Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Manisha Arkile"'
Autor:
Vijay M. Khedkar, Dhiman Sarkar, Pankaj B. Miniyar, Ashish S. Kumar, Dattatray D. Anuse, Manisha Arkile, Anand A. Mahajan, Mahesh A. Barmade
Publikováno v:
Letters in Drug Design & Discovery. 16:1264-1275
Background: Treating tuberculosis is a challenge due to the development of drug resistance. Hence, it is imperative to develop novel leads having high potency and efficacy to curb drug resistance. Methods: The present research work is focused on micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b69df8ebd0563b51b96360d02e7a651
https://doi.org/10.2174/1570180816666190329222636
https://doi.org/10.2174/1570180816666190329222636
Autor:
Prashant S. Kharkar, Hardik Manek, Dhiman Sarkar, Pradip K. Gadekar, Vijay M. Khedkar, Abhijit Roychowdhury, Vijayaparthasarathi Vijayakumar, Manisha Arkile, S. Sarveswari, Rajiv Sharma
Publikováno v:
European Journal of Medicinal Chemistry. 122:475-487
The design, synthesis and antimicrobial evaluation of a novel series of azaspiro analogues of linezolid (1) have been described. Linezolid comprises of a morpholine ring which is known for its metabolism-related liabilities. Therefore, the key modifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1848951c4d25976ed6a7a5b9b3deb05c
https://doi.org/10.1016/j.ejmech.2016.07.001
https://doi.org/10.1016/j.ejmech.2016.07.001
Publikováno v:
Planta Medica International Open. 3:e55-e59
A bioactivity-guided chemical examination of the acetone extract of the rhizomes of Alpinia galanga led to the isolation of six secondary metabolites, eucalyptol derivative (1) and phenylpropanoids (2–6). The structures of all of the isolated compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b19f013060d8975533509d1ead377060
https://doi.org/10.1055/s-0042-112226
https://doi.org/10.1055/s-0042-112226
Autor:
Pankaj B. Miniyar, Manisha Arkile, Kalyani D. Asgaonkar, Amar Yeware, Dhiman Sarkar, A. B. Dharme, Vijay M. Khedkar, Prakash C. Jha, Trupti S. Chitre
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 26:2224-2228
The persistence of Mycobacterium tuberculosis (MTB) in dormant stage assists the pathogen to develop resistance against current antimycobactrial drugs. To address this issue, we report herein the synthesis of N-(4-oxo-2 substituted thiazolidin-3 yl)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3c52b1bdde1c701eb9df15d9a5fe7ed
https://doi.org/10.1016/j.bmcl.2016.03.055
https://doi.org/10.1016/j.bmcl.2016.03.055
Autor:
Manisha Arkile, Laxman Nawale, Utkarsha U. Shedbalkar, Snehal Chopade, Dhiman Sarkar, Sweety A. Wadhwani, Balu A. Chopade, Richa Singh
Publikováno v:
International Journal of Nanomedicine
Richa Singh,1 Laxman Nawale,2 Manisha Arkile,2 Sweety Wadhwani,1 Utkarsha Shedbalkar,1 Snehal Chopade,1 Dhiman Sarkar,2 Balu Ananda Chopade1,3 1Department of Microbiology, Savitribai Phule Pune University, 2Combichem-Bioresource Center, Organic Chemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4049401918472e8872e7029444af52
http://europepmc.org/articles/PMC4862349
http://europepmc.org/articles/PMC4862349
Autor:
Amar Yeware, Manisha Arkile, Bapurao B. Shingate, Mubarak H. Shaikh, Dnyaneshwar D. Subhedar, Dhiman Sarkar
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 26:1704-1708
We have developed, highly efficient, one-pot, solvent-free, [Et3NH][HSO4] catalyzed multicomponent reaction protocol for the synthesis of 1,3-thiazolidin-4-ones in excellent yields. For the first time, the 1,3-thiazolidin-4-ones were evaluated in vit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b19485de75aa42e07085fc662461b32
https://doi.org/10.1016/j.bmcl.2016.02.056
https://doi.org/10.1016/j.bmcl.2016.02.056
Publikováno v:
Planta Medica Letters. 3:e20-e24
The new 14,15-dinor- cis -labdane diterpene, named (+)-14,15-dinor-9 α -hydroxy- cis -labd-11(E)-en-13-one ( 1 ), was isolated from the acetone extract of the aerial parts of Colebrookea oppositifolia , along with the known compounds alnustin ( 2 ),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6321ab85ab4ad2fcfc2cf2bcb086147
https://doi.org/10.1055/s-0042-102200
https://doi.org/10.1055/s-0042-102200
Autor:
Mubarak H. Shaikh, Firoz A. Kalam Khan, Dnyaneshwar D. Subhedar, Manisha Arkile, Laxman Nawale, Dhiman Sarkar, Bapurao B. Shingate, Jaiprakash N. Sangshetti
Publikováno v:
Journal of Heterocyclic Chemistry. 54:413-421
A library of 1,2,3-triazoles efficiently prepared via click chemistry and evaluated for their antifungal, antitubercular, antioxidant, cytotoxicity, molecular docking and ADME prediction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bba6559891857f975516db08686b2f9
https://doi.org/10.1002/jhet.2598
https://doi.org/10.1002/jhet.2598
Autor:
Ramrao A. Mane, Manisha Arkile, Lalit D. Khillare, Amarsinh R. Deshmukh, Dhiman Sarkar, Sambhaji T. Dhumal
Publikováno v:
Journal of Heterocyclic Chemistry. 54:125-130
Emergence of multidrug resistant and extensively drug resistant tuberculosis has prompted to develop new molecular entities to treat the disease. A series of new 4-thiazolidinones with pyrazinyl and thiazolyl scaffolds has been synthesized, and their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f083e0526df6b13807779e550d7aa572
https://doi.org/10.1002/jhet.2552
https://doi.org/10.1002/jhet.2552
Autor:
Ashish A. Chinchansure, Anurag Shukla, Swati P. Joshi, Dhiman Sarkar, Manisha Arkile, Dhanasekaran Shanmugam
Publikováno v:
Planta Medica Letters. 2:e35-e38
A phytochemical investigation of the acetone extract from the aerial parts of Leucas mollissima afforded one new (−) epi -marmelo lactone, (2 S , 4 R , 6 S )-2,6-dimethyl-6 hydroxy-7-ene-4-olide ( 1 ), along with five known compounds, schensianol A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1041aeb13dfd8cb0b92dd01be1ed997f
https://doi.org/10.1055/s-0035-1557830
https://doi.org/10.1055/s-0035-1557830