Nuclear Receptors : The Art and Science of Modulator Design and Discovery (2021)

個数:
  • ポイントキャンペーン

Nuclear Receptors : The Art and Science of Modulator Design and Discovery (2021)

  • 提携先の海外書籍取次会社に在庫がございます。通常3週間で発送いたします。
    重要ご説明事項
    1. 納期遅延や、ご入手不能となる場合が若干ございます。
    2. 複数冊ご注文の場合は、ご注文数量が揃ってからまとめて発送いたします。
    3. 美品のご指定は承りかねます。

    ●3Dセキュア導入とクレジットカードによるお支払いについて
  • ≪洋書のご注文について≫ 「海外取次在庫あり」「国内在庫僅少」および「国内仕入れ先からお取り寄せいたします」表示の商品でもクリスマス前(12/20~12/25)および年末年始までにお届けできないことがございます。あらかじめご了承ください。

  • 【入荷遅延について】
    世界情勢の影響により、海外からお取り寄せとなる洋書・洋古書の入荷が、表示している標準的な納期よりも遅延する場合がございます。
    おそれいりますが、あらかじめご了承くださいますようお願い申し上げます。
  • ◆画像の表紙や帯等は実物とは異なる場合があります。
  • ◆ウェブストアでの洋書販売価格は、弊社店舗等での販売価格とは異なります。
    また、洋書販売価格は、ご注文確定時点での日本円価格となります。
    ご注文確定後に、同じ洋書の販売価格が変動しても、それは反映されません。
  • 製本 Paperback:紙装版/ペーパーバック版/ページ数 679 p.
  • 言語 ENG
  • 商品コード 9783030784386
  • DDC分類 571.66

Full Description

Nuclear receptors are ligand activated transcription factors that control numerous biological functions. Consequently, altering activity of these receptors is proposed, and indeed documented, to affect many physiological and pathological conditions in experimental animals and humans. Thus, nuclear receptors have become a major target in the effort to treat numerous diseases.This book will shed light on and emphasize intricate processes involved in designing as well as discovering physiological and pharmacological modulators of these important proteins. World-renowned scientists will share with the reader their professional expertise and extensive experience acquired through decades working with nuclear receptors. Chapters address the various means and consequences of modulating nuclear receptor activity will be presented and discussed. These modulators cover a wide span of moieties ranging from synthetic chemicals to natural products. In addition, the classification of these chemicals ranges from pan agonists to selective agonists and inverse agonists to antagonists. They also include proteolytic means to obliterate the receptor in the event that modulating its activity through canonical pharmacological agents becomes less effective and/or less desirable due to anticipated or experienced toxicities. Modulation of receptor activity may also take place in the absence of a ligand or through manipulating the structure of the receptor itself by controlling posttranslational events.

Contents

1. Molecular Pharmacology of the Youngest Member of the Nuclear Receptor Family: The Mineralocorticoid Receptor.- 2. A Simple Method for Visual Assessment and Quantification of Altered Subcellular Localization of Nuclear Receptors.- 3. Multifaceted Effects of Ligand on Nuclear Receptor Mobility.- 4. Chemical Considerations in Discovery of Receptor Modulators.- 5. Structure-Based Design of Estrogen-Related Receptors Modulators.- 6. PPARα and δ ligand design - Honing the traditional empirical method with a more holistic overview.- 7. Pregnane X Receptor: understanding its function and activity at the molecular level.- 8. Ligand Design for the Vitamin D Receptor.- 9. What Makes a Good Antagonist: Lessons Learned from the Estrogen and Aryl Hydrocarbon Receptors.- 10. Design of Novel PPAR agonist for Neurodegenerative Disease.- 11. Functional bioassays lithograph ligand reflections in the PPARalpha sphere.- 12. Computational applications on Food Contact Chemicals as Nuclear Receptors binders.- 13. Alternation of Nuclear Hormone Receptor Signaling by Antiviral Drugs.- 14. Retinoic acid-related orphan receptor (ROR) inverse agonists: potential therapeutic strategies for multiple inflammatory diseases.- 15. Therapeutic Strategies to Target Activating Estrogen Receptor a Mutation.- 16. Androgen Receptors in the Pathology of Disease.- 17. Bilirubin: A Ligand of the PPARα Nuclear Receptor.- 18. Nuclear Receptor Ligands in Flavivirus Infection Control.- 19. Use of Nanotechnology to Improve 15d-PGJ2 Immunomodulatory Activities.- 20.Ligand-independent Activation of PPARs.- 21. PPAR Modulation Through Posttranslational Modification Control.- 22. Developing Inhibitors to the Amino-Terminus Domains of Steroid Hormone Receptors.- 23. Redirecting the cellular waste disposal machinery to target transcription.

最近チェックした商品