Статті в журналах з теми "Plamitic acid (16:O)"
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Tripathi, Pushpendra Kumar, Shraddha Gupta, Suruchi Rai, Ankur Shrivatava, Shalini Tripathi, Sima Singh, Ajay J. Khopade, and Prashant Kesharwani. "Curcumin loaded poly (amidoamine) dendrimer-plamitic acid core-shell nanoparticles as anti-stress therapeutics." Drug Development and Industrial Pharmacy 46, no. 3 (February 24, 2020): 412–26. http://dx.doi.org/10.1080/03639045.2020.1724132.
Повний текст джерелаLee, Byung Chul, Dong Hyun Kim, Iljung Lee, Yearn Seong Choe, Dae Yoon Chi, Kyung-Han Lee, Yong Choi, and Byung-Tae Kim. "16-Cyclopentadienyl Tricarbonyl99mTc 16-Oxo-hexadecanoic Acid: Synthesis and Evaluation of Fatty Acid Metabolism in Mouse Myocardium†." Journal of Medicinal Chemistry 51, no. 12 (June 2008): 3630–34. http://dx.doi.org/10.1021/jm800049h.
Повний текст джерелаProtiva, Jiří, Jaroslav Pecka, Eva Klinotová, and Miloš Procházka. "Synthesis of 16-(4-iodophenyl)hexadecanoic acid." Collection of Czechoslovak Chemical Communications 51, no. 4 (1986): 872–78. http://dx.doi.org/10.1135/cccc19860872.
Повний текст джерелаSanda, Fumio, Taizo Fujiyama та Takeshi Endo. "Stepwise Synthesis ofγ-Glutamic Acid 16-Mer". Macromolecular Chemistry and Physics 203, № 4 (1 березня 2002): 727–34. http://dx.doi.org/10.1002/1521-3935(20020301)203:4<727::aid-macp727>3.0.co;2-s.
Повний текст джерелаHAGEY, L. "16$alpha;-hydroxychenodeoxycholic acid, a new major bile acid in birds." Hepatology 18, no. 4 (October 1993): A305. http://dx.doi.org/10.1016/0270-9139(93)92745-l.
Повний текст джерелаSchneider, Silke, Marcel G. Wubbolts, Dominique Sanglard, and Bernard Witholt. "Production Of Alkanedioic Acids By Cytochrome P450Bm-3Monooxygenase: Oxidation Of 16-Hydroxyhexadecanoic Acid To Hexadecane-1, 16-Dioic Acid." Biocatalysis and Biotransformation 17, no. 3 (January 1999): 163–78. http://dx.doi.org/10.3109/10242429909040113.
Повний текст джерелаKataev, V. E., A. P. Timosheva, A. I. Nugmanov, A. T. Gubaidullin, I. Yu Strobykina, R. R. Shagidullin, L. V. Avvakumova, and O. I. Militsina. "Structure of 16-hydroxyisosteviol-derived dicarboxylic acid esters." Russian Journal of General Chemistry 77, no. 6 (June 2007): 1069–77. http://dx.doi.org/10.1134/s1070363207060217.
Повний текст джерелаRoy, Amlan K., James R. Hart, and Ajit J. Thakkar. "Clusters of glycolic acid and 16 water molecules." Chemical Physics Letters 434, no. 4-6 (February 2007): 176–81. http://dx.doi.org/10.1016/j.cplett.2006.12.010.
Повний текст джерелаSharpe, Ruben B. A., Dirk Burdinski, Jurriaan Huskens, Harold J. W. Zandvliet, David N. Reinhoudt, and Bene Poelsema. "Spreading of 16-Mercaptohexadecanoic Acid in Microcontact Printing." Langmuir 20, no. 20 (September 2004): 8646–51. http://dx.doi.org/10.1021/la0487040.
