Thiazole - A promising scaffold for antituberculosis agents and structure-activity relationships studies

被引:0
|
作者
Zhao, Xuanming [1 ]
Di, Jing [2 ]
Luo, Dingjie [3 ]
Verma, Rameshwari [4 ]
Verma, Santosh Kumar [4 ]
Verma, Shekhar [5 ]
Ravindar, Lekkala [6 ]
Koshle, Anubhuti [7 ]
Dewangan, Hitesh Kumar [7 ]
Gupta, Raksha [7 ]
Chandra, Sunita [7 ]
Deshpande, Samta [8 ]
Kamal [9 ]
Vaishnav, Yogesh [5 ]
Rakesh, Kadalipura P. [10 ]
机构
[1] Yulin Univ, Energy Engn Coll, Yulin 71900, Peoples R China
[2] Yulin Univ, Phys Educ Coll, Yulin 71900, Peoples R China
[3] Xian Traff Engn Inst, Sch Humanities & Management, Xian 710000, Peoples R China
[4] Yulin Univ, Sch Chem & Chem Engn, Yulin 719000, Shaanxi, Peoples R China
[5] Guru Ghasidas Vishwavidyalaya, Dept Pharm, Bilaspur 495009, Chhattisgarh, India
[6] Univ Kebangsaan Malaysia, Fac Sci & Technol, Dept Chem Sci, Bangi 43600, Selangor, Malaysia
[7] Shri Rawatpura Sarkar Univ, Dept Chem, Raipur 492015, Chhattisgarh, India
[8] Shri Shankaracharya Tech Campus, Dept Appl Phys, Bhilai Durg 490020, Chhattisgarh, India
[9] Indian Inst Technol Jammu, Dept Chem, Jammu 181221, India
[10] Univ North Carolina Chapel Hill, Biomed Res Imaging Ctr, Dept Radiol, Chapel Hill, NC 27599 USA
关键词
Thiazole; Heterocyclic; In vitro; In vivo; Antituberculosis; SAR; Drugs; IN-SILICO; ANTIMICROBIAL ACTIVITY; DRUG DISCOVERY; DERIVATIVES; DESIGN; TUBERCULOSIS; INHIBITORS; ANTIBACTERIAL; TOXICITY; SULFONYL;
D O I
10.1016/j.bioorg.2024.108035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Research on thiazole derivatives has been a popular topic in medicine and one of the most active fields in heterocyclic chemistry. Pharmacological and industrial researchers have been studying thiazole-containing derivatives in great detail because they have a lot of biological uses. These compounds are one of the best examples of a five-membered heterocyclic compound that has a lot of potential and has had a lot of success in recent decades. Investigating viable hybrid designs utilizing thiazole is critical for the development of new antituberculosis medications. This article offers a thorough overview of the latest advancements in thiazolecontaining hybrids, offering potential therapeutic applications as anti-TB drugs. We also discussed the structure-activity correlations (SAR) of the powerful thiazole moiety and its several functional groups, along with a few potential molecular targets.
引用
收藏
页数:15
相关论文
共 50 条
  • [21] STRUCTURE-ACTIVITY RELATIONSHIPS OF BENZOTHIADIAZINE COMPOUNDS AS HYPERGLYCEMIC AGENTS
    WALES, JK
    KREES, SV
    GRANT, AM
    VIKTORA, JK
    WOLFF, FW
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 1968, 164 (02): : 421 - &
  • [22] Structure-activity relationships of silybin derivatives as anticancer agents
    Vue, Bao
    Zhang, Sheng
    Parisis, Konstantinos
    Chen, Qiaohong
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 250
  • [23] Structure-activity relationship studies of thiazole agents with potential anti methicillin-resistance Staphylococcus aureus (MRSA) activity
    Wang, Jing
    Long, Sihui
    Liu, Ziwei
    Rakesh, Kadalipura P.
