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For: Noureddin SA, El-shishtawy RM, Al-footy KO. Curcumin analogues and their hybrid molecules as multifunctional drugs. European Journal of Medicinal Chemistry 2019;182:111631. [DOI: 10.1016/j.ejmech.2019.111631] [Cited by in Crossref: 37] [Cited by in F6Publishing: 32] [Article Influence: 12.3] [Reference Citation Analysis]
Number Citing Articles
1 López-Malo D, Villarón-Casares CA, Alarcón-Jiménez J, Miranda M, Díaz-Llopis M, Romero FJ, Villar VM. Curcumin as a Therapeutic Option in Retinal Diseases. Antioxidants (Basel) 2020;9:E48. [PMID: 31935797 DOI: 10.3390/antiox9010048] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
2 Stepanova VA, Guerrero A, Schull C, Christensen J, Trudeau C, Cook J, Wolmutt K, Blochwitz J, Ismail A, West JK, Wheaton AM, Guzei IA, Yao B, Kubatova A. Hybrid Synthetic and Computational Study of an Optimized, Solvent-Free Approach to Curcuminoids. ACS Omega 2022;7:7257-77. [PMID: 35252716 DOI: 10.1021/acsomega.1c07006] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Pawelski D, Walewska A, Ksiezak S, Sredzinski D, Radziwon P, Moniuszko M, Gandusekar R, Eljaszewicz A, Lazny R, Brzezinski K, Plonska-Brzezinska ME. Monocarbonyl Analogs of Curcumin Based on the Pseudopelletierine Scaffold: Synthesis and Anti-Inflammatory Activity. Int J Mol Sci 2021;22:11384. [PMID: 34768818 DOI: 10.3390/ijms222111384] [Reference Citation Analysis]
4 Insuasty D, Castillo J, Becerra D, Rojas H, Abonia R. Synthesis of Biologically Active Molecules through Multicomponent Reactions. Molecules 2020;25:E505. [PMID: 31991635 DOI: 10.3390/molecules25030505] [Cited by in Crossref: 35] [Cited by in F6Publishing: 11] [Article Influence: 17.5] [Reference Citation Analysis]
5 Polaquini CR, Marques BC, Ayusso GM, Morão LG, Sardi JCO, Campos DL, Silva IC, Cavalca LB, Scheffers DJ, Rosalen PL, Pavan FR, Ferreira H, Regasini LO. Antibacterial activity of a new monocarbonyl analog of curcumin MAC 4 is associated with divisome disruption. Bioorg Chem 2021;109:104668. [PMID: 33601139 DOI: 10.1016/j.bioorg.2021.104668] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Floris B, Galloni P, Conte V, Sabuzi F. Tailored Functionalization of Natural Phenols to Improve Biological Activity. Biomolecules 2021;11:1325. [PMID: 34572538 DOI: 10.3390/biom11091325] [Reference Citation Analysis]
7 Al Zahrani NA, El-Shishtawy RM, Elaasser MM, Asiri AM. Synthesis of Novel Chalcone-Based Phenothiazine Derivatives as Antioxidant and Anticancer Agents. Molecules 2020;25:E4566. [PMID: 33036301 DOI: 10.3390/molecules25194566] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
8 Luiza Koop B, Nascimento da Silva M, Diniz da Silva F, Thayres dos Santos Lima K, Santos Soares L, José de Andrade C, Ayala Valencia G, Rodrigues Monteiro A. Flavonoids, anthocyanins, betalains, curcumin, and carotenoids: Sources, classification and enhanced stabilization by encapsulation and adsorption. Food Research International 2022;153:110929. [DOI: 10.1016/j.foodres.2021.110929] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
9 Moreira J, Saraiva L, Pinto MM, Cidade H. Diarylpentanoids with antitumor activity: A critical review of structure-activity relationship studies. Eur J Med Chem 2020;192:112177. [PMID: 32172081 DOI: 10.1016/j.ejmech.2020.112177] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
10 Zahran RF, Geba ZM, Tabll AA, Mashaly MM. Therapeutic potential of a novel combination of Curcumin with Sulfamethoxazole against carbon tetrachloride-induced acute liver injury in Swiss albino mice. J Genet Eng Biotechnol 2020;18:13. [PMID: 32363509 DOI: 10.1186/s43141-020-00027-9] [Reference Citation Analysis]
11 Borah B, Dhar Dwivedi K, Chowhan LR. 4‐Hydroxycoumarin: A Versatile Substrate for Transition‐metal‐free Multicomponent Synthesis of Bioactive Heterocycles. Asian J Org Chem 2021;10:3101-26. [DOI: 10.1002/ajoc.202100550] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
