Synthesis of dispirooxindoles containing N-unsubstituted heterocyclic moieties and study of their anticancer activity
A A Beloglazkina
1
,
N A Karpov
1
,
S R Mefedova
1
,
V S Polyakov
1
,
D A Skvortsov
1
,
M A Kalinina
1, 2
,
V. A. Tafeenko
1
,
A G Majouga
1, 3
,
N. V. Zyk
1
,
Publication type: Journal Article
Publication date: 2019-05-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 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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Total citations:
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Citations from 2024:
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GOST
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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.
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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.
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RIS
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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 -
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BibTex (up to 50 authors)
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@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}
}
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MLA
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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, vol. 68, no. 5, May. 2019, pp. 1006-1013. http://link.springer.com/10.1007/s11172-019-2511-6.