Investigations on 3D-structure, properties and antibacterial activity of two new curcumin derivatives
暂无分享,去创建一个
D. Jonathan | G. Usha | M. Krishna Priya | D. Angeline Shirmila | Era. DravidaThendral | A. Anish Fathima | R. Yuvashri
[1] M. Wierzchowski,et al. Enhanced Cytotoxic Activity of PEGylated Curcumin Derivatives: Synthesis, Structure–Activity Evaluation, and Biological Activity , 2023, International journal of molecular sciences.
[2] M. Tahir,et al. Molecular duplexes featuring NH···N, CH···O and CH···π interactions in solid-state self-assembly of triazine-based compounds , 2022, Royal Society Open Science.
[3] Sangdun Choi,et al. Role of Plant-Derived Active Constituents in Cancer Treatment and Their Mechanisms of Action , 2022, Cells.
[4] Z. Zakaria,et al. Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation , 2022, Molecules.
[5] N. Dege,et al. Synthesis, solid state self-assembly driven by antiparallel π⋯π stacking and {⋯H–C–C–F}2 dimer synthons, and in vitro acetyl cholinesterase inhibition activity of phenoxy pendant isatins , 2022, RSC advances.
[6] Qi Zhang,et al. Curcumin combined with photodynamic therapy, promising therapies for the treatment of cancer. , 2021, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[7] S. Dhar,et al. Promising role of curcumin against viral diseases emphasizing COVID-19 management: A review on the mechanistic insights with reference to host-pathogen interaction and immunomodulation , 2021, Journal of Functional Foods.
[8] Yuji Sasanuma,et al. Molecular Design of Aromatic Polythionoesters , 2020, ACS omega.
[9] Yuelan Zhang,et al. Micronized curcumin fabricated by supercritical CO2 to improve antibacterial activity against Pseudomonas aeruginosa , 2020, Artificial cells, nanomedicine, and biotechnology.
[10] B. Revathi,et al. Synthesis, structure elucidation, spectroscopic analysis, thermal and NLO properties of A new piperidine derivative – (4-Methylphenyl) (4-methylpiperidin-1-yl) methanone , 2019, Optics & Laser Technology.
[11] P. Álvarez,et al. Latest in Vitro and in Vivo Assay, Clinical Trials and Patents in Cancer Treatment using Curcumin: A Literature Review , 2018, Nutrition and cancer.
[12] H. Napolitano,et al. The Influence of Methoxy and Ethoxy Groups on Supramolecular Arrangement of Two Methoxy-chalcones , 2017 .
[13] E. Tiekink,et al. 12-(3,4,5-Trimethoxyphenyl)-2,3,4,12-tetrahydro-1H-5-oxatetraphen-1-one: crystal structure and Hirshfeld surface analysis , 2016, Acta crystallographica. Section E, Crystallographic communications.
[14] H. Fun,et al. Crystal structures of 3,5-bis[(E)-3-hydroxybenzylidene]-1-methylpiperidin-4-one and 3,5-bis[(E)-2-chlorobenzylidene]-1-methylpiperidin-4-one , 2015, Acta crystallographica. Section E, Crystallographic communications.
[15] G. Sheldrick. SHELXT – Integrated space-group and crystal-structure determination , 2015, Acta crystallographica. Section A, Foundations and advances.
[16] K. Priyadarsini. The Chemistry of Curcumin: From Extraction to Therapeutic Agent , 2014, Molecules.
[17] P. Wadgaonkar,et al. Processable aromatic polyesters based on bisphenol derived from cashew nut shell liquid: synthesis and characterization , 2014, Journal of Polymer Research.
[18] K. Zandi,et al. A Review on Antibacterial, Antiviral, and Antifungal Activity of Curcumin , 2014, BioMed research international.
[19] P. Ramasamy,et al. Synthesis, crystal growth, structural, spectral, optical, thermal and dielectric studies of a new nonlinear optical material: 4-Hydroxy-l-proline-l-tartaric acid (1:1) ☆ , 2014 .
[20] G. De Sarro,et al. Pharmacokinetic drug-drug interaction and their implication in clinical management , 2013, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.
[21] G. Liang,et al. Discovery and evaluation of piperid-4-one-containing mono-carbonyl analogs of curcumin as anti-inflammatory agents. , 2013, Bioorganic & medicinal chemistry.
[22] Chengguang Zhao,et al. Promising curcumin-based drug design: mono-carbonyl analogues of curcumin (MACs). , 2013, Current pharmaceutical design.
[23] A. Abu Taha,et al. Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety , 2013, Iranian journal of pharmaceutical research : IJPR.
[24] S. Sudha,et al. Spectroscopic (FTIR, FT-Raman, NMR and UV) and molecular structure investigations of 1,5-diphenylpenta-1,4-dien-3-one: A combined experimental and theoretical study , 2012 .
