Design, synthesis and antistaphylococcal activity of marine pyrrole alkaloid derivatives

被引:19
|
作者
Rane, Rajesh A. [1 ]
Sahu, Niteshkumar U. [1 ]
Shah, Chetan P. [1 ]
Shah, Nishant K. [1 ]
机构
[1] NMIMS Univ, SPP Sch Pharm & Technol Management, Bombay 400056, Maharashtra, India
关键词
Antistaphylococcal activity; bromopyrrole alkaloids; hydrazide derivatives; METHICILLIN-RESISTANT; ANTIBIOFILM ACTIVITY; IN-VITRO; STAPHYLOCOCCI; BIOFILM; BROMOPYRROLE; DAPTOMYCIN; INHIBITORS; BACTERIA; MODEL;
D O I
10.3109/14756366.2013.793183
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
A novel set of 16 hybrids of bromopyrrole alkaloids with aroyl hydrazone were designed, synthesized and evaluated for antibacterial and antibiofilm activities against methicillin-resistant Staphylococcus aureus (MRSA; ATCC 43866), methicillin-susceptible Staphylococcus aureus (MSSA; ATCC 35556) and Staphylococcus epidermidis (SE, S. epidermidis ATCC 35984). Of the 16 tested hybrids, 14 exhibited equal or superior antibiofilm activity against MSSA and MRSA relative to standard vancomycin. Compound 4m showed highest potency with antibiofilm activity of 0.39 mu g/mL and 0.78 mu g/mL against MSSA and MRSA, respectively. Thus, this compound could act as a potential lead for further development of new antistaphylococcal drugs.
引用
收藏
页码:401 / 407
页数:7
相关论文
共 50 条
  • [31] Investigations of the Anticancer Activity and Mechanism of Action of the Derivatives of Marine Alkaloid Ascididemine
    Dyshlovoy, Sergey A.
    Kaune, Moritz
    Hauschild, Jessica
    Pelageev, Dmitry N.
    Rohlfing, Tina
    Bokemeyer, Carsten
    Stonik, Valentin A.
    von Amsberg, Gunhild
    MARINE DRUGS, 2020, 18 (01)
  • [32] Investigations of the anticancer activity and mechanism of action of derivatives of the marine alkaloid Ascididemine
    Kaune, M.
    Dyshlovoy, S.
    Hauschild, J.
    Rohlfing, T.
    Pelageev, D.
    Stonik, V.
    Bokemeyer, C.
    von Amsberg, G.
    ONCOLOGY RESEARCH AND TREATMENT, 2019, 42 : 46 - 46
  • [33] ETA(2)-PYRROLE COMPLEXES AS SYNTHONS TO ALKALOID DERIVATIVES
    HODGES, LM
    GONZALEZ, J
    KOONTZ, JI
    MYERS, WH
    HARMAN, WD
    JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (18): : 4788 - 4790
  • [34] A SYNTHESIS OF PYRROLE DERIVATIVES
    ROSENMUN.P
    GRUBEL, K
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1968, 7 (09) : 733 - &
  • [35] Synthesis of Pyrrole Derivatives
    Han, Fugen
    Lu, Ye
    Ji, Xiaoming
    Zhao, Mingqin
    Zhang, Xiaoyun
    Liu, Yun
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2010, 30 (07) : 1080 - 1083
  • [36] Synthesis and cytotoxic evaluation of new derivatives of the marine alkaloid variolin B
    Fresneda, PM
    Delgado, S
    Francesch, A
    Manzanares, I
    Cuevas, C
    Molina, P
    JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (03) : 1217 - 1221
  • [37] Total synthesis and bioactivity of the marine alkaloid pityriacitrin and some of its derivatives
    Zhang, Puyong
    Sun, Xiaofei
    Xu, Bin
    Bijian, Krikor
    Wan, Shengbiao
    Li, Guigen
    Alaoui-Jamali, Moulay
    Jiang, Tao
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2011, 46 (12) : 6089 - 6097
  • [38] Total Synthesis of a Pyrrole Lactone Alkaloid, Longanlactone
    Reddy, Chada Raji
    Reddy, Motatipally Damoder
    Dilipkumar, Uredi
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2014, 2014 (28) : 6310 - 6313
  • [39] RETRACTION: The synthesis and biological activity of marine alkaloid derivatives and analogues (Retraction of Vol 10, Pg 31909, 2020)
    Zhou, Shiyang
    Huang, Gangliang
    RSC ADVANCES, 2021, 11 (14) : 7896 - 7896
  • [40] Synthesis and structure-activity relationship study of aldose reductase inhibiting marine alkaloid lukianol A and its derivatives
    Ishibashi, Fumito
    Zha, Shijiao
    Kondo, Taiyo
    Sakamoto, Mayu
    Ueno, Mikinori
    Fukuda, Tsutomu
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2023, 87 (02) : 148 - 157