Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Shrikant V. Hese"'
Autor:
Sonali S. Kamble, Jasoda Choudhari, Ramakrishna Nimma, Totakura Venkata Santosh Kumar, Kapil K. Patil, Shrikant V. Hese, Bhaskar S. Dawane, Rajesh N. Gacche
Publikováno v:
Cancer Reports, Vol 5, Iss 10, Pp n/a-n/a (2022)
Abstract Background Natural products with targeted bioactivity have gained major attention in the field of cancer research owing to emerging anti‐cancer drug resistance and off target toxicities. Chloroxylon swietenia (Roxb.) DC is recognized as a
Externí odkaz:
https://doaj.org/article/e2d00c2f9c2e467f83e11d7f3daef3cc
Autor:
Madhav J. Hebade, Sambhaji T. Dhumal, Sonali S. Kamble, Tejshri R. Deshmukh, Vijay M. Khedkar, Shrikant V. Hese, Rajesh N. Gacche, Bhaskar S. Dawane
Publikováno v:
Polycyclic Aromatic Compounds. 43:2866-2887
A series of new substituted benzimidazole-thiazoles (9a–l) have been designed and synthesized using 2-aminothiazole as a starting material by using molecular hybridization approach. The newly synthesized compounds were characterized by 1H NMR, 13C
Autor:
Sonali S. Kamble, Jasoda Choudhari, Ramakrishna Nimma, Totakura Venkata Santosh Kumar, Kapil K. Patil, Shrikant V. Hese, Bhaskar S. Dawane, Rajesh N. Gacche
Publikováno v:
Cancer Reports. 5
Autor:
Rahul D. Kamble, Milind V. Gaikwad, Manojkumar R. Tapare, Shrikant V Hese, Shuddhodan N Kadam, Bhaskar S. Dawane, Ajay N Ambhore
An efficient and convenient method has been developed for the synthesis of 2- amino-5-oxo-4-phenyl-4, 5-dihydropyrano[3,2-c]chromene-3-carbonitrile derivatives from a one-pot multi-component reaction between 4-hydroxy-2H- chromen-2-one. Aromatic alde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::161330da9c17ed418c96a6c8f5794e56
https://zenodo.org/record/5920233
https://zenodo.org/record/5920233
Autor:
Sonali S, Kamble, Jasoda, Choudhari, Ramakrishna, Nimma, Totakura Venkata Santosh, Kumar, Kapil K, Patil, Shrikant V, Hese, Bhaskar S, Dawane, Rajesh N, Gacche
Publikováno v:
Cancer reports (Hoboken, N.J.). 5(10)
Natural products with targeted bioactivity have gained major attention in the field of cancer research owing to emerging anti-cancer drug resistance and off target toxicities. Chloroxylon swietenia (Roxb.) DC is recognized as a folklore medicinal pla
Autor:
Sonali S. Kamble, Sanjay S. Sawant, Shrikant V. Hese, Parshuram M. Pisal, Kamini T Bagul, Rajesh N. Gacche, Rohan J. Meshram, Rahul V. Pinjari, Vinod T. Kamble, Ajay S. Sawant
Publikováno v:
Computational Biology and Chemistry. 92:107484
N-(4-(substituted)-3-(trifluoromethyl) phenyl) isobutyramides and their N-ethyl analogues (flutamides) are versatile scaffolds with a wide spectrum of biological activities. A series of new N-(4-(substituted)-3-(trifluoromethyl) phenyl) isobutyramide
Autor:
Rajesh N. Gacche, Sonali S. Kamble, Bhaskar S. Dawane, Rohan J. Meshram, Kapil K. Patil, Shrikant V. Hese, Pratima P. Mogle, Rahul D. Kamble
Publikováno v:
Medicinal Chemistry Research. 26:805-818
Diabetes is embracing the human population in logarithmic fashion both in developed as well as developing countries. Aldose reductase is one of the important enzymes of polyol pathway of sugar metabolism in humans. Aldose reductase inhibition has bee
Autor:
Rahul D. Kamble, Shuddhodan N. Kadam, Ajay N. Ambhore, Shrikant V. Hese, Bhaskar S. Dawane, Madhav J. Hebade, Milind V. Gaikwad
Publikováno v:
European Journal of Chemistry. 7:431-435
The present report describes a microwave assisted convenient and efficient protocol for the synthesis of new 6-(4-substituted-phenyl)-3-methylimidazo[2,1- b ]thiazole-2-carbohydra- zide derivatives. The current method holds a tag of green synthesis b
Autor:
Rajesh N. Gacche, Rohan J. Meshram, Shuddhodan N. Kadam, Madhav J. Hebade, Sonali S. Kamble, Ajay N. Ambhore, Rahul D. Kamble, Milind V. Gaikwad, Bhaskar S. Dawane, Shrikant V. Hese
Publikováno v:
Computational biology and chemistry. 80
Development of novel, safe and effective drug candidates combating the emerging drug resistance has remained a major focus in the mainstream of anti-tuberculosis research. Here, we inspired to design and synthesize series of new pyridin-4-yl-1,3,4-ox