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This work described a comprehensive study to estimate chemical constituents of essential oils (EOs) extracted from different parts of the Callistemon citrinus viz: fruits, leaves and aerial part. The EOs were characterized using physicochemical parameters, and GC-FID/MS. It was observed that among different parts, aerial part has the highest oil yield (0.90 %) followed by leaves and fruits. Further, seventeen compounds were characterized, and represented total amount (97.2-99.5 %) with domination of monoterpenes (12.5-34.6 %) and oxygenated monoterpenes hydrocarbon (61.8-86.8 %). α-pinene (11.8-24.7 %), α-phellandrene (1.2-3.0 %), p-cymene (3.3-3.9 %) and 1,8-cineole (58.3-85.1 %) were found as major compounds in C. citrinus samples. These major compounds are the quality chemical markers of C. citrinus oil. The findings revealed significant quantitative variations in EO composition of samples and were also clearly supported by multivariate statistical analysis. Moreover, EOs were evaluated for glucosidase and colon cancer cell lines inhibitory activities, which were found promising.

Titel:	Comparative Studies of Essential Oil Composition and Biological Activities of Callistemon citrinus from Western Himalaya.
Autor/in / Beteiligte Person:	Vashisath, S ; Kapoor, S ; Kumari, V ; Butt, S ; Kumar, D
Zeitschrift:	Chemistry & biodiversity, Jg. 21 (2024-06-01), Heft 6, S. e202301129
Veröffentlichung:	Zürich, Switzerland : Hoboken, NJ : Verlag Helvetica Chimica Acta ; Distributed in the USA by Wiley, c2004-, 2024
Medientyp:	academicJournal
ISSN:	1612-1880 (electronic)
DOI:	10.1002/cbdv.202301129
Schlagwort:	Humans Plant Leaves chemistry Drug Screening Assays, Antitumor Cell Line, Tumor Cell Proliferation drug effects Fruit chemistry alpha-Glucosidases metabolism Glycoside Hydrolase Inhibitors pharmacology Glycoside Hydrolase Inhibitors chemistry Glycoside Hydrolase Inhibitors isolation & purification Monoterpenes isolation & purification Monoterpenes pharmacology Monoterpenes analysis Monoterpenes chemistry Oils, Volatile chemistry Oils, Volatile pharmacology Oils, Volatile isolation & purification Myrtaceae chemistry Antineoplastic Agents, Phytogenic pharmacology Antineoplastic Agents, Phytogenic chemistry Antineoplastic Agents, Phytogenic isolation & purification
Sonstiges:	Nachgewiesen in: MEDLINE Sprachen: English Publication Type: Journal Article; Comparative Study Language: English [Chem Biodivers] 2024 Jun; Vol. 21 (6), pp. e202301129. <i>Date of Electronic Publication: </i>2023 Oct 10. MeSH Terms: Oils, Volatile* / chemistry ; Oils, Volatile* / pharmacology ; Oils, Volatile* / isolation & purification ; Myrtaceae* / chemistry ; Antineoplastic Agents, Phytogenic* / pharmacology ; Antineoplastic Agents, Phytogenic* / chemistry ; Antineoplastic Agents, Phytogenic* / isolation & purification ; Humans ; Plant Leaves / chemistry ; Drug Screening Assays, Antitumor ; Cell Line, Tumor ; Cell Proliferation / drug effects ; Fruit / chemistry ; alpha-Glucosidases / metabolism ; Glycoside Hydrolase Inhibitors / pharmacology ; Glycoside Hydrolase Inhibitors / chemistry ; Glycoside Hydrolase Inhibitors / isolation & purification ; Monoterpenes / isolation & purification ; Monoterpenes / pharmacology ; Monoterpenes / analysis ; Monoterpenes / chemistry References: E. M. Abdelmalek, M. A. Ramadan, F. M. Darwish, M. H. Assaf, N. M. Mohamed, S. A. Ross, Med. Chem. Res. 2021, 30, 1031–1055. ; R. A. Larayetan, O. O. Okoh, A. Sadimenko, A. I. Okoh, BMC Complementary Altern. Med. 2017, 17, 1–9. ; F. Ahmed, M. S. Rahman, BMC Complementary Altern. Med. 2016, 16, 1–8. ; N. Zandi-Sohani, M. Hojjati, A. A. Carbonell-Barrachina, J. Essent. Oil-Bear. Plants. 