Повний текст джерелаle Bars, D., M. Apparu, P. M. Léo, M. Vidal, and C. Luu-Duc. "Synthesis of 16-iodo-[carboxyl-14C]hexadecanoic acid." Journal of Labelled Compounds and Radiopharmaceuticals 22, no. 9 (September 1985): 903–7. http://dx.doi.org/10.1002/jlcr.2580220905.
Повний текст джерелаDolgopalets, V. I., S. M. Volkov, M. A. Kisel', A. N. Kozhevko, and O. G. Kulinkovich. "ChemInform Abstract: Convenient Synthesis of 16-Oxooctadecanoic Acid." ChemInform 31, no. 37 (September 12, 2000): no. http://dx.doi.org/10.1002/chin.200037071.
Повний текст джерелаDentali, Steven J., and Joseph J. Hoffmann. "16-hydroxycarnosic acid, a diterpene from Salvia apiana." Phytochemistry 29, no. 3 (1990): 993–94. http://dx.doi.org/10.1016/0031-9422(90)80066-p.
Повний текст джерелаLivni, E., and D. R. Elmaleh. "Synthesis of 16-[18F]fluoro-betamethylhexadecanoic acid ([18F] FBMHA) and 16-[18F] fluorohexadecanoic acid ([18F] FHA) from the corresponding triflates." Journal of Labelled Compounds and Radiopharmaceuticals 26, no. 1-12 (January 1989): 231–32. http://dx.doi.org/10.1002/jlcr.25802601105.
Повний текст джерелаHanda, T., K. Tomita, and M. Nakagaki. "Nonideal mixing of 16-(9-anthroyloxy) palmitic acid and fatty acid in monolayer." Colloid and Polymer Science 265, no. 3 (March 1987): 250–56. http://dx.doi.org/10.1007/bf01412715.
Повний текст джерелаKitamura, Yoshiaki. "Synthesis of Nucleic Acid Mimics and Their Application in Nucleic Acid-based Medicine." YAKUGAKU ZASSHI 136, no. 11 (November 1, 2016): 1491–99. http://dx.doi.org/10.1248/yakushi.16-00180.
Повний текст джерелаJoseph, Joy, and Ching-San Lai. "An improved synthesis of [15N] 16-doxyl stearic acid." Journal of Labelled Compounds and Radiopharmaceuticals 24, no. 10 (October 1987): 1159–65. http://dx.doi.org/10.1002/jlcr.2580241003.
Повний текст джерелаCarballeira, Néstor M., and Mayra Pagán. "Total synthesis of the novel bacterial fatty acid 16-methyl-8(Z)-heptadecenoic acid." Chemistry and Physics of Lipids 113, no. 1-2 (November 2001): 23–27. http://dx.doi.org/10.1016/s0009-3084(01)00137-2.
Повний текст джерелаABSON, ANGELA, NIGEL J. P. BROOM, PHILIPPA A. COATES, JOHN S. ELDER, ANDREW K. FORREST, PETER C. T. HANNAN, AMANDA J. HICKS, et al. "Chemistry of Pseudomonic Acid. Part 16. Aryl and Heteroaryl Ketone Derivatives of Monic Acid." Journal of Antibiotics 49, no. 4 (1996): 390–94. http://dx.doi.org/10.7164/antibiotics.49.390.
Повний текст джерелаWang, Shuguang, Yongpeng Ma, Chengbin Wan, Chungyun Hse, Todd F. Shupe, Yujun Wang, and Changming Wang. "Immunolocalization of Endogenous Indole-3-Acetic Acid and Abscisic Acid in the Shoot Internodes of Fargesia yunnanensis Bamboo during Development." Journal of the American Society for Horticultural Science 141, no. 6 (November 2016): 563–72. http://dx.doi.org/10.21273/jashs03814-16.
Повний текст джерелаtaş, Recep, Muzaffer CAN, and Savaş SÖNMEZOĞLU. "Preparation and characterization of polyaniline microrods synthesized by using dodecylbenzene sulfonic acid and periodic acid." TURKISH JOURNAL OF CHEMISTRY 39 (2015): 589–99. http://dx.doi.org/10.3906/kim-1411-16.
