Статті в журналах з теми "Bioactive Indole Alkaloids"
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Khan, Neyaz A., Navdeep Kaur, Peter Owens, Olivier P. Thomas, and Aoife Boyd. "Bis-Indole Alkaloids Isolated from the Sponge Spongosorites calcicola Disrupt Cell Membranes of MRSA." International Journal of Molecular Sciences 23, no. 4 (February 11, 2022): 1991. http://dx.doi.org/10.3390/ijms23041991.
Повний текст джерелаKirsch, Gilbert, Eslam El-Sawy, and Ahmed Abdelwahab. "Utilization of 1H-Indole-3-carboxaldehyde as a Precursor for the Synthesis of Bioactive Indole Alkaloids." Synthesis 50, no. 23 (October 15, 2018): 4525–38. http://dx.doi.org/10.1055/s-0037-1610288.
Повний текст джерелаPan, Li, César Terrazas, Ulyana Muñoz Acuña, Tran Ngoc Ninh, Heebyung Chai, Esperanza J. Carcache de Blanco, Djaja D. Soejarto, Abhay R. Satoskar, and A. Douglas Kinghorn. "Bioactive indole alkaloids isolated from Alstonia angustifolia." Phytochemistry Letters 10 (December 2014): liv—lix. http://dx.doi.org/10.1016/j.phytol.2014.06.010.
Повний текст джерелаKlein-Júnior, Luiz C., Sylvian Cretton, Yvan Vander Heyden, André L. Gasper, Samad Nejad-Ebrahimi, Philippe Christen, and Amélia T. Henriques. "Bioactive Azepine-Indole Alkaloids from Psychotria nemorosa." Journal of Natural Products 83, no. 4 (March 9, 2020): 852–63. http://dx.doi.org/10.1021/acs.jnatprod.9b00469.
Повний текст джерелаLiu, Yan-Ping, Qing-Long Liu, Xiang-Lin Zhang, Hai-Yuan Niu, Chun-Yan Guan, Fu-Kang Sun, Wei Xu, and Yan-Hui Fu. "Bioactive monoterpene indole alkaloids from Nauclea officinalis." Bioorganic Chemistry 83 (March 2019): 1–5. http://dx.doi.org/10.1016/j.bioorg.2018.10.013.
Повний текст джерелаZhang, Yanyan, Ting Han, Qianliang Ming, Lingshang Wu, Khalid Rahman, and Luping Qin. "Alkaloids Produced by Endophytic Fungi: A Review." Natural Product Communications 7, no. 7 (July 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700742.
Повний текст джерелаBozkurt, Buket, Gulen I. Kaya, and Nehir U. Somer. "Chemical Composition and Enzyme Inhibitory Activities of Turkish Pancratium maritimum Bulbs." Natural Product Communications 14, no. 10 (October 2019): 1934578X1987290. http://dx.doi.org/10.1177/1934578x19872905.
Повний текст джерелаLee, Kit, Bing-Nan Zhou, David Kingston, Abraham Vaisberg, and Gerald Hammond. "Bioactive Indole Alkaloids from the Bark ofUncaria guianensis." Planta Medica 65, no. 08 (December 1999): 759–60. http://dx.doi.org/10.1055/s-2006-960860.
Повний текст джерелаRahman, M. Toufiqur, Jeffrey R. Deschamps, Gregory H. Imler, and James M. Cook. "Total Synthesis of Sarpagine-Related Bioactive Indole Alkaloids." Chemistry - A European Journal 24, no. 10 (January 23, 2018): 2354–59. http://dx.doi.org/10.1002/chem.201705575.
Повний текст джерелаAthipornchai, Anan. "A Review on Tabernaemontana spp.: Multipotential Medicinal Plant." Asian Journal of Pharmaceutical and Clinical Research 11, no. 5 (May 1, 2018): 45. http://dx.doi.org/10.22159/ajpcr.2018.v11i5.11478.
Повний текст джерелаSevik Kilicaslan, Ozlem, Sylvian Cretton, Luis Quirós-Guerrero, Merveilles A. Bella, Marcel Kaiser, Pascal Mäser, Joseph T. Ndongo, and Muriel Cuendet. "Isolation and Structural Elucidation of Compounds from Pleiocarpa bicarpellata and Their In Vitro Antiprotozoal Activity." Molecules 27, no. 7 (March 28, 2022): 2200. http://dx.doi.org/10.3390/molecules27072200.
