Plumbagin analogs-synthesis, characterization, and antitubercular activity

被引:6
|
作者
Nayak, Nishi [1 ]
Bajpai, Meenakshi [2 ]
Razdan, Balkishen [3 ]
机构
[1] Uttarakhand Tech Univ, Dehra Dun, Uttar Pradesh, India
[2] Uttarakhand Tech Univ, Fac Pharm, Dehra Dun, Uttar Pradesh, India
[3] BIT, Dept Pharmaceut Sci, Ranchi, Bihar, India
关键词
Ethambutol (R); isoniazid (h); plumbagin; rifampicin (r);
D O I
10.4103/2231-4040.126984
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Considering the emerging problem of drug resistance in tuberculosis, there is an urgent need of development of new analogs that are useful in curing drug resistant tuberculosis. In India, tuberculosis continues to remain one of the most pressing health problems. India is the highest tuberculosis burden country in the world, accounting one fifth of global incidence - estimated 2.0-2.5 million cases annually. In 2011, approximately 8.7 million new cases of tuberculosis and 1.4 million people die from tuberculosis each year worldwide. Current antitubercular therapies are successful against normal tuberculosis but it is not suitable for drug resistant tuberculosis. In this study Plumbagin analogs, obtained from Plumbago zeylanica (Family-Plumbaginaceae), have been synthesized. Out of the various synthesized analogs, the antitubercular activity of compound a and b was evaluated using standard H-37 Rv and S, H, R, and E sensitive M tuberculosis strains using LRF assay method. Compound a showed strong activity against both standard H-37 Rv and S, H, R and E sensitive M. tuberculosis strains as compared to standard Rifampicin. The other compounds are proved to be more active against standard H-37 Rv and S, H, R and E sensitive M. tuberculosis strain as compared to Rifampicin.
引用
收藏
页码:28 / 32
页数:5
相关论文
共 50 条
  • [1] Synthesis and Antitubercular Activity of Oleanolic Acid Analogs
    A. Mahapatra
    N. Chauhan
    D. R. Patel
    N. P. Kalia
    V. S. Rajput
    I. A. Khan
    [J]. Pharmaceutical Chemistry Journal, 2014, 48 : 39 - 43
  • [2] Synthesis and Antitubercular Activity of Oleanolic Acid Analogs
    Mahapatra, A.
    Chauhan, N.
    Patel, D. R.
    Kalia, N. P.
    Rajput, V. S.
    Khan, I. A.
    [J]. PHARMACEUTICAL CHEMISTRY JOURNAL, 2014, 48 (01) : 39 - 43
  • [3] Synthesis and antitubercular activity of tricyclic analogs of puupehenone
    Kraus, GA
    Nguyen, T
    Bae, J
    Hostetter, J
    Steadham, E
    [J]. TETRAHEDRON, 2004, 60 (19) : 4223 - 4225
  • [4] Synthesis and antitubercular activity of novel pyrazole–quinazolinone hybrid analogs
    Unnat Pandit
    Amit Dodiya
    [J]. Medicinal Chemistry Research, 2013, 22 : 3364 - 3371
  • [5] Synthesis and antitubercular activity of novel pyrazole-quinazolinone hybrid analogs
    Pandit, Unnat
    Dodiya, Amit
    [J]. MEDICINAL CHEMISTRY RESEARCH, 2013, 22 (07) : 3364 - 3371
  • [6] Synthesis of fluorinated analogs of antitubercular drugs.
    Kobarfard, F
    Kauffman, JM
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U664 - U664
  • [7] Synthesis and evaluation of sansanmycin analogs as antitubercular agents
    Giltrap, Andrew M.
    Tran, Anh T.
    Conroy, Trent
    Britton, Warwick J.
    Payne, Richard J.
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248
  • [8] SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL EVALUATION OF SOME NOVEL BENZOTHIAZOLE ANALOGS AS POTENTIAL ANTITUBERCULAR AGENTS
    Satyadev, Siddhanadham Arun
    Prava, Raj Kumar
    Mantha, Sowmya
    Koduru, Aparna
    Gowtami, Thimmysetty
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2021, 12 (01): : 576 - 586
  • [9] Synthesis and antitubercular activity of a series of hydrazone and nitrovinyl analogs derived from heterocyclic aldehydes
    Sonar, Vijayakumar N.
    Crooks, Peter A.
    [J]. JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2009, 24 (01) : 117 - 124
  • [10] New INH-pyrazole analogs: Design, synthesis and evaluation of antitubercular and antibacterial activity
    Nayak, Nagabhushana
    Ramprasad, Jurupula
    Dalimba, Udayakumar
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2015, 25 (23) : 5540 - 5545