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Polyketides metabolites from the marine sediment-derived fungus Thermomyces lanuginosus Tsikl. KMM 4681

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Polyketides metabolites from the marine sediment-derived fungus Thermomyces lanuginosus Tsikl. KMM 4681. / Sobolevskaya, Maria P.; Berdyshev, Dmitrii V.; Zhuravleva, Olesya I.; Denisenko, Vladimir A.; Dyshlovoy, Sergey A.; von Amsberg, Gunhild; Khudyakova, Yuliya V.; Kirichuk, Natalya N.; Afiyatullov, Shamil Sh.

In: PHYTOCHEM LETT, Vol. 41, 02.2021, p. 114-118.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Sobolevskaya, MP, Berdyshev, DV, Zhuravleva, OI, Denisenko, VA, Dyshlovoy, SA, von Amsberg, G, Khudyakova, YV, Kirichuk, NN & Afiyatullov, SS 2021, 'Polyketides metabolites from the marine sediment-derived fungus Thermomyces lanuginosus Tsikl. KMM 4681', PHYTOCHEM LETT, vol. 41, pp. 114-118. https://doi.org/10.1016/j.phytol.2020.11.014

APA

Sobolevskaya, M. P., Berdyshev, D. V., Zhuravleva, O. I., Denisenko, V. A., Dyshlovoy, S. A., von Amsberg, G., Khudyakova, Y. V., Kirichuk, N. N., & Afiyatullov, S. S. (2021). Polyketides metabolites from the marine sediment-derived fungus Thermomyces lanuginosus Tsikl. KMM 4681. PHYTOCHEM LETT, 41, 114-118. https://doi.org/10.1016/j.phytol.2020.11.014

Vancouver

Sobolevskaya MP, Berdyshev DV, Zhuravleva OI, Denisenko VA, Dyshlovoy SA, von Amsberg G et al. Polyketides metabolites from the marine sediment-derived fungus Thermomyces lanuginosus Tsikl. KMM 4681. PHYTOCHEM LETT. 2021 Feb;41:114-118. https://doi.org/10.1016/j.phytol.2020.11.014

Bibtex

@article{95cc4101a63e4d798d78663b44cd5ebf,
title = "Polyketides metabolites from the marine sediment-derived fungus Thermomyces lanuginosus Tsikl. KMM 4681",
abstract = "New 1,3,6-trihydroxy-7-(dihydroxypropyl)-anthraquinone (1) and 6-(3′-hydroxybutan-2′-yl)-3,5-dimethyltetrahydro-2H-pyran-2-one (2), along with three previously known compounds, 1,3-dihydroxy-6-hydroxymethyl-7-methoxyanthraquinone (3), 1,3-dihydroxy-6-methyl-7-methoxyanthraquinone (4) and biphenyl-2,2′-diyl-diacetate (5) were isolated from the lipophilic extract of the marine sediment-derived fungus Thermomyces lanuginosus KMM 4681. The structures of the isolated compounds were established based on spectroscopic data. The absolute configurations of the stereocentres of 1 were determined using the time-dependent density functional theory (TD-DFT) calculation of ECD spectra. The effects of 1-4 on viability and colony formation of drug-resistant prostate cancer 22Rv1 and human PNT-2 cells were examined.",
keywords = "Acetonide, Anthraquinone, Derivative, HPLC, NMR, Prostate cancer, Spectroscopy, Thermomyces lanuginosus, Time-dependent density functional theory (TD-DFT)",
author = "Sobolevskaya, {Maria P.} and Berdyshev, {Dmitrii V.} and Zhuravleva, {Olesya I.} and Denisenko, {Vladimir A.} and Dyshlovoy, {Sergey A.} and {von Amsberg}, Gunhild and Khudyakova, {Yuliya V.} and Kirichuk, {Natalya N.} and Afiyatullov, {Shamil Sh}",
note = "Funding Information: We thank the Collective Facilities Center “The Far Eastern Center for Structural Molecular Research (NMR/MS) PIBOC FEB RAS” (Dr. Natalya. Yu. Kim, Dr. Roman.S. Popov and Dr. Valery. P. Glazunov) for recording MS, CD, UV, and IR data. The study was carried out using the Collective Facilities Center “Collection of Marine Microorganisms PIBOC FEB RAS”. The study was supported by Russian Foundation for Basic Research (grant № 19-53-54002 ). Publisher Copyright: {\textcopyright} 2020 Phytochemical Society of Europe Copyright: Copyright 2020 Elsevier B.V., All rights reserved.",
year = "2021",
month = feb,
doi = "10.1016/j.phytol.2020.11.014",
language = "English",
volume = "41",
pages = "114--118",
journal = "PHYTOCHEM LETT",
issn = "1874-3900",
publisher = "Elsevier BV",