Повний текст джерелаPark, Jae Sung, Eunji Cho, Ji-Yeon Hwang, Sung Chul Park, Beomkoo Chung, Oh-Seok Kwon, Chung J. Sim, Dong-Chan Oh, Ki-Bong Oh, and Jongheon Shin. "Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge." Marine Drugs 19, no. 1 (December 23, 2020): 3. http://dx.doi.org/10.3390/md19010003.
Повний текст джерелаOliveros-Díaz, Andrés, Jesús Olivero-Verbel, Yina Pájaro-González, and Fredyc Díaz-Castillo. "Molecular Human Targets of Bioactive Alkaloid-Type Compounds from Tabernaemontana cymose Jacq." Molecules 26, no. 12 (June 21, 2021): 3765. http://dx.doi.org/10.3390/molecules26123765.
Повний текст джерелаSrivastava, Mukul, Shikha Kesharwani, Roohi Kesharwani, Dilip K. Patel, and S. N. Singh. "A REVIEW ON POTENTIAL BIOACTIVE CHEMICAL FROM RAUWOLFIA SERPENTINA: RESERPINE." International Journal of Research in Ayurveda and Pharmacy 12, no. 1 (March 2, 2021): 106–9. http://dx.doi.org/10.7897/2277-4343.120123.
Повний текст джерелаRamkissoon, Antonio, Mohindra Seepersaud, Anderson Maxwell, Jayaraj Jayaraman, and Adesh Ramsubhag. "Isolation and Antibacterial Activity of Indole Alkaloids from Pseudomonas aeruginosa UWI-1." Molecules 25, no. 16 (August 17, 2020): 3744. http://dx.doi.org/10.3390/molecules25163744.
Повний текст джерелаNoldin, Vânia Floriani, Domingos Tabajara de Oliveira Martins, César Marcos Marcello, Joaquim Corsino da Silva Lima, Franco Delle Monache, and Valdir Cechinel Filho. "Phytochemical and Antiulcerogenic Properties of Rhizomes from Simaba ferruginea St. Hill. (Simaroubaceae)." Zeitschrift für Naturforschung C 60, no. 9-10 (October 1, 2005): 701–6. http://dx.doi.org/10.1515/znc-2005-9-1007.
Повний текст джерелаWang, Zhijie, Yu Jiang, Xiujuan Xin, and Faliang An. "Bioactive indole alkaloids from insect derived endophytic Aspergillus lentulus." Fitoterapia 153 (September 2021): 104973. http://dx.doi.org/10.1016/j.fitote.2021.104973.
Повний текст джерелаOhashi, Leticia Hiromi, Douglas Costa Gontijo, Maria Fernanda Alves do Nascimento, Luciano Ferreira Margalho, Geraldo Célio Brandão, and Alaíde Braga de Oliveira. "Extraction and Fractionation Effects on Antiplasmodial Activity and Phytochemical Composition of Palicourea hoffmannseggiana." Planta Medica International Open 8, no. 01 (April 2021): e34-e42. http://dx.doi.org/10.1055/a-1375-6456.
Повний текст джерелаMunir, Samman, Aqsa Shahid, Bilal Aslam, Usman Ali Ashfaq, Muhammad Sajid Hamid Akash, Muhammad Akhtar Ali, Ahmad Almatroudi, Khaled S. Allemailem, Muhammad Shahid Riaz Rajoka, and Mohsin Khurshid. "The Therapeutic Prospects of Naturally Occurring and Synthetic Indole Alkaloids for Depression and Anxiety Disorders." Evidence-Based Complementary and Alternative Medicine 2020 (October 16, 2020): 1–11. http://dx.doi.org/10.1155/2020/8836983.
Повний текст джерелаArgade, Narshinha, and Pravat Mondal. "Formal Synthesis of Bioactive Indole Alkaloids Eburnamonine, Eburnaminol, and Vindeburnol." Synthesis 49, no. 08 (January 13, 2017): 1849–56. http://dx.doi.org/10.1055/s-0036-1588386.
