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Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol. / Nazimova, E. V.; Shtro, A. A.; Anikin, V. B. et al.

In: Chemistry of Natural Compounds, Vol. 53, No. 2, 01.03.2017, p. 260-264.

Research output: Contribution to journalArticlepeer-review

Harvard

Nazimova, EV, Shtro, AA, Anikin, VB, Patrusheva, OS, Il′ina, IV, Korchagina, DV, Zarubaev, VV, Volcho, KP & Salakhutdinov, NF 2017, 'Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol', Chemistry of Natural Compounds, vol. 53, no. 2, pp. 260-264. https://doi.org/10.1007/s10600-017-1966-7

APA

Nazimova, E. V., Shtro, A. A., Anikin, V. B., Patrusheva, O. S., Il′ina, I. V., Korchagina, D. V., Zarubaev, V. V., Volcho, K. P., & Salakhutdinov, N. F. (2017). Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol. Chemistry of Natural Compounds, 53(2), 260-264. https://doi.org/10.1007/s10600-017-1966-7

Vancouver

Nazimova EV, Shtro AA, Anikin VB, Patrusheva OS, Il′ina IV, Korchagina DV et al. Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol. Chemistry of Natural Compounds. 2017 Mar 1;53(2):260-264. doi: 10.1007/s10600-017-1966-7

Author

Nazimova, E. V. ; Shtro, A. A. ; Anikin, V. B. et al. / Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol. In: Chemistry of Natural Compounds. 2017 ; Vol. 53, No. 2. pp. 260-264.

BibTeX

@article{050e820749a54a17895c2645efc8f142,
title = "Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol",
abstract = "Influenza A (H1N1) antiviral activity of compounds with an octahydro-2H-chromene skeleton that were prepared by reacting the monoterpenoid (–)-isopulegol and thiophenecarboxaldehyde and its derivatives was studied for the first time. The 5-bromothiophene-2-carboxaldehyde derivative exhibited the greatest antiviral activity.",
keywords = "antiviral activity, clay, heterocyclic compounds, influenza A, monoterpenes, thiophenecarboxaldehyde",
author = "Nazimova, {E. V.} and Shtro, {A. A.} and Anikin, {V. B.} and Patrusheva, {O. S.} and Il′ina, {I. V.} and Korchagina, {D. V.} and Zarubaev, {V. V.} and Volcho, {K. P.} and Salakhutdinov, {N. F.}",
note = "Publisher Copyright: {\textcopyright} 2017, Springer Science+Business Media New York.",
year = "2017",
month = mar,
day = "1",
doi = "10.1007/s10600-017-1966-7",
language = "English",
volume = "53",
pages = "260--264",
journal = "Chemistry of Natural Compounds",
issn = "0009-3130",
publisher = "Springer New York",
number = "2",

}

RIS

TY - JOUR

T1 - Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol

AU - Nazimova, E. V.

AU - Shtro, A. A.

AU - Anikin, V. B.

AU - Patrusheva, O. S.

AU - Il′ina, I. V.

AU - Korchagina, D. V.

AU - Zarubaev, V. V.

AU - Volcho, K. P.

AU - Salakhutdinov, N. F.

N1 - Publisher Copyright: © 2017, Springer Science+Business Media New York.

PY - 2017/3/1

Y1 - 2017/3/1

N2 - Influenza A (H1N1) antiviral activity of compounds with an octahydro-2H-chromene skeleton that were prepared by reacting the monoterpenoid (–)-isopulegol and thiophenecarboxaldehyde and its derivatives was studied for the first time. The 5-bromothiophene-2-carboxaldehyde derivative exhibited the greatest antiviral activity.

AB - Influenza A (H1N1) antiviral activity of compounds with an octahydro-2H-chromene skeleton that were prepared by reacting the monoterpenoid (–)-isopulegol and thiophenecarboxaldehyde and its derivatives was studied for the first time. The 5-bromothiophene-2-carboxaldehyde derivative exhibited the greatest antiviral activity.

KW - antiviral activity

KW - clay

KW - heterocyclic compounds

KW - influenza A

KW - monoterpenes

KW - thiophenecarboxaldehyde

UR - http://www.scopus.com/inward/record.url?scp=85018495476&partnerID=8YFLogxK

U2 - 10.1007/s10600-017-1966-7

DO - 10.1007/s10600-017-1966-7

M3 - Article

AN - SCOPUS:85018495476

VL - 53

SP - 260

EP - 264

JO - Chemistry of Natural Compounds

JF - Chemistry of Natural Compounds

SN - 0009-3130

IS - 2

ER -

ID: 8969088