Статті в журналах з теми "Terpene-isolation"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Terpene-isolation".
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.
Lai, Shih-Ming, I.-Wen Chen, and Ming-Jyi Tsai. "Preparative isolation of terpene trilactones from Ginkgo biloba leaves." Journal of Chromatography A 1092, no. 1 (October 2005): 125–34. http://dx.doi.org/10.1016/j.chroma.2005.01.028.
Повний текст джерелаYang, Chang-Qing, Xiu-Ming Wu, Ju-Xin Ruan, Wen-Li Hu, Yin-Bo Mao, Xiao-Ya Chen, and Ling-Jian Wang. "Isolation and characterization of terpene synthases in cotton (Gossypium hirsutum)." Phytochemistry 96 (December 2013): 46–56. http://dx.doi.org/10.1016/j.phytochem.2013.09.009.
Повний текст джерелаColeman, W. M., Bert M. Gordon, and Brian M. Lawrence. "Examinations of the Matrix Isolation Fourier Transform Infrared Spectra of Organic Compounds: Part XII." Applied Spectroscopy 43, no. 2 (February 1989): 298–304. http://dx.doi.org/10.1366/0003702894203273.
Повний текст джерелаTrapp, Susan C., and Rodney B. Croteau. "Genomic Organization of Plant Terpene Synthases and Molecular Evolutionary Implications." Genetics 158, no. 2 (June 1, 2001): 811–32. http://dx.doi.org/10.1093/genetics/158.2.811.
Повний текст джерелаAwakawa, Takayoshi. "Enzymatic reactions in teleocidin B biosynthesis." Journal of Natural Medicines 75, no. 3 (March 6, 2021): 467–74. http://dx.doi.org/10.1007/s11418-021-01504-2.
Повний текст джерелаWeiss, Eve R., Jana Pika, and Robert J. Braddock. "Isolation and Identification of Terpene Chlorohydrins Found in Cold-Pressed Orange Oil." Journal of Agricultural and Food Chemistry 51, no. 8 (April 2003): 2277–82. http://dx.doi.org/10.1021/jf026122n.
Повний текст джерелаWang, Piao-Yi, Rong Ni, Ting-Ting Zhu, Chun-Jing Sun, Hong-Xiang Lou, Xuebin Zhang, and Ai-Xia Cheng. "Isolation and functional characterization of four microbial type terpene synthases from ferns." Plant Physiology and Biochemistry 155 (October 2020): 716–24. http://dx.doi.org/10.1016/j.plaphy.2020.08.037.
Повний текст джерелаHattan, Jun-ichiro, Kazutoshi Shindo, Tetsuya Sasaki, and Norihiko Misawa. "Isolation and Functional Characterization of New Terpene Synthase Genes from Traditional Edible Plants." Journal of Oleo Science 67, no. 10 (2018): 1235–46. http://dx.doi.org/10.5650/jos.ess18163.
Повний текст джерелаJasiem, Thamer Mouhi. "Isolation of terpene and pharmacognostical study of iraqi caper shrubs (Capparis spinosa) L." Research Journal of Pharmacy and Technology 11, no. 6 (2018): 2388. http://dx.doi.org/10.5958/0974-360x.2018.00441.9.
Повний текст джерелаFrench, Larry G. "Isolation and Structure Elucidation of the Terpene β-Thujone from Cedar Leaf Oil". Journal of Chemical Education 88, № 6 (червень 2011): 829–31. http://dx.doi.org/10.1021/ed100620b.
Повний текст джерелаWeyerstahl, Peter, Helga Marschall-Weyerstahl, Martin Schröder, and Vijay K. Kaul. "Terpenes and terpene derivatives, XXIV. Isolation and stereochemistry of the four artedouglasia oxides." Liebigs Annalen der Chemie 1988, no. 9 (September 14, 1988): 917–18. http://dx.doi.org/10.1002/jlac.198819880919.
Повний текст джерелаde Mesquita, Mariana L., José E. de Paula, Laila S. Espindola, Luiz A. L. Soares, Tania M. G. da Silva, Celso A. Camara, and Telma M. G. Da Silva. "Protoflavanones from the Wood Stem of Salvertia convallariodora." Natural Product Communications 12, no. 4 (April 2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200413.
