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Clinical data | |
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Other names | BNC210; BNC-210; IW2143; IW-2143; L-Isoleucyl-L-tryptophan |
Routes of administration | Oral |
Drug class | α7-Nicotinic acetylcholine receptor negative allosteric modulator |
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Pharmacokinetic data | |
Bioavailability | 69.4% (rat) [1] [2] |
Protein binding | 70–88% [1] [2] |
Elimination half-life | 6.2 hours (rat) [1] [2] |
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Chemical and physical data | |
Formula | C17H23N3O3 |
Molar mass | 317.389 g·mol−1 |
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Soclenicant (INN ), [3] also known by its developmental code names BNC210 and IW-2143 and as L-isoleucyl-L-tryptophan, is an antinicotinic agent which is under development for the treatment of anxiety disorders such as social phobia and generalized anxiety disorder, as well as for treatment of agitation, post-traumatic stress disorder (PTSD), and depressive disorders. [1] [4] [5] It is taken by mouth. [4]
The drug acts as a highly selective negative allosteric modulator (NAM) of the α7-nicotinic acetylcholine receptor (α7-nAChR). [1] [6] [4] [5] It produces anxiolytic-, anti-stress-, and antidepressant-like effects without causing sedation, memory or motor impairment, or physical dependence in rodents. [6] Chemically, soclenicant is a dipeptide of the amino acids L-tryptophan and L-isoleucine and can be considered a tryptamine derivative. [7]
Soclenicant is being developed by Bionomics. [4] It has also been developed by Ironwood Pharmaceuticals and EmpathBio. [4] [5] Bionomics was acquired by Neuphoria Therapeutics in December 2024. [4] As of December 2024, soclenicant is in phase 3 clinical trials for anxiety disorders, phase 2 trials for agitation and PTSD, and no recent development has been reported for depressive disorders. [4] [5] The drug received Fast Track designation from the United States Food and Drug Administration (FDA) in 2019. [8] It was first described in the literature, in a conference abstract, by 2007. [2]