Повний текст джерелаLin, Li Ping, and Ren Xiang Tan. "Bioactive Alkaloids from Indole-3-carbinol Exposed Culture of Daldiniaeschscholzii." Chinese Journal of Chemistry 36, no. 8 (June 13, 2018): 749–53. http://dx.doi.org/10.1002/cjoc.201800160.
Повний текст джерелаHadi, Surya. "MATARANINE A AND B: A NEW DIASTOMERIC INDOLE ALKALOID FROM Alstonia scholaris R.Br. OF LOMBOK ISLAND." Indonesian Journal of Chemistry 9, no. 3 (June 24, 2010): 466–69. http://dx.doi.org/10.22146/ijc.21517.
Повний текст джерелаPlazas, Erika, and Nicoletta Faraone. "Indole Alkaloids from Psychoactive Mushrooms: Chemical and Pharmacological Potential as Psychotherapeutic Agents." Biomedicines 11, no. 2 (February 5, 2023): 461. http://dx.doi.org/10.3390/biomedicines11020461.
Повний текст джерелаMatsuura, Hélio Nitta, Mariana Ritter Rau, and Arthur Germano Fett-Neto. "Oxidative stress and production of bioactive monoterpene indole alkaloids: biotechnological implications." Biotechnology Letters 36, no. 2 (September 24, 2013): 191–200. http://dx.doi.org/10.1007/s10529-013-1348-6.
Повний текст джерелаHuang, Yuxiang, Hexin Tan, Zhiying Guo, Xunxun Wu, Qinglei Zhang, Lei Zhang, and Yong Diao. "The biosynthesis and genetic engineering of bioactive indole alkaloids in plants." Journal of Plant Biology 59, no. 3 (June 2016): 203–14. http://dx.doi.org/10.1007/s12374-016-0032-5.
Повний текст джерелаMuhaimin, Muhaimin, Muhammad Irhash Shalihin, and Madyawati Latief. "Anti-Inflammatory Activity of an Indole Alkaloid Isolated from Bebuas (Premna serratifolia)." Journal of Pure and Applied Chemistry Research 10, no. 2 (August 31, 2021): 84–103. http://dx.doi.org/10.21776/ub.jpacr.2021.010.02.584.
Повний текст джерелаSu, Chun-Han, Yu-Chieh Cheng, Yu-Chia Chang, Ting-Hsuan Kung, Yu-Li Chen, Kuei-Hung Lai, Hsi-Lung Hsieh, Chun-Yu Chen, Tsong-Long Hwang, and Yu-Liang Yang. "Untargeted LC-MS/MS-Based Multi-Informative Molecular Networking for Targeting the Antiproliferative Ingredients in Tetradium ruticarpum Fruit." Molecules 27, no. 14 (July 12, 2022): 4462. http://dx.doi.org/10.3390/molecules27144462.
Повний текст джерелаYang, Jin, Lizhi Gong, Miaomiao Guo, Yu Jiang, Yi Ding, Zhijie Wang, Xiujuan Xin, and Faliang An. "Bioactive Indole Diketopiperazine Alkaloids from the Marine Endophytic Fungus Aspergillus sp. YJ191021." Marine Drugs 19, no. 3 (March 17, 2021): 157. http://dx.doi.org/10.3390/md19030157.
Повний текст джерелаBerner, Mathias, Arto Tolvanen, and Reija Jokela. "ChemInform Abstract: Acid-Catalyzed Epimerization of Bioactive Indole Alkaloids and Their Derivatives." ChemInform 33, no. 36 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200236271.
Повний текст джерелаChear, Nelson Jeng-Yeou, Tan Ai Fein Ching-Ga, Kooi-Yeong Khaw, Francisco León, Wen-Nee Tan, Siti R. Yusof, Christopher R. McCurdy, Vikneswaran Murugaiyah, and Surash Ramanathan. "Natural Corynanthe-Type Cholinesterase Inhibitors from Malaysian Uncaria attenuata Korth.: Isolation, Characterization, In Vitro and In Silico Studies." Metabolites 13, no. 3 (March 7, 2023): 390. http://dx.doi.org/10.3390/metabo13030390.
