Статті в журналах з теми "Y-lactones"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Y-lactones".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Burger, B. V., and P. J. Pretorius. "Notes: Mammalian Pheromone Studies, VI. Compounds from the Preorbital Gland of the Blue Duiker, Cephalophus monticola." Zeitschrift für Naturforschung C 42, no. 11-12 (December 1, 1987): 1355–57. http://dx.doi.org/10.1515/znc-1987-11-1238.
Повний текст джерелаYates, Edwin A., Bodo Philipp, Catherine Buckley, Steve Atkinson, Siri Ram Chhabra, R. Elizabeth Sockett, Morris Goldner, et al. "N-Acylhomoserine Lactones Undergo Lactonolysis in a pH-, Temperature-, and Acyl Chain Length-Dependent Manner during Growth of Yersinia pseudotuberculosis and Pseudomonas aeruginosa." Infection and Immunity 70, no. 10 (October 2002): 5635–46. http://dx.doi.org/10.1128/iai.70.10.5635-5646.2002.
Повний текст джерелаLoboiko, Yu V., Ye O. Barylo, and B. S. Barylo. "Assessment of macrocyclic lacton group products for ectoparasitosis of carp." Scientific Messenger of LNU of Veterinary Medicine and Biotechnologies 22, no. 98 (August 22, 2020): 16–21. http://dx.doi.org/10.32718/nvlvet9803.
Повний текст джерелаGutenberger, Guido, Siegfried Blechert та Eberhard Steckhan. "ChemInform Abstract: α-Cyano-y-lactones by Photoinduced Electron Transfer-Catalyzed Oxidation of α-Hydroxyalkylsilanes in the Presence of α-Cyano Acrylates." ChemInform 31, № 17 (8 червня 2010): no. http://dx.doi.org/10.1002/chin.200017109.
Повний текст джерелаDyszel, Jessica L., Jenee N. Smith, Darren E. Lucas, Jitesh A. Soares, Matthew C. Swearingen, Mathew A. Vross, Glenn M. Young, and Brian M. M. Ahmer. "Salmonella enterica Serovar Typhimurium Can Detect Acyl Homoserine Lactone Production by Yersinia enterocolitica in Mice." Journal of Bacteriology 192, no. 1 (October 9, 2009): 29–37. http://dx.doi.org/10.1128/jb.01139-09.
Повний текст джерелаda Silva, Cristiane França, Denise da Gama Jaen Batista, Julianna Siciliano De Araújo, Marcos Meuser Batista, Jessica Lionel, Elen Mello de Souza, Erica Ripoll Hammer, et al. "Activities of Psilostachyin A and Cynaropicrin against Trypanosoma cruziIn VitroandIn Vivo." Antimicrobial Agents and Chemotherapy 57, no. 11 (August 12, 2013): 5307–14. http://dx.doi.org/10.1128/aac.00595-13.
Повний текст джерелаHabyarimana, Fabien, Matthew C. Swearingen, Glenn M. Young, Stephanie Seveau, and Brian M. M. Ahmer. "Yersinia enterocolitica Inhibits Salmonella enterica Serovar Typhimurium and Listeria monocytogenes Cellular Uptake." Infection and Immunity 82, no. 1 (October 14, 2013): 174–83. http://dx.doi.org/10.1128/iai.00984-13.
Повний текст джерелаRossini, Carmen, and Rodolfo Ungerfeld. "Chemical profile of the cutaneous gland secretions from male pampas deer ( Ozotoceros bezoarticus )." Journal of Mammalogy 97, no. 1 (October 28, 2015): 167–78. http://dx.doi.org/10.1093/jmammal/gyv167.
Повний текст джерелаTomova, Teodora, Nina Doncheva, Anita Mihaylova, Ilia Kostadinov, Lyudmil Peychev, and Mariana Argirova. "An experimental study on phytochemical composition and memory enhancing effect of Ginkgo biloba seed extract." Folia Medica 63, no. 2 (April 30, 2021): 203–12. http://dx.doi.org/10.3897/folmed.63.e53060.