}

RIS

TY - JOUR

T1 - Polyketides metabolites from the marine sediment-derived fungus Thermomyces lanuginosus Tsikl. KMM 4681

AU - Sobolevskaya, Maria P.

AU - Berdyshev, Dmitrii V.

AU - Zhuravleva, Olesya I.

AU - Denisenko, Vladimir A.

AU - Dyshlovoy, Sergey A.

AU - von Amsberg, Gunhild

AU - Khudyakova, Yuliya V.

AU - Kirichuk, Natalya N.

AU - Afiyatullov, Shamil Sh

N1 - Funding Information: We thank the Collective Facilities Center “The Far Eastern Center for Structural Molecular Research (NMR/MS) PIBOC FEB RAS” (Dr. Natalya. Yu. Kim, Dr. Roman.S. Popov and Dr. Valery. P. Glazunov) for recording MS, CD, UV, and IR data. The study was carried out using the Collective Facilities Center “Collection of Marine Microorganisms PIBOC FEB RAS”. The study was supported by Russian Foundation for Basic Research (grant № 19-53-54002 ). Publisher Copyright: © 2020 Phytochemical Society of Europe Copyright: Copyright 2020 Elsevier B.V., All rights reserved.

PY - 2021/2

Y1 - 2021/2

N2 - New 1,3,6-trihydroxy-7-(dihydroxypropyl)-anthraquinone (1) and 6-(3′-hydroxybutan-2′-yl)-3,5-dimethyltetrahydro-2H-pyran-2-one (2), along with three previously known compounds, 1,3-dihydroxy-6-hydroxymethyl-7-methoxyanthraquinone (3), 1,3-dihydroxy-6-methyl-7-methoxyanthraquinone (4) and biphenyl-2,2′-diyl-diacetate (5) were isolated from the lipophilic extract of the marine sediment-derived fungus Thermomyces lanuginosus KMM 4681. The structures of the isolated compounds were established based on spectroscopic data. The absolute configurations of the stereocentres of 1 were determined using the time-dependent density functional theory (TD-DFT) calculation of ECD spectra. The effects of 1-4 on viability and colony formation of drug-resistant prostate cancer 22Rv1 and human PNT-2 cells were examined.

AB - New 1,3,6-trihydroxy-7-(dihydroxypropyl)-anthraquinone (1) and 6-(3′-hydroxybutan-2′-yl)-3,5-dimethyltetrahydro-2H-pyran-2-one (2), along with three previously known compounds, 1,3-dihydroxy-6-hydroxymethyl-7-methoxyanthraquinone (3), 1,3-dihydroxy-6-methyl-7-methoxyanthraquinone (4) and biphenyl-2,2′-diyl-diacetate (5) were isolated from the lipophilic extract of the marine sediment-derived fungus Thermomyces lanuginosus KMM 4681. The structures of the isolated compounds were established based on spectroscopic data. The absolute configurations of the stereocentres of 1 were determined using the time-dependent density functional theory (TD-DFT) calculation of ECD spectra. The effects of 1-4 on viability and colony formation of drug-resistant prostate cancer 22Rv1 and human PNT-2 cells were examined.

KW - Acetonide

KW - Anthraquinone

KW - Derivative

KW - HPLC

KW - NMR

KW - Prostate cancer

KW - Spectroscopy

KW - Thermomyces lanuginosus

KW - Time-dependent density functional theory (TD-DFT)

UR - http://www.scopus.com/inward/record.url?scp=85097448098&partnerID=8YFLogxK

U2 - 10.1016/j.phytol.2020.11.014

DO - 10.1016/j.phytol.2020.11.014

M3 - SCORING: Journal article

AN - SCOPUS:85097448098

VL - 41

SP - 114

EP - 118

JO - PHYTOCHEM LETT

JF - PHYTOCHEM LETT

SN - 1874-3900

ER -