Author(s):
Kouser Unnisa, Tahseen Sameena, Habeeba Sulthana, Hafsa Siddiqua, Maimunna Khatoon
Email(s):
kouserunnisa@yahoo.in
DOI:
10.5958/0974-4150.2017.00044.X 
Address:
Kouser Unnisa*, Tahseen Sameena, Habeeba Sulthana, Hafsa Siddiqua, Maimunna Khatoon
Department of Pharmaceutical Chemistry, Azad College of Pharmacy, Moinabad-Chilkur Road, Hyderabad-500075
*Corresponding Author
Published In:
Volume - 10,
Issue - 3,
Year - 2017
ABSTRACT:
Natural products derived from plants or microbes play a major role in drug discovery as a source of original bioactive structures and offer models for rational drug design. The promising natural anti-mycobacterials include carbazole alkaloids, such as Clausine and Micromeline isolated independently from several sources and were shown to have potent antitubercular activity. In recent years, carbazole alkaloids are playing important role in discovering new antitubercular leads against non-resistant and multi-drug resistant strains of M. tuberculosis. Few among them are 7-hydroxymukonal (IX, MIC 25lg/mL), Clausine K (MIC: 100lg/mL), and Micromeline (MIC: 31.5lg/mL). Knölker screened a series of carbazole alkaloids for their in vitro anti-TB activity. It appeared that anti-TB activity is highly sensitive to subtle changes in substitution around the carbazole ring system. Herein we report the synthesis of Nine Novel Carbazole linked propeonones in excellent yields via N-Methylation of Carbazole followed by Friedel’s crafts acylation of N-methyl carbazole. All the compounds were characterised by Spectroscopic methods.
Cite this article:
Kouser Unnisa, Tahseen Sameena, Habeeba Sulthana, Hafsa Siddiqua, Maimunna Khatoon. Design, Synthesis and Characterisation of Novel Carbazole Linked Propeonones. Asian J. Research Chem. 2017; 10(3):271-274. doi: 10.5958/0974-4150.2017.00044.X
Cite(Electronic):
Kouser Unnisa, Tahseen Sameena, Habeeba Sulthana, Hafsa Siddiqua, Maimunna Khatoon. Design, Synthesis and Characterisation of Novel Carbazole Linked Propeonones. Asian J. Research Chem. 2017; 10(3):271-274. doi: 10.5958/0974-4150.2017.00044.X Available on: https://www.ajrconline.org/AbstractView.aspx?PID=2017-10-3-5