19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum. / Traore, Maminata; Ziegler, Hanne Lindvig; Olsen, C Erik; Hassanata, Millogo-kone; Pierre, Guissou I; Nacoulma, Odile G; Guiguemdé, T Rober; Christensen, Søren Brøgger.

In: Natural Product Research, Vol. 23, No. 12, 2009, p. 1108-1111.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Traore, M, Ziegler, HL, Olsen, CE, Hassanata, M, Pierre, GI, Nacoulma, OG, Guiguemdé, TR & Christensen, SB 2009, '19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum', Natural Product Research, vol. 23, no. 12, pp. 1108-1111. https://doi.org/10.1080/14786410802401481

APA

Traore, M., Ziegler, H. L., Olsen, C. E., Hassanata, M., Pierre, G. I., Nacoulma, O. G., ... Christensen, S. B. (2009). 19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum. Natural Product Research, 23(12), 1108-1111. https://doi.org/10.1080/14786410802401481

Vancouver

Traore M, Ziegler HL, Olsen CE, Hassanata M, Pierre GI, Nacoulma OG et al. 19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum. Natural Product Research. 2009;23(12):1108-1111. https://doi.org/10.1080/14786410802401481

Author

Traore, Maminata ; Ziegler, Hanne Lindvig ; Olsen, C Erik ; Hassanata, Millogo-kone ; Pierre, Guissou I ; Nacoulma, Odile G ; Guiguemdé, T Rober ; Christensen, Søren Brøgger. / 19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum. In: Natural Product Research. 2009 ; Vol. 23, No. 12. pp. 1108-1111.

Bibtex

@article{c077353096d211de8bc9000ea68e967b,
title = "19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum",
abstract = "A bioactivity guided fractionation of roots of Canthium multiflorum led to the isolation of the new ursenoic acid derivative 19alpha-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid (1), which showed antiplasmodial effect without inducing change of the shape of membranes of erythrocytes.",
keywords = "Former Faculty of Pharmaceutical Sciences",
author = "Maminata Traore and Ziegler, {Hanne Lindvig} and Olsen, {C Erik} and Millogo-kone Hassanata and Pierre, {Guissou I} and Nacoulma, {Odile G} and Guiguemd{\'e}, {T Rober} and Christensen, {S{\o}ren Br{\o}gger}",
note = "Keywords: Canthium multiflorum; antiplasmodial triterpenoids; ursenoic acid; derivative; Rubiaceae; erythrocytes",
year = "2009",
doi = "10.1080/14786410802401481",
language = "English",
volume = "23",
pages = "1108--1111",
journal = "Natural Product Research",
issn = "1478-6419",
publisher = "Taylor & Francis",
number = "12",

}

RIS

TY - JOUR

T1 - 19a-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated from Canthium multiflorum

AU - Traore, Maminata

AU - Ziegler, Hanne Lindvig

AU - Olsen, C Erik

AU - Hassanata, Millogo-kone

AU - Pierre, Guissou I

AU - Nacoulma, Odile G

AU - Guiguemdé, T Rober

AU - Christensen, Søren Brøgger

N1 - Keywords: Canthium multiflorum; antiplasmodial triterpenoids; ursenoic acid; derivative; Rubiaceae; erythrocytes

PY - 2009

Y1 - 2009

N2 - A bioactivity guided fractionation of roots of Canthium multiflorum led to the isolation of the new ursenoic acid derivative 19alpha-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid (1), which showed antiplasmodial effect without inducing change of the shape of membranes of erythrocytes.

AB - A bioactivity guided fractionation of roots of Canthium multiflorum led to the isolation of the new ursenoic acid derivative 19alpha-hydroxy-3-oxo-ursa-1,12-dien-28-oic acid (1), which showed antiplasmodial effect without inducing change of the shape of membranes of erythrocytes.

KW - Former Faculty of Pharmaceutical Sciences

U2 - 10.1080/14786410802401481

DO - 10.1080/14786410802401481

M3 - Journal article

C2 - 19662575

VL - 23

SP - 1108

EP - 1111

JO - Natural Product Research

JF - Natural Product Research

SN - 1478-6419

IS - 12

ER -

ID: 14119460