Two naphthalene-containing compounds, 4-hydroxy-6,7-dimethoxy-1-(4-(trifluoromethyl)phenyl)-2-naphthoic acid (A) and 4-hydroxy-6,7-dimethoxy-1-phenyl-2-naphthoic acid (B), were prepared by several steps. Their bindings to human serum albumin (HSA) were studied by ultraviolet-visible (UV-vis) absorption, fluorescence, synchronous fluorescence, three-dimensional fluorescence, circular dichroism (CD) spectroscopies and molecular docking. The crystal data of these compounds show the structure of the compounds. The results show that the mechanism of the interaction between compound A and HSA is mixed-quenching (both dynamic and static quenching), while that of compound B and HSA is static quenching. The number of binding sites, binding constants and binding distance () were obtained. The interaction processes are spontaneous. A mainly interacts with HSA through typical hydrophobic interaction, and B binds to HSA mainly by the hydrogen bonds and van der Waals forces. The conformation of HSA changes slightly after the addition of the compounds. Besides, molecular docking method was used to study the interaction details between the compounds and HSA. This is helpful to understand the absorption and metabolism of these two compounds in the body, and provides a basis for designing naphthalene-containing drugs. Communicated by Ramaswamy H. Sarma.
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http://dx.doi.org/10.1080/07391102.2020.1764867 | DOI Listing |
Inorg Chem
June 2024
Department of Chemistry, Georgetown University, Washington, District of Columbia 20057, United States of America.
Three novel bismuth-organic compounds, with the general formula [Bi(HPDC)(PDC)]·(arene)·2HO (HPDC = 2,6-pyridinedicarboxylic acid; arene = pyrene, naphthalene, and azulene), that consist of neutral dinuclear Bi-pyridinedicarboxylate complexes and outer coordination sphere arene molecules were synthesized and structurally characterized. The structures of all three phases exhibit strong π-π stacking interactions between the Bi-bound PDC/HPDC and outer sphere organic molecules; these interactions effectively sandwich the arene molecules between bismuth complexes and thereby prevent molecular vibrations. Upon UV irradiation, the compounds containing pyrene and naphthalene displayed red and green emission, respectively, with quantum yields of 1.
View Article and Find Full Text PDFNat Chem
August 2024
Key Laboratory of Molecule Synthesis and Function Discovery, Fujian Province University, College of Chemistry at Fuzhou University, Fuzhou, Fujian, China.
Bioisosteric replacement has emerged as a clear strategy for drug-structure optimization. Naphthalene is the core element of many chiral pharmaceuticals and drug candidates. However, as a promising isostere of naphthalene, the chiral version of 1,2-benzazaborine has rarely been explored due to the lack of efficient synthetic methods.
View Article and Find Full Text PDFComb Chem High Throughput Screen
April 2024
Department of Pharmaceutical Sciences and Natural Products, Central University of Punjab, Ghudda, Bathinda, 151401, India.
Aim: Design, synthesis and molecular docking studies of quinoline/naphthalene containing pyrazoline derivatives as PI3K inhibitors.
Background: Phosphatidylinositol 3-kinases (PI3Ks) belong to the family of enzymes, which are associated with various cellular functions such as cell growth, proliferation, differentiation etc. Overexpression or any changes in these functions may result in various abnormalities, which in turn cause cancer.
Phytochemistry
December 2022
H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan; Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Crystals of previously described para-naphthoquinone abietane diterpenoids 12,16-dideoxy-aegyptinone B and 12-deoxy-salvipisone were obtained from Zhumeria majdae Rech.f. & Wendelbo.
View Article and Find Full Text PDFMolecules
November 2020
Department of Medicinal Chemistry, Faculty of Pharmacy, Minia University, El Minia 61519, Egypt.
Three new series of paracyclophanyl-dihydronaphtho[2,3-]thiazoles and paracyclophanyl-thiazolium bromides were designed, synthesized, and characterized by their spectroscopic data, along with X-ray analysis. One-dose assay results of anticancer activity indicated that - had the highest ability to inhibit the proliferation of different cancer cell lines. Moreover, the hybrids - were selected for five-dose analyses to demonstrate a broad spectrum of antitumor activity without apparent selectivity.
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