Pharmaceutical compound
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 .[ 2] [ 3] [ 4] [ 5] [ 6] [ 7] It is a member of the phenethylamine and 2C families of compounds .[ 4] [ 5] [ 7] The drug is being developed as a topical eye drop for treatment of inflammatory eye conditions .[ 2] [ 3] There is also interest in 2C-iBu and related drugs for treatment of systemic inflammation and neuroinflammation .[ 8] [ 9] [ 10] [ 11] [ 12] [ 5]
2C-iBu was not assessed or discovered by Alexander Shulgin and was not described in PiHKAL (Phenethylamines I Have Known and Loved ) (1991).[ 7] [ 13] 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).[ 1] 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.[ 1] The cited source for these observations, however, was only a 2006 personal communication with "M. Mueller."[ 1]
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.[ 4] [ 7] 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.[ 2] [ 3]
Pharmacology
2C-iBu is a highly potent and robustly efficacious serotonin 5-HT2A receptor agonist .[ 4] Its EC50 Tooltip half-maximal effective concentration values are 1.3 nM for calcium mobilization and 57.5 nM for β-arrestin-2 recruitment, whereas its Emax Tooltip maximal efficacy values are 103% for calcium mobilization and 77% for β-arrestin-2 recruitment relative to serotonin.[ 4] The drug showed higher potency and efficacy as a serotonin 5-HT2A receptor agonist than several other 2C drugs, including 2C-NP, 2C-B , 2C-I , 2C-H , and 2C-iP , whereas its activities were more comparable to or less than those of the DOx drugs DOIB , (R )-DOB , (R )-DOI , and DOiP .[ 4] 2C-iBu has also been assessed and found to bind to other serotonin receptors , including the serotonin 5-HT2C , 5-HT2B , 5-HT1B , 5-HT1D , 5-HT1A , 5-HT7 , and 5-HT6 receptors , in that order of affinity and with varying avidities.[ 4]
2C-iBu dose-dependently produces the head-twitch response (HTR), a behavioral proxy of psychedelic effects, in rodents.[ 4] In terms of ED50 Tooltip median effective dose , 2C-iBu is about 3-fold less potent than (R )-DOI in producing the HTR.[ 4] According to Eleusis, it is expected to have "greatly reduced" psychoactivity or hallucinogenic effects compared to related drugs like other members of the 2C family.[ 6] [ 14]
The drug is effective in an allergic asthma model in rodents and showed similar potency as (R )-DOI.[ 4] Due to its reduced potency in producing the HTR but retained anti-inflammatory potency, 2C-iBu is expected to show greater separation between the desired anti-inflammatory and the undesired psychedelic effects in humans compared to (R )-DOI.[ 4] In contrast to certain other anti-inflammatory drugs like corticosteroids , serotonin 5-HT2A receptor agonists like 2C-iBu are not immunosuppressants .[ 14]
Chemistry
2C-iBu, also known as 2,5-dimethoxy-4-isobutylphenethylamine, is a phenethylamine and 2C derivative .[ 4] [ 5] [ 7]
Related drugs to 2C-iBu include 2C-Bu (the butyl analogue ), 2C-tBu (the tert -butyl analogue), 2C-sBu (the sec -butyl analogue), and 2C-CPM (the cyclopropyl methyl analogue).[ 4] In addition, 2C-iBu is related to DOx drugs such as DOIB (DOiBu).[ 4] [ 15]
According to Charles D. Nichols , 2,5-dimethoxyamphetamine (2,5-DMA) has potent anti-inflammatory activity with weak or no hallucinogenic effects.[ 7] [ 15] Moreover, DOTFM has potent psychedelic effects with no anti-inflammatory activity.[ 7] [ 16] [ 17] Hence, it appears that the anti-inflammatory effects and psychedelic effects of serotonin 5-HT2A receptor agonists can be fully dissociated.[ 7]
The chemical synthesis of 2C-iBu has been described.[ 4] [ 1]
Clinical development
2C-iBu was developed as a novel anti-inflammatory drug by Charles D. Nichols and colleagues at Eleusis in the late 2010s.[ 7] [ 4] They are developing it for treatment of inflammatory conditions .[ 2] [ 3] Eleusis was acquired by and merged into Beckley Psytech in October 2022.[ 2] [ 18] [ 19] The drug has reached the preclinical research stage of development, but no recent development has been reported as of October 2023.[ 2] [ 3] Eleusis has licensed intellectual property surrounding 2C-iBu and has patent protection for 2C-iBu.[ 6] [ 4]
Legal status
2C-iBu is not a controlled substance in the United States as of 2020.[ 6]
See also
References
^ a b c d e f Shulgin A, Manning T, Daley PF (2011). "#60. DOM" . The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds . Vol. 1. Berkeley, CA: Transform Press. pp. 118– 129. ISBN 978-0-9630096-3-0 . OCLC 709667010 . 2c-IB: [...] (15) Synthesis (from 2,5-dimethoxyisobutylbenzene) (Mueller, 2006); although this compound was reported here, a structure-search in Chemical Abstracts does not produce a CAS registry number (16) Threshold activity in humans at 5 mg orally; long duration (about 20 hours; Mueller, 2006). [...] Mueller, M. (2006) Personal communication with A.T. Shulgin.
