76142-14-8Relevant academic research and scientific papers
Synthesis of C-methyl chalcones as HIV-integrase inhibitors - Computational approach
Vasu Babu,Navudu, Ramesh,Trimurtulu,Hari Babu
, p. 877 - 881 (2014/03/21)
Eight new 3-methyl chalcones (3a-h) were synthesized for active inhibition against HIV-integrase basing on docking studies on a series of titled compounds. The selected integrase (IN) enzyme is taken as an attractive target for therapeutic drug design. Th
STUDIES ON THE CONSTITUENTS OF OPHIOPOGONIS TUBERS. VII. SYNTHETIC STUDIES OF HOMOISOFLAVONIDS.
Tada, Akihiro,Saitoh, Tamotsu,Shoji, Junzo
, p. 2487 - 2493 (2007/10/02)
Several homoisoflavonoidal compounds, namely the monomethyl ethers ((IIIb) and (IVb)) of methylophiopogonones A and B, isoophiopogonone A monomethyl ether (VIIIb) and desmethylisoophiopogonone B (IXa), which were derived from the constituents of Ophiopogo
