Gotowa bibliografia na temat „Membranotropic compounds”
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Artykuły w czasopismach na temat "Membranotropic compounds"
Sokolova, S. M., G. N. Buzuk, M. Ya Lovkova i Yu V. Tyutekin. "Membranotropic Compounds and Alkaloid Accumulation in Plants". Doklady Biochemistry and Biophysics 402, nr 1-6 (maj 2005): 220–22. http://dx.doi.org/10.1007/s10628-005-0075-x.
Pełny tekst źródłaDubinin, Mikhail V., Vyacheslav A. Sharapov, Alena A. Semenova, Lyudmila V. Parfenova, Anna I. Ilzorkina, Ekaterina I. Khoroshavina, Natalia V. Belosludtseva, Sergey V. Gudkov i Konstantin N. Belosludtsev. "Effect of Modified Levopimaric Acid Diene Adducts on Mitochondrial and Liposome Membranes". Membranes 12, nr 9 (8.09.2022): 866. http://dx.doi.org/10.3390/membranes12090866.
Pełny tekst źródłaShabanov, Petr Dmitrievich, Anatoliy Ivanovich Vislobokov, Georgiy Nolianovich Shilov, P. M. Bulay i A. P. Lugovskii. "Changes in intracellular potentials and ionic currents of the mollusk and activity of Cl--channels under exposure to some inhibitory amino acids and new litium-containing compounds of them". Reviews on Clinical Pharmacology and Drug Therapy 13, nr 3 (15.09.2015): 39–47. http://dx.doi.org/10.17816/rcf13339-47.
Pełny tekst źródłaAkhmedov, Alan A., Dmitriy N. Shurpik, Zainab R. Latypova, Rustem R. Gamirov i Ivan I. Stoykov. "Synthetic meroterpenoids based on terpene alcohols: synthesis, self-assembly, and membranotropic properties". Butlerov Communications 63, nr 7 (31.07.2020): 11–18. http://dx.doi.org/10.37952/roi-jbc-01/20-63-7-11.
Pełny tekst źródłaLogashenko, E. B., I. L. Kuznetsova, E. I. Ryabchikova, V. V. Vlassov i M. A. Zenkova. "Mechanism of the toxicity of the artificial ribonucleases for the different human cancer cell lines". Biomeditsinskaya Khimiya 56, nr 2 (2010): 230–43. http://dx.doi.org/10.18097/pbmc20105602230.
Pełny tekst źródłaGaraev, T. M., T. V. Grebennikova, V. V. Avdeeva, V. V. Lebedeva i V. F. Larichev. "Antiviral properties of synthetic histidine derivatives containing membranotropic volumetrical carbocycles in their molecule against SARS-CoV-2 virus <i>in vitro</i>". Problems of Virology 68, nr 1 (11.03.2023): 18–25. http://dx.doi.org/10.36233/0507-4088-147.
Pełny tekst źródłaAvdeeva, V. V., T. M. Garaev, E. A. Malinina, K. Yu Zhizhin i N. T. Kuznetsov. "Physiologically Active Compounds Based on Membranotropic Cage Carriers–Derivatives of Adamantane and Polyhedral Boron Clusters (Review)". Russian Journal of Inorganic Chemistry 67, nr 1 (styczeń 2022): 28–47. http://dx.doi.org/10.1134/s0036023622010028.
Pełny tekst źródłaAmerkhanova, Syumbelya K., Alexandra D. Voloshina, Alla B. Mirgorodskaya, Anna P. Lyubina, Darya A. Kuznetsova, Rushana A. Kushnazarova, Vasilii A. Mikhailov i Lucia Ya Zakharova. "Antimicrobial Properties and Cytotoxic Effect of Imidazolium Geminis with Tunable Hydrophobicity". International Journal of Molecular Sciences 22, nr 23 (5.12.2021): 13148. http://dx.doi.org/10.3390/ijms222313148.
Pełny tekst źródłaKUKOVINETS, О. S., R. KH MUDARISOVA, A. A. VAKULSKAYA i A. R. ISAEVA. "TECHNOLOGY FOR OBTAINING NEW BIOLOGICALLY ACTIVE PECTIN MATERIALS MODIFIED WITH L-TRIPTOFAN". Fundamental and Applied Problems of Engineering and Technology, nr 4 (2021): 28–32. http://dx.doi.org/10.33979/2073-7408-2021-348-4-28-32.
Pełny tekst źródłaRoman’ko, M. Y. "Biochemical markers of safety of nano-particles of metals on the model of isolated subcultural fractions of eukaryotes". Regulatory Mechanisms in Biosystems 8, nr 4 (9.11.2017): 564–68. http://dx.doi.org/10.15421/021787.
Pełny tekst źródłaRozprawy doktorskie na temat "Membranotropic compounds"
Botcazon, Camille. "Etude du mode d'action de composés antifongiques membranotropes naturels sur deux Sclerotiniacées : cas des rhamnolipides et des fengycines". Electronic Thesis or Diss., Compiègne, 2023. https://bibliotheque.utc.fr/Default/doc/SYRACUSE/2023COMP2755.
Pełny tekst źródłaRhamnolipids (RLs) and fengycins (FGs), are compounds produced by bacteria displaying antifungal properties against the phytopathogenic fungi Sclerotinia sclerotiorum and Botrytis cinerea. However, the induced biocidal effects, and the involved mechanisms are poorly understood in fungi. Due to their amphiphilic properties, a membranotropic mode of action is proposed for these interesting compounds for biocontrol. The present work demonstrates that the two Sclerotiniaceae have opposite sensitivities to RLs and FGs. A microscopy study shows that RLs can induce programmed cell death (PCD) or necrotic cell death in both fungi depending on the concentration whereas FGs systematically induce PCD, probably by triggering autophagy. Lipidomic analyses (fatty acid, phospholipid and ergosterol contents) of S. sclerotiorum and B. cinerea strains differently sensitive to RLs and FGs allow to correlate the lipid contents of the fungi to their sensitivities. These data are used to study the interactions of RLs or FGs on biomimetic plasma membrane models of the two fungi. The dynamics show that the RLs monomers insert into the models without fluidizing them and that the FGs auto-aggregate themselves and insert into some models, inducing fluidization. Ergosterol and phosphatidic acids seems to disfavour this insertion while phosphatidylcholine and phosphatidylethanolamine seem to favour it.This work allows to better understand the antifungal mode of action of RLs and FGs, with a view to develop more effective biocontrol products for crop protection targeting specific pathogens