Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Raghunath B. Bhosale"'
Autor:
Nargisbano A. Peerzade, Shravan Y. Jadhav, Raghunath B. Bhosale, Vijay H. Masand, Rakhi G. Gawali, Sami A. Al-Hussain, Aamal A. Al-Mutairi, Magdi E.A. Zaki
Publikováno v:
Results in Chemistry, Vol 11, Iss , Pp 101793- (2024)
A series of methoxy substituted pyrazole based pyrazoline derivatives (4a-j) were synthesized in good to excellent yield from corresponding pyrazole-chalcones (3a-j). All synthesized derivatives were characterized and screened for their in vitro anti
Externí odkaz:
https://doaj.org/article/1e12073996314a35800c970846cf9399
Autor:
Bhaskar S. Dawane, Shankaraiah G. Konda, Vinod T. Kamble, Sanjay A. Chavan, Raghunath B. Bhosale, Shaikh Baseer M.
Publikováno v:
E-Journal of Chemistry, Vol 6, Iss S1, Pp S358-S362 (2009)
Thiazole derivatives were prepared by one-pot procedure by the reaction of α-haloketones, thiourea and substituted o-hydroxybenzaldehyde under environmentally solvent free conditions.
Externí odkaz:
https://doaj.org/article/75501ce7f6c04d808e0a081f55f512b2
Autor:
Dattatraya G. Raut, Raghunath B. Bhosale, Anjana S. Lawand, Mahesh G. Hublikar, Vikas D. Kadu, Sandeep B. Patil, Prafulla B. Choudhari
Publikováno v:
Recent Advances in Inflammation & Allergy Drug Discovery. 16:96-106
Background: Recently, researchers have worked on the development of new methods for the synthesis of bioactive heterocycles using polyethylene glycol as a green solvent. In this context, we report the synthesized 2-(2-hydrazinyl) thiazoles for their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c02f878772ea4148a2e266b9cded5a
https://doi.org/10.2174/2772270816666220902094019
https://doi.org/10.2174/2772270816666220902094019
Autor:
Dattatraya G. Raut, Raghunath B. Bhosale, Anjana S. Lawand, Mahesh G. Hublikar, Vikas D. Kadu, Sandeep B. Patil
Publikováno v:
Recent Advances in Inflammation & Allergy Drug Discovery. 16:19-25
Background: A literature survey revealed that many imidazo-thiadiazole molecules were used as key intermediates for the development of novel drugs. The synthesized imidazo-thiadiazole derivatives were tested for their in vitro antioxidant and anti-in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::378f7047898087d23e56bdb97064eab6
https://doi.org/10.2174/2772270816666220410130059
https://doi.org/10.2174/2772270816666220410130059
Autor:
Raghunath B. Bhosale, Amol A Kulkarni, Nargisbano A. Peerzade, Shravan Y. Jadhav, Bhushan D Varpe
Publikováno v:
Polycyclic Aromatic Compounds. 42:3939-3952
Present work involves the green and environmentally benign synthesis of 1,5-benzodiazepines using iodine as a catalyst and PEG-400 as a green solvent at room temperature that gives an excellent yie...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1d2dcac009346e585955ad0f3db7058
https://doi.org/10.1080/10406638.2021.1878244
https://doi.org/10.1080/10406638.2021.1878244
Autor:
Nargisbano A. Peerzade, Mahesh G. Hublikar, Raghunath B. Bhosale, Bhushan D Varpe, Amol A Kulkarni, Shravan Y. Jadhav
Publikováno v:
Russian Journal of Bioorganic Chemistry. 46:1128-1135
A new series of difluoro phenyl pyrazole chalcone was prepared by utilizing PEG 400 as a catalyst and investigated for their antifungal, anti-inflammatory, and antioxidant activity. The compounds 3-[3-(4-bromo-phenyl)-1-phenyl-1H-pyrazol-4-yl]-1-(2,4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62e80ede7095535091d087c790b8355f
https://doi.org/10.1134/s1068162020060102
https://doi.org/10.1134/s1068162020060102
Autor:
Raghunath B. Bhosale, Yueqing Gu, Niraj R. Rane, Parikshit Banerjee, Rohit Bavi, Zhang Hang, Sneha Bavi, Mahendra Jadhao, Byong-Hun Jeon, Aquib, Kisan M. Kodam
Publikováno v:
Molecular Therapy. Nucleic Acids
Molecular Therapy: Nucleic Acids, Vol 21, Iss, Pp 1074-1086 (2020)
Molecular Therapy: Nucleic Acids, Vol 21, Iss, Pp 1074-1086 (2020)
Aptamers are small, functional single-stranded DNA or RNA oligonucleotides that bind to their targets with high affinity and specificity. Experimentally, aptamers are selected by the systematic evolution of ligands by exponential enrichment (SELEX) m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84a33afdec1a94008d2b2cdf9b451de9
https://doi.org/10.1016/j.omtn.2020.07.038
https://doi.org/10.1016/j.omtn.2020.07.038
Autor:
A. S. Lawand, Vikas D. Kadu, Raghunath B. Bhosale, S. B. Patil, Mahesh G. Hublikar, Prafulla B. Choudhari, Dattatraya G. Raut
Publikováno v:
Current Chemical Biology. 14:58-68
Background: The present research work is focused on the development of alternative antioxidant and anti-inflammatory agents. The review of the literature reveals that many benzofused thiazole analogues have been used as lead molecules for the design
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::090550d67d07b3b37e46a36312e9088e
https://doi.org/10.2174/2212796813666191118100520
https://doi.org/10.2174/2212796813666191118100520
Publikováno v:
Asian Journal of Chemistry. 32:959-964
The objective of the present study was to synthesize a series of some novel quinoline based methoxy substituted chalcones and to evaluate their in vitro antimalarial, anti-inflammatory, antioxidant and antidiabetic activitites. The quinoline based ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3096bbda5e2beb79eb09ec72f4ad318b
https://doi.org/10.14233/ajchem.2020.22542
https://doi.org/10.14233/ajchem.2020.22542
Autor:
Dnyandev G. Bhosale, Vikas D. Kadu, Dattatraya G. Raut, S. B. Patil, Raghunath B. Bhosale, A. S. Lawand, Mahesh G. Hublikar
Publikováno v:
Polycyclic Aromatic Compounds. 42:70-79
A new series of 1-Thiazolyl-2-Pyrazolines 5a-g was accomplished by reacting pyrazolealdehyde with an appropriate aromatic ketone in the presence of PEG-300 as a solvent to yield chalcone. The chalc...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f50f016f1b1a5ca7512ddd134b5d4d3b
https://doi.org/10.1080/10406638.2020.1716028
https://doi.org/10.1080/10406638.2020.1716028