Synthesis of H4 pantetheine adducts for histone acetyltransferase inhibition

Abstract: Site-specific modifications of peptides provide a powerful tool for design of chemical probes and enzyme inhibitors. A convenient synthesis method was developed and used to produce H4K16-pantetheine bisubstrate analogs which could be employed as inhibitors of histone acetyltransferases in vivo and in vitro.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Synthesis of H4 pantetheine adducts for histone acetyltransferase inhibition ; volume:16 ; number:4-6 ; year:2010 ; pages:231-234
Heterocyclic communications ; 16, Heft 4-6 (2010), 231-234

Creator
Wu, Jiang
Zheng, Yujun George

DOI
10.1515/HC.2010.014
URN
urn:nbn:de:101:1-2501130541512.734231721710
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.20252151, 4:08 PM CET

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Associated

  • Wu, Jiang
  • Zheng, Yujun George

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