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Syntheses of alkyl-de-sanguinarine-N5-methyl derivatives and evaluation of in vitro growth inhibitory activities against cancer cell lines
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Qi-lin LI, An-jun DENG, Zheng YAN, Zhi-hong LI, Nan WANG, Hai-lin QIN*
Acta Pharmaceutica Sinica | 2018, 53(10) : 1689 - 1695
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Acta Pharmaceutica Sinica | 2018, 53(10): 1689-1695
Medicinal Chemistry
Syntheses of alkyl-de-sanguinarine-N5-methyl derivatives and evaluation of in vitro growth inhibitory activities against cancer cell lines
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Qi-lin LI, An-jun DENG, Zheng YAN, Zhi-hong LI, Nan WANG, Hai-lin QIN*
Affiliations
  • State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
Published: 2018-10-12 doi: 10.16438/j.0513-4870.2018-0645
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2, 3:7, 8-Bis(methylenedioxy)benzo[c]phenanthridine was synthesized in a strategy of converging synthesis with 6-bromo-2, 3-dihydroxybenzaldehyde, 5-nitronaphthalene-2, 3-diol, and dibromomethane, respectively, as starting materials. The reaction process included dioxy-de-dibromo nucleophilic substitution under alkaline condition, reduction reaction, Schiff base-forming reaction, and an arene radical cyclization step under the presence of Bu3SnH and AIBN as radical initiator, among others. The 2, 3:7, 8-bis(methylenedioxy)benzo[c] phenanthridine as intermediate was reacted with NaBH4 and different aliphatic acids as alkylation agent to afford 2, 3:7, 8-bis(methylenedioxy)-5, 6-dihydro-N5-alkylbenzo[c]phenanthridines. These dihydro-type products were aromatized using DDQ as oxidant under alkaline condition, and then, salinized using HCl as source of equilibrium anion to yield the series of target alkyl-de-sanguinarine-N5-methyl derivatives. All the synthesized alkyl-de-sanguinarine-N5-methyl derivatives exhibited significantly improved in vitro growth inhibitory activities against cancer cell lines as compared with sanguinarine and the positive control. In pharmacological experiments targeting five cancer cell lines, the target compounds showed activities five-fold active than that of sanguinarine. The findings of this study indicated that the structure modification strategy of substituting n-alkyls for the N5-methyl of natural sanguinarine can be used to improve the growth inhibitory activities against cancer cell lines through increasing liposolubility and steric hindrance to protect the active 5, 6-imine structure.

sanguinarine  /  alkyl-de-sanguinarine-N5-methyl derivative  /  converging synthesis  /  N-alkylation reaction  /  growth inhibitory activities against tumor cell lines
Qi-lin LI, An-jun DENG, Zheng YAN, Zhi-hong LI, Nan WANG, Hai-lin QIN. Syntheses of alkyl-de-sanguinarine-N5-methyl derivatives and evaluation of in vitro growth inhibitory activities against cancer cell lines[J]. Acta Pharmaceutica Sinica, 2018 , 53 (10) : 1689 -1695 . DOI: 10.16438/j.0513-4870.2018-0645
Year 2018 volume 53 Issue 10
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doi: 10.16438/j.0513-4870.2018-0645
  • Receive Date:2018-07-16
  • Online Date:2026-01-15
  • Published:2018-10-12
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  • Received:2018-07-16
  • Revised:2018-08-29
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    State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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