Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ch. Gangu Naidu"'
Publikováno v:
Tetrahedron Letters. 59:1670-1673
The first total synthesis was successfully achieved for biologically active 9,10-dihydrophenanthrene-1,5-diol. The key features of our synthetic approach are Perkin condensation, followed by bromination, palladium mediated intramolecular C-C bond cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9071714ef8531db1203d8b886b38adba
https://doi.org/10.1016/j.tetlet.2018.03.049
https://doi.org/10.1016/j.tetlet.2018.03.049
Autor:
A V Prasada Rao, Ch. Gangu Naidu, V Madhusudhan Rao, R. Nageswara Rao, K. Nagesh Kumar, Raju Padiya
Publikováno v:
Journal of chromatographic science. 56(10)
A sensitive, selective rapid bioanalytical assay method was developed and quantification of iloperidone (ILP) and olanzapine (OLZ) in rat plasma was done by mass spectrometry. Systematic sample preparation and extraction procedure were carried out by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867595e05093c3ff5e216b68083fa075
https://pubmed.ncbi.nlm.nih.gov/29982313
https://pubmed.ncbi.nlm.nih.gov/29982313
Publikováno v:
Biomedical Chromatography. 27:1733-1740
A stability-indicating reverse-phase high-performance liquid chromatography–mass spectrometric method was developed and validated for the assay of metaxalone through forced degradation under acidic, alkaline, photo, oxidative and peroxide stress co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::830de0a0245db43a8e9c4353e1b35841
https://doi.org/10.1002/bmc.2987
https://doi.org/10.1002/bmc.2987
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. :92-99
A validated stability indicating RP-HPLC assay of doxofylline was developed by separating its related substances and degradants on LichrocartC18 (250 mm × 4.6 mm; 5 μm) column using 10 mM ammonium acetate and acetonitrile as a mobile phase in a gra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96f923e6b57f03beb07057cde37eaf89
https://doi.org/10.1016/j.jpba.2013.02.004
https://doi.org/10.1016/j.jpba.2013.02.004
Publikováno v:
Biomedical Chromatography. 26:1534-1542
A highly selective, sensitive and rapid hydrophilic liquid interaction chromatographic method was developed and validated for determination of gemifloxacin on dried blood spots. The chromatographic separation was achieved on a reversed-phase zwitteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c22f96c3002fd5d3eec2a3a5db222276
https://doi.org/10.1002/bmc.2728
https://doi.org/10.1002/bmc.2728
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 56:471-478
A simple and rapid reversed phase liquid chromatographic method for separation and determination of the related substances of telmisartan (TLM) was developed and validated. The chromatographic separation was achieved on Lichrospher RP-18 column (250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b041266155f57b15990d2ed1f8f0e24c
https://doi.org/10.1016/j.jpba.2011.05.043
https://doi.org/10.1016/j.jpba.2011.05.043
Publikováno v:
Biomedical Chromatography. 25:1222-1229
A validated stability indicating RP-HPLC assay of gemifloxacin mesylate was developed by separating its related substances on an Inertsil-ODS3V-C18 (4.6 × 250 mm; 5 μm) column using 0.1% trifluoroaceticacid (pH 2.5) and methanol as a mobile phase i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94c2db4a8801c9341a4f93d1bdaeea2b
https://doi.org/10.1002/bmc.1594
https://doi.org/10.1002/bmc.1594
Publikováno v:
Biomedical chromatography : BMC. 27(12)
A stability-indicating reverse-phase high-performance liquid chromatography-mass spectrometric method was developed and validated for the assay of metaxalone through forced degradation under acidic, alkaline, photo, oxidative and peroxide stress cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9a67119569355a6c75e40283a066ed3
https://pubmed.ncbi.nlm.nih.gov/23881540
https://pubmed.ncbi.nlm.nih.gov/23881540
Publikováno v:
Journal of pharmaceutical and biomedical analysis.
A validated stability indicating RP-HPLC assay of doxofylline was developed by separating its related substances and degradants on LichrocartC18 (250 mm × 4.6 mm; 5 μm) column using 10 mM ammonium acetate and acetonitrile as a mobile phase in a gra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ae2ab7bc1806b4cb52a36577faee98c
https://pubmed.ncbi.nlm.nih.gov/23466440
https://pubmed.ncbi.nlm.nih.gov/23466440
Publikováno v:
Journal of pharmaceutical and biomedical analysis.
A rapid and highly sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method for determination of doxofylline on rat dried blood spots and urine was developed and validated. The chromatographic separation was achieved on a reverse p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcad1d4990c48850885cbfdfd23ceafa
https://pubmed.ncbi.nlm.nih.gov/23501441
https://pubmed.ncbi.nlm.nih.gov/23501441