• April 2, 2013 - N30 Announces Presentation of Preclinical Data at the Basic Science Meeting of the European Cystic Fibrosis Society
  • March 13, 2013 - N30 Announces First Patient Treated in Clinical Trial of N6022 in Cystic Fibrosis
  • October 8, 2012 - N30 Names Sherif Gabriel, Ph.D. as VP Research
  • August 27, 2012 - N30 Pharma Converts from LLC to C-Corp
  • February 21, 2012 - Board Adds Evan Loh, MD and John R. Moore
  • March 21, 2013 - S-nitrosoglutathione Reductase Inhibitors Modulate F508-del CFTR Protein Levels and Chloride Secretion In Vitro
  • March 20, 2013 - Small Molecule Inhibitors of GSNOR Possess Anti-Inflammatory and Bronchodilatory Actions in Mouse Models of Inflammatory Lung Disease and Modulate CFTR Function in F508del-CFTR Mice
  • November 11, 2011 - S-Nitrosoglutathione Reductase Inhibitors for the Prevention and Treatment of Experimental Colitis
  • August 28, 2011 - Structure – Activity Relationships of Pyrrole Based S-Nitrosoglutathione Reductase Inhibitors – Carboxamide Modification
  • July 14, 2011 - Heterozygous Deletion of S-Nitrosoglutathione Reductase in Mice Does Not Increase Nitrosative Inactivation of O6-Alkylguanine-DNA Alkyltransferase or Diethylnitrosamine-induced Hepatocarcinogenesis
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GSNOR Inhibitor Drugs

GSNOR Inhibitor Drugs

N30 Pharma has a broad portfolio of GSNOR inhibitor drug candidates that are potent, long lasting, and can be administered by a variety of routes, including oral, parenteral, inhalation and topical.

Key Chemical Series Expansion and Optimization Results
N6 Series 463 compounds 61 compounds <100 nM IC50
N7 Series 245 compounds 112 compounds <100 nM IC50
N9 Series 353 compounds 121 compounds <100 nM IC50

From the portfolio above, N30 Pharma has screened and selected a number of lead drug candidates that are currently in various stages of development.

Intravenous/Inhalation Oral
Lead N6022 N91115/69
Backup N6547 N91138
Lead Rationale
  • Low oral bioavailability
  • IC50 8 – 12 nM
  • Broad therapeutic index
  • Significant anti-inflammatory and bronchoprotective effects
  • High oral bioavailability
  • IC50 11-22 nM
  • Tox/ADME results support development
  • Chronic oral dosing
  • Sustained effects ≥ 24hrs
Status Phase 1 and 2 Clinical Studies IND enablement