41340-30-1Relevant articles and documents
Discovery of pyrano[3,4-b]indoles as potent and selective HCV NS5B polymerase inhibitors
Gopalsamy, Ariamala,Lim, Kitae,Ciszewski, Gregory,Park, Kaapjoo,Ellingboe, John W.,Bloom, Jonathan,Insaf, Shabana,Upeslacis, Janis,Mansour, Tarek S.,Krishnamurthy, Girija,Damarla, Murthy,Pyatski, Yelena,Ho, Douglas,Howe, Anita Y. M.,Orlowski, Mark,Feld, Boris,O'Connell, John
, p. 6603 - 6608 (2007/10/03)
A novel series of HCV NS5B RNA-dependent RNA polymerase inhibitors containing a pyrano-[3,4-b]indole scaffold is described leading to the discovery of compound 16, a highly potent and selective inhibitor that is active in the replicon system.
A novel class of potential antidepressants: 1 aminoalkyl 1,3,4,9 tetrahydropyrano [3,4 b]indoles
Humber,Demerson,Asselin,et al.
, p. 215 - 220 (2007/10/05)
A series of twenty four 1,3,4,9 tetrahydropyrano[3,4 b]indoles bearing baic side chains at positions 1 or 9 have been synthesized and their acute toxicities and antidepressant properties have been determined. One of the most active compounds was 1,9 dimethyl 1 [2 (dimethylamino)ethyl] 1,3,4,9 tetrahydropyrano[3,4 b]indole hydrochloride (AY 23,671), having an ED50 of 0.51 mg/kg i.p. in mice in preventing reserpine induced ptosis. The enantiomers of this compound were examined and were found to have the same order of activity as the racemate.