volume 68 issue 5 pages 1006-1013

Synthesis of dispirooxindoles containing N-unsubstituted heterocyclic moieties and study of their anticancer activity

Publication typeJournal Article
Publication date2019-05-01
scimago Q3
SJR0.305
CiteScore2.8
Impact factor
ISSN10665285, 15739171
General Chemistry
Abstract
A convenient method is proposed for the synthesis of N-unsubstituted spiroxindoles with different heterocyclic moieties (2-thiohydantoin, hydantoin, and thiazolidine) by the regio-selective 1,3-dipolar cycloaddition of azomethine ylides, generated from isatins and sarcosine, to arylidene derivatives of corresponding heterocycles. The cytotoxicity of compounds was tested by the MTT method against MCF7, A549, HEK, and VA13 cell lines and compared with the anticancer drug Nutlin-3a. The best bioactivity was observed for hydantoin-based dispiroindolinones, the most cytotoxic compound demonstrated selectivity against A549 lung cancer cells with an IC50 value of 6.6±1.6 μmol L−1.
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Beloglazkina A. A. et al. Synthesis of dispirooxindoles containing N-unsubstituted heterocyclic moieties and study of their anticancer activity // Russian Chemical Bulletin. 2019. Vol. 68. No. 5. pp. 1006-1013.
GOST all authors (up to 50) Copy
Beloglazkina A. A., Karpov N. A., Mefedova S. R., Polyakov V. S., Skvortsov D. A., Kalinina M. A., Tafeenko V. A., Majouga A. G., Zyk N. V., Beloglazkina E. K. Synthesis of dispirooxindoles containing N-unsubstituted heterocyclic moieties and study of their anticancer activity // Russian Chemical Bulletin. 2019. Vol. 68. No. 5. pp. 1006-1013.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1007/s11172-019-2511-6
UR - http://link.springer.com/10.1007/s11172-019-2511-6
TI - Synthesis of dispirooxindoles containing N-unsubstituted heterocyclic moieties and study of their anticancer activity
T2 - Russian Chemical Bulletin
AU - Beloglazkina, A A
AU - Karpov, N A
AU - Mefedova, S R
AU - Polyakov, V S
AU - Skvortsov, D A
AU - Kalinina, M A
AU - Tafeenko, V. A.
AU - Majouga, A G
AU - Zyk, N. V.
AU - Beloglazkina, E K
PY - 2019
DA - 2019/05/01
PB - Springer Nature
SP - 1006-1013
IS - 5
VL - 68
SN - 1066-5285
SN - 1573-9171
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Beloglazkina,
author = {A A Beloglazkina and N A Karpov and S R Mefedova and V S Polyakov and D A Skvortsov and M A Kalinina and V. A. Tafeenko and A G Majouga and N. V. Zyk and E K Beloglazkina},
title = {Synthesis of dispirooxindoles containing N-unsubstituted heterocyclic moieties and study of their anticancer activity},
journal = {Russian Chemical Bulletin},
year = {2019},
volume = {68},
publisher = {Springer Nature},
month = {may},
url = {http://link.springer.com/10.1007/s11172-019-2511-6},
number = {5},
pages = {1006--1013},
doi = {10.1007/s11172-019-2511-6}
}
MLA
Cite this
MLA Copy
Beloglazkina, A. A., et al. “Synthesis of dispirooxindoles containing N-unsubstituted heterocyclic moieties and study of their anticancer activity.” Russian Chemical Bulletin, vol. 68, no. 5, May. 2019, pp. 1006-1013. http://link.springer.com/10.1007/s11172-019-2511-6.