Synthesis, structure-activity relationship and biological evaluation of novel N-substituted matrinic acid derivatives as host heat-stress cognate 70 (Hsc70) down-regulators

Bioorg Med Chem Lett. 2011 Aug 15;21(16):4732-5. doi: 10.1016/j.bmcl.2011.06.071. Epub 2011 Jun 23.

Abstract

Oxymatrine (1) is a natural anti-hepatitis B virus (HBV) drug that down-regulates host heat-stress cognate 70 (Hsc70) expression through a mechanism different from that of nucleosides. Taking Hsc70 as a target against HBV, 26 novel N-substituted matrinic acid analogs were designed, synthesized and evaluated for their regulation of Hsc70 mRNA expression with 1 as the lead. The SAR analysis revealed that (i) the carboxyl group at the 11-position was required for activity; (ii) introducing of a substituent on the nitrogen atom at the 12-position of 3, especially substituted benzyl, might significantly improve the activity. Among these analogs, compound 9p possessing N-p-methoxylbenzyl afforded an increased anti-HBV effect in comparison with 1. We consider 9p a promising anti-HBV candidate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Butyrates / chemical synthesis
  • Butyrates / chemistry
  • Butyrates / pharmacology*
  • Down-Regulation / drug effects
  • HSC70 Heat-Shock Proteins / antagonists & inhibitors*
  • HSC70 Heat-Shock Proteins / metabolism
  • Hepacivirus / drug effects
  • Hepatitis B virus / drug effects
  • Molecular Conformation
  • Quinolizines / chemical synthesis
  • Quinolizines / chemistry
  • Quinolizines / pharmacology*
  • RNA, Messenger / drug effects
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • Anti-Bacterial Agents
  • Butyrates
  • HSC70 Heat-Shock Proteins
  • Quinolizines
  • RNA, Messenger