Повний текст джерелаBurger, Alain, Joan E. Clark, Masazumi Nishimoto, A. Scott Muerhoff, Bettie Sue Siler Masters, and Paul R. Ortiz de Montellano. "Mechanism-based inhibitors of prostaglandin .omega.-hydroxylase: (R)- and (S)-12-hydroxy-16-heptadecynoic acid and 2,2-dimethyl-12-hydroxy-16-heptadecynoic acid." Journal of Medicinal Chemistry 36, no. 10 (May 1993): 1418–24. http://dx.doi.org/10.1021/jm00062a014.
Повний текст джерелаKhairy, Mostafa A., and Fotouh R. Mansour. "Simultaneous Determination of Ursodeoxycholic Acid and Chenodeoxycholic Acid in Pharmaceutical Dosage Form by HPLC–UV Detection." Journal of AOAC INTERNATIONAL 100, no. 1 (January 1, 2017): 59–64. http://dx.doi.org/10.5740/jaoacint.16-0176.
Повний текст джерелаGhosh, Pranab, and Raju Subba. "ChemInform Abstract: Studies on the Reaction of 16-Dehydropregnenolone Acetate (16-DPA) with m-Chloroperbenzoic Acid." ChemInform 44, no. 51 (December 2, 2013): no. http://dx.doi.org/10.1002/chin.201351220.
Повний текст джерелаSiegel, Earl, and Suman Wason. "Boric Acid Toxicity." Pediatric Clinics of North America 33, no. 2 (April 1986): 363–67. http://dx.doi.org/10.1016/s0031-3955(16)35006-4.
Повний текст джерелаNakano, T., M. A. Maillo, A. C. Spinelli, Alfonso Martin, and A. Usubillaga. "Molecular rearrangements in derivatives of grandiflorenic acid [(-)-kaur-9(11),16-dien-19-oic acid]." Pure and Applied Chemistry 66, no. 10-11 (January 1, 1994): 2357–60. http://dx.doi.org/10.1351/pac199466102357.
Повний текст джерелаFitz, Wolfgang, and Duilio Arigoni. "Biosynthesis of 15,16-dimethyltriacontanedioic acid (diabolic acid) from [16-2H3]- and [14-2H2]-palmitic acids." Journal of the Chemical Society, Chemical Communications, no. 20 (1992): 1533. http://dx.doi.org/10.1039/c39920001533.
Повний текст джерелаShirasaka, Norifumi, Takuya Umehara, Tetsuo Murakami, Hajime Yoshizumi та Sakayu Shimizu. "Microbial conversion of palmitoleic acid to 9,12-hexadecadienoic acid (16:2ω4) by Trichoderma sp. AM076". Journal of the American Oil Chemists' Society 75, № 6 (червень 1998): 717–20. http://dx.doi.org/10.1007/s11746-998-0211-8.
Повний текст джерелаForsythe, C. E., M. A. French, Y. K. Goh, and M. T. Clandinin. "Cholesterolaemic influence of palmitic acid in the sn-1, 3 v. the sn-2 position with high or low dietary linoleic acid in healthy young men." British Journal of Nutrition 98, no. 2 (August 2007): 337–44. http://dx.doi.org/10.1017/s0007114507704993.
Повний текст джерелаRuiz-Rodado, Victor, Tyrone Dowdy, Jinkyu Yung, Ana Dios-Esponera, Adrian Lita, Tamalee Kramp, Kevin Camphausen, Mark Gilbert, and Mioara Larion. "DDRE-16. CYSTEINE IS AN ESSENTIAL AMINO ACID IN GLIOMAS." Neuro-Oncology Advances 3, Supplement_1 (March 1, 2021): i9. http://dx.doi.org/10.1093/noajnl/vdab024.038.
