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Готові списки джерел за темами / Thiozolidinone

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Добірка наукової літератури з теми "Thiozolidinone"

Автор: Grafiati

Опубліковано: 3 червня 2025

Оновлено: 31 липня 2025

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Статті в журналах з теми "Thiozolidinone"

1

Dakshayini, Chandrashekarachar1 Devaraju Kesagudu*2. "IMPORTANCE OF FURAN BASED COMPOUNDS AND THEIR BIOMEDICAL APPLICATIONS: AN OVERVIEW." INDO AMERICAN JOURNAL OF PHARMACEUTICAL RESEARCH 07, no. 01 (2017): 7541–449. https://doi.org/10.5281/zenodo.1007303.

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Furan based substituted compounds showed very promising biomaterials such as antimicrobial, anti cancer, antihyperglucemic and analgesic. The poly substituted compounds are employed as building blocks of synthesis of naturally occurring biomaterials which are important in medicinal chemistry. Some of the Benzo furan substituted compounds placed role in asthma, rheumatism and ulcers, Immune nanoparticle of furan based polymeric nanoparticle of biodegradable graft co-polymer to provide a reactive functional group for coupling chemistry of antibodies through Diels-Alder chemistry. Here we enlight

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2

Ekram Abdullah Basheer, Kalid Matny Al-jaanaby, and Feras Shauki Al-joboury. "Synthesis a Number of Heterocyclic Compounds Derived From Levofloxacin." Tikrit Journal of Pure Science 20, no. 5 (2023): 84–95. http://dx.doi.org/10.25130/tjps.v20i5.1244.

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In this paper, the preparation a number of heterocyclic compounds five membered rings like oxadiazole, imidazolidine, thiozolidine, tetrazole, azetidine 2-on. Hydrazide (1) was synthesized from the reaction of levofloxacin with hydrazine hydrate. Hydrazone compounds (2-9) were synthesized from the reaction (1) with a number of aldehydes, and 3-acetyl-1,3,4-oxadiazol (10-17) was prepared from the reaction of hydrazones (2-9) with acetic anhydride, 5-oxo-2-aryl imadazoldine derivative (18-25) were prepared from the reaction of hydrazone derivatives (2-9) with glycine, while the reaction of hydra

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3

Vellalacheruvu, Ramakrishna, Ramayanam Sai Leela, and L. K. Ravindranath. "Novel Route for Synthesis of Thiozolidine-2,4-Dione Derivatives as a Mannich Base." International Journal of Organic Chemistry 07, no. 03 (2017): 269–83. http://dx.doi.org/10.4236/ijoc.2017.73021.

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4

Mishra, Kunj B., Anand K. Agrahari, and Vinod K. Tiwari. "One-pot synthesis of oxazolidine-2-thione and thiozolidine-2-thione from sugar azido-alcohols." Carbohydrate Research 450 (October 2017): 1–9. http://dx.doi.org/10.1016/j.carres.2017.08.002.

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5

Singh, U., A. Verma, and H. R. Bhat. "Discovery of novel 1,3,5-triazine-thiozolidine (DDDL-251) based dual PI3K/mTOR inhibitor against breast cancer." Annals of Oncology 28 (November 2017): x3. http://dx.doi.org/10.1093/annonc/mdx652.007.

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6

SAMIA, R. EL-EZBAWY, and A. ALSHAIKH MONIRA. "Synthesis and Antibacterial Activity of New Diaryisulphicles containing Quinolyl, Pyrryl, 4-Thiazolidinone and/or Azetidin-2-one Moieties." Journal of Indian Chemical Society Vol. 67, May 1990 (1990): 398–400. https://doi.org/10.5281/zenodo.6163557.

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Анотація:

Chemistry Department, Faculty of Science, Assiut University, Assiut, Egypt Chemistry Department, Girls College of Education, Jeddah, Saudi Arabia <em>Manuscript received 3 August 1989, accepted 1 January 1990</em> Condensation of quinoline-4-carboxaldehyde and/or pyrrole-2-carboxaldebyde with 4-a minodiaryl sulphides (1) gave 4-[<em>N</em>-(ρ-(diarylthio] formimidoyliquinolines (2) and 2-[<em>N</em>-(ρ-(diarylthio)]formimidoyl]pyrroles (3) in good yields. Cyclocondensation of mercaptoacetic acid with azometbines yielded 3-[ρ-(diarylthio]-244-quinoly1)-4- thiazolidinone (4) and 3-[&

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7

Hindi, Shymaa A., and Sahar S. Hassan. "Synthesis, Characterization and Theoretical Treatments for Complexes of Co+2, Ni+2, Zn+2 and Cd+2 Ions with Mixed Ligands of Cef and Glycine." Research Journal of Chemistry and Environment 28, no. 8 (2024): 66–80. http://dx.doi.org/10.25303/288rjce066080.

