Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Madhava, Golla"'
Autor:
Arun Kumar Awasthi, Lalit Kumar, Punit Tripathi, Madhava Golla, Cirandur Suresh Reddy, Pramod Kumar
Publikováno v:
Journal of Pharmaceutical Analysis, Vol 9, Iss 3, Pp 170-177 (2019)
Pantoprazole sodium, a substituted benzimidazole derivative, is an irreversible proton pump inhibitor which is primarily used for the treatment of duodenal ulcers, gastric ulcers, and gastroesophageal reflux disease (GERD). The monographs of European
Externí odkaz:
https://doaj.org/article/9351c82ef1d04a10b5835b2392fa1641
Autor:
Arun Kumar Awasthi, Lalit Kumar, Punit Tripathi, Madhava Golla, Mushtaq A. Aga, Cirandur Suresh Reddy, Pramod Kumar
Publikováno v:
ACS Omega, Vol 2, Iss 9, Pp 5460-5469 (2017)
Externí odkaz:
https://doaj.org/article/674bfd06eac6499f9ceb319ebb8eecdf
Autor:
Cirandur Suresh Reddy, Madhava Golla, Punit Tripathi, Pradeep Kumar, Lalit Kumar, Arun Kumar Awasthi
Publikováno v:
Journal of Pharmaceutical Analysis
Journal of Pharmaceutical Analysis, Vol 9, Iss 3, Pp 170-177 (2019)
Journal of Pharmaceutical Analysis, Vol 9, Iss 3, Pp 170-177 (2019)
Pantoprazole sodium, a substituted benzimidazole derivative, is an irreversible proton pump inhibitor which is primarily used for the treatment of duodenal ulcers, gastric ulcers, and gastroesophageal reflux disease (GERD). The monographs of European
Autor:
Rajasekhar Maram, Rasheed Syed, Subba Rao Devineni, Bhanu Kiran Rayalacheru, Madhava Golla, Chamarthi Naga Raju
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 192:794-798
The synthesis of a new series of P-heterocyclic compounds, substituted 2-aminomethyl-2-oxo-2λ5-perhydro-[1,3,2]oxazaphospholo[3,4-a]pyridine derivatives 8(a-j), was accomplished. A key intermediate, 2-(chloromethyl)-2-oxo-2λ5-perhydro-[1,3,2]oxazap
Autor:
Madhu Sudhana Saddala, Subba Rao Devineni, Madhava Golla, Naga Raju Chamarthi, Janardhan Avilala, Thaslim Basha Shaik, Narasimha Golla
Publikováno v:
Medicinal Chemistry Research. 26:999-1009
Synthesis of a series of new ethyl phosphoramidates 9a–j of acyclovir through phosphorylation of hydroxy group followed by substitution of numerous amines/amino acid esters 7a–j was accomplished. The structures of newly synthesized compounds were
Autor:
Subba Rao Devineni, Naga Raju Chamarthi, Gnana Kumari Pothuru, Madhava Golla, Munichandra Reddy Sivala, Venkatesh Medarametla
Publikováno v:
Journal of Chemical Sciences. 128:1303-1313
An efficient, environmentally benign and green method was developed for the synthesis of α-aminophosphonates by one-pot three-component reaction (Kabachnik-Fields reaction) of amine (4-(4-chlorophenoxy)aniline), aldehydes and diethyl phosphite using
Autor:
Balaji Meriga, Naga Raju Chamarthi, Usha Rani Asupathri, Madhu Sudhana Saddala, Subba Rao Devineni, Madhava Golla
Publikováno v:
Medicinal Chemistry Research. 25:751-768
A series of new class of P-heterocycle encompassing urea and thiourea derivatives, N-(substitutedphenyl)-N′-(2-oxo-2,3-dihydro-1H-2λ5-[1,3,2]diazaphospholo[4,5-b]pyridin-2-yl)ureas 11a–e/thioureas 11f–k, was accomplished from the precursor int
Publikováno v:
Journal of the Serbian Chemical Society, Vol 79, Iss 3, Pp 283-289 (2014)
Series of novel urea and thiourea derivatives of valaciclovir were efficiently synthesized in high yields and their antiviral activity was evaluated. (S)-2-((2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)methoxy)ethyl 2-amino-3- methylbutanoate (valaciclov
Autor:
Venkata Ramana Katla, Rasheed Syed, Naresh Kondapalli, Subba Rao Devineni, Madhava Golla, Naga Raju Chamarthi
Publikováno v:
Journal of Chemical Sciences. 126:117-125
An expeditious neat procedure was developed for the synthesis of a series of new methyl phenyl heterocyclic phosphinates (3a–l) through Michaelis–Arbuzov reaction by the reaction of various heterocyclic halides (Cl or Br) (1a–l) with dimethyl p
Autor:
Rasheed Syed, Nanda Kumar Yellapu, Jyothi Kumar Mv, Kuruva Chandra Sekhar, Naga Raju Chamarthi, Madhava Golla, Appa Rao Chippada
Publikováno v:
DARU Journal of Pharmaceutical Sciences
Background Chronic and oral administration of benzylamine improves glucose tolerance. Picolylamine is a selective functional antagonist of the human adenosine A2B receptor. Phosphonic diamide derivatives enhance the cellular permeability and in turn