Transport of six tyrosine kinase inhibitors: active or passive?
Transport of erlotinib, gefitinib, sorafenib, sunitinib, dasatinib and crizotinib can be active or passive, which was studied by measuring uptake at low (4 °C; passive) and normal temperature (37 °C; active and passive) and by the use of specific organic cation transporter (OCT) inhibitors. Intrace...
Main Authors: | Richard J. Honeywell, Sarina Hitzerd, Ietje Kathmann, Godefridus J. Peters |
---|---|
Format: | Article |
Language: | English |
Published: |
International Association of Physical Chemists (IAPC)
2016-03-01
|
Series: | ADMET and DMPK |
Online Access: | http://pub.iapchem.org/ojs/index.php/admet/article/view/275 |
Similar Items
-
Subcellular localization of several structurally different tyrosine kinase inhibitors
by: Richard Honeywell, et al.
Published: (2018-09-01) -
Adaptation of a human gut epithelial model in relation to the assessment of clinical pharmacokinetic parameters for selected tyrosine kinase inhibitors
by: Richard Honeywell, et al.
Published: (2015-03-01) -
Epithelial Transfer of the Tyrosine Kinase Inhibitors Erlotinib, Gefitinib, Afatinib, Crizotinib, Sorafenib, Sunitinib, and Dasatinib: Implications for Clinical Resistance
by: Richard J. Honeywell, et al.
Published: (2020-11-01) -
Transporter and Lysosomal Mediated (Multi)drug Resistance to Tyrosine Kinase Inhibitors and Potential Strategies to Overcome Resistance
by: Daniel J. de Klerk, et al.
Published: (2018-12-01) -
ADME/DMPK in the development and use of tyrosine and serine-threonine kinase inhibitors
by: Godefridus J. Peters, et al.
Published: (2016-10-01)