Повний текст джерелаEchavarria, Ana, Haydelba D'Armas Regnault, Nubia Lisbeth, Lisbeth Matute, Carmita Jaramillo, Luisa Rojas de Astudillo, and Ricardo Benitez. "Evaluación de la capacidad antioxidante y metabolitos secundarios de extractos de dieciséis plantas medicinales / Evaluation of antioxidant capacity and secondary metabolites of sixteen medicinal plants extracts." Ciencia Unemi 9, no. 20 (December 20, 2016): 29. http://dx.doi.org/10.29076/issn.2528-7737vol9iss20.2016pp29-35p.
Повний текст джерелаJacobi, Christoph A., Alexandra Bach, Leo Eberl, Anette Steidle, and Jürgen Heesemann. "Detection of N-(3-Oxohexanoyl)-l-Homoserine Lactone in Mice Infected with Yersinia enterocolitica Serotype O8." Infection and Immunity 71, no. 11 (November 2003): 6624–26. http://dx.doi.org/10.1128/iai.71.11.6624-6626.2003.
Повний текст джерелаAli, Md Ashraf, Shuji Noguchi, Miteki Watanabe, Yasunori Iwao, and Shigeru Itai. "The antitumour drug 7-ethyl-10-hydroxycamptothecin monohydrate and its solid-state hydrolysis mechanism on heating." Acta Crystallographica Section C Structural Chemistry 72, no. 10 (September 23, 2016): 743–47. http://dx.doi.org/10.1107/s2053229616014492.
Повний текст джерелаXia, Zhengxiang, Jincheng Yao, and Jingyu Liang. "Two new sesquiterpene lactones from Sonchus arvensis." Chemistry of Natural Compounds 48, no. 1 (March 2012): 47–50. http://dx.doi.org/10.1007/s10600-012-0155-y.
Повний текст джерелаCardona, M. Luz, Isabel Fernández, José R. Pedro, and Beatriz Pérez. "Sesquiterpene lactones and flavonoids from Centaurea aspera." Phytochemistry 30, no. 7 (January 1991): 2331–33. http://dx.doi.org/10.1016/0031-9422(91)83643-y.
Повний текст джерелаAtkinson, Steve, Chien-Yi Chang, R. Elizabeth Sockett, Miguel Cámara, and Paul Williams. "Quorum Sensing in Yersinia enterocolitica Controls Swimming and Swarming Motility." Journal of Bacteriology 188, no. 4 (February 15, 2006): 1451–61. http://dx.doi.org/10.1128/jb.188.4.1451-1461.2006.
Повний текст джерелаAdekenov, S. M. "Sesquiterpene lactones from endemic species of the family Asteraceae." Chemistry of Natural Compounds 49, no. 1 (March 2013): 158–62. http://dx.doi.org/10.1007/s10600-013-0543-y.
Повний текст джерелаUsmanova, Liliia, Olga Bakulina, Dmitry Dar’in, and Mikhail Krasavin. "Spontaneous formation of tricyclic lactones following the Castagnoli–Cushman reaction." Chemistry of Heterocyclic Compounds 53, no. 4 (April 2017): 474–79. http://dx.doi.org/10.1007/s10593-017-2076-y.
Повний текст джерелаMa, Guoyi, Li Chong, Zuqiang Li, Andrew H. T. Cheung, and Martin H. N. Tattersall. "Anticancer activities of sesquiterpene lactones from Cyathocline purpurea in vitro." Cancer Chemotherapy and Pharmacology 64, no. 1 (November 9, 2008): 143–52. http://dx.doi.org/10.1007/s00280-008-0863-y.
Повний текст джерелаShen, Jianzhong, Suxia Zhang, Congming Wu, Haiyang Jiang, Zhanhui Wang, and Linli Cheng. "Determination of Six Resorcylic Acid Lactones in Feed by GC–MS." Chromatographia 71, no. 1-2 (November 5, 2009): 163–65. http://dx.doi.org/10.1365/s10337-009-1399-y.
Повний текст джерелаHummel, G., and R. R. Schmidt. "ChemInform Abstract: Efficient Synthesis of lactoneo Series Antigen Lewis Y (Ley)." ChemInform 30, no. 35 (June 13, 2010): no. http://dx.doi.org/10.1002/chin.199935258.
