Academic literature on the topic 'Primary Moiety for The Synthesis of Anti-Inflammatory Agents'

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Journal articles on the topic "Primary Moiety for The Synthesis of Anti-Inflammatory Agents"

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Archana, Singh, Prasad Virendra, Rajkhowa Sanchayita, D. Tripathi Vishwa, and K. Tiwari Vinod. "Synthesis of glycosylated aminothiol from D-glucose as promising anti-tubercular agent." Journal of Indian Chemical Society Vol. 97, Feb 2020 (2020): 213–25. https://doi.org/10.5281/zenodo.5651696.

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Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi-221 005, Uttar Pradesh, India <em>E-mail</em>: tiwari_chem@yahoo.co.in, vinod.tiwari@bhu.ac.in Department of Chemistry, Gauhati University, Guwahati-781 014, Assam, India Department of Chemistry, M. K. College, L. N.Mithila University, Darbhanga-846 004, Bihar, India <em>Manuscript received online 29 September 2019, revised and accepted 18 January 2020</em> A facile method for a series of novel glycosylated &beta;-aminothiols by employing TBAB/NEt<sub>3</sub> -catalyzed ring opening of thiirane ring of D-glucose-
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Sharkey, D. J., та S. A. Robertson. "229.Seminal plasma TGFβ activates pro-inflammatory cytokine synthesis in human cervical epithelial cells". Reproduction, Fertility and Development 16, № 9 (2004): 229. http://dx.doi.org/10.1071/srb04abs229.

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Exposure to semen at intercourse in women elicits an inflammation-like response characterised by recruitment of inflammatory cells and expression of pro-inflammatory cytokines including GM-CSF, interleukin-6 (IL-6) and IL-8 (1). Studies in animal models have implicated TGFβ as the major active moiety in seminal plasma, and we have shown previously that TGFβ1 and TGFβ3 are present in high concentrations in human seminal plasma (&gt;100 ng/mL), while TGFβ2 is less abundant. To investigate the physiological significance of each of the three TGFβ isoforms as pro-inflammatory agents in human semina
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Pei, Shanshan, Kevin Callahan, Mohammad Minhajuddin, et al. "Targeting Redox Homeostasis As a Means to Selectively Eradicate Primary Human Leukemia Cells,." Blood 118, no. 21 (2011): 3506. http://dx.doi.org/10.1182/blood.v118.21.3506.3506.

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Abstract Abstract 3506 Many studies have indicated that induction of oxidative stress is one component of the mechanism by which anti-leukemia agents function. However, little is known about the differences between leukemic and normal redox homeostasis, and whether these agents achieve their selective toxicity to leukemia through specifically targeting leukemic redox homeostasis. Hence, the present study performed a detailed analysis of CD34+ cells derived from normal bone marrow (NBM) or primary acute myelogenous leukemia (AML) specimens. By evaluating the expression profiles of redox regulat
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Madadi, Nikhil R., Narsimha R. Penthala, Amit Ketkar, et al. "Synthesis and Evaluation of 2-Naphthaleno trans-Stilbenes and Cyanostilbenes as Anticancer Agents." Anti-Cancer Agents in Medicinal Chemistry 18, no. 4 (2018): 556–64. http://dx.doi.org/10.2174/1871521409666170412115703.

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Background: Naphthalene is a good structural replacement for the isovanillin moiety (i.e. the 3- hydroxy-4-methoxyphenyl unit) in the combretastatin A-4 molecule, a natural product structurally related to resveratrol, which consistently led to the generation of highly cytotoxic naphthalene analogues when combined with a 3,4,5-trimethoxyphenyl or related aromatic system. Also, the naphthalene ring system is present in many current drug molecules that are utilized for anti-tumor, anti-arrhythmia and antioxidant therapy. Objective: In our continuing quest to improve the potencies of naturally occ
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Allart-Simon, Ingrid, Aurélie Moniot, Nicolo Bisi, et al. "Pyridazinone derivatives as potential anti-inflammatory agents: synthesis and biological evaluation as PDE4 inhibitors." RSC Medicinal Chemistry 12, no. 4 (2021): 584–92. http://dx.doi.org/10.1039/d0md00423e.