Повний текст джерелаShimizu, Ken-ichi, Toshiki Kan-no, Tsuyoshi Hatamachi, Shin-ichi Komai, Tatsuya Kodama, and Yoshie Kitayama. "Stereoselective hydrogenation of linoleic acid over Ir/FSM-16 catalyst." Applied Catalysis A: General 228, no. 1-2 (March 2002): 75–82. http://dx.doi.org/10.1016/s0926-860x(01)00954-1.
Повний текст джерелаMoribe, Kunikazu, Ryo Kinoshita, Kenjirou Higashi, Yuichi Tozuka, and Keiji Yamamoto. "Coloration Phenomenon of Mefenamic Acid in Mesoporous Silica FSM-16." CHEMICAL & PHARMACEUTICAL BULLETIN 58, no. 2 (2010): 214–18. http://dx.doi.org/10.1248/cpb.58.214.
Повний текст джерелаMcGinty, D., C. S. Letizia, and A. M. Api. "Fragrance material review on 16-hydroxy-7-hexadecenoic acid lactone." Food and Chemical Toxicology 49 (December 2011): S149—S151. http://dx.doi.org/10.1016/j.fct.2011.07.013.
Повний текст джерелаJabeen, Nabila, Misbah Mushtaq, Muhammad Danish, Muhammad Nawaz Tahir, and Muhammad Asam Raza. "Crystal structure of 2-benzenesulfonamido-3-hydroxypropanoic acid." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (October 31, 2015): o902—o903. http://dx.doi.org/10.1107/s2056989015020149.
Повний текст джерелаTian, Shi-Lin, Li Li, Yue-Qin Tian, S. N. M. Shah, and Zhen-Hui Gong. "Effects of Abscisic Acid on Capsanthin Levels in Pepper Fruit." Journal of the American Society for Horticultural Science 141, no. 6 (November 2016): 609–16. http://dx.doi.org/10.21273/jashs03898-16.
Повний текст джерелаAyub, Ricardo Antonio, and André Belmont Pereira. "Brassinosteroid Combined With Indolbutyric Acid in Blueberry Micropropagation." Journal of Agricultural Science 14, no. 5 (April 15, 2022): 59. http://dx.doi.org/10.5539/jas.v14n5p59.
Повний текст джерелаLeclercq, Alexandre, Annie Guiyoule, Mohamed El Lioui, Elisabeth Carniel, and Jacques Decallonne. "High Homogeneity of the Yersinia pestisFatty Acid Composition." Journal of Clinical Microbiology 38, no. 4 (2000): 1545–51. http://dx.doi.org/10.1128/jcm.38.4.1545-1551.2000.
Повний текст джерелаSilaban, Bernita. "KOMPOSISI ASAM LEMAK CACING LAUT SIASIA (SIPUNCULUS, SP) DARI PERAIRAN PANTAI PULAU NUSALAUT." BIOPENDIX: Jurnal Biologi, Pendidikan dan Terapan 4, no. 1 (October 7, 2017): 10–16. http://dx.doi.org/10.30598/biopendixvol4issue1page10-16.
Повний текст джерелаValcheva-Kuzmanova, S., A. Georgieva, I. Belcheva, S. Belcheva, and R. Tashev. "Investigation of the effects of chlorogenic acid, ferulic acid, gallic acid and quercetin on pain sensitivity threshold in rats." European Neuropsychopharmacology 26 (October 2016): S222. http://dx.doi.org/10.1016/s0924-977x(16)31077-x.
Повний текст джерелаBolsoni-Lopes, Andressa, William T. Festuccia, Talita S. M. Farias, Patricia Chimin, Francisco L. Torres-Leal, Priscilla B. M. Derogis, Paula B. de Andrade та ін. "Palmitoleic acid (n-7) increases white adipocyte lipolysis and lipase content in a PPARα-dependent manner". American Journal of Physiology-Endocrinology and Metabolism 305, № 9 (1 листопада 2013): E1093—E1102. http://dx.doi.org/10.1152/ajpendo.00082.2013.
