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  • 1
    Online Resource
    Online Resource
    Wiley ; 2020
    In:  Journal of Heterocyclic Chemistry Vol. 57, No. 1 ( 2020-01), p. 428-435
    In: Journal of Heterocyclic Chemistry, Wiley, Vol. 57, No. 1 ( 2020-01), p. 428-435
    Abstract: A novel series of 11 C‐3– and N‐1–substituted oxoacetamide indole derivatives were synthesized by reacting with various aromatic amines and alkyl halides. These compounds were characterized by using various spectral techniques, ie , 1 HNMR, 1 HNMR‐D 2 O, 13 CNMR, UV, elemental analysis, IR, and mass spectrometery. In vitro , antimicrobial studies of resultant compounds were carried out against two bacterial strains, Pseudomonas aeruginosa and Pseudomonas oryzihabitans using disc plate method. All the tested compounds showed vital efficiency as antimicrobial agents against both the bacterial strains. The results revealed that synthesized indole derivative 2‐(1‐(3‐bromopropyl)‐1 H ‐indol‐3‐yl)‐ N ‐(2‐nitrophenyl)‐2‐oxoacetamide displayed the best antimicrobial activity as compared with all other synthesized compounds.
    Type of Medium: Online Resource
    ISSN: 0022-152X , 1943-5193
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2042274-X
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  • 2
    Online Resource
    Online Resource
    Diva Enterprises Private Limited ; 2022
    In:  Agricultural Research Journal Vol. 59, No. 5 ( 2022), p. 945-952
    In: Agricultural Research Journal, Diva Enterprises Private Limited, Vol. 59, No. 5 ( 2022), p. 945-952
    Type of Medium: Online Resource
    ISSN: 2395-1435 , 2395-146X
    Language: English
    Publisher: Diva Enterprises Private Limited
    Publication Date: 2022
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  • 3
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2024
    In:  Mini-Reviews in Organic Chemistry Vol. 21, No. 4 ( 2024-06), p. 477-493
    In: Mini-Reviews in Organic Chemistry, Bentham Science Publishers Ltd., Vol. 21, No. 4 ( 2024-06), p. 477-493
    Abstract: Natural products are secondary metabolites obtained from plants, animals, and microorganisms with diverse chemical structures resulting in diverse biological functions and drug-like properties. Objective: This review article summarizes in detail the occurrence, detection, isolation, various pharmacological properties, metabolism, and toxicity of a natural compound i.e., 5-Allyl-1-methoxy- 2,3-methylenedioxybenzene commonly known as Myristicin. Methods: A relevant literature search was made using the keywords essential oil, mace, myristicin, nutmeg, and pharmacological activities from different databases such as PubMed, Sci Finder, Science Direct, and Google Scholar. The literature search results presented articles from 1963 to 2022. Thereafter, the articles were carefully screened and selected for review. Results: Myristicin, an alkoxy-substituted allylbenzene is present in major to minor amounts in the essential oils obtained from different plant parts and exhibits various pharmacological properties such as antimicrobial, antioxidant, antiproliferative, anti-inflammatory, insecticidal, and hepatoprotective. It forms 10 metabolites by reduction, demethylation, hydroxylation, ring formation, ring-opening, and conjugate formation. In the liver, myristicin has been metabolized by Cytochrome P450 complex enzymes to generate active metabolite (1ˈ hyroxymyristicin) responsible for cytotoxic, genotoxic and apoptotic effects (150 μM). But, myristicin at 600 μM does not produce enough 1ʼ-hydroxymyristicin to give the final toxicant. Conclusion: Myristicin poses no major risk to human health through the consumption of herbs and spices due to its presence in low amounts. It has great potential to be used in the traditional system of medicine. We hope that this review will provide complete knowledge about myristicin on a single platform.
    Type of Medium: Online Resource
    ISSN: 1570-193X
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2024
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  • 4
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2016
    In:  Current Organic Synthesis Vol. 13, No. 4 ( 2016-08-10), p. 484-503
    In: Current Organic Synthesis, Bentham Science Publishers Ltd., Vol. 13, No. 4 ( 2016-08-10), p. 484-503
    Type of Medium: Online Resource
    ISSN: 1570-1794
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2016
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  • 5
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2023
    In:  Current Organic Chemistry Vol. 27, No. 11 ( 2023-06), p. 941-961
    In: Current Organic Chemistry, Bentham Science Publishers Ltd., Vol. 27, No. 11 ( 2023-06), p. 941-961
    Abstract: Heterocyclic compounds containing nitrogen have emerged as crucial entities in the realm of medicinal chemistry. Among these, Schiff bases derived from indole or compounds incorporating an indole moiety have demonstrated a wide range of biological properties, including antibacterial, anticancer, antitumor and antimicrobial activities. The diverse characteristics exhibited by Schiff bases have stimulated the exploration of their antimicrobial potential, with the aim of developing more effective drugs to save precious lives. This review article focuses on the synthesis of various Schiff bases derived from the indole moiety and their antimicrobial activities. The extensive body of work in synthesizing these Schiff bases and evaluating their antimicrobial properties is comprehensively discussed. The insights provided in this review can serve as a valuable resource for researchers engaged in the development of efficient drugs.