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Mamatha, S. V., S. L. Belagali, and Mahesh Bhat. "Synthesis and SAR Evaluation of Mercaptotriazolo derivatives as anti-inflammatory agents." International Journal of ChemTech Research 13, no. 1 (2020): 187–98. http://dx.doi.org/10.20902/ijctr.2019.130123.

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A new series of benzothiazole appended triazole derivatives were synthesized. Characterization is done by FT-IR, Mass, 1H and 13C NMR spectroscopic techniques. The newly synthesized compounds were screened for antioxidant and anti inflammatory activities. Experimental data hypothesized compound 7b as highly potent cytotoxicant with lengthened activity. Structure–activity relation interrelates the biological activity and chemical moiety of the molecule. Structurally, 7b is a benzothiazolyltriazole having a pyrrolidine group (five membered ring) attached to two CH2 groups and methyl substituent
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R. Makwana, Hetal, and Atul H. Makwana. "SYNTHESIS AND CHARACTERIZATION OF 1-(BENZOYL)-4- (ARYLIDENE)-3-METHYL-1H-PYRAZOL-5(4H)-ONES DERIVATIVES AND THEIR BIOLOGICAL ACTIVITIES." RASAYAN Journal of Chemistry 17, no. 04 (2024): 2062–66. https://doi.org/10.31788/rjc.2024.1748574.

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Pyrazole and its derivatives are considered pharmacologically active and itgives various types of biological activities. The presence of this nucleus in pharmacological agents of diverse therapeutic categories such as a potent anti-inflammatory, anti-microbial, andanalgesic, has proved the pharmacological potential of the pyrazole moiety.
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Sahoo, Biswa M., Bera Venkata V. Ravi Kumar, Bimal K. Banik, and Preetismita Borah. "Green Efficient Synthesis of Oxadiazole Derivatives as Analgesic and Antiinflammatory Agents." Current Green Chemistry 7, no. 2 (2020): 163–78. http://dx.doi.org/10.2174/2213346107999200427080057.

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Non-steroidal anti-inflammatory drugs (NSAIDs) act as a major class of therapeutic agents. The biological activity of NSAIDs is due to the suppression of prostaglandin biosynthesis by inhibiting cyclooxygenase (COX) enzyme. COX is an endogenous enzyme, which catalyzes the conversion of arachidonic acid into prostaglandins. But the significant side effect by NSAIDs is the formation of gastric ulcers, irritation and GI bleeding. Therefore, alternative drugs that can overcome these limitations are necessary. Towards the goal, oxadiazole derivatives are designed and synthesized following a green c
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Vlachou, Evangelia-Eirini N., and Konstantinos E. Litinas. "An Overview on Pyranocoumarins: Synthesis and Biological Activities." Current Organic Chemistry 23, no. 24 (2020): 2679–721. http://dx.doi.org/10.2174/1385272823666191025151236.

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Pyrano- and dipyranocoumarins are classes of naturally occurring organic compounds with very interesting biological activities. This review focuses on the synthetic strategies for the synthesis of pyranocoumarins and dipyranocoumarins and the biological properties of those compounds. The synthesis involves the formation of the pyran ring, at first, from a coumarin or the formation of pyranone moiety from an existing pyran. Pyranocoumarins and dipyranocoumarins present anti-HIV, anti-cancer, neuroprotective, antidiabetic, antibacterial, antifungal, anti-inflammatory activities. Especially khell
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Vashisht, Ketan, Pooja Sethi, Anshul Bansal, et al. "Path of Pyrazoles from Synthetic Factors to Anti-inflammatory Potential: A Review." Asian Journal of Chemistry 36, no. 6 (2024): 1217–31. http://dx.doi.org/10.14233/ajchem.2024.31652.

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Pyrazoles, a class of heterocyclic compounds, have garnered considerable attention in drug development due to their intriguing properties, particularly those containing a pyrazole moiety. Pyrazole, a pivotal chemical in the creation of potent bioactive agents, encompasses five heterocyclic members. The discovery of certain pyrazole compounds exhibiting robust biological activities has spurred interest in this field of inquiry. Heterocyclic compounds incorporating nitrogen and its derivatives have historically served as crucial sources of medicinal compounds. Given that the heterocyclic group c
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Book chapters on the topic "Primary Moiety for The Synthesis of Anti-Inflammatory Agents"

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Tiwari, Aditi, Anjaneyulu Bendi, and Anirudh Singh Bhathiwal. "Carbazoles and their Derivatives as Anti-inflammatory agents." In Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815223460124010010.

