Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Munna Prasad Gupt"'
Autor:
Sarvesh Kumar Pandey, Umesh Yadava, M.L. Sharma, Anjali Upadhyay, Munna Prasad Gupt, Ashish Ranjan Dwivedi, Aaqila Khatoon
Publikováno v:
Results in Chemistry, Vol 5, Iss , Pp 100726- (2023)
A series of 3-substituted-spiro-(1,3-dithiolan-2,2′-thiazolidin)-4-ones(2) designed as antimicrobial agents and have been synthesized by the reaction between [1,3]dithiolan-2-ylidene-(substituted-phenyl)amine (1) and mercaptoacetic acid. The reacti
Externí odkaz:
https://doaj.org/article/240d9be043a243259a32de7478416611
Autor:
Karan Singh Saini, Hamidullah, Arindam Bhattacharjee, Kalyan Mitra, Sonam Dwivedi, Rama Pati Tripathi, Munna Prasad Gupt, Arya Ajay, Rituraj Konwar, Sharmistha Das, Himangsu K. Bora, N. Devender
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 65:275-287
Autophagy is considered as an important cell death mechanism that closely interacts with other common cell death programs like apoptosis. Critical role of autophagy in cell death makes it a promising, yet challenging therapeutic target for cancer. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aa3fe3a7687c71cd8ecf6da0ad4da54
https://doi.org/10.1016/j.biocel.2015.06.016
https://doi.org/10.1016/j.biocel.2015.06.016
Autor:
Brijesh Kumar, Munna Prasad Gupt, Ravi Sankar Ampapathi, Rituraj Konwar, Hamidullah, Arya Ajay, Vikas Bajpai, Mahabir Prasad Kaushik, Rama Pati Tripathi, Shrikant Sharma
Publikováno v:
Organic Letters. 14:4306-4309
A new approach to synthesize a homologous series of 14-, 15-, and 16-membered drug-like, macrocyclic glycoconjugates involving TBAHS promoted azide-propenone intramolecular cycloaddition in designed C-glycopyranosyl butenones from a simple sugar d-gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b6a68e4c90cac2e6c1be7a302d33676
https://doi.org/10.1021/ol3022275
https://doi.org/10.1021/ol3022275
Autor:
Vinita Chaturvedi, Kishore K. Srivastava, Munna Prasad Gupt, Shailandra K. Pandey, Niyati Rai, Jawahar Lal, Brijesh Kumar, Anil Kumar Dwivedi, Varsha Gupta, Namrata Anand, Rama Pati Tripathi, K. Kumar G. Ramakrishna, Ravishankar Ramachandran, Praveen K. Shukla, Prapunjika Sharma, Shubhra Singh, S. B. Pandey
A series of 1-[(4-benzyloxyphenyl)-but-3-enyl]-1H-azoles has been identified as potent antitubercular agents against Mycobacterium tuberculosis. Synthesis of compounds involved acid catalyzed ring-opening of cyclopropyl ring of phenyl cyclopropyl met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e5b8f7c4f6bdb0a1e4c4bef640b9761
https://europepmc.org/articles/PMC4027561/
https://europepmc.org/articles/PMC4027561/
Publikováno v:
Molecular diversity. 16(2)
Diversity-oriented synthesis of structurally different, novel and small drug like molecules based on 1,4,5-trisubstituted 1,2,3-triazoles is developed in a streamlined sequence of different sets of reactions. The method involves the use of simple, re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d4962bb2ed5919588a80da4772ad450
https://pubmed.ncbi.nlm.nih.gov/22528271
https://pubmed.ncbi.nlm.nih.gov/22528271