Повний текст джерелаAtolani, Olubunmi, and Gabriel A. Olatunji. "Isolation and evaluation of antiglycation potential of polyalthic acid (furano-terpene) from Daniella oliveri." Journal of Pharmaceutical Analysis 4, no. 6 (December 2014): 407–11. http://dx.doi.org/10.1016/j.jpha.2014.05.002.
Повний текст джерелаOkoth, Dorothy A., Joachim J. Hug, Ronald Garcia, Cathrin Spröer, Jörg Overmann, and Rolf Müller. "2-Hydroxysorangiadenosine: Structure and Biosynthesis of a Myxobacterial Sesquiterpene–Nucleoside." Molecules 25, no. 11 (June 9, 2020): 2676. http://dx.doi.org/10.3390/molecules25112676.
Повний текст джерелаПрокопчук (Prokopchuk), Денис (Denis) Игоревич (Igorevich), Олег (Oleg) Игоревич (Igorevich) Покровский (Pokrovskiy), Ольга (Ol'ga) Олеговна (Olegovna) Паренаго (Parenago), Саида (Saida) Амирановна (Аmiranovna) Багателия (Bagatelia), Алхас (Аlkhas) Анатольевич (Аnatol'evich) Марколия (Markolia), Сергей (Sergej) Александрович (Аleksandrovich) Покрышкин (Pokryshkin), and Валерий (Valerij) Васильевич (Vasil'evich) Лунин (Lunin). "COMPARISON OF THE QUALITATIVE COMPOSITION OF LAURUS NOBILIS LEAVES EXTRACTS OBTAINED BY SUPERCRITICAL FLUID EXTRACTION AND MICROWAVE-ASSISTED EXTRACTION." chemistry of plant raw material, no. 3 (March 20, 2018): 169–77. http://dx.doi.org/10.14258/jcprm.2018033758.
Повний текст джерелаKung, Chen, Chao, Wu, Lin, and Chen. "Analysis of Volatile Constituents in Platostoma palustre (Blume) Using Headspace Solid-Phase Microextraction and Simultaneous Distillation-Extraction." Foods 8, no. 9 (September 14, 2019): 415. http://dx.doi.org/10.3390/foods8090415.
Повний текст джерелаJ. Fradi, Ahmed. "Evaluation the Effectiveness of Different Concentrations Phenols, Alkaloids and Terpenes Extracted from Pimpinella anisum against Phytophthora Fungi." Ibn AL- Haitham Journal For Pure and Applied Sciences 35, no. 2 (April 20, 2022): 1–6. http://dx.doi.org/10.30526/35.2.2746.
Повний текст джерелаGarson, Mary J., Annette F. Dexter, Lynette K. Lambert, and Vicky Liokas. "Isolation of the Bioactive Terpene 7-Deacetoxy-olepupuane from the Temperate Marine Spong Dysidea Sp." Journal of Natural Products 55, no. 3 (March 1992): 364–67. http://dx.doi.org/10.1021/np50081a013.
Повний текст джерелаSulastri, Lilik, Ristanti Mega Lestari, and Partomuan Simanjuntak. "Isolasi Dan Identifikasi Senyawa Kimia Monoterpen Dari Fraksi Etilasetat Daun Keji Beling (Strobilanthes crispa (L.) Blume) Yang Mempunyai Daya Sitotoksik." Jurnal Fitofarmaka Indonesia 8, no. 1 (January 29, 2021): 12–17. http://dx.doi.org/10.33096/jffi.v8i1.721.
Повний текст джерелаKatavic, Peter L., Pinus Jumaryatno, John N. A. Hooper, Joanne T. Blanchfield, and Mary J. Garson. "Oxygenated Terpenoids from the Australian Sponges Coscinoderma matthewsi and Dysidea sp., and the Nudibranch Chromodoris albopunctata." Australian Journal of Chemistry 65, no. 5 (2012): 531. http://dx.doi.org/10.1071/ch12010.
Повний текст джерелаKatavic, Peter L., Pinus Jumaryatno, John N. A. Hooper, Joanne T. Blanchfield, and Mary J. Garson. "Note of clarification about: Oxygenated Terpenoids from the Australian Sponges Coscinoderma matthewsi and Dysidea sp., and the Nudibranch Chromodoris albopunctata [vol. 65, pp. 531–538]." Australian Journal of Chemistry 66, no. 11 (2013): 1461. http://dx.doi.org/10.1071/ch12010_nc.
