Anticancer Agents from Natural Products

Name: Anticancer Agents from Natural Products
Brand: Taylor & Francis Ltd
SKU: 9781032917535
Price: 380.73 RON
Availability: InStock

Autor: David J. Newman, Gordon M. Cragg

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Editura: Taylor & Francis Ltd

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380.73 lei

The approach to drug discovery from natural sources has yielded many important new pharmaceuticals i...

Informații despre carte

Autor

David J. Newman, Gordon M. Cragg

Limbă

engleză

Legare

Carte - Carte broșată

Publicat

2024

Pagini

784

EAN

9781032917535

ISBN

1032917539

Enbook ID

46440182

Editura

Taylor & Francis Ltd

Greutate

453

Dimensiuni

178 x 254

Descriere completă

The approach to drug discovery from natural sources has yielded many important new pharmaceuticals inaccessible by other routes. In many cases the isolated natural product may not be an effective drug for any of several reasons, but it nevertheless may become a drug through chemical modification or have a novel pharmacophore for future drug design. In summarizing the status of natural products as cancer chemotherapeutics, Anticancer Agents from Natural Products, Second Edition covers the:

History of each covered drug—a discussion of its mechanism on action, medicinal chemistry, synthesis, and clinical applications
Potential for novel drug discovery through the use of genome mining as well as future developments in anticancer drug discovery
Important biosynthetic approaches to "unnatural" natural products

Anticancer Agents from Natural Products, Second Edition discusses how complex target-oriented synthesis—enabled by historic advances in methodology—has enormously expanded the scope of the possible. This book covers the current clinically used anticancer agents that are either natural products or are clearly derived from natural product leads. It also reviews drug candidates currently in clinical development since many of these will be clinically used drugs in the future.

Examples include the drugs etoposide and teniposide derived from the lead compound podophyllotoxin; numerous analogs derived from taxol; topotecan, derived from camptothecin; and the synthetic clinical candidates, E7389 and HTI-286, developed from the marine leads, halichondrin B and hemiasterlin.

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