Повний текст джерелаSerdyuk, Olga, Igor Trushkov, Maxim Uchuskin, and Vladimir Abaev. "Indolylvinyl Ketones: Building Blocks for the Synthesis of Natural Products and Bioactive Compounds." Synthesis 51, no. 04 (January 24, 2019): 787–815. http://dx.doi.org/10.1055/s-0037-1611702.
Повний текст джерелаScheidt, Karl A., and Eric R. Miller. "Enantioselective Syntheses of Yohimbine Alkaloids: Proving Grounds for New Catalytic Transformations." Synthesis 54, no. 05 (November 2, 2021): 1217–30. http://dx.doi.org/10.1055/a-1684-2942.
Повний текст джерелаYang, Mengquan, Bowen Yao, and Rongmei Lin. "Profiles of Metabolic Genes in Uncaria rhynchophylla and Characterization of the Critical Enzyme Involved in the Biosynthesis of Bioactive Compounds-(iso)Rhynchophylline." Biomolecules 12, no. 12 (November 30, 2022): 1790. http://dx.doi.org/10.3390/biom12121790.
Повний текст джерелаCheng, Gui-Guang, Dan Li, Bo Hou, Xiao-Nian Li, Lu Liu, Ying-Ying Chen, Paul-Keilah Lunga, et al. "Melokhanines A–J, Bioactive Monoterpenoid Indole Alkaloids with Diverse Skeletons from Melodinus khasianus." Journal of Natural Products 79, no. 9 (September 2016): 2158–66. http://dx.doi.org/10.1021/acs.jnatprod.6b00011.
Повний текст джерела-, Prabhavathi, and Anuradha Mal. "Nutraceutical properties of Vinca rosea." Biomedicine 42, no. 3 (July 3, 2022): 427–33. http://dx.doi.org/10.51248/.v42i3.1459.
Повний текст джерелаJennings, Laurence K., Neyaz M. D. Khan, Navdeep Kaur, Daniel Rodrigues, Christine Morrow, Aoife Boyd, and Olivier P. Thomas. "Brominated Bisindole Alkaloids from the Celtic Sea Sponge Spongosorites calcicola." Molecules 24, no. 21 (October 29, 2019): 3890. http://dx.doi.org/10.3390/molecules24213890.
Повний текст джерелаChen, Min, Chang-Lun Shao, Xiu-Mei Fu, Ru-Fang Xu, Juan-Juan Zheng, Dong-Lin Zhao, Zhi-Gang She, and Chang-Yun Wang. "Bioactive Indole Alkaloids and Phenyl Ether Derivatives from a Marine-Derived Aspergillus sp. Fungus." Journal of Natural Products 76, no. 4 (March 25, 2013): 547–53. http://dx.doi.org/10.1021/np300707x.
Повний текст джерелаYuan, Hai-Lian, Yun-Li Zhao, Xu-Jie Qin, Ya-Ping Liu, Hao-Fei Yu, Pei-Feng Zhu, Qiong Jin, Xing-Wei Yang, and Xiao-Dong Luo. "Anti-inflammatory and analgesic activities of Neolamarckia cadamba and its bioactive monoterpenoid indole alkaloids." Journal of Ethnopharmacology 260 (October 2020): 113103. http://dx.doi.org/10.1016/j.jep.2020.113103.
Повний текст джерелаMarques, Dayan de Araújo, Fernando Berton Zanchi, and Geisa Paulino Caprini Evaristo. "Ethnopharmacological review, phytochemistry and bioactivity of the genus Geissospermum (Apocynaceae)." Research, Society and Development 12, no. 2 (February 3, 2023): e18912240047. http://dx.doi.org/10.33448/rsd-v12i2.40047.
Повний текст джерелаNandagopal, Pavitra, Anthony Nyangson Steven, Liong-Wai Chan, Zaidah Rahmat, Haryati Jamaluddin, and Nur Izzati Mohd Noh. "Bioactive Metabolites Produced by Cyanobacteria for Growth Adaptation and Their Pharmacological Properties." Biology 10, no. 10 (October 18, 2021): 1061. http://dx.doi.org/10.3390/biology10101061.
