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Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis. / Prima, Darya O.; Vorontsova, Elena V.; Makarov, Arkady G. et al.

In: Mendeleev Communications, Vol. 27, No. 5, 01.09.2017, p. 439-442.

Research output: Contribution to journalArticlepeer-review

Harvard

Prima, DO, Vorontsova, EV, Makarov, AG, Makarov, AY, Bagryanskaya, IY, Mikhailovskaya, TF, Slizhov, YG & Zibarev, AV 2017, 'Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis', Mendeleev Communications, vol. 27, no. 5, pp. 439-442. https://doi.org/10.1016/j.mencom.2017.09.002

APA

Prima, D. O., Vorontsova, E. V., Makarov, A. G., Makarov, A. Y., Bagryanskaya, I. Y., Mikhailovskaya, T. F., Slizhov, Y. G., & Zibarev, A. V. (2017). Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis. Mendeleev Communications, 27(5), 439-442. https://doi.org/10.1016/j.mencom.2017.09.002

Vancouver

Prima DO, Vorontsova EV, Makarov AG, Makarov AY, Bagryanskaya IY, Mikhailovskaya TF et al. Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis. Mendeleev Communications. 2017 Sept 1;27(5):439-442. doi: 10.1016/j.mencom.2017.09.002

Author

Prima, Darya O. ; Vorontsova, Elena V. ; Makarov, Arkady G. et al. / Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis. In: Mendeleev Communications. 2017 ; Vol. 27, No. 5. pp. 439-442.

BibTeX

@article{c101008ec60945cda89456f16612a132,
title = "Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis",
abstract = "The title compounds synthesized from halogenated arene-1,2-diamines revealed, together with the latter, cytotoxicity towards the Hep2 (laryngeal epidermoid carcinoma) cells. The cytotoxicity was high and was accompanied by pronounced apoptotic activity at low concentrations for fluorinated diazoles, triazoles and selenadiazoles.",
author = "Prima, {Darya O.} and Vorontsova, {Elena V.} and Makarov, {Arkady G.} and Makarov, {Alexander Yu} and Bagryanskaya, {Irina Yu} and Mikhailovskaya, {Tatiana F.} and Slizhov, {Yuri G.} and Zibarev, {Andrey V.}",
year = "2017",
month = sep,
day = "1",
doi = "10.1016/j.mencom.2017.09.002",
language = "English",
volume = "27",
pages = "439--442",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "5",

}

RIS

TY - JOUR

T1 - Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis

AU - Prima, Darya O.

AU - Vorontsova, Elena V.

AU - Makarov, Arkady G.

AU - Makarov, Alexander Yu

AU - Bagryanskaya, Irina Yu

AU - Mikhailovskaya, Tatiana F.

AU - Slizhov, Yuri G.

AU - Zibarev, Andrey V.

PY - 2017/9/1

Y1 - 2017/9/1

N2 - The title compounds synthesized from halogenated arene-1,2-diamines revealed, together with the latter, cytotoxicity towards the Hep2 (laryngeal epidermoid carcinoma) cells. The cytotoxicity was high and was accompanied by pronounced apoptotic activity at low concentrations for fluorinated diazoles, triazoles and selenadiazoles.

AB - The title compounds synthesized from halogenated arene-1,2-diamines revealed, together with the latter, cytotoxicity towards the Hep2 (laryngeal epidermoid carcinoma) cells. The cytotoxicity was high and was accompanied by pronounced apoptotic activity at low concentrations for fluorinated diazoles, triazoles and selenadiazoles.

UR - http://www.scopus.com/inward/record.url?scp=85030125084&partnerID=8YFLogxK

U2 - 10.1016/j.mencom.2017.09.002

DO - 10.1016/j.mencom.2017.09.002

M3 - Article

AN - SCOPUS:85030125084

VL - 27

SP - 439

EP - 442

JO - Mendeleev Communications

JF - Mendeleev Communications

SN - 0959-9436

IS - 5

ER -

ID: 9896293