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Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors

Timothy Haemers, Jochen Wiesner, Sara Van Poecke UGent, Jan Goeman UGent, Dajana Henschker, Ewald Beck, Hassan Jomaa and Serge Van Calenbergh UGent (2006) BIOORGANIC & MEDICINAL CHEMISTRY LETTERS. 16(7). p.1888-1891
Please use this url to cite or link to this publication:
author
organization
alternative title
Synthesis of alpha-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors
year
type
journalArticle (original)
publication status
published
subject
keyword
2C-methyl-D-erithrytol 4-phosphate pathway, fosmidomycin, 1-deoxy-D-xylulose-5-phosphate reductoisomerase, VIVO ANTIMALARIAL ACTIVITY, ESTER PRODRUGS, 5-PHOSPHATE REDUCTOISOMERASE, ISOPRENOID BIOSYNTHESIS, NONMEVALONATE PATHWAY, FR900098, MALARIA, DRUGS
journal title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Bioorg. Med. Chem. Lett.
volume
16
issue
7
pages
1888 - 1891
Web of Science type
Article
Web of Science id
000236402500025
JCR category
CHEMISTRY, MEDICINAL
JCR impact factor
2.538 (2006)
JCR rank
11/35 (2006)
JCR quartile
2 (2006)
ISSN
0960-894X
DOI
10.1016/j.bmcl.2005.12.082
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
351053
handle
http://hdl.handle.net/1854/LU-351053
date created
2006-04-18 12:05:00
date last changed
2016-12-19 15:43:10
@article{351053,
  author       = {Haemers, Timothy and Wiesner, Jochen and Van Poecke, Sara and Goeman, Jan and Henschker, Dajana and Beck, Ewald and Jomaa, Hassan and Van Calenbergh, Serge},
  issn         = {0960-894X},
  journal      = {BIOORGANIC \& MEDICINAL CHEMISTRY LETTERS},
  keyword      = {2C-methyl-D-erithrytol 4-phosphate pathway,fosmidomycin,1-deoxy-D-xylulose-5-phosphate reductoisomerase,VIVO ANTIMALARIAL ACTIVITY,ESTER PRODRUGS,5-PHOSPHATE REDUCTOISOMERASE,ISOPRENOID BIOSYNTHESIS,NONMEVALONATE PATHWAY,FR900098,MALARIA,DRUGS},
  language     = {eng},
  number       = {7},
  pages        = {1888--1891},
  title        = {Synthesis of \ensuremath{\alpha}-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors},
  url          = {http://dx.doi.org/10.1016/j.bmcl.2005.12.082},
  volume       = {16},
  year         = {2006},
}

Chicago
Haemers, Timothy, Jochen Wiesner, Sara Van Poecke, Jan Goeman, Dajana Henschker, Ewald Beck, Hassan Jomaa, and Serge Van Calenbergh. 2006. “Synthesis of Α-substituted Fosmidomycin Analogues as Highly Potent Plasmodium Falciparum Growth Inhibitors.” Bioorganic & Medicinal Chemistry Letters 16 (7): 1888–1891.
APA
Haemers, Timothy, Wiesner, J., Van Poecke, S., Goeman, J., Henschker, D., Beck, E., Jomaa, H., et al. (2006). Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 16(7), 1888–1891.
Vancouver
1.
Haemers T, Wiesner J, Van Poecke S, Goeman J, Henschker D, Beck E, et al. Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS. 2006;16(7):1888–91.
MLA
Haemers, Timothy, Jochen Wiesner, Sara Van Poecke, et al. “Synthesis of Α-substituted Fosmidomycin Analogues as Highly Potent Plasmodium Falciparum Growth Inhibitors.” BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 16.7 (2006): 1888–1891. Print.