Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Eruva Vamshi Krishna"'
Autor:
Komal G. Sangu, Saiprasad Dasugari varakala, Eruva Vamshi Krishna, Abdul Akhir, Deepanshi Saxena, Mohammad Naiyaz Ahmad, Sidharth Chopra, Sunil Misra, Dharmarajan Sriram, Haridas B. Rode
Publikováno v:
ChemistrySelect. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4653202a46924d466490601e85f0137d
https://doi.org/10.1002/slct.202204186
https://doi.org/10.1002/slct.202204186
Autor:
Vijayan N Azger Dusthackeer, Manjulika Shukla, Eruva Vamshi Krishna, Vagolu Siva Krishna, Vitthal B. Makane, Haridas B. Rode, Sunil Misra, Balakrishnan Mahizhaveni, Dharmarajan Sriram, Sidharth Chopra
Publikováno v:
Future Medicinal Chemistry. 11:499-510
Aim: In recent times, heterocyclic chemotypes are being explored for the development of new antimycobacterials that target the drug-resistant tuberculosis. Here, we are disclosing the 5-substitued 2-mercapto-1,3,4-oxadiazoles as potent antitubercular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e5cad0f4197117b50fa9e580dc61b3
https://doi.org/10.4155/fmc-2018-0378
https://doi.org/10.4155/fmc-2018-0378
Autor:
Abimbola P. Oluyori, Tirunagari Harini, Komal G. Sangu, Eruva Vamshi Krishna, Surender S. Jadav, Sunil Misra, Haridas B. Rode
Publikováno v:
Archiv der Pharmazie. 355:2200102
Novel almazole D-amide conjugates, esters, and N-alkylated analogs were synthesized and investigated for their anticancer activity against seven cancer cell lines. Among the series, compounds 5g and 5m showed significant anticancer activities against
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62d170d33c1074d6015c153780b0edad
https://doi.org/10.1002/ardp.202200102
https://doi.org/10.1002/ardp.202200102
Autor:
Manjulika Shukla, Saradhi Kalari, Estharla Madhu Rekha, Uattam B. Karale, Dattatraya A. Babar, Sunil Misra, Grace Kaul, Eruva Vamshi Krishna, Vitthal B. Makane, Haridas B. Rode, Dharmarajan Sriram, Sidharth Chopra
Publikováno v:
Archiv der Pharmazie. 353:2070019
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e701597ec1c4a161232c9ce58cfa3e2
https://doi.org/10.1002/ardp.202070019
https://doi.org/10.1002/ardp.202070019
Autor:
Manjulika Shukla, Uattam B. Karale, Saradhi Kalari, Dattatraya A. Babar, Eruva Vamshi Krishna, Grace Kaul, Dharmarajan Sriram, Sidharth Chopra, Haridas B. Rode, Vitthal B. Makane, Sunil Misra, Estharla Madhu Rekha
Publikováno v:
Archiv der Pharmazie. 353:2000192
A facile strategy was developed for the synthesis of biologically important 4,5-dihydropyrrolo[1,2-a]quinoxalines and pyrrolo[1,2-a]quinoxalin]-2-ones by treating 2-(1H-pyrrol-1-yl)anilines with imidazo[1,2-a]pyridine-3-carbaldehyde or isatin, using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a09de0ba4cdd29e67e9559df0977d21
https://doi.org/10.1002/ardp.202000192
https://doi.org/10.1002/ardp.202000192