نتایج جستجو برای: adme

تعداد نتایج: 990  

Journal: :Drug discovery today 2006
Tobias Wunberg Martin Hendrix Alexander Hillisch Mario Lobell Heinrich Meier Carsten Schmeck Hanno Wild Berthold Hinzen

Drug-like and lead-like hits derived from HTS campaigns provide good starting points for lead optimization. However, too strong emphasis on potency as hit-selection parameter might hamper the success of such projects. A detailed absorption, distribution, metabolism, excretion and toxicology (ADME-Tox) profiling is needed to help identify hits with a minimum number of (known) liabilities. This i...

Journal: :Journal of clinical pharmacology 2008
J Andrew Williams Tommy Andersson Tommy B Andersson Rebecca Blanchard Martin Otto Behm Nadine Cohen Timi Edeki Monique Franc Kathleen M Hillgren Keith J Johnson David A Katz Mark N Milton Bernard P Murray Joseph W Polli Deb Ricci Lisa A Shipley Subrahmanyam Vangala Steven A Wrighton

Pharmacogenomic (PGx) research on the absorption, distribution, metabolism, and excretion (ADME) properties of drugs has begun to have impact for both drug development and utilization. To provide a cross-industry perspective on the utility of ADME PGx, the Pharmaceutical Research and Manufacturers of America (PhRMA) conducted a survey of major pharmaceutical companies on their PGx practices and...

2014
Timothy M. Chapman Simon A. Osborne Claire Wallace Kristian Birchall Nathalie Bouloc Hayley M. Jones Keith H. Ansell Debra L. Taylor Barbara Clough Judith L. Green Anthony A. Holder

A structure-guided design approach using a homology model of Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1) was used to improve the potency of a series of imidazopyridazine inhibitors as potential antimalarial agents. This resulted in high affinity compounds with PfCDPK1 enzyme IC50 values less than 10 nM and in vitro P. falciparum antiparasite EC50 values down to 12 nM, alt...

2017
Ai-Ming Yu Magnus Ingelman-Sundberg Nathan J. Cherrington Lauren M. Aleksunes Ulrich M. Zanger Wen Xie Hyunyoung Jeong Edward M. Morgan Peter J. Turnbaugh Curtis D. Klaassen Aadra P. Bhatt Matthew R. Redinbo Pengying Hao David J. Waxman Li Wang Xiao-bo Zhong

Variations in drug metabolism may alter drug efficacy and cause toxicity; better understanding of the mechanisms and risks shall help to practice precision medicine. At the 21st International Symposium on Microsomes and Drug Oxidations held in Davis, California, USA, in October 2-6, 2016, a number of speakers reported some new findings and ongoing studies on the regulation mechanisms behind var...

2014
Dejan Caglič Michelle C. Krutein Kristin M. Bompiani Deborah J. Barlow Galit Benoni Jeffrey C. Pelletier Allen B. Reitz Luke L. Lairson Karen L. Houseknecht Garry R. Smith Tobin J. Dickerson

Botulinum neurotoxins (BoNT) are the most potent toxins known and a significant bioterrorist threat. Few small molecule compounds have been identified that are active in cell-based or animal models, potentially due to toxin enzyme plasticity. Here we screened commercially available quinolinols, as well as synthesized hydroxyquinolines. Seventy-two compounds had IC50 values below 10 μM, with the...

Journal: :The Journal of antibiotics 2004
Michael R Leadbetter Stacy M Adams Bettina Bazzini Paul R Fatheree Dane E Karr Kevin M Krause Bernice M T Lam Martin S Linsell Matthew B Nodwell John L Pace Kelly Quast Jeng-Pyng Shaw Elizabeth Soriano Sean G Trapp Jenny D Villena Terry X Wu Burton G Christensen J Kevin Judice

Novel derivatives of N-decylaminoethylvancomycin (2), containing appended hydrophilic groups were synthesized and their antibacterial activity and ADME properties were evaluated. The compounds were prepared by reacting amines with the C-terminus (C-) of 2 using PyBOP mediated amide formation, or with the resorcinol-like (R-) position of 2 using a Mannich aminomethylation reaction. These analogs...

2016
JE Edwards C LaCerte T Peyret NH Gosselin JF Marier AF Hofmann D Shapiro

Obeticholic acid (OCA), a semisynthetic bile acid, is a selective and potent farnesoid X receptor (FXR) agonist in development for the treatment of chronic nonviral liver diseases. Physiologic pharmacokinetic models have been previously used to describe the absorption, distribution, metabolism, and excretion (ADME) of bile acids. OCA plasma levels were measured in healthy volunteers and cirrhot...

2017
M Vrana D Whittington V Nautiyal B Prasad

The purpose of this study was to create an open access repository of validated liquid chromatography tandem mass spectrometry (LC-MS/MS) multiple reaction monitoring (MRM) methods for quantifying 284 important proteins associated with drug absorption, distribution, metabolism, and excretion (ADME). Various in silico and experimental approaches were used to select surrogate peptides and optimize...

2014
Lidija R Jevrić Sanja O Podunavac-Kuzmanović Jaroslava V Švarc-Gajić Strahinja Z Kovačević Bratislav Ž Jovanović

The properties relevant to pharmacokinetics and pharmacodynamics of four series of synthesized s-triazine derivatives have been studied by Quantitative structure-retention relationship (QSRR) approach. The chromatographic behavior of these compounds was investigated by using reversed-phase high performance thin-layer chromatography (RP-HPTLC). Chromatographic retention (R M (0)) was correlated ...

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