Повний текст джерелаLi, Huanhuan, Hongji Li, Shuo Chen, Wenhui Wu, and Peng Sun. "Isolation and Identification of Pentalenolactone Analogs from Streptomyces sp. NRRL S-4." Molecules 26, no. 23 (December 5, 2021): 7377. http://dx.doi.org/10.3390/molecules26237377.
Повний текст джерелаYuping, Tang, and Lou Fengchang. "SEPARATION AND ISOLATION OF TERPENE LACTONES FROM GINKGO BILOBA L. BY DIRECT HIGH PERFORMANCE LIQUID CHROMATOGRAPHY." Journal of Liquid Chromatography & Related Technologies 23, no. 18 (January 2000): 2897–900. http://dx.doi.org/10.1081/jlc-100101241.
Повний текст джерелаSuciati, Lynette K. Lambert, Benjamin P. Ross, Myrna A. Deseo, and Mary J. Garson. "Phytochemical Study of Fagraea spp. Uncovers a New Terpene Alkaloid with Anti-Inflammatory Properties." Australian Journal of Chemistry 64, no. 4 (2011): 489. http://dx.doi.org/10.1071/ch10421.
Повний текст джерелаJørgensen, Lars, Steven J. McKerrall, Christian A. Kuttruff, Felix Ungeheuer, Jakob Felding, and Phil S. Baran. "14-Step Synthesis of (+)-Ingenol from (+)-3-Carene." Science 341, no. 6148 (August 1, 2013): 878–82. http://dx.doi.org/10.1126/science.1241606.
Повний текст джерелаOladimeji, Olawale H., and Kufre E. Eberefiak. "Isolation and antimicrobial analysis of a steroidal terpene from the butanol fraction of Byrophyllum pinnatum (Lam.) Oken." European Chemical Bulletin 6, no. 7 (July 12, 2017): 292. http://dx.doi.org/10.17628/ecb.2017.6.292-294.
Повний текст джерелаVezzaro, Alice, Sandra T. Krause, Alberto Nonis, Angelo Ramina, Jörg Degenhardt, and Benedetto Ruperti. "Isolation and characterization of terpene synthases potentially involved in flavor development of ripening olive (Olea europaea) fruits." Journal of Plant Physiology 169, no. 9 (June 2012): 908–14. http://dx.doi.org/10.1016/j.jplph.2012.01.021.
Повний текст джерелаNurhayati, Awik Puji Dyah, Rarastoeti Pratiwi, Subagus Wahyuono, and Istriyati . "PROLIFERATION INHIBITORY ACTIVITY OF THE ACTIVE FRACTION MARINE SPONGE Cinachyrella sp. AGAINST CELL LINE T47D." KnE Life Sciences 2, no. 1 (September 20, 2015): 663. http://dx.doi.org/10.18502/kls.v2i1.243.
Повний текст джерелаJones, Christopher G., Christopher I. Keeling, Emilio L. Ghisalberti, Elizabeth L. Barbour, Julie A. Plummer, and Jörg Bohlmann. "Isolation of cDNAs and functional characterisation of two multi-product terpene synthase enzymes from sandalwood, Santalum album L." Archives of Biochemistry and Biophysics 477, no. 1 (September 2008): 121–30. http://dx.doi.org/10.1016/j.abb.2008.05.008.
Повний текст джерелаGuidoti, Daniela Granella Gomes, David Teixeira Guidoti, Adriano Lopes Romero, Ana Lúcia Tasca Gois Ruiz, Mary Ann Foglio, João Ernesto de Carvalho, and Carmem Lúcia de Mello Sartori Cardoso da Rocha. "Kaurenoic acid from Annona squamosa L. exhibits antiproliferative effect on human tumor cell lines and induces apoptosis in Aspergillus nidulans." Revista Fitos 13, no. 2 (September 10, 2019): 122–36. http://dx.doi.org/10.17648/2446-4775.2019.716.
Повний текст джерелаEl Midaoui, Adil, Farid Khallouki, Réjean Couture, Florina Moldovan, Mahmoud Ali Ismael, Brice Ongali, Marie Yvonne Akoume, et al. "Thymus atlanticus: A Source of Nutrients with Numerous Health Benefits and Important Therapeutic Potential for Age-Related Diseases." Nutrients 15, no. 18 (September 21, 2023): 4077. http://dx.doi.org/10.3390/nu15184077.
