26847-68-7

Upstream product

• 67-56-1 methanol 
• 26691-61-2 6,7-dimethoxy-3-benzyloxy-9-phenanthrenecarboxylic acid 
• 26691-59-8 9-Cyan-3-benzyloxy-6,7-dimethoxy-phenanthren 
• 1449298-72-9 3-hydroxy-6,7-dimethoxy-9-phenanthrenecarboxylic acid methyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 26691-62-3 [3-(benzyloxy)-6,7-dimethoxy-9-phenanthryl]methanol 
• 26691-63-4 9-Chlormethyl-3-benzyloxy-6,7-dimethoxy-phenanthren 
• 1422707-31-0 methyl (2S)-1-{[3-(benzyloxy)-6,7-dimethoxy-9-phenanthryl]methyl}-5-oxopyrrolidine-2-carboxylate 
• 1422707-32-1 methyl (2R)-1-{[3-(benzyloxy)-6,7-dimethoxy-9-phenanthryl]methyl}-5-oxopyrrolidine-2-carboxylate 
• 1223487-18-0 (2S)-1-{[3-(benzyloxy)-6,7-dimethoxy-9-phenanthryl]methyl}-5-oxopyrrolidine-2-carboxylic acid 
• 1223487-20-4 (2R)-1-{[3-(benzyloxy)-6,7-dimethoxy-9-phenanthryl]methyl}-5-oxopyrrolidine-2-carboxylic acid 
• 1223487-21-5 (13aS)-3-(benzyloxy)-6,7-dimethoxy-13,13a-dihydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline-11,14(9H,12H)-dione 
• 1223487-22-6 (13aR)-3-(benzyloxy)-6,7-dimethoxy-13,13a-dihydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline-11,14(9H,12H)-dione 
• 1338360-74-9 (13aS)-3-(benzyloxy)-6,7-dimethoxy-12,13,13a,14-tetrahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline-11(9H)-one 
• 1422707-33-2 (13aR)-3-(benzyloxy)-6,7-dimethoxy-12,13,13a,14-tetrahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline-11(9H)-one 
• 1422707-34-3 (13aS)-3-(benzyloxy)-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline 
• 1422707-35-4 (13aR)-3-(benzyloxy)-6,7-dimethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline 
• 26691-61-2 6,7-dimethoxy-3-benzyloxy-9-phenanthrenecarboxylic acid 

Relevant academic research and scientific papers

Stereospecific synthesis and biological evaluation of monodesmethyl metabolites of (+)-13a-(S)-deoxytylophorinine as potential antitumor agents

Three major monodesmethyl metabolites of (+)-13a-(S)-deoxytylophorinine were synthesized stereospecifically and their configurations at C-13a were determined. Biological assays revealed that one of the metabolites, 3-O-desmethyl-13a-(S)-deoxytylophorinine

Phenanthroquinolizidine Phenanthroindolizidine alkaloid derivatives and salts thereof and their preparation, anti-plant-virus and anti-cancer activity

Provided are phenanthroindolizidine alkaloid derivates and salt thereof as well as preparation, a plant-virus resisting activity, and an anti-cancer activity of phenanthroindolizidine alkaloid derivates and salt thereof. The derivates and the salt thereof have a good plant-virus resisting activity, which is capable of well restraining a tobacco mosaic virus (TMV), and meanwhile, have a good anti-cancer activity, which is capable of well restraining the human lung adenocarcinoma A-549 and the human leukemia HL-60.