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  • Produktbild: RAS Drug Discovery
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RAS Drug Discovery Past, Present and Future

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Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

01.11.2024

Herausgeber

Adrian Gill + weitere

Verlag

Elsevier Science & Technology

Seitenzahl

568

Maße (L/B/H)

23,5/19,1/2,9 cm

Gewicht

450 g

Sprache

Englisch

ISBN

978-0-443-21861-3

Beschreibung

Portrait

Adrian has over 25 years of drug discovery and development experience in senior roles across a diverse range of disease areas in both large pharma and biotech environments and been heavily involved in the identification of multiple clinical candidates across a variety of disease areas. He is a co-inventor of RMC-4630, Revolution Medicines first development candidate selectively targeting SHP2 and RMC-5552, a bi-steric inhibitor which selectively targets mTORC1. Adrian has been instrumental in the design and development of four more recent RAS(ON) development candidates from the Revolution Medicines tri-complex inhibitor platform and is also a co-inventor of RMC-6236 (RAS MULTI inhibitor), RMC-6291(KRASG12C inhibitor), RMC-8839 (KRASG13C inhibitor) and RMC-9805(KRASG12D inhibitor).

Adrian has authored over 25 publications in peer-reviewed journals, is a named inventor on over 45 issued and pending small molecule patent applications and has given multiple invited presentations at national and international conferences. Adrian received his Ph.D. in organic chemistry from the University of Sussex, U.K. and has a bachelor’s degree in applied chemistry from the University of Salford, U.K. Adrian is a member of the Royal Society of Chemistry, the SCI, the American Chemical Society and an invited member of the AACR Chemistry in Cancer Research (CICR) Steering Committee. Adrian is also a member of XPose Therapeutics and Curve Therapeutics scientific advisory boards and an honorary Prof. of Drug Discovery at the Sussex University Drug Discovery Center, UK.

Professor Kevan is currently an Investigator of the Howard Hughes Medical Institute, Chair of the Department of Cellular and Molecular Pharmacology at UCSF and a Professor of Chemistry at UC Berkeley. He was inducted into the National Academy of Sciences (2010), the Institute of Medicine (2011), and the American Academy of Arts and Sciences (2011). His lab is most well-known for drugging the "undruggable" oncogene K-Ras (G12C) in 2013. In May of 2021 the drug sotorasib which binds to the same pocket on K-Ras (G12C) was approved for the treatment of lung cancer patients with this mutation. The field of K-Ras drug discovery is expanding quickly to hunt for drugs to target the other K-Ras mutants such as those which drive colon and pancreatic cancers which collectively represent almost 20% of all cancer patients world-wide. Kevan has been a co-founder of a number companies from their inception to public offering or acquisition and he is a co-founder of several currently private companies.

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

01.11.2024

Herausgeber

Verlag

Elsevier Science & Technology

Seitenzahl

568

Maße (L/B/H)

23,5/19,1/2,9 cm

Gewicht

450 g

Sprache

Englisch

ISBN

978-0-443-21861-3

EU-Ansprechpartner

Zeitfracht Medien GmbH
Ferdinand-Jühlke-Straße 7
99095 Erfurt
DE
produktsicherheit@zeitfracht.de

Herstelleradresse

Elsevier Science & Technology
London Wall 125
EC2Y 5AS London
GB
tradeorders@elsevier.com

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Die Leseprobe wird geladen.
  • Produktbild: RAS Drug Discovery
  • Produktbild: RAS Drug Discovery
  • 1. Introduction to KRAS Biology
    2. Historical context and background to RAS drug discovery: the first 25 years of RAS targeting focused on FTase inhibitors
    3. KRAS in vitro assays - biochem, biophysics and cell based
    4. KRAS in vivo models and pharmacology
    5. RAS Structural Biology: The Journey from Structures to Therapeutic Advances

    Section 1: First generation KRAS G12C OFF inhibitors
    6. ARS-1620 SAR journey
    7. Sotorasib/AMG510 SAR journey
    8. Adagrasib/MRTX849 SAR journey
    9. Novartis SAR journey - JDQ 443
    10. Jacobio SAR Journey - JAB-21822
    11. KRAS degraders

    Section 2: Second generation G12C inhibitors and new modalities
    12. KRAS ON inhibitors using Tri-complex inhibitors - RMC-4998/6291 story

    Section 3: Beyond KRAS G12C
    13. Pan-KRAS inhibitors
    14. RAS-multi - RMC-7977 story
    15. G12S/R stories
    16. G12D stories
    17. MRTX1133 (small molecule)
    18. RMC-9945 (G12D covalent inhibitor)
    19. KRAS combinations (preclinical and clinical)
    20. The immune-oncology potential of KRAS inhibitors
    21. KRAS Competitive Intelligence/G12C, G12D, pan/multi-RAS Chapter
    22. Conclusions and future of RAS Drug Discovery
    23. LUMAKRAS® (sotorasib): SAR Journey & Path to the Clinic