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dc.contributor.authorFueloep, Ferenc
dc.contributor.authorOkyar, Alper
dc.contributor.authorToth, Gabor K.
dc.contributor.authorLevi, Francis
dc.contributor.authorKrajcsi, Peter
dc.contributor.authorRAJNAI, Zsuzsanna
dc.contributor.authorMehn, Dora
dc.contributor.authorBEERY, Erzsebet
dc.contributor.authorJani, Marton
dc.date.accessioned2021-03-03T14:52:06Z
dc.date.available2021-03-03T14:52:06Z
dc.date.issued2010
dc.identifier.citationRAJNAI Z., Mehn D., BEERY E., Okyar A., Jani M., Toth G. K. , Fueloep F., Levi F., Krajcsi P., "ATP-Binding Cassette B1 Transports Seliciclib (R-Roscovitine), a Cyclin-Dependent Kinase Inhibitor", DRUG METABOLISM AND DISPOSITION, cilt.38, sa.11, ss.2000-2006, 2010
dc.identifier.issn0090-9556
dc.identifier.otherav_3bdc50a5-b3dc-4e5f-96ed-16b328c42e69
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44185
dc.identifier.urihttps://doi.org/10.1124/dmd.110.032805
dc.description.abstractSeliciclib, a cyclin-dependent kinase inhibitor, is a promising candidate to treat a variety of cancers. Pharmacokinetic studies have shown high oral bioavailability but limited brain exposure to the drug. This study shows that seliciclib is a high-affinity substrate of ATP-binding cassette B1 (ABCB1) because it activates the ATPase activity of the transporter with an EC50 of 4.2 mu M and shows vectorial transport in MDCKII-MDR1 cells, yielding an efflux ratio of 8. This interaction may be behind the drug's limited penetration of the blood-brain barrier. ABCB1 overexpression, on the other hand, does not confer resistance to the drug in the models tested. These findings should be considered when treatment strategies using seliciclib are designed.
dc.language.isoeng
dc.subjectEczacılık
dc.subjectTemel Bilimler
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.titleATP-Binding Cassette B1 Transports Seliciclib (R-Roscovitine), a Cyclin-Dependent Kinase Inhibitor
dc.typeMakale
dc.relation.journalDRUG METABOLISM AND DISPOSITION
dc.contributor.department, ,
dc.identifier.volume38
dc.identifier.issue11
dc.identifier.startpage2000
dc.identifier.endpage2006
dc.contributor.firstauthorID70422


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