Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Dirk van Papendorp"'
Autor:
Lisa Repsold, Thandi Mqoco, Elize Wolmarans, Sandra Nkandeu, Joji Theron, Tomek Piorkowski, Peet du Toit, Dirk van Papendorp, Annie Margaretha Joubert
Publikováno v:
Biological Research, Vol 47, Iss 0, Pp 1-7 (2014)
BACKGROUND: Novel, in silico-designed anticancer compounds were synthesized in our laboratory namely, 2-ethyl-3-O-sulphamoyl-estra-1,3,5(10),15-tetraen-17-ol (ESE-15-ol) and 2-ethyl-3-O-sulphamoyl-estra-1,3,5(10)16-tetraene (ESE-16). These compounds
Externí odkaz:
https://doaj.org/article/2a43e687de674add8279c3c7fc6d2e1d
Publikováno v:
Biomedical Research. 29
Much research over the past five decades has focussed on the repair and replacement of bone. Recently, the research focus has shifted to nanotechnology since it provides a platform from which to alter and possibly improve materials’ properties. In
Autor:
Sandra D. Nkandeu, Anna Margaretha Joubert, Marianne J. Cronjé, Iman van den Bout, Dirk van Papendorp
Publikováno v:
Pharmacology. 102(1-2)
Background: 2-Methoxyestradiol (2ME2) is an endogenous metabolite of 17-β-estradiol with anti-proliferative and anti-angiogenic properties. Due to 2ME2’s rapid metabolism and low oral bioavailability in in vivo settings, 2ME2 analogues have been d
Publikováno v:
Biomedical Research. 23:249-253
Electrotherapy has been used for a variety of clinical conditions with varying results. In 1982 it was shown that a small DC current leads to an increase in ATP generation. ATP has been implicated as a peripheral mediator of pain. This study compared
Autor:
E.M. Nolte, Renaud Prudent, Peet J. Du Toit, Anne Elisabeth Theron, Annie M. Joubert, Rivak Punchoo, Sumari Marais, Yvette Hlophe, Dirk van Papendorp, Iman van den Bout, Laurence Lafanechère
Publikováno v:
Cancer Chemotherapy and Pharmacology
Cancer Chemotherapy and Pharmacology, Springer Verlag, 2015, 75 (2), pp.431-437. ⟨10.1007/s00280-014-2653-z⟩
Cancer Chemotherapy and Pharmacology, Springer Verlag, 2015, 75 (2), pp.431-437. ⟨10.1007/s00280-014-2653-z⟩
2-Methoxyestradiol (2ME) is a promising anti-cancer agent that disrupts the integrity and dynamics of the spindle network. In order to overcome the pharmacokinetic constraints of this compound, a panel of sulphamoylated estradiol analogues were in si
Autor:
Tomek Piorkowski, Sandra D. Nkandeu, J. J. Theron, Peet J. Du Toit, T.V. Mqoco, Lisa Repsold, Elize Wolmarans, Annie M. Joubert, Dirk van Papendorp
Publikováno v:
Biological Research v.47 2014
SciELO Chile
CONICYT Chile
instacron:CONICYT
Biological Research
Biological Research, Volume: 47, Pages: 1-7, Published: 2014
Biological Research, Vol 47, Iss 0, Pp 1-7 (2014)
SciELO Chile
CONICYT Chile
instacron:CONICYT
Biological Research
Biological Research, Volume: 47, Pages: 1-7, Published: 2014
Biological Research, Vol 47, Iss 0, Pp 1-7 (2014)
BACKGROUND: Novel, in silico-designed anticancer compounds were synthesized in our laboratory namely, 2-ethyl-3-O-sulphamoyl-estra-1,3,5(10),15-tetraen-17-ol (ESE-15-ol) and 2-ethyl-3-O-sulphamoyl-estra-1,3,5(10)16-tetraene (ESE-16). These compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ba7643b6bcec26f2ae7d21f02cbfd7
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602014000100039
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602014000100039
Autor:
Dirk van Papendorp, Robert C. Habbersett, Yulin Shou, Bruce E. Lehnert, J.C. Seegers, Mona-Liza Lottering, Christina J.S. Grobler
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 62:253-267
The endogenous metabolite, 2-methoxyestradiol (2ME), is an inhibitor of tubulin polymerization and is therefore toxic to dividing fast-growing tumor cells. Transformed cells are not equally susceptible to the effects of 2ME. In this study the effects
Publikováno v:
Cell biochemistry and function. 27(4)
The influence of 2-methoxyestradiol(2-ME) was investigated oncell numbers, morphology, cellcycleprogression,and apoptosis inductionin an oesophageal carcinoma cell line (WHCO3). Dose-dependent studies (1 � 10 � 9 M‐1 � 10 � 6 M) revealed th