Monanchocidin

Standard

Monanchocidin : a new apoptosis-inducing polycyclic guanidine alkaloid from the marine sponge Monanchora pulchra. / Guzii, Alla G; Makarieva, Tatyana N; Denisenko, Vladimir A; Dmitrenok, Pavel S; Kuzmich, Alexandra S; Dyshlovoy, Sergey A; Krasokhin, Vladimir B; Stonik, Valentin A.

In: ORG LETT, Vol. 12, No. 19, 01.10.2010, p. 4292-5.

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

Harvard

Guzii, AG, Makarieva, TN, Denisenko, VA, Dmitrenok, PS, Kuzmich, AS, Dyshlovoy, SA, Krasokhin, VB & Stonik, VA 2010, 'Monanchocidin: a new apoptosis-inducing polycyclic guanidine alkaloid from the marine sponge Monanchora pulchra', ORG LETT, vol. 12, no. 19, pp. 4292-5. https://doi.org/10.1021/ol101716x

APA

Guzii, A. G., Makarieva, T. N., Denisenko, V. A., Dmitrenok, P. S., Kuzmich, A. S., Dyshlovoy, S. A., Krasokhin, V. B., & Stonik, V. A. (2010). Monanchocidin: a new apoptosis-inducing polycyclic guanidine alkaloid from the marine sponge Monanchora pulchra. ORG LETT, 12(19), 4292-5. https://doi.org/10.1021/ol101716x

Vancouver

Bibtex

@article{489ce75cad1d4a14984d03feeca275a3,
title = "Monanchocidin: a new apoptosis-inducing polycyclic guanidine alkaloid from the marine sponge Monanchora pulchra",
abstract = "Monanchocidin (1), a guanidine alkaloid with an unprecedented skeleton system derived from a polyketide precursor, (ω-3)-hydroxy fatty acid, and containing a 2-aminoethyl- and 3-aminopropyl-substituted morpholine hemiketal ring, has been isolated from the sponge Monanhora pulchra. The structure of 1 was assigned on the basis of detailed analysis of 1D and 2D NMR spectra, mass spectrometry, and results of chemical transformations. Compound 1 shows pro-apoptotic and cytoxic activities.",
keywords = "Animals, Apoptosis, Cell Line, Guanidine, Humans, Mice, Molecular Structure, Oxidation-Reduction, Porifera, Journal Article, Research Support, Non-U.S. Gov't",
author = "Guzii, {Alla G} and Makarieva, {Tatyana N} and Denisenko, {Vladimir A} and Dmitrenok, {Pavel S} and Kuzmich, {Alexandra S} and Dyshlovoy, {Sergey A} and Krasokhin, {Vladimir B} and Stonik, {Valentin A}",
year = "2010",
month = oct,
day = "1",
doi = "10.1021/ol101716x",
language = "English",
volume = "12",
pages = "4292--5",
journal = "ORG LETT",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "19",

}

RIS

TY - JOUR

T1 - Monanchocidin

T2 - a new apoptosis-inducing polycyclic guanidine alkaloid from the marine sponge Monanchora pulchra

AU - Guzii, Alla G

AU - Makarieva, Tatyana N

AU - Denisenko, Vladimir A

AU - Dmitrenok, Pavel S

AU - Kuzmich, Alexandra S

AU - Dyshlovoy, Sergey A

AU - Krasokhin, Vladimir B

AU - Stonik, Valentin A

PY - 2010/10/1

Y1 - 2010/10/1

N2 - Monanchocidin (1), a guanidine alkaloid with an unprecedented skeleton system derived from a polyketide precursor, (ω-3)-hydroxy fatty acid, and containing a 2-aminoethyl- and 3-aminopropyl-substituted morpholine hemiketal ring, has been isolated from the sponge Monanhora pulchra. The structure of 1 was assigned on the basis of detailed analysis of 1D and 2D NMR spectra, mass spectrometry, and results of chemical transformations. Compound 1 shows pro-apoptotic and cytoxic activities.

AB - Monanchocidin (1), a guanidine alkaloid with an unprecedented skeleton system derived from a polyketide precursor, (ω-3)-hydroxy fatty acid, and containing a 2-aminoethyl- and 3-aminopropyl-substituted morpholine hemiketal ring, has been isolated from the sponge Monanhora pulchra. The structure of 1 was assigned on the basis of detailed analysis of 1D and 2D NMR spectra, mass spectrometry, and results of chemical transformations. Compound 1 shows pro-apoptotic and cytoxic activities.

KW - Animals

KW - Apoptosis

KW - Cell Line

KW - Guanidine

KW - Humans

KW - Mice

KW - Molecular Structure

KW - Oxidation-Reduction

KW - Porifera

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.1021/ol101716x

DO - 10.1021/ol101716x

M3 - SCORING: Journal article

C2 - 20804151

VL - 12

SP - 4292

EP - 4295

JO - ORG LETT

JF - ORG LETT

SN - 1523-7060

IS - 19

ER -