Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Bhukya, Supriya"'
Autor:
Bhukya, Supriya1, Swain, Sonam1,2, Mounika, Darna2,3, Honnanayakanavar, Jyoti2,4, Harish, Battu2,4, Behera, Purna Chandra2,3, Alli, Vidya Jyothi2,3, Jadav, Surender Singh2,3, Addlagatta, Anthony1,2 anthony@csiriict.in, Suresh, Surisetti2,4 surisetti@iict.res.in, Jain, Nishant1,2 nishant.iict@gov.in
Publikováno v:
International Journal of Pharmaceutical Investigation. Apr-Jun2024, Vol. 14 Issue 2, p436-453. 18p.
Autor:
Natani, Sirisha, Dhople, Vishnu M., Parveen, Asha, Sruthi, K.K., Khilar, Priyanka, Bhukya, Supriya, Ummanni, Ramesh
Publikováno v:
In BBA - Molecular Cell Research September 2021 1868(10)
Autor:
Dasari, Chandrashekhar, Reddy, Karthik Reddy Kami, Natani, Sirisha, Murthy, T.R.L., Bhukya, Supriya, Ummanni, Ramesh
Publikováno v:
In BBA - Molecular Cell Research August 2019 1866(8):1298-1309
Autor:
B. Poornima, Devi Amujuri, Bhukya Supriya, K. Suresh Babu, Bandi Siva, K. Bharathi, Ramesh Ummanni
Publikováno v:
Phytochemistry Letters. 45:184-189
In continuation of our efforts in the exploration of Indian flora and development of new natural product-based therapeutics, bio-activity directed investigation of Schisandra grandiflora led to the isolation of two new widdarane-sesquiterpenes (1 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c86bd3258d2b8e9cc0f8f4da8b2a0318
https://doi.org/10.1016/j.phytol.2021.08.009
https://doi.org/10.1016/j.phytol.2021.08.009
Autor:
Ramprasad, Jurupula, Kumar Sthalam, Vinay, Linga Murthy Thampunuri, Rama, Bhukya, Supriya, Ummanni, Ramesh, Balasubramanian, Sridhar, Pabbaraja, Srihari
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 15 October 2019 29(20)
Autor:
Ahmed Kamal, Anthony Addlagatta, Sumit S. Chourasiya, Rakesh Mishra, G. Bharath Kumar, Yerramsetty Suresh, Chandan Kishor, Anver Basha Shaik, Nishant Jain, Ananthamurthy Nagabhushana, Bhukya Supriya
Publikováno v:
European Journal of Medicinal Chemistry. 92:501-513
A series of twenty one compounds with pyrazole and oxindole conjugates were synthesized by Knoevenagel condensation and investigated for their antiproliferative activity on different human cancer cell lines. The conjugates are comprised of a four rin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c49a86bfeed3cbc2a312f27fd52858e8
https://doi.org/10.1016/j.ejmech.2013.10.077
https://doi.org/10.1016/j.ejmech.2013.10.077
Autor:
Chada Raji Reddy, Bhukya Supriya, Muppidi Subbarao, Jonnalagadda Vijaykumar, Ramesh Ummanni, Reddi Rani Valleti, Nilesh Sasane, Surender Singh Jadav
Publikováno v:
Anti-cancer agents in medicinal chemistry. 18(12)
Background: The anti-mitotic activity of podophyllotoxin derivative targeting tubulin enzyme proved them as strong polymerization inhibitors. The introduction of heteroatom along with different heteroaryl systems in naturally obtained lignans created
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0aad197ecc2eb8cda88304b989ad2274
https://pubmed.ncbi.nlm.nih.gov/30019651
https://pubmed.ncbi.nlm.nih.gov/30019651
Autor:
Jerald Mahesh Kumar, M V Surekha, Karthik Reddy Kami Reddy, Chandrashekhar Dasari, Bhukya Supriya, Divya Duscharla, N Sai Ram, Ramesh Ummanni
Publikováno v:
Angiogenesis. 21(1)
Tissue microarray analysis confirmed higher dimethylarginine dimethylaminohydrolase-1 (DDAH1) expression in prostate cancer (PCa) compared to benign and normal prostate tissues. DDAH1 regulates nitric oxide (NO) production by degrading endogenous nit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38f1df4a76ad337e8c150269368de2c7
https://pubmed.ncbi.nlm.nih.gov/29150732
https://pubmed.ncbi.nlm.nih.gov/29150732
Akademický článek
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Autor:
Nishant Jain, Deepa Ramesh, Anthony Addlagatta, Chandan Kishor, A. Suresh Kumar, M. Amarnath Reddy, T. Ramalinga Murthy, Bhukya Supriya, Bojja Sreedhar, Shasi V. Kalivendi
Publikováno v:
European Journal of Medicinal Chemistry. 60:305-324
Two new series of compounds E-2,3,4-trimethoxy-6-styrylbiphenyls and 2,3,4-trimethoxy-6-(1-phenylvinyl)biphenyls were designed, synthesized and evaluated for antitubulin activity. A common intermediate 4,5,6-trimethoxybiphenyl-2-carbaldehydes was emp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c6980226ef74521c3f4651a3beab2ee
https://doi.org/10.1016/j.ejmech.2012.12.008
https://doi.org/10.1016/j.ejmech.2012.12.008