Theoretical results:
 - Successfully synthesized 17 quinoline substances of the new podophyllotoxin
 - NMR, MS spectrometer... confirm the structure of the newly synthesized substances
- 01 in vitro cytotoxicity profile on some experimental cancer cell lines of 17 synthesized substances.
Applied results: 
- 01 process of synthesizing 17 laboratory-scale clean substances
- Successfully synthesized 17 quinoline derivatives of new podophyllotoxin, 15-20mg each

- Presenting a new method of successfully synthesizing new thiore derivatives of podophyllotoxin under mild conditions without solvents and catalysts.
- Conducted bioactivity screening and molecular docking simulation of newly synthesized substances
- Analyzed the effect of structure, group of substances, bulkiness or position of groups on the activity of derivatives and confirmed through correlation on molecular docking model.

- Scientific papers in referred journals (list):
+ 01 International paper in the Journal of Heterocylic chemistry: Multicomponent 
synthesis of new 5-thiourea-4-aza-2.3 didehydropodophyllotoxins as potent 
cytotoxic agents.
+ 01 domestic article published in Vietnam Journal of Science and Technology: 
Synthesis and cytotoxicity of new 4-aza-2.3 didehydropodophyllotoxins.
- Other products (if applicable): Other products (currently kept at the Pharmaceutical Research and Development Department, Institute of Chemistry)
+ 01 Process of synthesizing 17 laboratory-scale clean substances
+ 17 new podophyllotoxin quinoline derivatives, each 15-20 mg
+ Profiles proving the structure of 17 quinoline clean substances of new podophylloin (MS, NMR, IR spectrometers...)
+ Results of activity testing of 17 substances with 2 cancer cell lines HepG2 and MCF7
+ 01 set of molecular docking image profiles of derivatives