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Andreas Reichel

Researcher at Bayer HealthCare Pharmaceuticals

Publications -  64
Citations -  2111

Andreas Reichel is an academic researcher from Bayer HealthCare Pharmaceuticals. The author has contributed to research in topics: Blood–brain barrier & P-glycoprotein. The author has an hindex of 23, co-authored 60 publications receiving 1915 citations. Previous affiliations of Andreas Reichel include King's College London & Schering AG.

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Addressing central nervous system (CNS) penetration in drug discovery: basics and implications of the evolving new concept.

TL;DR: Despite enormous efforts, achieving a safe and efficacious concentration profile in the brain remains one of the big challenges in central nervous system (CNS) drug discovery and development.
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Interaction of Poly(butylcyanoacrylate) Nanoparticles with the Blood-Brain Barrier in vivo and in vitro

TL;DR: The hypothesis that the mechanism of blood-brain barrier transport of drugs by polysorbate 80-coated nanoparticles is one of endocytosis followed by possible transcytosis is supported.
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Closing the gaps: a full scan of the intestinal expression of p-glycoprotein, breast cancer resistance protein, and multidrug resistance-associated protein 2 in male and female rats.

TL;DR: All transporters showed considerable intra- and interindividual variability, especially at the protein level, making it problematic to take transporter expressions of small sections exemplary for general assumptions on intestinal abundances.
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The role of blood-brain barrier studies in the pharmaceutical industry.

TL;DR: This review will elaborate on the specific needs in terms of BBB-related issues across the different drug discovery and development phases, i.e. target identification and validation, lead generation and optimization, candidate selection and profiling, preclinical development and clinical studies.
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The lab oddity prevails: discovery of pan-CDK inhibitor (R)-S-cyclopropyl-S-(4-{[4-{[(1R,2R)-2-hydroxy-1-methylpropyl]oxy}-5-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)sulfoximide (BAY 1000394) for the treatment of cancer

TL;DR: Lead optimization of a high‐throughput screening hit led to the rapid identification of aminopyrimidine ZK 304709, a multitargeted CDK and VEGF‐R inhibitor that displayed a promising preclinical profile, but failed in phase I studies due to dose‐limited absorption and high inter‐patient variability.