    Type of Medium: Online Resource
    ISSN: 1385-2728
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2023
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  • 6
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2018
    In:  Letters in Organic Chemistry Vol. 15, No. 10 ( 2018-08-08), p. 870-877
    In: Letters in Organic Chemistry, Bentham Science Publishers Ltd., Vol. 15, No. 10 ( 2018-08-08), p. 870-877
    Type of Medium: Online Resource
    ISSN: 1570-1786
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2018
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  • 7
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2020
    In:  Current Organic Chemistry Vol. 24, No. 23 ( 2020-12-28), p. 2755-2781
    In: Current Organic Chemistry, Bentham Science Publishers Ltd., Vol. 24, No. 23 ( 2020-12-28), p. 2755-2781
    Abstract: Owing to the growing demand for compelling antimicrobial agents, chalcones and their heterocyclic derivatives have engrossed prodigious attention of medicinal chemists as an effective clinical template for the synthesis of such agents on account of their structural diversity and molecular flexibility. Chalcones are considered as a fortunate scaffold in the field of both synthetic as well as natural product chemistry. They are reflected as a remarkable section of logically occurring pharmacophores that possess a comprehensive scale of biological activities, such as anti-cancer, anti-malarial, anti-viral and anti-inflammatory, rendering them with a high degree of assortment and noble therapeutic profile. They act as a crucial intermediate for the synthesis of novel heterocyclic skeletons holding biodynamic behavior. This review emphasizes on different aspects of chalcones including their natural sources, recent synthetic methodologies and evaluation of their anti-microbial potential. It is expected as a persuasive compilation on chalcones that may benefit the experts to design potent and less toxic chalcone referents as medicinal agents.
    Type of Medium: Online Resource
    ISSN: 1385-2728
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2020
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  • 8
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2022
    In:  Current Organic Chemistry Vol. 26, No. 7 ( 2022-04), p. 651-678
    In: Current Organic Chemistry, Bentham Science Publishers Ltd., Vol. 26, No. 7 ( 2022-04), p. 651-678
    Abstract: Heterocycles constitute a wider class of organic compounds which contribute significantly to every facet of pure and applied chemistry. Indole, one of the bicyclic heterocyclic compounds containing nitrogen atom, witnessed unparalleled biological activity such as antiviral, antibacterial, anticancer, anti-depressant and antifungal activities. Different biological activities exhibited by indole derivatives provide the impulsion to explore its activity against anti-phytopathogenic microbes to save the plants from pests and disease, as food security will once again become a rigid demand. This review mainly focuses on various methods related to the synthesis of indole derivatives and its role in agriculture.
    Type of Medium: Online Resource
    ISSN: 1385-2728
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2022
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  • 9
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2019
    In:  Current Organic Synthesis Vol. 16, No. 1 ( 2019-02-04), p. 17-37
    In: Current Organic Synthesis, Bentham Science Publishers Ltd., Vol. 16, No. 1 ( 2019-02-04), p. 17-37
    Abstract: Heterocyclic compounds containing nitrogen have been known to possess a very important role in the field of medicinal chemistry. Indole and its derivatives displayed a wide range of biological properties such as anti-inflammatory, analgesic, anti-microbial, anti-convulsant, antidepressant, anti-diabetic, antihelmintic and anti-allergic activities etc. The diverse biological activities exhibited by compounds containing indole moiety has provided the impetus to explore its anti-microbial activity in order to save the valuable life of patients. 〈 /P 〉 〈 P 〉 Objective: The review focuses on the advances in the synthesis of indole derivatives and antimicrobial properties exhibited by them. Conclusion: A great deal of work has been done in order to synthesize indole derivatives and to evaluate antimicrobial potential, as indicated by the review. The information provided in this article may be helpful for the researchers for the development of efficient antimicrobial drugs.
    Type of Medium: Online Resource
    ISSN: 1570-1794
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2019
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  • 10
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2022
    In:  Current Organic Synthesis Vol. 19, No. 1 ( 2022-02), p. 31-55
    In: Current Organic Synthesis, Bentham Science Publishers Ltd., Vol. 19, No. 1 ( 2022-02), p. 31-55
    Abstract: Barbituric acid and its derivatives have gained significant attention for several years as an indispensable class of compounds in the pharmaceutical industry due to their various biological activities, such as anticonvulsants, hypnotics, anti-diabetic, antiviral, anti-AIDS, anti-cancer, anti-microbial, and antioxidant, etc. A plethora of studies has shed light on the properties, synthesis, and reactivity of these compounds. The depiction of multiple biological activities by barbiturates compelled us, and by virtue of which herein we have mediated over the progress of synthesis of numerous kinds of compounds derived from barbituric acid with well-known and typical examples from 2016 to the present. Objective: This review focuses on the advancements in methods of synthesis of barbituric acid derivatives and their applications as antimicrobial agents. Conclusion: This review will help future researchers to analyze the previous studies and explore new compounds for the development of efficient antimicrobial drugs.
    Type of Medium: Online Resource
    ISSN: 1570-1794
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2022
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