2012, 15, 703–707. ; M. Ramachandran, K. Baskar, M. Jayakumar, PLoS One 2022, 17. ; S. Alvarez, M. J. Sanchez-Blanco, Plant Biol. 2014, 16, 757–764. ; J. W. Wrigley, M. Fagg, Australian Native Plants, Concise Edition, 2007. ; A. Lopez-Mejia, L. G. Ortega-Perez, D. Godinez-Hernandez, B. Nateras-Marin, E. Melendez-Herrera, P. Rios-Chavez, J. Cancer Res. Clin. Oncol. 2019, 145, 1417–1426. ; R. A. Larayetan, Y. Abdulrazaq, O. O. Okoh, Asian J. Chem. 2020, 32, 612–618. ; S. Netala, R. Penmetsa, S. Nakka, B. L. Polisetty, Int. J. Pharm. Pharm. Sci. 2015, 7, 427–430. ; S. Sampath, V. Veeramani, G. S. Krishnakumar, U. Sivalingam, S. L. Madurai, R. Chellan, Biomed. Pharmacother. 2017, 93, 296–307. ; V. Pendyala, S. Thaakur, Asian J. Pharm. Clin. Res. 2017, 10, 232–234. ; F. Ahmed, M. S. Rahman, M. A. Al-Mansur, M. A. Rashid, Dhaka Univ. J. Pharm. Sci. 2016, 15, 1–5. ; S. A. El-Refai, A. F. Atia, S. F. Mahmoud, J. Helminthol. 2019, 93, 424–433. ; H. A. Gad, I. M. Ayoub, M. Wink, PLoS One 2019, 14. ; A. Shaha, V. R. Salunkhe, Pharmacogn. Rev. 2014, 6. ; N. S. Radulovic, P. J. Randjelovic, N. M. Stojanovic, N. D. Cakic, G. A. Bogdanovic, A. V. Zivanovic, Food Res. Int. 2015, 77, 280–289. ; D. Kumar, M. Sukapaka, G. K. Babu, Y. Padwad, PLoS One 2015, 10. ; N. Zandi-Sohani, M. Hojjati, A. A. Carbonell-Barrachina, Neotrop. Entomol. 2013, 42, 89–94. ; O. O. Oyedeji, O. A. Lawal, F. O. Shode, A. O. Oyedeji, Molecules. 2009, 14, 1990–1998. ; R. Gogoi, T. Begum, N. Sarma, S. Kumar Pandey, M. Lal, J. Food Biochem. 2021, 45. ; S. A. Adefegha, T. A. Olasehinde, G. Oboh, J. Oleo Sci. 2017, 66, 51–63. ; A. K. Maurya, S. Vashisath, G. Aggarwal, V. Yadav, V. K. Agnihotri, Chem. Biodiversity 2022, 19. ; J. J. Granados-Romero, A. I. Valderrama-Treviño, E. H. Contreras-Flores, B. Barrera-Mera, M. Herrera Enríquez, K. Uriarte-Ruíz, J. C. Ceballos-Villalba, A. G. Estrada-Mata, C. Alvarado Rodríguez, G. Arauz-Pena, Int. J. Refract. Hard Met. 2017, 5. ; N. M. Alhoshani, N. S. Al-Johani, N. Alkeraishan, S. Alarifi, S. Alkahtani, Saudi J. Biol. Sci. 2022, 29. ; A. T. Rufino, M. Ribeiro, F. Judas, L. Salgueiro, M. C. Lopes, C. Cavaleiro, A. F. Mendes, J. Nat. Prod. 2014, 77, 264–269. ; H. Worth, C. Schacher, U. Dethlefsen, Respiratory Research. 2009, 10, 1–7. ; D. Kumar, V. Kumari, S. Afr. J. Bot. 2023, 153, 102–108. ; S. E. Stein, Mass Spectral Database and Software, Version 3.02, National Institute of Standards and Technology (NIST), Gaithersburg, MD, 1990. ; R. P. Adams, Identification of Essential oil Components by Gas Chromatography Mass Spectrometry, ed. 4.1, Allured Publ Crop Carol Steam, IL, 2017. ; S. Vashisath, A. K. Maurya, V. K. Agnihotri, J. Essent. Oil Res. 2021, 6, 592–600. Grant Information: HCP-0007 CSIR-New Delhi; 5362 CSIR-IHBT Contributed Indexing: Keywords: GC/GCMS; chemical composition; cytotoxicity activity; physicochemical properties; α-glucosidase activity Substance Nomenclature: 0 (Oils, Volatile) ; 0 (Antineoplastic Agents, Phytogenic) ; EC 3.2.1.20 (alpha-Glucosidases) ; 0 (Glycoside Hydrolase Inhibitors) ; 0 (Monoterpenes) Entry Date(s): Date Created: 20230920 Date Completed: 20240618 Latest Revision: 20240618 Update Code: 20240619

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Comparative Studies of Essential Oil Composition and Biological Activities of Callistemon citrinus from Western Himalaya.