Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672

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Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672. / Yurchenko, Anton N; Smetanina, Olga F; Ivanets, Elena V; Kalinovsky, Anatoly I; Khudyakova, Yuliya V; Kirichuk, Natalya N; Popov, Roman S; Bokemeyer, Carsten; von Amsberg, Gunhild; Chingizova, Ekaterina A; Afiyatullov, Shamil Sh; Dyshlovoy, Sergey A.

In: MAR DRUGS, Vol. 14, No. 7, 27.06.2016, p. E122.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Yurchenko, AN, Smetanina, OF, Ivanets, EV, Kalinovsky, AI, Khudyakova, YV, Kirichuk, NN, Popov, RS, Bokemeyer, C, von Amsberg, G, Chingizova, EA, Afiyatullov, SS & Dyshlovoy, SA 2016, 'Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672', MAR DRUGS, vol. 14, no. 7, pp. E122. https://doi.org/10.3390/md14070122

APA

Yurchenko, A. N., Smetanina, O. F., Ivanets, E. V., Kalinovsky, A. I., Khudyakova, Y. V., Kirichuk, N. N., Popov, R. S., Bokemeyer, C., von Amsberg, G., Chingizova, E. A., Afiyatullov, S. S., & Dyshlovoy, S. A. (2016). Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672. MAR DRUGS, 14(7), E122. https://doi.org/10.3390/md14070122

Vancouver

Yurchenko AN, Smetanina OF, Ivanets EV, Kalinovsky AI, Khudyakova YV, Kirichuk NN et al. Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672. MAR DRUGS. 2016 Jun 27;14(7):E122. https://doi.org/10.3390/md14070122

Bibtex

@article{270fac326158470d8500f64a0f7360a9,
title = "Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672",
abstract = "Three new epidithiodiketopiperazines pretrichodermamides D-F (1-3), together with the known N-methylpretrichodermamide B (4) and pretrichodermamide С (5), were isolated from the lipophilic extract of the marine algae-derived fungus Penicillium sp. KMM 4672. The structures of compounds 1-5 were determined based on spectroscopic methods. The absolute configuration of pretrichodermamide D (1) was established by a combination of modified Mosher's method, NOESY data, and biogenetic considerations. N-Methylpretrichodermamide B (5) showed strong cytotoxicity against 22Rv1 human prostate cancer cells resistant to androgen receptor targeted therapies.",
keywords = "Journal Article",
author = "Yurchenko, {Anton N} and Smetanina, {Olga F} and Ivanets, {Elena V} and Kalinovsky, {Anatoly I} and Khudyakova, {Yuliya V} and Kirichuk, {Natalya N} and Popov, {Roman S} and Carsten Bokemeyer and {von Amsberg}, Gunhild and Chingizova, {Ekaterina A} and Afiyatullov, {Shamil Sh} and Dyshlovoy, {Sergey A}",
year = "2016",
month = jun,
day = "27",
doi = "10.3390/md14070122",
language = "English",
volume = "14",
pages = "E122",
journal = "MAR DRUGS",
issn = "1660-3397",
publisher = "MDPI AG",
number = "7",

}

RIS

TY - JOUR

T1 - Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672

AU - Yurchenko, Anton N

AU - Smetanina, Olga F

AU - Ivanets, Elena V

AU - Kalinovsky, Anatoly I

AU - Khudyakova, Yuliya V

AU - Kirichuk, Natalya N

AU - Popov, Roman S

AU - Bokemeyer, Carsten

AU - von Amsberg, Gunhild

AU - Chingizova, Ekaterina A

AU - Afiyatullov, Shamil Sh

AU - Dyshlovoy, Sergey A

PY - 2016/6/27

Y1 - 2016/6/27

N2 - Three new epidithiodiketopiperazines pretrichodermamides D-F (1-3), together with the known N-methylpretrichodermamide B (4) and pretrichodermamide С (5), were isolated from the lipophilic extract of the marine algae-derived fungus Penicillium sp. KMM 4672. The structures of compounds 1-5 were determined based on spectroscopic methods. The absolute configuration of pretrichodermamide D (1) was established by a combination of modified Mosher's method, NOESY data, and biogenetic considerations. N-Methylpretrichodermamide B (5) showed strong cytotoxicity against 22Rv1 human prostate cancer cells resistant to androgen receptor targeted therapies.

AB - Three new epidithiodiketopiperazines pretrichodermamides D-F (1-3), together with the known N-methylpretrichodermamide B (4) and pretrichodermamide С (5), were isolated from the lipophilic extract of the marine algae-derived fungus Penicillium sp. KMM 4672. The structures of compounds 1-5 were determined based on spectroscopic methods. The absolute configuration of pretrichodermamide D (1) was established by a combination of modified Mosher's method, NOESY data, and biogenetic considerations. N-Methylpretrichodermamide B (5) showed strong cytotoxicity against 22Rv1 human prostate cancer cells resistant to androgen receptor targeted therapies.

KW - Journal Article

U2 - 10.3390/md14070122

DO - 10.3390/md14070122

M3 - SCORING: Journal article

C2 - 27355960

VL - 14

SP - E122

JO - MAR DRUGS

JF - MAR DRUGS

SN - 1660-3397

IS - 7

ER -