Повний текст джерелаCateni, Francesca, Patrizia Nitti, Sara Drioli, Giuseppe Procida, Renzo Menegazzi та Maurizio Romano. "γ- and δ-lactones as fumarate esters analogues and their neuroprotective effects". Medicinal Chemistry Research 30, № 4 (16 січня 2021): 913–24. http://dx.doi.org/10.1007/s00044-020-02698-y.
Повний текст джерелаBelovodskii, A. V., E. E. Shul’ts, M. M. Shakirov, V. E. Romanov, B. Zh Elmuradov, Kh M. Shakhidoyatov, and G. A. Tolstikov. "Synthesis of hybrid molecules containing fragments of sesquiterpene lactones and plant alkaloids." Chemistry of Natural Compounds 46, no. 6 (January 2011): 880–85. http://dx.doi.org/10.1007/s10600-011-9774-y.
Повний текст джерелаSpring, Otmar, David Vargas, and Nikolaus H. Fischer. "Sesquiterpene lactones and benzofurans in glandular trichomes of three Pappobolus species." Phytochemistry 30, no. 6 (January 1991): 1861–67. http://dx.doi.org/10.1016/0031-9422(91)85029-y.
Повний текст джерелаBuschmann, H. "Sesquiterpene lactones as a result of interspecific hybridization in Helliathus species." Phytochemistry 39, no. 2 (May 1995): 367–71. http://dx.doi.org/10.1016/0031-9422(94)00870-y.
Повний текст джерелаMukhopadhyay, Triptikumar, S. R. Nadkarni, M. V. Patel, R. G. Bhat, K. R. Desikan, B. N. Ganguli, R. H. Rupp, H. W. Fehlhaber, and H. Kogler. "Maclafungin, a new antifungal macrocyclic lactone from Actinomycete sp. Y-8521050." Tetrahedron 54, no. 44 (October 1998): 13621–28. http://dx.doi.org/10.1016/s0040-4020(98)00838-2.
Повний текст джерелаCĂTANĂ, Laura, Raul CĂTANĂ, Roxana CORA, Ştefan RĂILEANU, and Mihai CERNEA. "In Vitro Study of Benzimidazole Derivatives, Tetrahydropyrimidines and Macrocyclic Lactones Therapeutic Efficacy in Dog Hookworms." Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca. Veterinary Medicine 75, no. 2 (December 16, 2018): 199. http://dx.doi.org/10.15835/buasvmcn-vm:2018.0019.
Повний текст джерелаYang, Nian-Yun, Jin-Ao Duan, Da-Wei Qian, and Li-Juan Tian. "Simultaneous Quantification of Four Sesquiterpene Lactones in Eupatorium lindleyanum DC. by RP-LC." Chromatographia 70, no. 1-2 (April 28, 2009): 205–9. http://dx.doi.org/10.1365/s10337-009-1123-y.
Повний текст джерелаBailly, Christian, and Gérard Vergoten. "Japonicone A and related dimeric sesquiterpene lactones: molecular targets and mechanisms of anticancer activity." Inflammation Research 71, no. 3 (January 16, 2022): 267–76. http://dx.doi.org/10.1007/s00011-021-01538-y.
Повний текст джерелаZhao, Ran, Hanmin Zhang, Xiang Zou, and Fenglin Yang. "Effects of Inhibiting Acylated Homoserine Lactones (AHLs) on Anammox Activity and Stability of Granules’." Current Microbiology 73, no. 1 (April 9, 2016): 108–14. http://dx.doi.org/10.1007/s00284-016-1031-y.
Повний текст джерелаNishide, Kiyoharu, Ryuichi Kurosaki, Kouichi Hosomi, Hitoshi Imazato, Takehisa Inoue, Manabu Node, Toshiumi Ohmori та Kaoru Fuji. "An Asymmetric Nitroolefination of α-Alkyl-γ-and δ-Lactones with Modified Nitroenamines". Tetrahedron 51, № 40 (жовтень 1995): 10857–66. http://dx.doi.org/10.1016/0040-4020(95)00683-y.
