The recent discovery of a promising pharmacological scaffold derived from carvacrol: A review

被引:6
作者
Retnosari, Rini [1 ,2 ,3 ]
Ali, Amatul Hamizah [1 ]
Zainalabidin, Satirah [4 ]
Ugusman, Azizah [5 ]
Oka, Natsuhisa [2 ,6 ,7 ,8 ]
Latip, Jalifah [1 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Sci & Technol, Dept Chem Sci, Ukm Bangi 43600, Selangor, Malaysia
[2] Gifu Univ, Int Joint Dept Mat Sci & Engn Natl Univ Malaysia &, Grad Sch Engn, 1-1 Yanagido, Gifu 5011193, Japan
[3] Univ Negeri Malang, Dept Chem, Jl Semarang 5, Malang, Indonesia
[4] Univ Kebangsaan Malaysia, Fac Hlth Sci, Ctr Toxicol & Hlth Risk Studies CORE, Programme Biomed Sci, Kuala Lumpur 50300, Malaysia
[5] Univ Kebangsaan Malaysia, Fac Med, Dept Physiol, Kuala Lumpur 56000, Malaysia
[6] Gifu Univ, Fac Engn, Dept Chem & Biomol Sci, 1-1 Yanagido, Gifu 5011193, Japan
[7] Gifu Univ, Inst Glyco Core Res iGCORE, Gifu 5011193, Japan
[8] Gifu Univ, Ctr One Med Innovat Translat Res Com, 1-1 Yanagido, Gifu 5011193, Japan
关键词
Carvacrol; Pharmacophore; Pharmacological activities; Structural -activity relationship; OREGANO ESSENTIAL OIL; IN-VITRO; ANTIMICROBIAL ACTIVITY; INFLAMMATORY RESPONSE; ANTIBACTERIAL ACTIVITY; BIOLOGICAL-ACTIVITIES; ANTIFUNGAL ACTIVITY; COMPOUND CARVACROL; OXIDATIVE STRESS; MICE INVOLVEMENT;
D O I
10.1016/j.bmcl.2024.129826
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Carvacrol, called CA, is a dynamic phytoconstituent characterized by a phenol ring abundantly sourced from various natural reservoirs. This versatile scaffold serves as a pivotal template for the design and synthesis of novel drug molecules, harboring promising biological activities. The active sites positioned at C-4, C-6, and the hydroxyl group (-OH) of CA offer fertile ground for creating potent drug candidates from a pharmacological standpoint. In this comprehensive review, we delve into diverse synthesis pathways and explore the biological activity of CA derivatives. We aim to illuminate the potential of these derivatives in discovering and developing efficacious treatments against a myriad of life-threatening diseases. By scrutinizing the structural modifications and pharmacophore placements that enhance the activity of CA derivatives, we aspire to inspire the innovation of novel therapeutics with heightened potency and effectiveness.
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页数:28
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共 124 条
[1]   Identification and structure-activity relationship study of carvacrol derivatives as Mycobacterium tuberculosis chorismate mutase inhibitors [J].
Alokam, Reshma ;
Jeankumar, Variam Ullas ;
Sridevi, Jonnalagadda Padma ;
Matikonda, Siddharth Sai ;
Peddi, Santosh ;
Alvala, Mallika ;
Yogeeswari, Perumal ;
Sriram, Dharmarajan .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2014, 29 (04) :547-554
[2]   Acetylcholinesterase inhibition by nootkatone and carvacrol in arthropods [J].
Anderson, J. A. ;
Coats, J. R. .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2012, 102 (02) :124-128
[3]   Comparative efficacy and toxic effects of carvacryl acetate and carvacrol on sheep gastrointestinal nematodes and mice [J].
Andre, Weibson P. P. ;
Ribeiro, Wesley L. C. ;
Cavalcante, Gessica S. ;
dos Santos, Jessica M. L. ;
Macedo, Iara T. F. ;
de Paula, Haroldo C. B. ;
de Freitas, Rivelilson M. ;
de Morais, Selene M. ;
de Melo, Janaina V. ;
Bevilaqua, Claudia M. L. .
VETERINARY PARASITOLOGY, 2016, 218 :52-58
[4]   Natural Product-Based 1,2,3-Triazole/Sulfonate Analogues as Potential Chemotherapeutic Agents for Bacterial Infections [J].
Aneja, Babita ;
Azam, Mudsser ;
Alam, Shadab ;
Perwez, Ahmad ;
Maguire, Ronan ;
Yadava, Umesh ;
Kavanagh, Kevin ;
Daniliuc, Constantin G. ;
Rizvi, M. Moshahid A. ;
Haq, Qazi Mohd. Rizwanul ;
Abid, Mohammad .
ACS OMEGA, 2018, 3 (06) :6912-6930
[5]   Carvacrol suppresses the expression of inflammatory marker genes in D-galactosamine-hepatotoxic rats [J].
Aristatile, Balakrishnan ;
Al-Assaf, Abdullah H. ;
Pugalendi, Kodukkur Viswanathan .
ASIAN PACIFIC JOURNAL OF TROPICAL MEDICINE, 2013, 6 (03) :205-211
[6]   Anti-proliferative effects of carvacrol on a human metastatic breast cancer cell line, MDA-MB 231 [J].
Arunasree, K. M. .
PHYTOMEDICINE, 2010, 17 (8-9) :581-588
[7]   Carvacrol derivatives as mushroom tyrosinase inhibitors; synthesis, kinetics mechanism and molecular docking studies [J].
Ashraf, Zaman ;
Rafiq, Muhammad ;
Nadeem, Humaira ;
Hassan, Mubashir ;
Afzal, Samina ;
Waseem, Muhammad ;
Afzal, Khurram ;
Latip, Jalifah .
PLOS ONE, 2017, 12 (05)
[8]   The effect of carvacrol on healthy neurons and N2a cancer cells: some biochemical, anticancerogenicity and genotoxicity studies [J].
Aydin, Elanur ;
Turkez, Hasan ;
Keles, M. Sait .
CYTOTECHNOLOGY, 2014, 66 (01) :149-157
[9]   Design, synthesis and biological activities of novel 5-isopropyl-2-methylphenolhydrazide-based sulfonamide derivatives [J].
Bagul, Suresh D. ;
Rajput, Jamatsing D. ;
Tadavi, Samina K. ;
Bendre, Ratnamala S. .
RESEARCH ON CHEMICAL INTERMEDIATES, 2017, 43 (04) :2241-2252
[10]   Synthesis of Carvacrol Derivatives as Potential New Anticancer Agent against Lung Cancer [J].
Bansal, Anu ;
Saleh-E-In, Md. Moshfekus ;
Kar, Pallab ;
Roy, Ayan ;
Sharma, Neeta Raj .
MOLECULES, 2022, 27 (14)