Повний текст джерелаMierza, Vriezka, Antolin Antolin, Audi Ichsani, Nurma Dwi, Sridevi Sridevi, and Syfa Dwi. "Research Article: Isolasi dan Identifikasi Senyawa Terpenoid." Jurnal Surya Medika 9, no. 2 (August 27, 2023): 134–41. http://dx.doi.org/10.33084/jsm.v9i2.5681.
Повний текст джерелаSchroeder, Daniel R., and Frank R. Stermitz. "Isolation and synthesis of bishordeninyl terpene alkaloids. Some experiments relating to the natural occurrence of formal Diels-Alder adducts." Tetrahedron 41, no. 19 (January 1985): 4309–20. http://dx.doi.org/10.1016/s0040-4020(01)97202-3.
Повний текст джерелаОленников (Olennikov), Даниил (Daniil) Николаевич (Nikolaevich), and Нина (Nina) Игоревна (Igorevna) Кащенко (Kashchenko). "PHYTOECDYSTEROIDS OF SERRATULA L. AND KLASEA CASS. GENERA: CHEMODIVERSITY, METHODS OF ISOLATION AND ANALYSIS." chemistry of plant raw material, no. 4 (September 14, 2017): 123–35. http://dx.doi.org/10.14258/jcprm.2017042016.
Повний текст джерелаLee, Sae-Byuk, and Heui-Dong Park. "Isolation and Investigation of Potential Non-Saccharomyces Yeasts to Improve the Volatile Terpene Compounds in Korean Muscat Bailey A Wine." Microorganisms 8, no. 10 (October 8, 2020): 1552. http://dx.doi.org/10.3390/microorganisms8101552.
Повний текст джерелаWeyerstahl, Peter, Christian Christiansen, and Helga Marschall. "Terpenes and Terpene Derivatives, XXX. Isolation and Synthesis of Isohumbertiol, the First Naturally Occurring Sesquiterpene Alcohol with a Humbertiane Skeleton." Liebigs Annalen der Chemie 1992, no. 12 (December 22, 1992): 1325–28. http://dx.doi.org/10.1002/jlac.1992199201218.
Повний текст джерелаChang, Yung-Jin, Seung-Hwan Song, Si-Hyung Park, and Soo-Un Kim. "Amorpha-4,11-diene Synthase of Artemisia annua: cDNA Isolation and Bacterial Expression of a Terpene Synthase Involved in Artemisinin Biosynthesis." Archives of Biochemistry and Biophysics 383, no. 2 (November 2000): 178–84. http://dx.doi.org/10.1006/abbi.2000.2061.
Повний текст джерелаKABORE, Ibrahim, Mamounata DIAO, Samson GUENNE, Amana METUOR-DABIRE, Hemayoro SAMA, Alin CIOBICA, Adama HILOU, Martin KIENDREBEOGO, and Mamoudou H. DICKO. "Phytochemistry and Alternative use of Sweeteners in Metabolic Diseases." Annals of the Academy of Romanian Scientists Series on Biological Sciences 11, no. 1 (2022): 109–19. http://dx.doi.org/10.56082/annalsarscibio.2022.1.109.
Повний текст джерелаMaksimovic, Svetolik, Vanja Tadic, Jasna Ivanovic, Tanja Radmanovic, Stoja Milovanovic, Milica Stankovic, and Irena Zizovic. "Utilization of the integrated process of supercritical extraction and impregnation for incorporation of Helichrysum italicum extract into corn starch xerogel." Chemical Industry and Chemical Engineering Quarterly 24, no. 2 (2018): 191–200. http://dx.doi.org/10.2298/ciceq170223031m.
Повний текст джерелаZou, Ran, Xin Li, Xiaochen Chen, Yue-Wei Guo, and Baofu Xu. "Chemical and biosynthetic potential of Penicillium shentong XL-F41." Beilstein Journal of Organic Chemistry 20 (March 15, 2024): 597–606. http://dx.doi.org/10.3762/bjoc.20.52.
Повний текст джерелаSmit, Samuel J., Melané A. Vivier, and Philip R. Young. "Seeing the Forest through the (Phylogenetic) Trees: Functional Characterisation of Grapevine Terpene Synthase (VviTPS) Paralogues and Orthologues." Plants 10, no. 8 (July 26, 2021): 1520. http://dx.doi.org/10.3390/plants10081520.