Повний текст джерелаKoukoulitsa, Catherine, George D. Geromichalos, and Helen Skaltsa. "VolSurf analysis of pharmacokinetic properties for several antifungal sesquiterpene lactones isolated from Greek Centaurea sp." Journal of Computer-Aided Molecular Design 19, no. 8 (August 2005): 617–23. http://dx.doi.org/10.1007/s10822-005-9018-y.
Повний текст джерелаDaferner, Michael, Sarah Mensch, Timm Anke, and Olov Sterner. "Hypoxysordarin, a New Sordarin Derivative from Hypoxylon croceum." Zeitschrift für Naturforschung C 54, no. 7-8 (August 1, 1999): 474–80. http://dx.doi.org/10.1515/znc-1999-7-803.
Повний текст джерелаMUKHOPADHYAY, T., S. R. NADKARNI, M. V. PATEL, R. G. BHAT, K. R. DESIKAN, B. N. GANGULI, R. H. RUPP, H. W. FEHLHABER, and H. KOGLER. "ChemInform Abstract: Maclafungin, a New Antifungal Macrocyclic Lactone from Actinomycete sp. Y-8521050." ChemInform 30, no. 9 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199909268.
Повний текст джерелаGuan, Hong, Song You, Li Yang, Xu Wang, and Rui Ni. "Newly Detected Specific Hydrogenation of the Conjugated Double Bond of Unsaturated Alkaloid Lactones by Aspergillus sp." Biotechnology Letters 27, no. 16 (August 2005): 1189–93. http://dx.doi.org/10.1007/s10529-005-0015-y.
Повний текст джерелаWindmüller, R. "Efficient synthesis of lactoneo series antigens H, Lewis X (Lex), and Lewis Y (Ley)." Tetrahedron Letters 35, no. 41 (October 10, 1994): 7927–30. http://dx.doi.org/10.1016/s0040-4039(00)78387-0.
Повний текст джерелаDalla Lana, Daiane F., Ânderson R. Carvalho, William Lopes, Marilene H. Vainstein, Luciano S. P. Guimarães, Mário L. Teixeira, Luis F. S. de Oliveira та ін. "Structure-based design of δ-lactones for new antifungal drug development: susceptibility, mechanism of action, and toxicity". Folia Microbiologica 64, № 4 (7 лютого 2019): 509–19. http://dx.doi.org/10.1007/s12223-018-00675-y.
Повний текст джерелаPriya, Kumutha, Joanita Sulaiman, Kah Yan How, Wai-Fong Yin, and Kok-Gan Chan. "Production of N-acyl homoserine lactones by Chromobacterium haemolyticum KM2 isolated from the river water in Malaysia." Archives of Microbiology 200, no. 7 (May 23, 2018): 1135–42. http://dx.doi.org/10.1007/s00203-018-1526-y.
Повний текст джерелаWindmüller, Rainer, and Richard R. Schmidt. "Efficient synthesis of lactoneo series antigens H, Lewis X (Lex), and Lewis Y (Ley)1." Tetrahedron Letters 35, no. 43 (October 1994): 7927–30. http://dx.doi.org/10.1016/0040-4039(94)80013-8.
Повний текст джерелаAlzérreca, Arnaldo. "New approach to l'C-modified riboside scaffold via stereoselective functionalization of D-(+)-ribonic-y-lactone." Journal of Heterocyclic Chemistry 40, no. 2 (March 2003): 317–20. http://dx.doi.org/10.1002/jhet.5570400218.
Повний текст джерелаSAÚDE-GUIMARÃES, DÊNIA A., DÉLIO S. RASLAN, EGLER CHIARI, and ALAÍDE B. DE OLIVEIRA. "Complete assignments of NMR data and assessment of trypanocidal activity of new eremantholide C derivatives." Anais da Academia Brasileira de Ciências 86, no. 4 (December 2014): 1563–72. http://dx.doi.org/10.1590/0001-3765201420140167.