Повний текст джерелаLimbadri, Salendra, Xiaowei Luo, Xiuping Lin, Shengrong Liao, Junfeng Wang, Xuefeng Zhou, Bin Yang, and Yonghong Liu. "Bioactive Novel Indole Alkaloids and Steroids from Deep Sea-Derived Fungus Aspergillus fumigatus SCSIO 41012." Molecules 23, no. 9 (September 18, 2018): 2379. http://dx.doi.org/10.3390/molecules23092379.
Повний текст джерелаPham, Hong Ngoc Thuy, Quan Van Vuong, Michael C. Bowyer, and Christopher J. Scarlett. "Phytochemicals Derived from Catharanthus roseus and Their Health Benefits." Technologies 8, no. 4 (December 21, 2020): 80. http://dx.doi.org/10.3390/technologies8040080.
Повний текст джерелаTlhapi, Dorcas, Isaiah Ramaite, Teunis Van Ree, Chinedu Anokwuru, Taglialatela-Scafati Orazio, and Heinrich Hoppe. "Isolation, Chemical Profile and Antimalarial Activities of Bioactive Compounds from Rauvolfia caffra Sond." Molecules 24, no. 1 (December 21, 2018): 39. http://dx.doi.org/10.3390/molecules24010039.
Повний текст джерелаChen, Min, Chang-Lun Shao, Xiu-Mei Fu, Ru-Fang Xu, Juan-Juan Zheng, Dong-Lin Zhao, Zhi-Gang She, and Chang-Yun Wang. "Correction to Bioactive Indole Alkaloids and Phenyl Ether Derivatives from a Marine-Derived Aspergillus sp. Fungus." Journal of Natural Products 76, no. 6 (June 19, 2013): 1229. http://dx.doi.org/10.1021/np400465r.
Повний текст джерелаPazos, Mariana, Estefania Dibello, Juan Manuel Mesa, Dalibor Sames, Marcelo Alberto Comini, Gustavo Seoane, and Ignacio Carrera. "Iboga Inspired N-Indolylethyl-Substituted Isoquinuclidines as a Bioactive Scaffold: Chemoenzymatic Synthesis and Characterization as GDNF Releasers and Antitrypanosoma Agents." Molecules 27, no. 3 (January 27, 2022): 829. http://dx.doi.org/10.3390/molecules27030829.
Повний текст джерелаIbrahim, Sabrin R. M., Sana A. Fadil, Haifa A. Fadil, Rawan H. Hareeri, Hossam M. Abdallah, and Gamal A. Mohamed. "Genus Smenospongia: Untapped Treasure of Biometabolites—Biosynthesis, Synthesis, and Bioactivities." Molecules 27, no. 18 (September 14, 2022): 5969. http://dx.doi.org/10.3390/molecules27185969.
Повний текст джерелаLin, Li Ping, and Ren Xiang Tan. "Back Cover: Bioactive Alkaloids from Indole-3-carbinol Exposed Culture of Daldiniaeschscholzii (Chin. J. Chem. 8/2018)." Chinese Journal of Chemistry 36, no. 8 (July 13, 2018): 780. http://dx.doi.org/10.1002/cjoc.201880085.
Повний текст джерелаLiang, Chuxin, Chang Chen, Pengfei Zhou, Lv Xu, Jianhua Zhu, Jincai Liang, Jiachen Zi, and Rongmin Yu. "Effect of Aspergillus flavus Fungal Elicitor on the Production of Terpenoid Indole Alkaloids in Catharanthus roseus Cambial Meristematic Cells." Molecules 23, no. 12 (December 11, 2018): 3276. http://dx.doi.org/10.3390/molecules23123276.
Повний текст джерелаPatowary, Rimzim, and Chaman Lal Sharma. "ETHNOPHARMACOLOGICAL PROPERTIES AND THERAPEUTIC USES OF OPHIORRHIZA MUNGOS LINN : A REVIEW." International Journal of Advanced Research 11, no. 03 (March 31, 2023): 230–35. http://dx.doi.org/10.21474/ijar01/16412.
Повний текст джерелаEstrada, Omar, Juan M. González-Guzmán, María M. Salazar-Bookman, Alfonso Cardozo, Eva Lucena, and Claudia P. Alvarado-Castillo. "Hypotensive and Bradycardic Effects of Quinovic Acid Glycosides from Aspidosperma fendleri in Spontaneously Hypertensive Rats." Natural Product Communications 10, no. 2 (February 2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000216.
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