Повний текст джерелаHeger, Dominik, Alexis J. Eugene, Sean R. Parkin, and Marcelo I. Guzman. "Crystal structure of zymonic acid and a redetermination of its precursor, pyruvic acid." Acta Crystallographica Section E Crystallographic Communications 75, no. 6 (May 24, 2019): 858–62. http://dx.doi.org/10.1107/s2056989019007072.
Повний текст джерелаABSON, A., N. J. P. BROOM, P. A. COATES, J. S. ELDER, A. K. FORREST, P. C. T. HANNAN, A. J. HICKS, et al. "ChemInform Abstract: Chemistry of Pseudomonic Acid. Part 16. Aryl and Heteroaryl Ketone Derivatives of Monic Acid." ChemInform 27, no. 39 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199639261.
Повний текст джерелаKatz, Julian. "Acid Secretion and Suppression." Medical Clinics of North America 75, no. 4 (July 1991): 877–87. http://dx.doi.org/10.1016/s0025-7125(16)30418-7.
Повний текст джерелаConger, John D. "Acute Uric Acid Nephropathy." Medical Clinics of North America 74, no. 4 (July 1990): 859–71. http://dx.doi.org/10.1016/s0025-7125(16)30522-3.
Повний текст джерелаIsmaila, Shina Sadiq, Yahaya Sani, Ali Audu Sani, Saminu Murtala Yakasai, Hajara Momoh, and Sa’adatu Eri Mohammed. "Determination of fatty acids and physicochemical properties of neem (Azadrachta indica L) seed oil extracts." Dutse Journal of Pure and Applied Sciences 8, no. 1a (May 5, 2022): 149–60. http://dx.doi.org/10.4314/dujopas.v8i1a.16.
Повний текст джерелаGeers, J., R. Appleby, and J. Walters. "Ursodeoxycholic Acid Increases Obeticholic Acid Stimulation of FGF19 in Human Ileal Explants." Journal of Hepatology 64, no. 2 (2016): S440. http://dx.doi.org/10.1016/s0168-8278(16)00724-8.
Повний текст джерелаThomas, Maciej, Simona Kliś, Krzysztof Barbusiński, and Marek Chyc. "Removal of Acid Red 27, Reactive Black 5 and Acid Green 16 from Aqueous Solutions using Potassium Ferrate(VI)." Fibres and Textiles in Eastern Europe 27, no. 4(136) (August 31, 2019): 71–75. http://dx.doi.org/10.5604/01.3001.0013.1821.
Повний текст джерелаKarpova, Tatiana R., Evgeniy A. Buluchevskiy, and Alexander V. Lavrenov. "Mesoporous composite materials based on acid-activated montmorillonites." Vestnik Тomskogo gosudarstvennogo universiteta. Khimiya, no. 15 (December 1, 2019): 15–28. http://dx.doi.org/10.17223/24135542/16/2.
Повний текст джерелаTarng, D. C., T. P. Huang, and Y. H. Wei. "Erythropoietin and iron: the role of ascorbic acid." Nephrology Dialysis Transplantation 16, suppl 5 (July 1, 2001): 35–39. http://dx.doi.org/10.1093/ndt/16.suppl_5.35.
Повний текст джерелаGuba, Gusar, Bakibayev, Tazhbayev, and Minayeva. "Dehydration/polycondensation of lactic acid under microwave irradiation." Bulletin of the Karaganda University. "Chemistry" series 93, no. 1 (March 29, 2019): 8–16. http://dx.doi.org/10.31489/2019ch1/8-16.
Повний текст джерелаYagi, Shusuke, Takeshi Soeki, Ken-ichi Aihara, Daiju Fukuda, Takayuki Ise, Muneyuki Kadota, Sachiko Bando, et al. "Low Serum Levels of Eicosapentaenoic Acid and Docosahexaenoic Acid are Risk Factors for Cardiogenic Syncope in Patients with Brugada Syndrome." International Heart Journal 58, no. 5 (2017): 720–23. http://dx.doi.org/10.1536/ihj.16-278.
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