Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mithilesh M. Rathore"'
Autor:
Magdi E. A. Zaki, Sami A. Al-Hussain, Syed Nasir Abbas Bukhari, Vijay H. Masand, Mithilesh M. Rathore, Sumer D. Thakur, Vaishali M. Patil
Publikováno v:
Pharmaceuticals, Vol 15, Iss 3, p 303 (2022)
Cancer is a major life-threatening disease with a high mortality rate in many countries. Even though different therapies and options are available, patients generally prefer chemotherapy. However, serious side effects of anti-cancer drugs compel us t
Externí odkaz:
https://doaj.org/article/2a52a34d377f4626a4be8a451c70b320
Publikováno v:
Medicinal Chemistry Research. 28:2270-2278
In the present work, QSAR (quantitative structure−activity relationship) analysis has been executed for RG7834 analogs. RG7834 is a first-in- class selective and orally available dihydroquinolizinone (DHQ)-based small molecule Hepatitis B virus exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a17d7e42e8d3ba4e4650228d970b89d
https://doi.org/10.1007/s00044-019-02455-w
https://doi.org/10.1007/s00044-019-02455-w
Synthesis and biological activities of piperazine derivatives as antimicrobial and antifungal agents
Publikováno v:
Organic Communications, Vol 10, Iss 3, Pp 228-238 (2017)
Apart from thiazole, benzimidazole, and tetrazole family, some of the piperazine analogs also show significant pharmacophoric activities. The synthesis of piperazine through intermediate 3 occurred via coupling of substituted benzenethiol with chloro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d5c05b62ec5d8aca16b4343f519c06d
https://doi.org/10.25135/acg.oc.23.17.05.026
https://doi.org/10.25135/acg.oc.23.17.05.026
Autor:
Mithilesh M. Rathore, Nahed N. E. El-Sayed, Nandkishor Gawhale, Vijay H. Masand, Sumersingh D. Thakur
Publikováno v:
Molecular informaticsReferences. 38(8-9)
In the present work, 2D- and 3D-quantitative structure-activity relationship (QSAR) analysis has been employed for a diverse set of eighty-nine quinoxalinones to identify the pharmacophoric features with significant correlation with the aldose reduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c7fa80025a859b32f0bb79e78e6b715
https://pubmed.ncbi.nlm.nih.gov/31131980
https://pubmed.ncbi.nlm.nih.gov/31131980