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Анотація:

Metal complexes of mixed ligands were prepared from a derivative of Cefepime and the amino acid glycine. The suggested structures of metal complexes of Cefepime derivatives and glycine with Co+2, Ni+2, Cu+2, Zn+2 and Cd+2 results were characterized by the Fourier-transform infrared spectroscopy, UV–visible spectroscopy and 1HNMR spectrum (300 MHZ, DMSO-d6), micro elemental analysis, magnetic moment, conductivity etc. The obtained results suggested that Cefepime reacted with metal ions as a bidentate ligand through the nitrogen of the β-lactam thiozolidine and carboxylate ion forming a five-mem

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8

Laohakunjit, Natta, Orapin Kerdchoechuen, Frank B. Matta, Juan L. Silva, and William E. Holmes. "Postharvest Survey of Volatile Compounds in Five Tropical Fruits Using Headspace-solid Phase Microextraction (HS-SPME)." HortScience 42, no. 2 (2007): 309–14. http://dx.doi.org/10.21273/hortsci.42.2.309.

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The volatiles of longon (Lansium domesticum Corr. var Dongon), mangosteen (Garcinia mangostana L. var Native), durian (Durio zibethinus L. var Monthong), rambutan (Nephelium lappaceum L. var Rong-rien), and sapodilla (Manilkara zapota van Royer var Kai) were identified by headspace-solid phase microextraction with the gas chromatography-mass spectrometry technique. The headspace volatiles of fresh, unheated, salted out with NaCl, and NaCl + heated samples were determined. Salting out gave the highest number of volatile components with the longon headspace. High temperature did not have much af

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9

Akram Hassan, Nadeem, and Muthanna Saadi Farhan. "Synthesis, Characterization and Anti-Inflammatory Evaluation of New Amino Acids Derivatives of Naproxen." Research Journal of Pharmacy and Technology, August 26, 2024, 3560–66. http://dx.doi.org/10.52711/0974-360x.2024.00556.

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Анотація:

Naproxen is well known as a nonsteroidal anti-inflammatory agent that belongs to propionic acid analogs and has the non-selective inhibitory property for both COX1 and COX2, and its side effects belong to the non-selective inhibitory of COX1 in addition to the anti-inflammatory action via COX2 inhibitory. The study aimed to design and synthesize a new Schiff baseof benzaldehyde and thiozolidinone derivative with amino acids spacers like Phenylalanine analogs P4, and Histidine (H5). In silico, the study design was done via auto dock vina soft wave and visualized by UCSF chimera. All analogs sho

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10

Tongkhan, Sukanya, Widchaya Radchatawedchakoon, Senee Kruanetr, and Uthai Sakee. "Design, Synthesis, and Bioactivity Assessment of Novel 2‐Phenyl Indole Derivatives Incorporating 4‐Thiazolidinone‐5‐carboxylic Acid as Promising Anti‐cancer Agents." ChemistrySelect 8, no. 45 (2023). http://dx.doi.org/10.1002/slct.202303591.

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Анотація:

AbstractWe conducted a study to create new chemical compounds using indole derivatives, specifically incorporating thiosemicarbazone (8 a–e) and 4‐thiozolidinone‐5‐carboxylic acid (9 a–e) structures. We then tested these compounds against various bacteria and cancer cells. In our antibacterial tests, the compounds showed moderate inhibitory effects on bacterial growth. However, when we examined their effects on cancer cells, we observed specific patterns of activity. Notably, compounds 9 c and 9 d were highly toxic to NCI‐H187 cancer cells, while compounds 8 c, 9 b, 9 c, 9 d, and 9 e exhibited

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Дисертації з теми "Thiozolidinone"

1

Abdillahi, Ismail. "Synthèse des pyrimidinones, des 1,3-thiazolidin-4-ones et des thiéno [3,2-d] [1,3] thiazoles à partir d'analogues thiophéniques d'acide anthranilique." Thesis, Metz, 2011. http://www.theses.fr/2011METZ003S/document.

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Анотація:

Dans le cadre de recherches sur les analogues thiophéniques de l’acide anthranilique, nous avons préparé ceux-ci soit au départ de béta-chloroacrylonitriles par une suite de condensation et de cyclisation, soit à partir de dérivés cétoniques en utilisant la méthode de Gewald. L’accès aux béta-chloroacrylonitriles béta-substitués utilise une séquence réactionnelle développée au laboratoire. Nous avons ensuite utilisé la présence de fonction amine ou acide (sous forme d’ester) pour la synthèse des systèmes condensés tels les pyrimidinones par condensation avec le chlorhydrate de chloroformamide,

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