^ a b c d e f g "ELE 02" . AdisInsight . 28 October 2023. Retrieved 16 February 2025 .
^ a b c d e f "Delving into the Latest Updates on ELE-02 with Synapse" . Synapse . 23 January 2025. Retrieved 16 February 2025 .
^ a b c d e f g h i j k l m n o p q r s WO published 2020210823 , Nichols CD , Billac G, Nichols DE , "Compounds and methods for treating inflammatory disorders", published 15 October 2020
^ a b c d Raz S (February 2020). Eleusis Drug Development Overview . LSX World Congress 2020.
^ a b c d Newvine C (8 July 2020). "Eleusis Draws on Research Into Psychedelics To Develop New Medicines for Inflammation" . Lucid News - Psychedelics, Consciousness Technology, and the Future of Wellness . Retrieved 16 February 2025 .
^ a b c d e f g h i Hamilton Morris (14 November 2021). "PODCAST 33: An interview with Dr. Charles D. Nichols" . The Hamilton Morris Podcast (Podcast). Patreon. Event occurs at 48:22–53:56. Retrieved 20 January 2025 .
^ Nichols DE, Johnson MW, Nichols CD (February 2017). "Psychedelics as Medicines: An Emerging New Paradigm". Clin Pharmacol Ther . 101 (2): 209– 219. doi :10.1002/cpt.557 . PMID 28019026 .
^ Flanagan TW, Nichols CD (2022). "Psychedelics and Anti-inflammatory Activity in Animal Models". Disruptive Psychopharmacology . Current Topics in Behavioral Neurosciences. Vol. 56. pp. 229– 245. doi :10.1007/7854_2022_367 . ISBN 978-3-031-12183-8 . PMID 35546383 .
^ Nichols CD (November 2022). "Psychedelics as potent anti-inflammatory therapeutics" . Neuropharmacology . 219 : 109232. doi :10.1016/j.neuropharm.2022.109232 . PMID 36007854 . {{cite journal }}
: CS1 maint: article number as page number (link )
^ Flanagan TW, Nichols CD (August 2018). "Psychedelics as anti-inflammatory agents" (PDF) . Int Rev Psychiatry . 30 (4): 363– 375. doi :10.1080/09540261.2018.1481827 . PMID 30102081 .
^ Thompson C, Szabo A (December 2020). "Psychedelics as a novel approach to treating autoimmune conditions". Immunol Lett . 228 : 45– 54. doi :10.1016/j.imlet.2020.10.001 . hdl :10852/80687 . PMID 33035575 .
^ Shulgin AT , Shulgin A (1991). PiHKAL: A Chemical Love Story (1st ed.). Berkeley, CA: Transform Press. ISBN 978-0-9630096-0-9 . OCLC 25627628 .
