Errata, Volume 24, 2004

EKYUHO HAN, C BUTLER, H ZHANG, JM SEVERIN… - ar.iiarjournals.org
Volume 25, Number 1A, pages 101-106: In all of the experiments in which flavopiridol was
used, the concentrations were in nanomolar and not micromolar. The concentrations of all of …

Flavopiridol. National Cancer Institute.

HK Wang - Current opinion in investigational drugs (London …, 2001 - europepmc.org
Flavopiridol is a synthetic flavonoid inhibitor of cyclin-dependent kinases, which is under
development by Aventis Pharma (formerly Hoechst Marion Roussel) and the National …

Development and validation of a sensitive liquid chromatography/mass spectrometry method for quantitation of flavopiridol in plasma enables accurate estimation of …

MA Phelps, DM Rozewski, JS Johnston… - … of Chromatography B, 2008 - Elsevier
A high-performance liquid chromatographic assay with tandem mass spectrometric
detection was developed and validated for quantitation of the broad spectrum kinase …

A high‐performance liquid chromatography method using ultraviolet detection for the quantitation of flavopiridol from human plasma

S Zhai, E Sausville, WD Figg - Biomedical Chromatography, 2002 - Wiley Online Library
Flavopiridol is an inhibitor of cyclin‐dependent kinase, a key regulator of cell cycle, and is
currently under clinical trials. We developed and validated an HPLC assay method for the …

Flavopiridol Hoechst AG.

MJ Zvelebil - Idrugs: the Investigational Drugs Journal, 1998 - europepmc.org
Hoechst is developing flavopiridol, a synthetic flavonoid based on an extract from an Indian
plant, for the potential treatment of cancer. Flavopiridol, a cyclin-dependent kinase inhibitor …

Clinical pharmacology of flavopiridol following a 72-hour continuous infusion

MA Rudek, KS Bauer Jr, RM Lush III… - Annals of …, 2003 - journals.sagepub.com
Background Flavopiridol, a novel flavone derivative, inhibits cyclin-dependent kinase-1. We
initiated a Phase I trial in patients with refractory solid tumors to determine the maximum …

Determination of flavopiridol (L86 8275; NSC 649890) in human plasma by reversed-phase liquid chromatography with electrochemical detection

SF Stinson, K Hill, TJ Siford, LR Phillips… - Cancer chemotherapy and …, 1998 - Springer
Purpose: Flavopiridol is a flavone which inhibits several cyclin-dependent kinases, and
exhibits potent growth-inhibitory activity against a number of human tumor cell lines both in …

Determination of flavopiridol (L 86 8275) in rat serum using ion-pair reversed-phase high-performance liquid chromatography

PK Inamdar, RD Yeole - Drug development and industrial …, 1997 - Taylor & Francis
A specific, sensitive, and simple high-performance liquid chromatographic method has been
developed for assaying flavopiridol in rat serum for preliminary bioavailability and …

Parenteral formulation of flavopiridol (NSC-649890)

RM Dannenfelser, Y Surakitbanharn… - PDA Journal of …, 1996 - journal.pda.org
Flavopiridol [5, 7-dihydroxy-8-(4-N-methyl-2-hydroxypyridyl)-6′-chloroflavone
hydrochloride] is a flavonoid with weak electrolyte properties and an intrinsic aqueous …

A novel liposomal formulation of flavopiridol

X Yang, X Zhao, MA Phelps, L Piao… - International journal of …, 2009 - Elsevier
Flavopiridol has shown promising activities in hematologic and solid tumor models, as well
as in clinical trials in chronic lymphocytic leukemia patients. Flavopiridol has relatively low …