Skip to Main Content

We have a new app!

Take the Access library with you wherever you go—easy access to books, videos, images, podcasts, personalized features, and more.

Download the Access App here: iOS and Android. Learn more here!


The first edition of Goodman & Gilman, published in 1941, helped to organize the field of pharmacology, giving it intellectual validity and an academic identity. That edition began: “The subject of pharmacology is a broad one and embraces the knowledge of the source, physical and chemical properties, compounding, physiological actions, absorption, fate, and excretion, and therapeutic uses of drugs. A drug may be broadly defined as any chemical agent that affects living protoplasm, and few substances would escape inclusion by this definition.” In practice, of course, a chemical or biological agent is considered a legal drug only if it has been approved as such by a national regulatory agency, such as the U.S. Food and Drug Administration (FDA) or the European Medicines Agency; these approved compounds are the focus of this book.

This first nine chapters of this book, General Principles, provide the underpinnings for these definitions of pharmacology and drugs by exploring the physiological, biochemical, and molecular mechanisms of drug action. This section covers drug invention, development, and regulation, as well as how drugs act in biological systems, i.e., pharmacodynamics, pharmacokinetics (including drug transport and metabolism), the influence of the gastrointestinal microbiome, and pharmacogenetics, with brief forays into pharmacovigilance and drug toxicity and poisoning. Subsequent sections deal with the use of specific classes of drugs as therapeutic agents in human subjects. The present chapter is an introduction to pharmaceuticals, their development, and the activities of the pharmaceutical industry and government surrounding the discovery, production, and use of therapeutic agents. The processes of discovery and invention of drugs have changed substantially with the general progress of biomedical sciences, the advent and improvement of computer-aided drug design, and technical advances in biochemistry and molecular biology. Some of these new capabilities are reviewed below.



ADME: absorption, distribution, metabolism, and excretion

BLA: Biologics License Application

CADD: computer-aided drug discovery

DEL: DNA-encoded compound library

DHHS: U.S. Department of Health and Human Services

DMPK: drug metabolism and pharmacokinetics

FBDD: fragment-based drug discovery

FDA: U.S. Food and Drug Administration

GPU: graphics processing unit

HCV: hepatitis C virus

HDL: high-density lipoprotein

HMG-CoA: 3-hydroxy-3-methylglutaryl coenzyme A

HTS: high-throughput screening

IND: Investigational New Drug

LDL: low-density lipoprotein

mRNA: messenger RNA

NDA: New Drug Application

NIH: National Institutes of Health

NMEs: new molecular entities

PDUFA: Prescription Drug User Fee Act

SBDD: structure-based drug design

siRNA: small interfering RNA


Early Experiences With Plants

The human fascination—and sometimes infatuation—with chemicals that alter biological function is ancient and begins with our long experience with and dependence on plants. Because most plants are root-bound, many produce defensive compounds that animals learn to avoid and humans to exploit or abuse. Thus, the prior of an Arabian convent came to appreciate coffee (caffeine) after noting the ...

Pop-up div Successfully Displayed

This div only appears when the trigger link is hovered over. Otherwise it is hidden from view.