis of the indolo[3,2-j]phenanthridine alkaloid, calothrixin B." Tetrahedron Letters 47, no. 33 (August 2006): 5859–61. http://dx.doi.org/10.1016/j.tetlet.2006.06.077.
Full textBernardo, Paul H., Christina L. L. Chai, Maurice Le Guen, Geoffrey D. Smith, and Paul Waring. "Structure–activity delineation of quinones related to the biologically active Calothrixin B." Bioorganic & Medicinal Chemistry Letters 17, no. 1 (January 2007): 82–85. http://dx.doi.org/10.1016/j.bmcl.2006.09.090.
Full textMohanakrishnan, Arasambattu, Bose Ramalingam, Nachiappan Moorthy, and Elangovan Vellaichamy. "Synthesis of Thia-Analogues of Calothrixin B Involving FeCl3-Mediated Domino Reaction." Synlett 28, no. 01 (September 12, 2016): 133–37. http://dx.doi.org/10.1055/s-0036-1588072.
Full textYang, Xiaohong, Jiangsheng Gao, Jian Guo, Zimeng Zhao, Shao-Lin Zhang, and Yun He. "Anti-lung cancer activity and inhibitory mechanisms of a novel Calothrixin A derivative." Life Sciences 219 (February 2019): 20–30. http://dx.doi.org/10.1016/j.lfs.2018.12.052.
Full textTohyama, Shigeo, Tominari Choshi, Kohji Matsumoto, Akira Yamabuki, Kouichiro Ikegata, Junko Nobuhiro, and Satoshi Hibino. "A new total synthesis of an indolo[3,2-j]phenanthridine alkaloid calothrixin B." Tetrahedron Letters 46, no. 32 (August 2005): 5263–64. http://dx.doi.org/10.1016/j.tetlet.2005.06.042.
Full textTohyama, Shigeo, Tominari Choshi, Kohji Matsumoto, Akira Yamabuki, Yuhzo Hieda, Junko Nobuhiro, and Satoshi Hibino. "ChemInform Abstract: Total Synthesis of Bioactive Indolo[3,2-j]phenanthridine Alkaloid, Calothrixin B." ChemInform 42, no. 19 (April 14, 2011): no. http://dx.doi.org/10.1002/chin.201119189.
Full textT. Parvatkar, Prakash. "Recent Progress Towards the Total Synthesis and Biological Studies of Calothrixin A and B." Current Organic Chemistry 20, no. 8 (March 3, 2016): 839–55. http://dx.doi.org/10.2174/1385272819666150803235103.
Full textMori-Quiroz, Luis M., Madeline M. Dekarske, Austin B. Prinkki, and Michael D. Clift. "Correction to “Exploiting Alkylquinone Tautomerization for the Total Synthesis of Calothrixin A and B”." Journal of Organic Chemistry 83, no. 11 (May 16, 2018): 6243. http://dx.doi.org/10.1021/acs.joc.8b01110.
Full textHatae, Noriyuki, Risa Satoh, Hitomi Chiba, Takahiro Osaki, Takashi Nishiyama, Minoru Ishikura, Takumi Abe, et al. "N-Substituted calothrixin B derivatives inhibited the proliferation of HL-60 promyelocytic leukemia cells." Medicinal Chemistry Research 23, no. 11 (June 15, 2014): 4956–61. http://dx.doi.org/10.1007/s00044-014-1061-6.
Full textAthbi, Ahmed M., Eqbal J. AL-Assedi, and Areej F. AL-Nassir. "solation and identification of an alkaloidic compound similar to Calothrixin-A from green alga Cladophora crispata (Roth.) Kützing." IRAQI JOURNAL OF AQUACULTURE 8, no. 1 (2011): 53–80. http://dx.doi.org/10.21276/ijaq.2011.8.1.4.
Full textBhosale, Shrikar M., Aadil A. Momin, Shrikant Kunjir, P. R. Rajamohanan, and Radhika S. Kusurkar. "Unexpected observations during the total synthesis of calothrixin B–sodium methoxide as a source of hydride." Tetrahedron Letters 55, no. 1 (January 2014): 155–62. http://dx.doi.org/10.1016/j.tetlet.2013.10.140.
Full textDoan, Nga Thanh, Peter R. Stewart, and Geoffrey D. Smith. "Inhibition of bacterial RNA polymerase by the cyanobacterial metabolites 12-epi-hapalindole E isonitrile and calothrixin A." FEMS Microbiology Letters 196, no. 2 (March 2001): 135–39. http://dx.doi.org/10.1111/j.1574-6968.2001.tb10554.x.
Full textLong, Qun, Xiao Xiao, Ping Yi, Yuancui Liu, Krishnapriya M. Varier, Qing Rao, Jingrui Song, et al. "L20, a Calothrixin B analog, induces intrinsic apoptosis on HEL cells through ROS/γ-H2AX/p38 MAPK pathway." Biomedicine & Pharmacotherapy 137 (May 2021): 111336. http://dx.doi.org/10.1016/j.biopha.2021.111336.
Full textDeng, Chengdan, Yuancui Liu, Mei Xu, Kaiqiang Xie, and Sheng Liu. "Exploiting an intramolecular Diels–Alder cyclization/dehydro-aromatization sequence for the total syntheses of ellipticines and calothrixin B." Organic & Biomolecular Chemistry 19, no. 6 (2021): 1395–403. http://dx.doi.org/10.1039/d0ob02527e.