    Verma, Rameshwari
    Verma, Santosh Kumar
    Kumar, Kothanahally S. Sharath
    PROCESS BIOCHEMISTRY, 2023, 132 : 13 - 29
  • [24] FURTHER STUDIES IN STRUCTURE-ACTIVITY RELATIONSHIPS OF HEMICHOLINIUMS
    HAARSTAD, VB
    SEIBOLD, CT
    ZACHARIS, H
    PHARMACOLOGIST, 1971, 13 (02): : 283 - &
  • [25] Structure-activity relationships, biological evaluation and structural studies of novel pyrrolonaphthoxazepines as antitumor agents
    Brindisi, Margherita
    Ulivieri, Cristina
    Alfano, Gloria
    Gemma, Sandra
    de Asis Balaguer, Francisco
    Khan, Tuhina
    Grillo, Alessandro
    Chemi, Giulia
    Menchon, Gregory
    Prota, Andrea E.
    Olieric, Natacha
    Lucena-Agell, Daniel
    Barasoain, Isabel
    Fernando Diaz, J.
    Nebbioso, Angela
    Conte, Mariarosaria
    Lopresti, Ludovica
    Magnano, Stefania
    Amet, Rebecca
    Kinsella, Paula
    Zisterer, Daniela M.
    Ibrahim, Ola
    O'Sullivan, Jeff
    Morbidelli, Lucia
    Spaccapelo, Roberta
    Baldari, Cosima
    Butini, Stefania
    Novellino, Ettore
    Campiani, Giuseppe
    Altucci, Lucia
    Steinmetz, Michel O.
    Brogi, Simone
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2019, 162 : 290 - 320
  • [26] Synthesis and structure-activity relationships studies of brartemicin analogs as anti-invasive agents
    Jiang, Yong-Li
    Miyanaga, Satoshi
    Han, Xiu-Zhen
    Tang, Long-Qiang
    Igarashi, Yasuhiro
    Saiki, Ikuo
    Liu, Zhao-Peng
    JOURNAL OF ANTIBIOTICS, 2013, 66 (09): : 531 - 537
  • [27] Sojourn of Nitrogenous Heterocycles as Promising Antileishmanial Agents: Medicinal Perspectives and Structure-Activity Relationship Studies
    Nehra, Bhupender
    Kumar, Manoj
    Singh, Sumitra
    Chawla, Viney
    Chawla, Pooja A.
    CHEMISTRY AFRICA-A JOURNAL OF THE TUNISIAN CHEMICAL SOCIETY, 2024, 7 (07): : 3485 - 3529
  • [28] Structure-activity relationships and hepatic safety risks of thiazole agonists of the thrombopoietin receptor
    Antipas, Amy S.
    Blumberg, Laura C.
    Brissette, William H.
    Brown, Matthew F.
    Casavant, Jeffrey M.
    Doty, Jonathan L.
    Driscoll, James
    Harris, Thomas M.
    Jones, Christopher S.
    McCurdy, Sandra P.
    McElroy, Eric
    Mitton-Fry, Mark
    Munchhof, Michael J.
    Reim, David A.
    Reiter, Lawrence A.
    Ripp, Sharon L.
    Shavnya, Andrei
    Smeets, Marc I.
    Trevena, Kristen A.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (14) : 4069 - 4072
  • [29] Synthesis, biological evaluation and structure-activity relationships of 4-substituted methoxybenzoyl aryl thiazole (SMART) as anticancer agents
    Lu, Yan
    Li, Chien-Ming
    Wang, Zhao
    Chen, Jianjun
    Dalton, James T.
    Li, Wei
    Miller, Duane D.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2010, 240
  • [30] Pyrrole: A Decisive Scaffold for the Development of Therapeutic Agents and Structure-Activity Relationship
    Ganesh, Bharathi Hassan
    Raj, Anirudh G.
    Aruchamy, Baladhandapani
    Nanjan, Pandurangan
    Drago, Carmelo
    Ramani, Prasanna
    CHEMMEDCHEM, 2024, 19 (01)