Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Vankadari, Srinivasa Rao"'
Autor:
Thongolla, Ramesha, Pulabala, Ramesh, Gogula, Sailam Sri, Shenoy, Thripthi Nagesh, Salam, Abdul Ajees Abdul, Vankadari, Srinivasa Rao, Rondla, Rohini, Puchakayala, Muralidhar Reddy
Publikováno v:
In Journal of Molecular Structure 15 March 2024 1300
Autor:
Nadipolla Naresh Reddy, Sung-Jen Hung, Merugu Kumara Swamy, Ananthula Sanjeev, Vankadari Srinivasa Rao, Rondla Rohini, Atcha Krishnam Raju, Kuthati Bhaskar, Anren Hu, Puchakayala Muralidhar Reddy
Publikováno v:
Molecules, Vol 26, Iss 7, p 1952 (2021)
Angiogenesis inhibition is a key step towards the designing of new chemotherapeutic agents. In a view to preparing new molecular entities for cancer treatment, eighteen 1,2,3-triazole-uracil ensembles 5a–r were designed and synthesized via the clic
Externí odkaz:
https://doaj.org/article/f2a1fc8377bf4c8f99c7d98ae512a0f5
Publikováno v:
Molecules, Vol 24, Iss 17, p 3038 (2019)
A series of 2-hydroxy-3-chrysino dithiocarbamate derivatives (3a−k) were designed, synthesized, and characterized for their structure determination by 1H NMR, 13C NMR, and HRMS (ESI) spectral data. They were screened for their in vitro biological a
Externí odkaz:
https://doaj.org/article/f2a089d803ea4ecdbdb8260fb97981f4
Autor:
Vankadari Srinivasa Rao, Mutheneni Srinivasa Rao, Pulabala Ramesh, Puchakayala Muralidhar Reddy, Katragadda Suresh Babu
Publikováno v:
Letters in Drug Design & Discovery. 17:873-883
Background:: Most of the currently available pharmaceutical drugs are either natural products or analogues of natural products. Flavonoids are plant based natural polyphenolic compounds which exhibit a wide range of biological activities. Chrysin, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::444096e83b21ff2c18c22ec8a3d38e91
https://doi.org/10.2174/1570180816666190913183623
https://doi.org/10.2174/1570180816666190913183623
Autor:
Rondla Rohini, Puchakayala Muralidhar Reddy, N. Naresh Reddy, Kuthati Bhaskar, Ananthula Sanjeev, Atcha Krishnam Raju, Sung-Jen Hung, Anren Hu, Vankadari Srinivasa Rao, Merugu Kumara Swamy
Publikováno v:
Molecules
Molecules, Vol 26, Iss 1952, p 1952 (2021)
Volume 26
Issue 7
Molecules, Vol 26, Iss 1952, p 1952 (2021)
Volume 26
Issue 7
Angiogenesis inhibition is a key step towards the designing of new chemotherapeutic agents. In a view to preparing new molecular entities for cancer treatment, eighteen 1,2,3-triazole-uracil ensembles 5a–r were designed and synthesized via the clic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cda8469971003a0b97e9450c5a0ed80
https://pubmed.ncbi.nlm.nih.gov/33808444
https://pubmed.ncbi.nlm.nih.gov/33808444
Publikováno v:
Molecules
Volume 24
Issue 17
Molecules, Vol 24, Iss 17, p 3038 (2019)
Volume 24
Issue 17
Molecules, Vol 24, Iss 17, p 3038 (2019)
A series of 2-hydroxy-3-chrysino dithiocarbamate derivatives (3a&ndash
k) were designed, synthesized, and characterized for their structure determination by 1H NMR, 13C NMR, and HRMS (ESI) spectral data. They were screened for their in vitro bio
k) were designed, synthesized, and characterized for their structure determination by 1H NMR, 13C NMR, and HRMS (ESI) spectral data. They were screened for their in vitro bio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3292ae7faf2723d6b1eef04e8fe027c8