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Armin Heckel

Researcher at Boehringer Ingelheim

Publications -  142
Citations -  3856

Armin Heckel is an academic researcher from Boehringer Ingelheim. The author has contributed to research in topics: Cyclin-dependent kinase & Alkyl. The author has an hindex of 22, co-authored 142 publications receiving 3654 citations. Previous affiliations of Armin Heckel include Neurocrine Biosciences.

Papers
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The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint.

TL;DR: The data suggest that Aurora B is required to generate unattached kinetochores on monooriented chromosomes, which in turn could promote bipolar attachment as well as maintain checkpoint signaling.
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BIBF 1120: Triple Angiokinase Inhibitor with Sustained Receptor Blockade and Good Antitumor Efficacy

TL;DR: Although BIBF 1120 is rapidly metabolized in vivo by methylester cleavage, resulting in a short mean residence time, once daily oral dosing is fully efficacious in xenograft models, preclinical findings suggest that long-term clinical outcomes may improve with blockade of additional proangiogenic receptor tyrosine kinases.
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Design, Synthesis, and Evaluation of Indolinones as Triple Angiokinase Inhibitors and the Discovery of a Highly Specific 6-Methoxycarbonyl-Substituted Indolinone (BIBF 1120)

TL;DR: Preclinical findings suggest that blockade of additional pro-angiogenic kinases, such as fibroblast and platelet-derived growth factor receptors (FGFR and PDGFR), may improve the efficacy of pharmacological cancer treatment.
Journal ArticleDOI

Inhibition of CDK5 is protective in necrotic and apoptotic paradigms of neuronal cell death and prevents mitochondrial dysfunction

TL;DR: Testing a new class of CDK inhibitors, it is found that inhibitory activity against CDK5, but not cell cycle-relevant CDKs, confers neuroprotection, and the firstCDK5-selective small molecule inhibitor is presented, lacking unwanted cytostatic effects due to cross-inhibition of mitoticCDKs.
Patent

6-position substituted indoline, production and use thereof as a medicament

TL;DR: In this paper, a 6-substituted indoline of formula (I), wherein R1 to R5 and X are as defined in claim 1, isomers and salts of a compound, in particular physiologically compatible salts of said compound having pharmacologically important characteristics, in addition inhibiting action on different receptor-tyrosine kinases and cyclin/CDK complexes.