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Walter A. Korfmacher

Researcher at Schering-Plough

Publications -  96
Citations -  5103

Walter A. Korfmacher is an academic researcher from Schering-Plough. The author has contributed to research in topics: Mass spectrometry & Tandem mass spectrometry. The author has an hindex of 38, co-authored 95 publications receiving 4947 citations. Previous affiliations of Walter A. Korfmacher include Applied Biosystems & Merck & Co..

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Direct analysis of drug candidates in tissue by matrix‐assisted laser desorption/ionization mass spectrometry

TL;DR: The anti-tumor drug SCH 226374 was unambiguously determined in mouse tumor tissue using MALDI-QqTOFMS (QSTAR) by monitoring the dissociation of the protonated drug at m/z 695.4 and images revealing the spatial localization of SCH 226 374 in tumor tissue and compound A in brain tissue were acquired.
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Investigation of matrix effects in bioanalytical high-performance liquid chromatography/tandem mass spectrometric assays: application to drug discovery

TL;DR: This report demonstrates that matrix effects can also be caused by exogenous materials, such as polymers contained in different brands of plastic tubes, or Li-heparin, a commonly used anticoagulant, and finds the APCI mode to be more sensitive to matrix effects than the ESI mode.
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Discovery of (1R,5S)-N-[3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]- 3-[2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl]- 6,6-dimethyl-3-azabicyclo[3.1.0]hexan-2(S)-carboxamide (SCH 503034), a selective, potent, orally bioavailable hepatitis C virus NS3 protease inhibitor: a potential therapeutic agent for the treatment of hepatitis C infection

TL;DR: The SAR leading to the discovery of 70 (SCH 503034), a novel, potent, selective, orally bioavailable NS3 protease inhibitor that has been advanced to clinical trials in human beings for the treatment of hepatitis C viral infections is described.
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Foundation review: Principles and applications of LC-MS in new drug discovery

TL;DR: A summary of the key components of HPLC-MS systems, as well as an overview of major application areas that use this technique as part of the drug discovery process, will be described here.