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Chemically programmed antibodies: Endothelin receptor targeting covx-bodies (tm)

Academic Article
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Overview

authors

  • Doppalapudi, V. R.
  • Tryder, N.
  • Li, L. N.
  • Aja, T.
  • Griffith, D.
  • Liao, F. F.
  • Roxas, G.
  • Ramprasad, M. P.
  • Bradshaw, C.
  • Barbas III, Carlos

publication date

  • 2007

journal

  • Bioorganic & Medicinal Chemistry Letters  Journal

abstract

  • Aryl sulfonamide-based endothelin antagonists were synthesized and covalently linked to the reactive lysine of the m38C2 antibody to create a series of CovX-Bodies. These chemically programmed antibodies behaved as potent endothelin receptor antagonists in vitro and had antitumor efficacy in a prostate cancer xenograft model which, on a molar basis, far exceeded the activity of the parent small molecule.

subject areas

  • Animals
  • Antibodies
  • Antineoplastic Agents
  • CHO Cells
  • Cricetinae
  • Cricetulus
  • Endothelin A Receptor Antagonists
  • Endothelin B Receptor Antagonists
  • Humans
  • Indicators and Reagents
  • Mice
  • Mice, Nude
  • Molecular Conformation
  • Neoplasm Transplantation
  • Receptors, Endothelin
  • Structure-Activity Relationship
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Research

keywords

  • CovX-Body (TM)
  • aldolase antibody
  • antitumor efficacy
  • endothelin-A
  • endothelin-A (ETA) antagonists
  • monoclonal antibodies
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Identity

International Standard Serial Number (ISSN)

  • 0960-894X

Digital Object Identifier (DOI)

  • 10.1016/j.bmcl.2006.10.009

PubMed ID

  • 17055724
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Additional Document Info

start page

  • 501

end page

  • 506

volume

  • 17

issue

  • 2

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