Synthesis and antimicrobial evaluation of indole containing derivatives of 1,3,4-thiadiazole, 1,2,4-triazole and their open-chain counterparts

被引:0
|
作者
Tsotinis, A
Varvaresou, A
Calogeropoulou, T
SiatraPapastaikoudi, T
Tiligada, A
机构
[1] UNIV ATHENS,DEPT PHARM,DIV PHARMACEUT CHEM,GR-15771 ATHENS,GREECE
[2] NATL HELLEN RES FDN,INST ORGAN & PHARMACEUT CHEM,ATHENS,GREECE
[3] UNIV ATHENS,SCH MED,DEPT EXPT PHARMACOL,GR-15771 ATHENS,GREECE
来源
ARZNEIMITTEL-FORSCHUNG/DRUG RESEARCH | 1997年 / 47卷 / 03期
关键词
indoles; 1,3,4-thiadiazoles, antimicrobial evaluation, synthesis; 1,2,4-triazoles, antimicrobial evaluation, synthesis;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The increasing clinical importance of drug-resistant bacterial pathogens has lent additional urgency to microbiological and antibacterial research. New indolic derivatives of triazoles, thiadiazoles and their respective open-chain thiosemicarbazides were evaluated for antibacterial and antifungal activity. The microorganisms used were the Gram-negative bacteria Escherichia coli ATCC 35218 and Pseudomonas aeruginosa ATCC 27853, the Gram-positive bacteria Staphylococcus aureus ATCC 25923 and Bacillus subtilis BBL 12084 and the yeasts Candida and Saccharomyces cerevisiae ATCC 2366. The most potent compounds were indole derivatives (12a-c) bearing 1,2,4-triazo-thien-5-yl moiety, which exhibit interesting antibacterial and antifungal activities.
引用
收藏
页码:307 / 310
页数:4
相关论文
共 50 条
  • [21] Synthesis and antibacterial activity of substituted thiosemicarbazides and of 1,3,4-thiadiazole or 1,2,4-triazole derivatives
    Spalinska, K
    Foks, H
    Kedzia, A
    Wierzbowska, M
    Kwapisz, E
    Gebska, A
    Ziólkowska-Klinkosz, M
    PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 2006, 181 (03) : 609 - 625
  • [22] Synthesis, Biological Evaluation and In Silico Studies of 1,2,4-Triazole and 1,3,4-Thiadiazole Derivatives as Antiherpetic Agents
    Goma'a, Hebat-Allah M.
    Ghaly, Mariam A.
    Abou-zeid, Laila A.
    Badria, Farid A.
    Shehata, Ihsan A.
    El-Kerdawy, Mohamed M.
    CHEMISTRYSELECT, 2019, 4 (21): : 6421 - 6428
  • [23] Synthesis and Antimicrobial Activities of 1,2,4-Triazole and 1,3,4-Thiadiazole Derivatives of 5-Amino-2-Hydroxybenzoic Acid
    Hussain, Sabir
    Sharma, Jyoti
    Amir, Mohd
    E-JOURNAL OF CHEMISTRY, 2008, 5 (04) : 963 - 968
  • [24] Synthesis and antimicrobial activity of new 1,2,4-triazole, 1,3,4-oxadiazole, 1,3,4-thiadiazole, thiopyrane, thiazolidinone, and azepine derivatives
    Abu-Hashem, Ameen Ali
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2021, 58 (01) : 74 - 92
  • [25] Synthesis of 1,2,4-triazole, 1,3,4-thiadiazole and 1,3,4-oxadiazole derivatives of 6-nitrobenzimidazole
    Xu, PF
    Yang, YP
    Wu, SZ
    Zhang, ZY
    INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 1998, 37 (02): : 127 - 131
  • [26] Synthesis, cytotoxicity and effects of some 1,2,4-triazole and 1,3,4-thiadiazole derivatives on immunocompetent cells
    Mavrova, Anelia Ts.
    Wesselinova, Diana
    Tsenov, Yordan A.
    Denkova, Pavletta
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (01) : 63 - 69
  • [27] Synthesis and Biological Evaluation of Benzoxazolone-Thiosemicarbazide, 1,2,4-Triazole, 1,3,4-Thiadiazole Derivatives as Cholinesterase Inhibitors
    Aslan, Ebru Kocak
    Saglik, Begum Nurpelin
    Ozkay, Yusuf
    Palaska, Erhan
    CHEMISTRYSELECT, 2023, 8 (35):
  • [28] Synthesis characterization and docking studies of 1,3,4-thiadiazole and 1,2,4-triazole containing 3-methoxyquinoxalines
    Rachala, Muralidhar Reddy
    Eppakayala, Laxminarayana
    Ananthoj, Kishre Kumar
    Maringanti, Thirumala Chary
    INDIAN JOURNAL OF CHEMISTRY, 2022, 61 (04): : 438 - 441
  • [29] SYNTHESIS OF 1,2,4-TRIAZOLE AND 1,3,4-THIADIAZOLE DERIVATIVES FROM METHYL 2-METHYLDITHIOCARBAZATE AND HETEROCUMULENES
    MOLINA, P
    TARRAGA, A
    ESPINOSA, A
    SYNTHESIS-STUTTGART, 1989, (12): : 923 - 929
  • [30] 1,3,4-Oxadiazole, 1,3,4-thiadiazole and 1,2,4-triazole derivatives as potential antibacterial agents
    Othman, Adil A.
    Kihel, Mebrouk
    Amara, Sarah
    ARABIAN JOURNAL OF CHEMISTRY, 2019, 12 (07) : 1660 - 1675