12 Zahran RF, Geba ZM, Tabll AA, Mashaly MM. Therapeutic potential of a novel combination of Curcumin with Sulfamethoxazole against carbon tetrachloride-induced acute liver injury in Swiss albino mice. J Genet Eng Biotechnol 2020;18:13. [PMID: 32363509 DOI: 10.1186/s43141-020-00027-9] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
13 El-Shishtawy RM, Rahman MM, Ali Sheikh T, Nadeem Arshad M, Al-Zahrani FAM, Asiri AM. A New Cr3+ Electrochemical Sensor Based on ATNA/Nafion/Glassy Carbon Electrode. Materials (Basel) 2020;13:E2695. [PMID: 32545677 DOI: 10.3390/ma13122695] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
14 Noureddin SA, El-shishtawy RM, Al-footy KO. Synthesis of new symmetric cyclic and acyclic halocurcumin analogues typical precursors for hybridization. Res Chem Intermed 2020;46:5307-23. [DOI: 10.1007/s11164-020-04264-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Priyadarshi R, Ezati P, Rhim J. Recent Advances in Intelligent Food Packaging Applications Using Natural Food Colorants. ACS Food Sci Technol 2021;1:124-38. [DOI: 10.1021/acsfoodscitech.0c00039] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
16 Ibáñez MD, Blázquez MA. Curcuma longa L. Rhizome Essential Oil from Extraction to Its Agri-Food Applications. A Review. Plants (Basel) 2020;10:E44. [PMID: 33379197 DOI: 10.3390/plants10010044] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
17 Al Zahrani NA, El-shishtawy RM, Asiri AM. Recent developments of gallic acid derivatives and their hybrids in medicinal chemistry: A review. European Journal of Medicinal Chemistry 2020;204:112609. [DOI: 10.1016/j.ejmech.2020.112609] [Cited by in Crossref: 22] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
18 Nagwa M. Fawzy, Sarhan AE, Elhefny EA, Nasef AM, Aly MS. Synthesis, Cytotoxicity Evaluation, and Molecular Docking Studies of Novel Pyrrole Derivatives of Khellin and Visnagin via One-Pot Condensation Reaction with Curcumin. Russ J Bioorg Chem 2020;46:1117-27. [DOI: 10.1134/s1068162020060072] [Reference Citation Analysis]
19 Shen D, Hu Q, Sun J, Pang X, Li X, Lu Y. Effect of oxidized dextran on the stability of gallic acid-modified chitosan-sodium caseinate nanoparticles. Int J Biol Macromol 2021;192:360-8. [PMID: 34634328 DOI: 10.1016/j.ijbiomac.2021.09.209] [Reference Citation Analysis]
20 Chibhabha F, Yang Y, Ying K, Jia F, Zhang Q, Ullah S, Liang Z, Xie M, Li F. Non-invasive optical imaging of retinal Aβ plaques using curcumin loaded polymeric micelles in APPswe/PS1ΔE9 transgenic mice for the diagnosis of Alzheimer's disease. J Mater Chem B 2020;8:7438-52. [PMID: 32662804 DOI: 10.1039/d0tb01101k] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 12.0] [Reference Citation Analysis]
21 Forero-doria O, Guzmán L, Jiménez-aspee F, Echeverría J, Wehinger S, Valenzuela C, Araya-maturana R, Martínez-cifuentes M. An In Vitro and In Silico Study of Antioxidant Properties of Curcuminoid N-alkylpyridinium Salts: Initial Assessment of Their Antitumoral Properties. Antioxidants 2022;11:1104. [DOI: 10.3390/antiox11061104] [Reference Citation Analysis]
22 Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL. Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery. Chem Rev 2021;121:3495-560. [PMID: 33164487 DOI: 10.1021/acs.chemrev.0c00922] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 6.5] [Reference Citation Analysis]
23 Zhao J, Li Y, He D, Hu X, Li K, Yang Q, Fang C, Zhong C, Yang J, Tan Q, Zhang J. Natural Oral Anticancer Medication in Small Ethanol Nanosomes Coated with a Natural Alkaline Polysaccharide. ACS Appl Mater Interfaces 2020;12:16159-67. [PMID: 32186843 DOI: 10.1021/acsami.0c02788] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
24 Nebbioso M, Franzone F, Greco A, Gharbiya M, Bonfiglio V, Polimeni A. Recent Advances and Disputes About Curcumin in Retinal Diseases. Clin Ophthalmol 2021;15:2553-71. [PMID: 34177257 DOI: 10.2147/OPTH.S306706] [Reference Citation Analysis]
25 Shabbir U, Rubab M, Tyagi A, Oh DH. Curcumin and Its Derivatives as Theranostic Agents in Alzheimer's Disease: The Implication of Nanotechnology. Int J Mol Sci 2020;22:E196. [PMID: 33375513 DOI: 10.3390/ijms22010196] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
