Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Minal S. Jaiswal"'
Autor:
Ravindra L. Bakal, Rahul D. Jawarkar, J.V. Manwar, Minal S. Jaiswal, Arabinda Ghosh, Ajaykumar Gandhi, Magdi E.A. Zaki, Sami Al-Hussain, Abdul Samad, Vijay H. Masand, Nobendu Mukerjee, Syed Nasir Abbas Bukhari, Praveen Sharma, Israa Lewaa
Publikováno v:
Saudi Pharmaceutical Journal, Vol 30, Iss 6, Pp 693-710 (2022)
The aldose reductase (AR) enzyme is an important target enzyme in the development of therapeutics against hyperglycaemia induced health complications such as retinopathy, etc. In the present study, a quantitative structure activity relationship (QSAR
Externí odkaz:
https://doaj.org/article/ba4aae211c9d47b48aa45d035a421f88
Autor:
Chetan M. Jain, Ravindra L. Bakal, Prashant J. Burange, Nitin I. Kochar, Jagdish V. Manwar, Rahul D. Jawarkar, Minal S. Jaiswal, Israa Lewaa
Publikováno v:
Bulletin of the National Research Centre, Vol 46, Iss 1, Pp 1-17 (2022)
Abstract Background A wound may define as an interruption within the continuity of the epithelial lining of the skin or mucosa that occurs as a result of physical or thermal damage. Wound healing is an intricate process that is highly synchronized ce
Externí odkaz:
https://doaj.org/article/4e2291ab2c1a4d95abc5d0a14912b00b
Autor:
R. D. Jawarkar, R. L. Bakal, P. N. Khatale, Israa Lewaa, Chetan M. Jain, Jagdish V. Manwar, Minal S. Jaiswal
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-24 (2021)
Abstract Background Telomerase reverse transcriptase (TERT) and human telomeric G-quadruplex DNA are amongst the favorable target for researchers to discover novel and more effective anticancer agents. To understand and elucidate structure activity r
Externí odkaz:
https://doaj.org/article/aea501f2e5bc41f4ae3358eb9f160c10
Autor:
Jagdish V. Manwar, Minal S. Jaiswal, P. N. Khatale, Ravindra L. Bakal, Chetan M. Jain, Israa Lewaa, Rahul D. Jawarkar
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-24 (2021)
Background Telomerase reverse transcriptase (TERT) and human telomeric G-quadruplex DNA are amongst the favorable target for researchers to discover novel and more effective anticancer agents. To understand and elucidate structure activity relationsh