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Heterocyclic compounds refer to a defining class of organic compounds with vast biological applications. Heterocyclic compounds are of great significance to life for the reason that they are abundantly present in nature, such as in the form of antibiotics, hormones, vitamins, and many more. Among heterocyclic compounds, nitrogen-based heterocycles are of special biological use because of their boundless medicinal and biological applications. Carbazoles are one of several nitrogen-based, biologically active heterocyclic compounds with the chemical formula C12H9N. Carbazole moiety has diverse ph
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"multiple donors. Three women had normal pregnancies and deliveries at term. Several groups have replicated this work with spouse leukocytes and successful deliveries result in more than 50% of the women treated. Crohn's Disease Crohn's disease is an inflammatory condition of the gastrointestinal tract which presents with diarrhea and crampy abdominal pain. Recurrence of disease following surgery is common -nearly half of the patients will develop symptoms of recurrence within ten years of surgical resection of all diseased bowel. Immune function is abnormal and patients are often treated with immunosuppressive steroids. Transfused patients have significantly decreased total lymphocyte and t-cell counts following surgery despite being clinically well. Increasing numbers of units of blood received are associated with progressively lower numbers of lymphocytes at follow-up. Several groups have studied the effect of blood transfusion on the outcome Crohn's disease because the immunosuppressive effects of transfusion might benefit patients in the same way steroids affect the course to the disease. Most of the studies observed that untransfused patients exhibited higher rates of recurrence than transfused patients (37-40). The studies suggest that transfusion may influence the course of diseases which are thought to have an immune or autoimmune basis and clinically respond to steroids. Crohn's disease patients with more severe disease, those with lower hemoglobins and serum albumins, undergoing resection of more bowel, should have higher recurrence rates. Yet, these patients when transfused have recurrence rates comparable to untransfused patients with higher hemoglobins and albumins and less bowel resected. Wound Healing It has recently been recognized that lymphocytes contribute to wound healing which is primarily mediated by macrophages. Lymphocytes secrete lymphokines which enhance fibroblast replication, migration and collagen synthesis. In vivo depletion of lymphocytes impairs skin wound healing. Since transfusions inhibit lymphocyte function, transfusion-induced inhibition of lymphocyte function should lead to impaired wound healing (41). Rats undergoing ileocolic resection with primary anastomosis and transfusion with saline, syngeneic or allogeneic blood were sacrificed three and seven days following surgery and the bursting pressure of the anastomosis measured. Bursting pressure was significantly lower following transfusion with syngeneic or allogeneic blood in comparison to saline. Hydroxyproline content of the anastomoses was reduced and anastomotic abscesses were common in the transfused animals. This study clearly implicates blood transfusion in impaired wound healing. D iabetes In man, insulin dependent diabetes mellitus is associated with decreases in both the number and functional activity of suppresser T lymphocytes. In the Bio-Breeding rat, diabetes develops when the animals develop pancreatic insulitis, suggesting a cell-mediated immune pathogenesis. Diabetes is prevented in these animals by treating them with immunosuppressive agents such as anti-lymphocyte serum, steroids, cyclosporin, irradiation, neonatal thymectomy, or blood transfusion (42)." In Transfusion Immunology and Medicine. CRC Press, 1995. http://dx.doi.org/10.1201/9781482273441-28.

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Conference papers on the topic "Primary Moiety for The Synthesis of Anti-Inflammatory Agents"

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van den Berg, E. A., E. Sprengers, M. Jaye, W. Burgess, and V. W. M. van Hinsbergh. "REGULATION OF PLASMINOGEN ACTIVATOR INHIBITOR-1 mRNA IN HUMAN ENDOTHELIAL CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642856.

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Cultured human endothelial cells (HEC) increase their production of plasminogen activator inhibitor (PAI-1) upon stimulation with endotoxin and IL-1, agents that are known to cause an increase in PAI-1 levels in vivo. In order to study the regulation of PAI-1 synthesis at the mRNA level, we isolated a cDNA clone for the human PAI-1 gene from an endothelial expression cDNA library in λ gt 11 by screening with a PAI-1 specific antibody. Three positive cross-hybridizing clones were isolated. The longest insert (1500 bp) was partially sequenced (1000 bp). The sequence was identical to the PAI-1 se
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