Synthesis and cytotoxic activity evaluation of maleopimaric and dihydroquinopimaric esters and amides

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Аннотация

The new 1-, 1,4- and 1,4,20-diethoxyphosphoryl-containing esters were synthesized as a result of interaction of dihydroquinopimaric acid methyl ester hydroxyl derivatives with diethylchlorophosphite, A study of the cytotoxic activity in vitro on 60 cell lines of nine different human tumors of methyl ester of dihydroquinopimaric acid with diethoxyphosphoryl, furan and indole fragments, as well as diterpene amides with linear, heterocyclic and aromatic amines residues showed that diethoxyphosphoryl and benzylamine substituents are of key importance for the manifestation of the cytotoxic effect. Diethoxyphosphoryl derivatives (XIX) and (XVII), and benzylamide (IX) showed cytotoxic activity against one, seven and four cell lines of breast cancer, leukemia, non-small cell lung cancer, melanoma and prostate cancer, respectively. The greatest activity was demonstrated by maleopimaric acid benzylamide (XIII), which effectively inhibited the growth of 19 cell lines of eight cancer types and had a significant cytotoxic effect against all studied leukemia cell lines.

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Авторлар туралы

E. Tretyakova

Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: tretyakovaelv@gmail.com
Ресей, prosp. Oktyabrya 71, Ufa, 450054

S. Sharafutdinova

Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences; Ufa University of Science and Technology

Email: tretyakovaelv@gmail.com
Ресей, prosp. Oktyabrya 71, Ufa, 450054; Ufa, ul. Zaki Validi 32, 450076

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Әрекет
1. JATS XML
2. Fig. 1. Methyl dihydroquinopimarate esters (I–V) [16] and amides of dihydroquinopimaric (VI–IX) and maleopimaric (X–XIII) acids [17]. Reagents and conditions: (EtO)2POCl, DMAP, pyridine, 0–23°C, 3 h.

Жүктеу (117KB)
3. Scheme 1. Synthesis of diethoxyphosphoryl derivatives (XVII–XIX).

Жүктеу (113KB)

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