𝔖 Scriptorium
✦   LIBER   ✦

πŸ“

Transporters as Drug Carriers: Structure, Function, Substrates (Methods and Principles in Medicinal Chemistry)

✍ Scribed by Gerhard Ecker, Peter Chiba, Raimund Mannhold, Hugo Kubinyi, Gerd Folkers


Year
2009
Tongue
English
Leaves
451
Series
Methods and Principles in Medicinal Chemistry 44
Edition
1
Category
Library

⬇  Acquire This Volume

No coin nor oath required. For personal study only.

✦ Synopsis


This reference handbook is the first to provide a comprehensive overview, systematically characterizing all known transporters involved in drug elimination and resistance. Combining recent knowledge on all known classes of drug carriers, from microbes to man, it begins with a look at human and mammalian transporters. This is followed by microbial, fungal and parasitic transporters with special attention given to transport across those physiological barriers relevant for drug uptake, distribution and excretion.As a result, this key resource lays the foundations for understanding and investigating the molecular mechanisms for multidrug resistance in cancer cells, microbial resistance to antibiotics and pharmacokinetics in general. For anyone working with antibiotics and cancer chemotherapeutics, as well as being of prime interest to biochemists and biophysicists.


πŸ“œ SIMILAR VOLUMES


Transporters as Drug Carriers: Structure
✍ Raimund Mannhold, Hugo Kubinyi, Gerd Folkers(eds.) πŸ“‚ Library πŸ“… 2009 🌐 English

This reference handbook is the first to provide a comprehensive overview, systematically characterizing all known transporters involved in drug elimination and resistance. Combining recent knowledge on all known classes of drug carriers, from microbes to man, it begins with a look at human and mamma

Nuclear Receptors as Drug Targets (Metho
✍ Eckhard Ottow, Hilmar Weinmann, Raimund Mannhold, Hugo Kubinyi, Gerd Folkers πŸ“‚ Library πŸ“… 2008 πŸ› Wiley-VCH 🌐 English

Edited by two experts working at the pioneering pharmaceutical company and major global player in hormone-derived drugs, this handbook and reference systematically treats the drug development aspects of all human nuclear receptors, including recently characterized receptors such as PPAR, FXR and LXR

Chemokine Receptors as Drug Targets (Met
✍ Martine J. Smit, Sergio A. Lira, Rob Leurs, Raimund Mannhold, Hugo Kubinyi, Gerd πŸ“‚ Library πŸ“… 2010 πŸ› Wiley-VCH 🌐 English

Opening with a general introduction on chemokine function and chemokine receptor biology, the handbook goes on to cover the known implications of these signaling molecules in human diseases, such as cancer, neural disorders, and viral infection, including HIV/AIDS. The second half of the book system

Protein Kinases as Drug Targets (Methods
✍ Bert Klebl, Gerhard MΓΌller, Michael Hamacher, Raimund Mannhold, Hugo Kubinyi, Ge πŸ“‚ Library πŸ“… 2011 πŸ› Wiley-VCH 🌐 English

This timely guide to kinase inhibitor drug discovery is the first to cover the entire drug pipeline, from target identification to compound development and clinical application. Edited by pioneers in the field, on the drug development side this ready reference discusses classical medicinal chemistry

Voltage-Gated Ion Channels as Drug Targe
✍ David J. Triggle, Murali Gopalakrishnan, David Rampe, Wei Zheng, Raimund Mannhol πŸ“‚ Library πŸ“… 2006 πŸ› Wiley-VCH 🌐 English

Edited by the most prominent person in the field and top researchers at US pharmaceutical companies, this is a unique resource for drug developers and physiologists seeking a molecular-level understanding of ion channel pharmacology.After an introduction to the topic, the authors evaluate the struct

Chemogenomics in Drug Discovery: A Medic
✍ Hugo Kubinyi, Gerhard Muller, Raimund Mannhold, Gerd Folkers πŸ“‚ Library πŸ“… 2004 πŸ› Wiley-VCH Verlag GmbH & Co. 🌐 English

Chemogenomics brings together the most powerful concepts in modern chemistry and biology, linking combinatorial chemistry with genomics and proteomics.The first reference devoted to the topic, this up-to-date resource covers all stages of the early drug discovery process, from target selection to co