26 Hosseini-Zare MS, Sarhadi M, Zarei M, Thilagavathi R, Selvam C. Synergistic effects of curcumin and its analogs with other bioactive compounds: A comprehensive review. Eur J Med Chem 2021;210:113072. [PMID: 33310285 DOI: 10.1016/j.ejmech.2020.113072] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
27 Gairola K, Gururani S, Bahuguna A, Garia V, Pujari R, Dubey SK. Natural products targeting cancer stem cells: Implications for cancer chemoprevention and therapeutics. J Food Biochem 2021;45:e13772. [PMID: 34028051 DOI: 10.1111/jfbc.13772] [Reference Citation Analysis]
28 Borges GA, Elias ST, Amorim B, de Lima CL, Coletta RD, Castilho RM, Squarize CH, Guerra ENS. Curcumin downregulates the PI3K-AKT-mTOR pathway and inhibits growth and progression in head and neck cancer cells. Phytother Res 2020;34:3311-24. [PMID: 32628350 DOI: 10.1002/ptr.6780] [Cited by in Crossref: 8] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
29 Insuasty D, García S, Abonia R, Insuasty B, Quiroga J, Nogueras M, Cobo J, Borosky GL, Laali KK. Design, synthesis, and molecular docking study of novel quinoline-based bis-chalcones as potential antitumor agents. Arch Pharm (Weinheim) 2021;354:e2100094. [PMID: 34050547 DOI: 10.1002/ardp.202100094] [Reference Citation Analysis]
30 Vigato AA, Machado IP, del Valle M, da Ana PA, Sepulveda AF, Yokaichiya F, Franco MKKD, Loiola MC, Tófoli GR, Cereda CMS, de Sairre MI, de Araujo DR. Monoketonic Curcuminoid-Lidocaine Co-Deliver Using Thermosensitive Organogels: From Drug Synthesis to Epidermis Structural Studies. Pharmaceutics 2022;14:293. [DOI: 10.3390/pharmaceutics14020293] [Reference Citation Analysis]
31 Panda SS, Girgis AS, Thomas SJ, Capito JE, George RF, Salman A, El-Manawaty MA, Samir A. Synthesis, pharmacological profile and 2D-QSAR studies of curcumin-amino acid conjugates as potential drug candidates. Eur J Med Chem 2020;196:112293. [PMID: 32311607 DOI: 10.1016/j.ejmech.2020.112293] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 4.5] [Reference Citation Analysis]
32 Kong M, Xie K, Lv M, Li J, Yao J, Yan K, Wu X, Xu Y, Ye D. Anti-inflammatory phytochemicals for the treatment of diabetes and its complications: Lessons learned and future promise. Biomed Pharmacother 2021;133:110975. [PMID: 33212375 DOI: 10.1016/j.biopha.2020.110975] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
33 Chainoglou E, Siskos A, Pontiki E, Hadjipavlou-Litina D. Hybridization of Curcumin Analogues with Cinnamic Acid Derivatives as Multi-Target Agents Against Alzheimer's Disease Targets. Molecules 2020;25:E4958. [PMID: 33114751 DOI: 10.3390/molecules25214958] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
34 Lim L, Dang M, Roy A, Kang J, Song J. Curcumin Allosterically Inhibits the Dengue NS2B-NS3 Protease by Disrupting Its Active Conformation. ACS Omega 2020;5:25677-86. [PMID: 33073093 DOI: 10.1021/acsomega.0c00039] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 7.0] [Reference Citation Analysis]
35 Omidi S, Kakanejadifard A. A review on biological activities of Schiff base, hydrazone, and oxime derivatives of curcumin. RSC Adv 2020;10:30186-202. [DOI: 10.1039/d0ra05720g] [Cited by in Crossref: 20] [Cited by in F6Publishing: 7] [Article Influence: 10.0] [Reference Citation Analysis]
36 Roy S, Priyadarshi R, Ezati P, Rhim JW. Curcumin and its uses in active and smart food packaging applications - a comprehensive review. Food Chem 2021;375:131885. [PMID: 34953241 DOI: 10.1016/j.foodchem.2021.131885] [Cited by in Crossref: 18] [Cited by in F6Publishing: 8] [Article Influence: 18.0] [Reference Citation Analysis]
37 Gagandeep, Singh M, Kidawi S, Das US, Velpandian T, Singh R, Rawat DS. Monocarbonyl curcuminoids as antituberculosis agents with their moderate in-vitro metabolic stability on human liver microsomes. J Biochem Mol Toxicol 2021;35:1-10. [PMID: 33751730 DOI: 10.1002/jbt.22754] [Reference Citation Analysis]