^ a b Lekhtman A (8 July 2020). "Researcher Charles Nichols Studies the Impact of Psychedelic Substances on Inflammation" . Lucid News - Psychedelics, Consciousness Technology, and the Future of Wellness . Retrieved 16 February 2025 .
^ a b Flanagan TW, Billac GB, Landry AN, Sebastian MN, Cormier SA, Nichols CD (April 2021). "Structure-Activity Relationship Analysis of Psychedelics in a Rat Model of Asthma Reveals the Anti-Inflammatory Pharmacophore" . ACS Pharmacol Transl Sci . 4 (2): 488– 502. doi :10.1021/acsptsci.0c00063 . PMC 8033619 . PMID 33860179 . The nature of the 4-position substituent of phenethylamine psychedelics has been previously linked to 5-HT2 receptor selectivity as well as agonist properties at 5-HT2 receptors.40 Analysis of the 4-position demonstrated that the identity of the moiety at this position was rather flexible. Fully efficacious substitutions at the 4-position included the halogens iodine and bromine (R)-DOI (Figure 3), 2C-B (Figure 7A), methoxy (TMA-2) (Figure 7G), short-chain hydrocarbons (R)-DOM (Figure 7H), (R)-DOET) (Figure 7I), and a branched hydrocarbon (DOiBu) (Figure 7J). [...] In a comparison of PenH-AUC values determined for each drug as a proxy measure of anti-inflammatory efficacy (Figure 8A) to either EC50 or EMax for calcium mobilization downstream of 5- HT2A receptor activation (Table 1), [...]
^ Flanagan TW, Billac G, Nichols CD (2022). "Differential Regulation of Inflammatory Responses Following 5-HT 2 Receptor Activation in Pulmonary Tissues" . The FASEB Journal . 36 (S1). doi :10.1096/fasebj.2022.36.S1.R2617 . ISSN 0892-6638 .
^ Flanagan TW, Foster TP, Galbato TE, Lum PY, Louie B, Song G, et al. (February 2024). "Serotonin-2 Receptor Agonists Produce Anti-inflammatory Effects through Functionally Selective Mechanisms That Involve the Suppression of Disease-Induced Arginase 1 Expression" . ACS Pharmacology & Translational Science . 7 (2): 478– 492. doi :10.1021/acsptsci.3c00297 . PMC 10863441 . PMID 38357283 . The effects of (R)-DOTFM were examined in the head-twitch response (HTR) assay. (R)-DOTFM produced a strong HTR with a potent ED 50 of 0.60 μmol/kg. These values are equivalent to (R)-DOI, as previously determined.
^ Gunther M (26 October 2022). "What's the Future of Eleusis Therapeutics After Acquisition by Beckley Psytech?" . Lucid News - Psychedelics, Consciousness Technology, and the Future of Wellness . Retrieved 17 February 2025 .
^ "Beckley Psytech Strengthens Pipeline and Development Team With Acquisition of Eleusis Therapeutics Limited" . Psychedelic Alpha . 24 October 2022. Retrieved 17 February 2025 .