[25] M. K. Kim,et al. Aromatic Hydroxyl Group Plays a Critical Role in Antibacterial Activity of the Curcumin Analogues , 2012, Natural product communications.
[26] N. Škalko-Basnet,et al. Curcumin: An Anti-Inflammatory Molecule from a Curry Spice on the Path to Cancer Treatment , 2011, Molecules.
[27] R. Roden,et al. α,β-Unsaturated carbonyl system of chalcone-based derivatives is responsible for broad inhibition of proteasomal activity and preferential killing of human papilloma virus (HPV) positive cervical cancer cells. , 2011, Journal of medicinal chemistry.
[28] A. Cavalli,et al. Polyamine conjugation of curcumin analogues toward the discovery of mitochondria-directed neuroprotective agents. , 2010, Journal of medicinal chemistry.
[29] D. K. Agrawal,et al. Curcumin and its analogues: Potential anticancer agents , 2009, Medicinal research reviews.
[30] F. Abas,et al. Synthesis and biological evaluation of curcumin-like diarylpentanoid analogues for anti-inflammatory, antioxidant and anti-tyrosinase activities. , 2009, European journal of medicinal chemistry.
[31] Jian Xiao,et al. Exploration and synthesis of curcumin analogues with improved structural stability both in vitro and in vivo as cytotoxic agents. , 2009, Bioorganic & medicinal chemistry.
[32] B. Aggarwal,et al. Biological activities of curcumin and its analogues (Congeners) made by man and Mother Nature. , 2008, Biochemical pharmacology.
[33] Jian Xiao,et al. Synthesis and anti-bacterial properties of mono-carbonyl analogues of curcumin. , 2008, Chemical & pharmaceutical bulletin.
[34] Robert A Newman,et al. Bioavailability of curcumin: problems and promises. , 2007, Molecular pharmaceutics.
[35] B. Aggarwal,et al. Role of pro-oxidants and antioxidants in the anti-inflammatory and apoptotic effects of curcumin (diferuloylmethane). , 2007, Free radical biology & medicine.
[36] Cleidson Valgas,et al. Screening methods to determine antibacterial activity of natural products , 2007 .
[37] K. N. Babu,et al. Curcumin — Biological and Medicinal Properties , 2007 .
[38] B. Aggarwal,et al. Curcumin: Getting Back to the Roots , 2005, Annals of the New York Academy of Sciences.
[39] R. Bonomo,et al. The threat of antibiotic resistance in Gram-negative pathogenic bacteria: beta-lactams in peril! , 2005, Current opinion in microbiology.
[40] R. C. Moellering. Vancomycin-resistant enterococci. , 1998, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[41] Louis J. Farrugia,et al. ORTEP-3 for Windows - a version of ORTEP-III with a Graphical User Interface (GUI) , 1997 .
[42] H. Timmerman,et al. 1,5-Diphenyl-1,4-pentadiene-3-ones and cyclic analogues as antioxidative agents. Synthesis and structure-activity relationship , 1997 .
[43] T. Nakamura,et al. In vitro and in vivo antifungal activities of ER-30346, a novel oral triazole with a broad antifungal spectrum , 1996, Antimicrobial agents and chemotherapy.
[44] M. Shibazaki,et al. YM-47522, a novel antifungal antibiotic produced by Bacillus sp. II. Structure and relative stereochemistry. , 1996, The Journal of antibiotics.
[45] J Davies,et al. Inactivation of antibiotics and the dissemination of resistance genes. , 1994, Science.
[46] Giovanni Luca Cascarano,et al. Completion and refinement of crystal structures with SIR92 , 1993 .
[47] Gautam R. Desiraju,et al. Crystal structures of polynuclear aromatic hydrocarbons. Classification, rationalization and prediction from molecular structure , 1989 .
[48] F. L. Hirshfeld. Bonded-atom fragments for describing molecular charge densities , 1977 .
[49] D. Cremer,et al. General definition of ring puckering coordinates , 1975 .
[50] D. N. Ingebrigtson,et al. Infrared Analysis of Solids by Potassium Bromide Pellet Technique , 1954 .
[51] K. S. Kumar,et al. Turmeric: a herbal and traditional medicine. , 2009 .
[52] N. S. Karthikeyan,et al. Synthesis, crystal structure, and anticancer properties of cyclic monocarbonyl analogs of curcumin , 2009, Medicinal Chemistry Research.
[53] Ricky A. Sharma,et al. Pharmacokinetics and pharmacodynamics of curcumin. , 2007, Advances in experimental medicine and biology.
[54] Jesús Silva Sánchez. [Resistance to antibiotics]. , 2006, Revista latinoamericana de microbiologia.