Synthesis, structural elucidation and biological evaluations of new guanidine-containing terpenoids as anticancer agents

Using sclareol and sclareolide as starting materials, the guanidine derivatives of 12-amino-11-dihomodrimane-8α-ol and 13-amino-14,15-bis-dinorlabd-8(9)-ene were synthesized by the reaction of the corresponding amines with sodium hydrogencyanamide in ethanol - water solution. Monoacyl- and diacylgua...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Duca Gheorghe
Aricu Aculina
Kuchkova Kaleria
Secara Elena
Barba Alic
Dragalin Ion
Ungur Nicon
Spengler Gabriella
Dokumentumtípus: Cikk
Megjelent: 2018
Sorozat:NATURAL PRODUCT LETTERS 33 No. 21
doi:10.1080/14786419.2018.1516658

mtmt:30409871
Online Access:http://publicatio.bibl.u-szeged.hu/16129
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520 3 |a Using sclareol and sclareolide as starting materials, the guanidine derivatives of 12-amino-11-dihomodrimane-8α-ol and 13-amino-14,15-bis-dinorlabd-8(9)-ene were synthesized by the reaction of the corresponding amines with sodium hydrogencyanamide in ethanol - water solution. Monoacyl- and diacylguanidines were prepared from activated with N,N-carbonyldiimidazole Δ8,9-bicyclohomofarnesenoic acid by the reaction with guanidine. Their structures were confirmed by the 1H and 13C NMR, IR spectral and elemental analysis data. The compounds 12, 13 and 15 were screened for their antiproliferative and cytotoxicity activities against Colo 205, Colo 320 and MRC 5 human lung fibroblasts with respect to standard drug, Cisplatin. The compounds 12 and 15 exhibits excellent results than positive control. Hence these two compounds may be act as drug lead molecules in cancer chemotherapy. 
700 0 1 |a Aricu Aculina  |e aut 
700 0 1 |a Kuchkova Kaleria  |e aut 
700 0 1 |a Secara Elena  |e aut 
700 0 1 |a Barba Alic  |e aut 
700 0 1 |a Dragalin Ion  |e aut 
700 0 1 |a Ungur Nicon  |e aut 
700 0 1 |a Spengler Gabriella  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/16129/1/Aricu_newguanidinecontainingterpenoidsasanticanceragents_2018.pdf  |z Dokumentum-elérés