Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Priyanka N. Makhal"'
Publikováno v:
Heliyon, Vol 9, Iss 3, Pp e14569- (2023)
Inflammation is a complicated physiological process that results in a variety of disorders. Several inflammatory mediators are produced during this process, which is responsible for long-term inflammatory conditions like osteoarthritis, rheumatoid ar
Externí odkaz:
https://doaj.org/article/7ddb822516944135a9679e86a446ab11
Publikováno v:
International Journal of Plant Based Pharmaceuticals, Vol 2, Iss 1, Pp 118-127 (2022)
Anthocyanins are flavonoid containing polyphenolic phytochemicals. They are widely present in plants and accounts for different color shades displayed by the plant organs. A broad range of health-revitalizing effects is attributed to anthocyanins, co
Externí odkaz:
https://doaj.org/article/c5f5ec66005d4b9caf6890fe0b9233f2
Autor:
Priyanka N. Makhal, Srinivas Reddy Dannarm, Arbaz Sujat Shaikh, Rezwan Ahmed, Shrilekha Chilvery, Lahu N. Dayare, Rajesh Sonti, Chandraiah Godugu, Venkata Rao Kaki
Publikováno v:
Chemical Communications. 59:3767-3770
Woollins’ reagent was used for the synthesis of novel 2,5-disubstituted selenazolines with excellent regio- and chemoselectivity that show potential antiproliferative activity, paving the way for developing selenazoline-based anticancer agents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cab1a65cf0989a9ae7d0fc98bb0b91b
https://doi.org/10.1039/d2cc06782j
https://doi.org/10.1039/d2cc06782j
Matrix Metalloproteinases-9 (MMP-9) is one of the important targets that play a vital role in various diseases such as cancer, Alzheimer’s, arthritis, etc. Traditionally, MMP-9 inhibitors have been unable to achieve selectivity to get around this t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a6c41354ff61517ad536f276216aa1e
Publikováno v:
ChemistrySelect. 6:663-679
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34e4f4399bc9ac547035b0e26a0d5bad
https://doi.org/10.1002/slct.202004029
https://doi.org/10.1002/slct.202004029
Autor:
Priyanka N. Makhal, Srinivas Reddy Dannarm, Arbaz Sujat Shaikh, Rajesh Sonti, Venkata Rao Kaki
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd4aebecbb1c7bb42951ecfa5af4bc74
https://doi.org/10.1002/slct.202200933
https://doi.org/10.1002/slct.202200933
Autor:
Arbaz Sujat Shaikh, Gaddam Kiranmai, G. Parimala Devi, Priyanka N. Makhal, Dilep Kumar Sigalapalli, Ramya Tokala, Venkata Rao Kaki, Nagula Shankaraiah, Narayana Nagesh, Bathini Nagendra Babu, Neelima D. Tangellamudi
Publikováno v:
Bioorganicmedicinal chemistry letters. 65
The design and synthesis of a new series of mercaptoacetamide-linked pyrimidine-1,3,4-oxadiazole hybrids was accomplished. The in vitro cytotoxic potential of these new compounds was evaluated against lung cancer (A549), prostate cancer (PC-3, DU-145
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f37fb8771f4116013cfa50f01aac7e0a
https://pubmed.ncbi.nlm.nih.gov/35339645
https://pubmed.ncbi.nlm.nih.gov/35339645
Publikováno v:
European journal of medicinal chemistry. 225
Inflammation is a most complex pathological process that gives birth to different diseases. Different inflammatory mediators are released during an inflammation responsible for acute pain and chronic inflammatory diseases like cancer, asthma, rheumat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec66a875b168f9d4ad2cf49b8353df6
https://pubmed.ncbi.nlm.nih.gov/34479036
https://pubmed.ncbi.nlm.nih.gov/34479036
Autor:
G. Parimala Devi, Dilep Kumar Sigalapalli, Neelima D. Tangellamudi, Uttam Chand Banerjee, Nagendra Babu Bathini, Priyanka N. Makhal, Manasa Kadagathur, Preeti Grewal
Publikováno v:
Bioorganic chemistry. 99
We present here-in the molecular design and chemical synthesis of a novel series of diindoloazepinone derivatives as DNA minor groove binding agents with selective topoisomerase I inhibition. The in vitro cytotoxicity of the synthesized compounds was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f47ea7f660f1acfa18c8e5a054180d7
https://pubmed.ncbi.nlm.nih.gov/32272367
https://pubmed.ncbi.nlm.nih.gov/32272367