2C-iBu
| Clinical data | |
|---|---|
| Other names | 2,5-Dimethoxy-4-isobutylphenethylamine; 4-Isobutyl-2,5-dimethoxyphenethylamine; 2C-iBu; 2C-IB; ELE-02; ELE02; ELEU02 |
| Routes of administration | Oral; Ophthalmic |
| Drug class | Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen; Anti-inflammatory drug |
| Pharmacokinetic data | |
| Protein binding | 74% |
| Duration of action | 20 hours |
| Identifiers | |
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| PubChem CID | |
| Chemical and physical data | |
| Formula | C14H23NO2 |
| Molar mass | 237.343 g·mol−1 |
| 3D model (JSmol) | |
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2,5-Dimethoxy-4-isobutylphenethylamine (2C-iBu or 2C-IB), also known by its developmental code name ELE-02, is a serotonin 5-HT2A receptor agonist, serotonergic psychedelic, and anti-inflammatory drug which is under development for the treatment of inflammation. It is a member of the phenethylamine and 2C families of compounds. The drug is being developed as a topical eye drop for treatment of inflammatory eye conditions. There is also interest in 2C-iBu and related drugs for treatment of systemic inflammation and neuroinflammation.
2C-iBu was not assessed or discovered by Alexander Shulgin and was not described in PiHKAL (Phenethylamines I Have Known and Loved) (1991). However, he did include 2C-iBu (as "2C-IB") as a DOM analogue in a table in The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds (2011). In addition, he stated in a footnote that a 5 mg oral dose of 2C-iBu produces threshold activity and has a long duration of about 20 hours. The cited source for these observations, however, was only a 2006 personal communication with "M. Mueller."
2C-iBu was subsequently more thoroughly characterized by Charles D. Nichols and colleagues at Louisiana State University School of Medicine as a novel anti-inflammatory drug in the late 2010s. Eleusis has licensed 2C-iBu intellectual property from LSU and the drug has reached the preclinical research stage of development, but no recent development has been reported as of October 2023.