Drugs of Natural Origin is a unique multidisciplinary book suitable for undergraduate and graduate students and teachers in the area of natural product science, but also as a complementary book for disciplines like medicinal chemistry, biochemistry and pharmacology. The book can also serve society as a scientific source for the understanding of a sustainable use of natural products in the development of new drugs, scientifically based herbal remedies, and environmentally friendly biomolecules. During evolution, molecules have been developed for specific functions in nature. These bioactive substances have a potential as new drug candidates in drug development, but also as pharmacological tools, intermediates or templates for synthesis of drugs. This book deals with terrestrial and marine bioactive substances of plant, microbial or animal origin. The occurrence, biosynthesis, isolation, chemistry and medical use are described together with basic research strategies. An increased understanding of the medical importance of bioactive natural products has developed in society. Since the publication of the sixth edition, six years ago, considerable progress has been achieved in the study of biosynthetic pathways, mainly based on gene technology. The revolution in high-throughput sequencing technology has given an increasing access to microbial genome sequences, which opens up new possibilities in the discovery of novel bioactive natural products. This development is reflected in a substantial revision and expansion of the book, but also removal of some sections containing products remotely associated with drugs. The new book also contains description of novel drugs marketed since the publication of the previous edition, especially in the field of diabetes, cancer and infection.

Drugs of Natural Origin provides a multidisciplinary approach suitable for those working in the area of natural product development. It brings together research on the sustainable use of natural products in the development of new drugs, scientifically based herbal remedies, and environmentally adapted biomolecules. During evolution, molecules evolved to perform specific functions in nature. By understanding their natural function, we can develop ways to make use of these bioactive substances a potential new drug candidates and also as pharmacological tools, intermediates, or templates for the synthesis of novel drugs. This book examines terrestrial and marine bioactive substances drawn from plant, microbial, and animal origin. Their occurrence, biosynthesis, isolation, chemistry, and medical use are described, together with basic research strategies. Development in the field of natural products of medical importance continues to expand. Since the publication of the 5th edition of this book, five years ago, new concepts such as chemo- and bioinformatics, phylogenetics and systems biology with the new ”omics” techniques (genomics, proteomics and metabolomics) have emerged. Herbal remedies have become subject to more rigid legislation aiming to improve their quality and efficacy, both as over-the-counter preparations for self-medication and as constituents of conventional drugs. This development is reflected in a substantial revision and expansion of the book. This edition also describes many new drugs marketed since the publication of the previous edition. Students and professors in the area of natural product research,as well as complementary disciplines like medicinal chemistry, biochemistry, and pharmacology will find much relevant information in this books.

This timely guide covers all aspects of litigation involving drugs, medical devices, vaccines and other FDA-regulated prescription products.

FDLI's popular reference book, A Practical Guide to FDA's Food and Drug Law and Regulation, Seventh Edition, provides an introduction to the laws and regulations governing development, marketing, and sale of FDA-regulated products, including topics on food, drugs, medical devices, biologics, dietary supplements, cosmetics, new animal drugs, cannabis, and tobacco and nicotine products. Structured to serve as a reference and as a teaching tool, the book offers practical legal and regulatory fundamentals, and each chapter builds sequentially from the last to provide an accessible overview of the key topics relevant to practitioners of food and drug law and regulation. This book is a standard legal text in law schools and graduate regulatory programs and has been cited as a reference in judicial opinions (including the U.S. Supreme Court). This Seventh Edition includes new sections on controlled substances, compounded drugs, and cannabis and cannabis-derived compounds. It also incorporates the latest amendments to the Federal Food, Drug, and Cosmetic Act, as well as FDA regulations and guidances.