Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vishnu Basetti"'
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 30:127288
Modifications at C6 and C7 positions of 3-cyanoquinolines 6 and 7 led to potent inhibitors of the ErbB family of kinases particularly against EGFRWT and Her4 enzymes in the radioisotope filter binding assay. The lead (4, SAB402) displayed potent dual
Publikováno v:
Heterocyclic Communications. 20:207-214
A tandem strategy for the synthesis of 7,12-dihydro-1,3,6,7,12-pentaazapleiadenes and 4-(2-aminophenoxy)pyrido[4,3-d]pyrimidin-5(6H)-ones from readily available starting materials has been developed.
Publikováno v:
Tetrahedron Letters. 54:2014-2017
A novel methodology for the synthesis of tetracyclic benzo-pyridonaphthyridines, forming a C–C and a C–N bond in concentrated sulfuric acid at 70 °C in a one-pot is reported. The key substrates (9a–m) are prepared by reacting 2-chloro-6-(4-flu
Publikováno v:
ChemInform. 46
Department of Discovery Chemistry, Aurigene Discovery Technologies Ltd., Hyderabad-500 049, Telangana, India E-mail : vijay_p@aurigene.com, potluri.vijay@gmail.com JNT University, Kukatpally, Hyderabad-500 072, Telangana, India new tandem three-step
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e9384f14885fb99721c35d1a569ab21
Autor:
Chandrasekhar Venna, Ravikrishna Vallakati, Aravinda B. Pulipaka, Sriram Rajgopal, Vamsee Krishna Chintakunta, Manohar Sharma Vedula, Venkateswarlu Akella, Sravan Kumar Teepireddy, Ajaya Kumar Reka, Venkata Adiseshu Kattuboina, Akash Khandelwal, Ramanujam Rajagopalan, Sreenu Jinnapally, Vijay V. Upreti, Prem Kumar Mamnoor, Gopalakrishnan Bulusu, Vishnu Basetti, Srinivas Rao Mamidi
Publikováno v:
European Journal of Medicinal Chemistry. 38:811-824
New styryl sulfone compounds have been synthesized and evaluated for their anti-proliferative activity. Among the compounds synthesized, one compound ( 7k ) has shown 51% tumor growth inhibition in mice implanted with HT-29 human carcinoma at 400 mg
ChemInform Abstract: A Facile Synthesis of Tetracyclic Benzo-pyridonaphthyridines by Domino Reaction
Publikováno v:
ChemInform. 44
The three-step synthesis of title compounds (VI), which represent alkaloid skeletons, is based on the acid-mediated cyclization of key precursors (V).