Full textLiao, Xianjiu, Chunlei Zhu, Haiyan Zhang, Xuemin Li, Xiaoqing Wen, Shao-Lin Zhang, and Yizhong Shen. "Investigation on the binding of cyanobacterial metabolite calothrixin A with human serum albumin for evaluating its potential toxicology." Food and Chemical Toxicology 155 (September 2021): 112396. http://dx.doi.org/10.1016/j.fct.2021.112396.
Full textCollet, Sylvain, André Guingant, Lucie Maingot, Frédéric Thuaud, Drissa Sissouma, and Michel Evain. "Synthesis of a Calothrixin B Isomer with a Novel 7H-Indolo[2,3-j]phenanthridine-7,13(8H)-dione Structure." Synlett 2008, no. 2 (January 2008): 263–67. http://dx.doi.org/10.1055/s-2007-1000933.
Full textBhosale, Shrikar M., Aadil A. Momin, Shrikant Kunjir, P. R. Rajamohanan, and Radhika S. Kusurkar. "ChemInform Abstract: Unexpected Observations During the Total Synthesis of Calothrixin B-Sodium Methoxide as a Source of Hydride." ChemInform 45, no. 20 (April 28, 2014): no. http://dx.doi.org/10.1002/chin.201420036.
Full textLee, Sungjong, Kyung-Hee Kim, and Cheol-Hong Cheon. "Total Syntheses of Arcyriaflavin A and Calothrixin B Using 2,2′-Bisindole-3-acetic Acid Derivative as a Common Intermediate." Organic Letters 19, no. 11 (May 18, 2017): 2785–88. http://dx.doi.org/10.1021/acs.orglett.7b00687.
Full textLin, Kai, Yong Jian, Peng Zhao, Chun-shen Zhao, Wei-dong Pan, and Sheng Liu. "A rapid construction of a specific quino[4,3-b] carbazolone system and its application for the synthesis of calothrixin B." Organic Chemistry Frontiers 5, no. 4 (2018): 590–94. http://dx.doi.org/10.1039/c7qo00864c.
Full textSingh, Shweta, Ramesh Samineni, Srihari Pabbaraja, and Goverdhan Mehta. "A General Carbazole Synthesis via Stitching of Indole–Ynones with Nitromethanes: Application to Total Synthesis of Carbazomycin A, Calothrixin B, and Staurosporinone." Organic Letters 21, no. 9 (April 23, 2019): 3372–76. http://dx.doi.org/10.1021/acs.orglett.9b01111.
Full textRickards, Rodney W., Jennifer M. Rothschild, Anthony C. Willis, Nola M. de Chazal, Julie Kirk, Kiaran Kirk, Kevin J. Saliba, and Geoffrey D. Smith. "Calothrixins A and B, novel pentacyclic metabolites from Calothrix cyanobacteria with potent activity against malaria parasites and human cancer cells." Tetrahedron 55, no. 47 (November 1999): 13513–20. http://dx.doi.org/10.1016/s0040-4020(99)00833-9.
Full textRickards, Rodney W., Jennifer M. Rothschild, Anthony C. Willis, Nola M. de Chazal, Julie Kirk, Kiaran Kirk, Kevin J. Saliba, and Geoffrey D. Smith. "ChemInform Abstract: Calothrixins A (I) and B (II), Novel Pentacyclic Metabolites from Calothrix Cyanobacteria with Potent Activity Against Malaria Parasites and Human Cancer Cells." ChemInform 31, no. 6 (June 11, 2010): no. http://dx.doi.org/10.1002/chin.200006222.
Full textMal, Dipakranjan, Joyeeta Roy, and Kumar Biradha. "Regiodivergent and short total synthesis of calothrixins." Org. Biomol. Chem. 12, no. 41 (August 21, 2014): 8196–203. http://dx.doi.org/10.1039/c4ob01309c.
Full textDethe, Dattatraya H., and Ganesh M. Murhade. "Diversity-Oriented Synthesis of Calothrixins and Ellipticines." European Journal of Organic Chemistry 2014, no. 31 (September 19, 2014): 6953–62. http://dx.doi.org/10.1002/ejoc.201402837.
Full textAbe, Takumi, Toshiaki Ikeda, Reiko Yanada, and Minoru Ishikura. "Concise Total Synthesis of Calothrixins A and B." Organic Letters 13, no. 13 (July 2011): 3356–59. http://dx.doi.org/10.1021/ol201107a.
Full textBerrendero, Esther, Elvira Perona, and Pilar Mateo. "Phenotypic variability and phylogenetic relationships of the genera Tolypothrix and Calothrix (Nostocales, Cyanobacteria) from running water." International Journal of Systematic and Evolutionary Microbiology 61, no. 12 (December 1, 2011): 3039–51. http://dx.doi.org/10.1099/ijs.0.027581-0.
Full textThajamanbi, Moirangthem, Jayashree Rout, and Nooruddin Thajuddin. "Isolation and Characterization of Two Cyanobacterial Strains Calothrix Sp. and Microchaete Sp. from Rice Fields of Karimganj District, Assam, North East India." Current World Environment 11, no. 2 (August 25, 2016): 399–405. http://dx.doi.org/10.12944/cwe.11.2.07.
Full textXu, Su, Bhavitavya Nijampatnam, Shilpa Dutta, and Sadanandan Velu. "Cyanobacterial Metabolite Calothrixins: Recent Advances in Synthesis and Biological Evaluation." Marine Drugs 14, no. 1 (January 12, 2016): 17. http://dx.doi.org/10.3390/md14010017.
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