Повний текст джерелаWEYERSTAHL, P., C. CHRISTIANSEN, and H. MARSCHALL. "ChemInform Abstract: Terpenes and Terpene Derivatives. Part 30. Isolation and Synthesis of Isohumbertiol, the First Naturally Occurring Sesquiterpene Alcohol with a Humbertiane Skeleton." ChemInform 24, no. 15 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199315239.
Повний текст джерелаAlicandri, Enrica, Stefano Covino, Bartolomeo Sebastiani, Anna Rita Paolacci, Maurizio Badiani, Francesco Manti, Carmelo Peter Bonsignore, Agostino Sorgonà, and Mario Ciaffi. "Diterpene Resin Acids and Olefins in Calabrian Pine (Pinus nigra subsp. laricio (Poiret) Maire) Oleoresin: GC-MS Profiling of Major Diterpenoids in Different Plant Organs, Molecular Identification and Expression Analysis of Diterpene Synthase Genes." Plants 10, no. 11 (November 5, 2021): 2391. http://dx.doi.org/10.3390/plants10112391.
Повний текст джерелаKlimek, Katarzyna, Katarzyna Tyśkiewicz, Malgorzata Miazga-Karska, Agnieszka Dębczak, Edward Rój, and Grazyna Ginalska. "Bioactive Compounds Obtained from Polish “Marynka” Hop Variety Using Efficient Two-Step Supercritical Fluid Extraction and Comparison of Their Antibacterial, Cytotoxic, and Anti-Proliferative Activities In Vitro." Molecules 26, no. 8 (April 19, 2021): 2366. http://dx.doi.org/10.3390/molecules26082366.
Повний текст джерелаUmaña, Eduardo, Godofredo Solano, Gabriel Zamora, and Giselle Tamayo-Castillo. "Costa Rican Propolis Chemical Compositions: Nemorosone Found to Be Present in an Exclusive Geographical Zone." Molecules 28, no. 20 (October 14, 2023): 7081. http://dx.doi.org/10.3390/molecules28207081.
Повний текст джерелаTran, Thi Diem Huong, Ngoc Tuyet Nguyen, and Thi Hong Thuong Nguyen. "Isolation and in silico analysis of a transcript variant for a putative terpene synthase (HbTPS6L-X1) from the bark tissues of rubber Hevea brasiliensis RRIV 209." Ministry of Science and Technology, Vietnam 65, no. 12 (December 25, 2023): 70–76. http://dx.doi.org/10.31276/vjst.65(12).70-76.
Повний текст джерелаHsu, Chih-Yao, Pung-Ling Huang, Chih-Ming Chen, Chi-Tang Mao, and Shu-Miaw Chaw. "Tangy Scent in Toona sinensis (Meliaceae) Leaflets: Isolation, Functional Characterization, and Regulation of TsTPS1 and TsTPS2, Two Key Terpene Synthase Genes in the Biosynthesis of the Scent Compound." Current Pharmaceutical Biotechnology 13, no. 15 (December 10, 2012): 2721–32. http://dx.doi.org/10.2174/138920112804724864.
Повний текст джерелаSundaraj, Yasotha, Hasdianty Abdullah, Nima Ghahremani Nezhad, Kenneth Francis Rodrigues, Suriana Sabri та Syarul Nataqain Baharum. "Cloning, Expression and Functional Characterization of a Novel α-Humulene Synthase, Responsible for the Formation of Sesquiterpene in Agarwood Originating from Aquilaria malaccensis". Current Issues in Molecular Biology 45, № 11 (10 листопада 2023): 8989–9002. http://dx.doi.org/10.3390/cimb45110564.
Повний текст джерелаIyekowa, Osaro, and Mary Olire Edema. "Chemosuppressive activities in in vivo studies of Plasmodium falciparum-infected mice using isolated oil of Stigmaphyllon ovatum (Amazon vine) Cav." Ovidius University Annals of Chemistry 28, no. 1 (February 23, 2017): 1–6. http://dx.doi.org/10.1515/auoc-2017-0001.
Повний текст джерелаAbbott, Eric, Dawn Hall, Bjoern Hamberger, and Joerg Bohlmann. "Laser microdissection of conifer stem tissues: Isolation and analysis of high quality RNA, terpene synthase enzyme activity and terpenoid metabolites from resin ducts and cambial zone tissue of white spruce (Picea glauca)." BMC Plant Biology 10, no. 1 (2010): 106. http://dx.doi.org/10.1186/1471-2229-10-106.
Повний текст джерела