Discovery of ITI-333, a Novel Orally Bioavailable Molecule Targeting Multiple Receptors for the Treatment of Pain and Other Disorders

• Published in: Journal of medicinal chemistry Vol. 67; no. 11; pp. 9355 - 9373
• Main Authors: Li, Peng, Zhang, Qiang, Zheng, Hailin, Qiao, Yupu, Snyder, Gretchen L., Martin, Terry, Yao, Wei, Zhang, Lei, Davis, Robert E.
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 13.06.2024; Amer Chemical Soc
• Subjects: Administration, Oral; Analgesics - chemical synthesis; Analgesics - chemistry; Analgesics - pharmacology; Analgesics - therapeutic use; Animals; Biological Availability; Chemistry, Medicinal; Drug Discovery; Humans; Life Sciences & Biomedicine; Male; Mice; Pain - drug therapy; Pharmacology & Pharmacy; Pyridines - chemical synthesis; Pyridines - chemistry; Pyridines - pharmacokinetics; Pyridines - pharmacology; Pyridines - therapeutic use; Pyrroles - chemical synthesis; Pyrroles - chemistry; Pyrroles - pharmacokinetics; Pyrroles - pharmacology; Rats; Rats, Sprague-Dawley; Receptors, Opioid, mu - agonists; Receptors, Opioid, mu - metabolism; Science & Technology; Structure-Activity Relationship; INDUCED VENTILATORY DEPRESSION; UNITED-STATES; DRUG; PRAZOSIN; POSITIVE ALLOSTERIC MODULATORS; ALPHA-1-ADRENERGIC ANTAGONIST; MU-OPIOID RECEPTOR; DEPENDENCE
• ISSN: 0022-2623; 1520-4804; 1520-4804
• DOI: 10.1021/acs.jmedchem.4c00480

Development of more efficacious medications with improved safety profiles to manage and treat multiple forms of pain is a critical element of healthcare. To this end, we have designed and synthesized a novel class of tetracyclic pyridopyrroloquinoxalinone derivatives with analgesic properties. The receptor binding profiles and analgesic properties of these tetracyclic compounds were studied. Systematic optimizations of this novel scaffold culminated in the discovery of the clinical candidate, (6bR,10aS)-8-[3-(4-fluorophenoxy)­propyl]-6b,7,8,9,10,10a-hexahydro-1H-pyrido­[3′,4′:4,5]­pyrrolo­[1,2,3-de]­quinoxalin-2­(3H)-one (compound 5, ITI-333), which exhibited potent binding affinity to serotonin 5-HT2A (K i = 8.3 nM) and μ-opioid receptors (MOR, K i = 11 nM) and moderate affinity to adrenergic α1A (K i = 28 nM) and dopamine D1 (K i = 50 nM) receptors. ITI-333 acts as a 5-HT2A receptor antagonist, a MOR partial agonist, and an adrenergic α1A receptor antagonist. ITI-333 exhibited dose-dependent analgesic effects in rodent models of acute pain. Currently, this investigational new drug is in phase I clinical development.