Повний текст джерелаHogardt, Michael, Maximilian Roeder, Anna Maria Schreff, Leo Eberl, and Jürgen Heesemann. "Expression of Pseudomonas aeruginosa exoS is controlled by quorum sensing and RpoS." Microbiology 150, no. 4 (April 1, 2004): 843–51. http://dx.doi.org/10.1099/mic.0.26703-0.
Повний текст джерелаWINDMUELLER, R., and R. R. SCHMIDT. "ChemInform Abstract: Efficient Synthesis of lactoneo Series Antigens H, Lewis X (Lex), and Lewis Y (Ley)." ChemInform 26, no. 13 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199513267.
Повний текст джерелаShen, Bingbing, Yupei Yang, Dan Wan, Huanghe Yu, Yuan Cai, Xionglong Wang, Daifeng Tang, Chunyu Tang, and Shuihan Zhang. "Sesquiterpene lactones isolated from Carpesium abrotanoides L. by LC–MS combined with HSCCC inhibit liver cancer through suppression of the JAK2/STAT3 signaling pathway." Medicinal Chemistry Research 31, no. 3 (February 2, 2022): 436–45. http://dx.doi.org/10.1007/s00044-021-02838-y.
Повний текст джерелаHummel, Gerd, and Richard R. Schmidt. "A versatile synthesis of the lactoneo-series antigens — synthesis of sialyl dimer Lewis X and of dimer Lewis Y." Tetrahedron Letters 38, no. 7 (February 1997): 1173–76. http://dx.doi.org/10.1016/s0040-4039(97)00006-3.
Повний текст джерелаSoulère, Laurent, Nicolas Guiliani, Yves Queneau, Carlos A. Jerez, and Alain Doutheau. "Molecular insights into quorum sensing in Acidithiobacillus ferrooxidans bacteria via molecular modelling of the transcriptional regulator AfeR and of the binding mode of long-chain acyl homoserine lactones." Journal of Molecular Modeling 14, no. 7 (May 14, 2008): 599–606. http://dx.doi.org/10.1007/s00894-008-0315-y.
Повний текст джерелаHUMMEL, G., and R. R. SCHMIDT. "ChemInform Abstract: A Versatile Synthesis of the lactoneo-Series Antigens - Synthesis of Sialyl Dimer Lewis X and of Dimer Lewis Y." ChemInform 28, no. 22 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199722223.
Повний текст джерелаYap, Mee-Ngan, Ching-Hong Yang, and Amy O. Charkowski. "The Response Regulator HrpY of Dickeya dadantii 3937 Regulates Virulence Genes Not Linked to the hrp Cluster." Molecular Plant-Microbe Interactions® 21, no. 3 (March 2008): 304–14. http://dx.doi.org/10.1094/mpmi-21-3-0304.
Повний текст джерелаWeissman, Kira J., Gordon C. Kearney, Peter F. Leadlay та James Staunton. "Structural elucidation studies of polyketide tetrasubstituted δ-lactones by gas chromatography/tandem mass spectrometry and electrospray mass spectrometry". Rapid Communications in Mass Spectrometry 13, № 21 (15 листопада 1999): 2103–8. http://dx.doi.org/10.1002/(sici)1097-0231(19991115)13:21<2103::aid-rcm760>3.0.co;2-y.
Повний текст джерелаCárdenas-Laverde, Diego, Sebastián Rincón-Aceldas, and Ericsson Coy-Barrera. "Identification of Antifungal Compounds from Piper Plants Against Fusarium oxysporum: An Untargeted Metabolite Profiling-Based Approach." Natural Product Communications 17, no. 4 (April 2022): 1934578X2210899. http://dx.doi.org/10.1177/1934578x221089995.
Повний текст джерелаMilagre, Matheus Marques, Renata Tupinambá Branquinho, Maira Fonseca Gonçalves, GMP de Assis, Maykon Tavares de Oliveira, LES Reis, Dênia Antunes Saúde-Guimarães, and Marta de Lana. "Activity of the sesquiterpene lactone goyazensolide against Trypanosoma cruzi in vitro and in vivo." Parasitology 147, no. 1 (September 23, 2019): 108–19. http://dx.doi.org/10.1017/s0031182019001276.
Повний текст джерела