Inhibitors of protein kinase C. 2. Substituted bisindolylmaleimides with improved potency and selectivity

PD Davis, LH Elliott, W Harris, CH Hill… - Journal of medicinal …, 1992 - ACS Publications
A hypothetical mode ofinhibition of protein kinase C (PKC) by the natural product
staurosporine has been used as a basis for thedesign of substituted bisindolylmaleimides …

[HTML][HTML] Inhibition of protein kinase C-alpha expression in human A549 cells by antisense oligonucleotides inhibits induction of intercellular adhesion molecule 1 …

NM Dean, R McKay, TP Condon, CF Bennett - Journal of Biological …, 1994 - Elsevier
We have identified 20-mer phosphorothioate oligodeoxynucleotides which potently (IC50
values of 100-200 nM) and specifically inhibit protein kinase C (PKC)-alpha mRNA and …

The NS5A/NS5 Proteins of Viruses from Three Genera of the Family Flaviviridae Are Phosphorylated by Associated Serine/Threonine Kinases

KE Reed, AE Gorbalenya, CM Rice - Journal of virology, 1998 - Am Soc Microbiol
Phosphorylation of the expressed NS5A protein of hepatitis C virus (HCV), a member of the
Hepacivirus genus of the family Flaviviridae, has been demonstrated in mammalian cells …

Inhibitors of protein kinases: CGP 41251, a protein kinase inhibitor with potential as an anticancer agent

D Fabbro, E Buchdunger, J Wood, J Mestan… - Pharmacology & …, 1999 - Elsevier
CGP 41251 was originally identified as an inhibitor of protein kinase C (PKC), inhibiting
mainly the conventional PKC subtypes, and subsequently shown to inhibit the vascular …

Protein kinase C isozymes as potential targets for anticancer therapy

J Hofmann - Current Cancer Drug Targets, 2004 - ingentaconnect.com
Protein kinase C (PKC) comprises a family of isozymes (α, βI, βII, γ δ, ε, θ, & eegr;, λ/ι
[mouse/human], and ζ) which are involved in signal transduction from membrane receptors …

Chemical synthesis and biological properties of pyridine epothilones

KC Nicolaou, R Scarpelli, B Bollbuck, B Werschkun… - Chemistry & biology, 2000 - cell.com
Background: Numerous analogs of the antitumor agents epothilones A and B have been
synthesized in search of better pharmacological profiles. Insights into the structure–activity …

Staurosporine-induced conformational changes of cAMP-dependent protein kinase catalytic subunit explain inhibitory potential

L Prade, RA Engh, A Girod, V Kinzel, R Huber… - Structure, 1997 - cell.com
Background: Staurosporine inhibits most protein kinases at low nanomolar concentrations.
As most tyrosine kinases, along with many serine/threonine kinases, are either proto …

[HTML][HTML] Dramatic inhibition of retinal and choroidal neovascularization by oral administration of a kinase inhibitor

MS Seo, N Kwak, H Ozaki, H Yamada… - The American journal of …, 1999 - Elsevier
The most common cause of new blindness in young patients is retinal neovascularization,
and in the elderly is choroidal neovascularization. Therefore, there has been a great deal of …

Protein kinase C inhibitors as novel anticancer drugs

MR Jirousek, PG Goekjian - Expert opinion on investigational …, 2001 - Taylor & Francis
The role of PKC isoforms in signal transduction pathways involved in regulation of the cell
cycle, apoptosis, angiogenesis, differentiation, invasiveness, senescence and drug efflux …

The potential of protein kinase C as a target for anticancer treatment

A Basu - Pharmacology & therapeutics, 1993 - Elsevier
Many investigators have embarked upon the search for novel cellular targets for the
treatment of cancer. A popular therapeutic strategy is to intervene with the components of …