38 Peng Y, Ao M, Dong B, Jiang Y, Yu L, Chen Z, Hu C, Xu R. Anti-Inflammatory Effects of Curcumin in the Inflammatory Diseases: Status, Limitations and Countermeasures. Drug Des Devel Ther 2021;15:4503-25. [PMID: 34754179 DOI: 10.2147/DDDT.S327378] [Reference Citation Analysis]
39 Wu Q, Ou H, Shang Y, Zhang X, Wu J, Fan F. Nanoscale Formulations: Incorporating Curcumin into Combination Strategies for the Treatment of Lung Cancer. Drug Des Devel Ther 2021;15:2695-709. [PMID: 34188448 DOI: 10.2147/DDDT.S311107] [Reference Citation Analysis]
40 Allegri P, Cimino L, Davis JL, Tugal-Tutkun I; Norflo Oro study group. Assessment of the Anti-inflammatory Effects of NORFLO® ORO in Acute Relapses of HLA-B27-associated Autoimmune Uveitis: A Multicenter, Randomized, Placebo-controlled, Double-blind Clinical Study. Ocul Immunol Inflamm 2022;:1-10. [PMID: 35353651 DOI: 10.1080/09273948.2022.2039210] [Reference Citation Analysis]
41 Dean Liang, Zhiguo Wen, Wanli Han, Wenming Li, Longfei Pan, Ruipeng Zhang. Curcumin protects against inflammation and lung injury in rats with acute pulmonary embolism with the involvement of microRNA-21/PTEN/NF-κB axis. Mol Cell Biochem 2021;476:2823-35. [PMID: 33730297 DOI: 10.1007/s11010-021-04127-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
42 Razavi MS, Ebrahimnejad P, Fatahi Y, D'Emanuele A, Dinarvand R. Recent Developments of Nanostructures for the Ocular Delivery of Natural Compounds. Front Chem 2022;10:850757. [PMID: 35494641 DOI: 10.3389/fchem.2022.850757] [Reference Citation Analysis]
43 Shabaninejad Z, Pourhanifeh MH, Movahedpour A, Mottaghi R, Nickdasti A, Mortezapour E, Shafiee A, Hajighadimi S, Moradizarmehri S, Sadeghian M, Mousavi SM, Mirzaei H. Therapeutic potentials of curcumin in the treatment of glioblstoma. Eur J Med Chem 2020;188:112040. [PMID: 31927312 DOI: 10.1016/j.ejmech.2020.112040] [Cited by in Crossref: 23] [Cited by in F6Publishing: 21] [Article Influence: 11.5] [Reference Citation Analysis]
44 Chen T, Zhu G, Meng X, Zhang X. Recent developments of small molecules with anti-inflammatory activities for the treatment of acute lung injury. European Journal of Medicinal Chemistry 2020;207:112660. [DOI: 10.1016/j.ejmech.2020.112660] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
45 Chalikonda G, Lee H, Sheik A, Huh YS. Targeting key transcriptional factor STAT3 in colorectal cancer. Mol Cell Biochem 2021;476:3219-28. [PMID: 33866491 DOI: 10.1007/s11010-021-04156-8] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
46 Chen Y, Du F, Tang L, Xu J, Zhao Y, Wu X, Li M, Shen J, Wen Q, Cho CH, Xiao Z. Carboranes as unique pharmacophores in antitumor medicinal chemistry. Mol Ther Oncolytics 2022;24:400-16. [PMID: 35141397 DOI: 10.1016/j.omto.2022.01.005] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
47 Subhedar DD, Shaikh MH, Nagargoje AA, Akolkar SV, Bhansali SG, Sarkar D, Shingate BB. Amide-Linked Monocarbonyl Curcumin Analogues: Efficient Synthesis, Antitubercular Activity and Molecular Docking Study. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2020.1852288] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
48 Benreka S, Zradni F, Madi F, Kirsch G, Kasmi-mir S. Synthesis of thiazolylidenethiazoloquinazolinone hybrids from monocarbonyl curcumin analogues. Characterization, bio-evaluation and DFT study. Journal of Sulfur Chemistry 2022;43:53-77. [DOI: 10.1080/17415993.2021.1971669] [Reference Citation Analysis]
49 Gagandeep, Kumar P, Kandi SK, Mukhopadhyay K, Rawat DS. Synthesis of novel monocarbonyl curcuminoids, evaluation of their efficacy against MRSA, including ex vivo infection model and their mechanistic studies. Eur J Med Chem 2020;195:112276. [PMID: 32279050 DOI: 10.1016/j.ejmech.2020.112276] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
50 Rampogu S, Lee G, Park JS, Lee KW, Kim MO. Molecular Docking and Molecular Dynamics Simulations Discover Curcumin Analogue as a Plausible Dual Inhibitor for SARS-CoV-2. Int J Mol Sci 2022;23:1771. [PMID: 35163692 DOI: 10.3390/ijms23031771] [Reference Citation Analysis]