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PRX-08066
Rauwolscine
Ritanserin
RS-127445
Sarpogrelate
SB-200646
SB-204741
SB-206553
SB-215505
SB-221284
SB-228357
SDZ SER-082
Tegaserod
Tetracyclic antidepressants (e.g., amoxapine , mianserin , mirtazapine )
Trazodone
Typical antipsychotics (e.g., chlorpromazine )
TIK-301
Yohimbine
5-HT2C
Agonists: 2Cs (e.g., 2C-B , 2C-E , 2C-I , 2C-T-2 , 2C-T-7 , 2C-T-21 )
5-Methoxytryptamines (5-MeO-DET , 5-MeO-DiPT , 5-MeO-DMT , 5-MeO-DPT , 5-MT )
α-Alkyltryptamines (e.g., 5-Cl-αMT , 5-Fl-αMT , 5-MeO-αET , 5-MeO-αMT , α-Me-5-HT , αET , αMT )
A-372159
AL-38022A
Alstonine
CP-809101
Dimemebfe
DOx (e.g., DOB , DOC , DOI , DOM )
Ergolines (e.g., ALD-52 , cabergoline , dihydroergotamine , ergine (LSA) , ergotamine , lisuride , LA-SS-Az , LSB , LSD , LSD-Pip , LSH , LSP , pergolide )
Flumexadol
Lorcaserin
MDxx (e.g., MDA (tenamfetamine) , MDMA (midomafetamine) , MDOH , MMDA )
MK-212
ORG-12962
ORG-37684
Oxaflozane
PHA-57378
Phenethylamines (e.g., lophophine , mescaline )
Piperazines (e.g., aripiprazole , BZP , mCPP , quipazine , TFMPP )
PNU-22394
PNU-181731
Ro60-0175
Ro60-0213
Serotonin (5-HT)
Tryptamines (e.g., 5-BT , 5-CT , bufotenin , DET , DiPT , DMT , DPT , psilocin , psilocybin , tryptamine )
Vabicaserin
WAY-629
WAY-161503
YM-348
Antagonists: Adatanserin
Agomelatine
Atypical antipsychotics (e.g., asenapine , clorotepine , clozapine , fluperlapine , iloperidone , melperone , olanzapine , paliperidone , quetiapine , risperidone , sertindole , ziprasidone , zotepine )
Captodiame
CEPC
Cinanserin
Cyproheptadine
Deramciclane
Desmetramadol
Dotarizine
Eltoprazine
Ergolines (e.g., amesergide , bromocriptine , LY-53857 , LY-215840 , mesulergine , metergoline , methysergide , sergolexole )
Etoperidone
Fluoxetine
FR-260010
Irindalone
Ketanserin
Ketotifen
Latrepirdine (dimebolin)
Medifoxamine
Metitepine (methiothepin)
Nefazodone
Pirenperone
Pizotifen
Propranolol
Ritanserin
RS-102221
S-14671
SB-200646
SB-206553
SB-221284
SB-228357
SB-242084
SB-243213
SDZ SER-082
Tedatioxetine
Tetracyclic antidepressants (e.g., amoxapine , aptazapine , esmirtazapine , maprotiline , mianserin , mirtazapine )
TIK-301
Tramadol
Trazodone
Tricyclic antidepressants (e.g., amitriptyline , nortriptyline )
Typical antipsychotics (e.g., chlorpromazine , loxapine , pimozide , pipamperone , thioridazine )
Xylamidine
5-HT3 –7
5-HT3
Agonists: Alcohols (e.g., butanol , ethanol (alcohol) , trichloroethanol )
m-CPBG
Phenylbiguanide
Piperazines (e.g., BZP , mCPP , quipazine )
RS-56812
Serotonin (5-HT)
SR-57227
SR-57227A
Tryptamines (e.g., 2-Me-5-HT , 5-CT , bufotenidine (5-HTQ) )
Volatiles/gases (e.g., halothane , isoflurane , toluene , trichloroethane )
YM-31636
Antagonists: Alosetron
Anpirtoline
Arazasetron
AS-8112
Atypical antipsychotics (e.g., clozapine , olanzapine , quetiapine )
Azasetron
Batanopride
Bemesetron (MDL-72222)
Cilansetron
CSP-2503
Dazopride
Dolasetron
Galanolactone
Granisetron
Lerisetron
Memantine
Ondansetron
Palonosetron
Ramosetron
Renzapride
Ricasetron
Tedatioxetine
Tetracyclic antidepressants (e.g., amoxapine , mianserin , mirtazapine )
Thujone
Tropanserin
Tropisetron
Typical antipsychotics (e.g., loxapine )
Volatiles/gases (e.g., nitrous oxide , sevoflurane , xenon )
Vortioxetine
Zacopride
Zatosetron
5-HT4
5-HT5A
5-HT6
Agonists: Ergolines (e.g., dihydroergocryptine , dihydroergotamine , ergotamine , lisuride , LSD , mesulergine , metergoline , methysergide )
Hypidone
Serotonin (5-HT)
Tryptamines (e.g., 2-Me-5-HT , 5-BT , 5-CT , 5-MT , Bufotenin , E-6801 , E-6837 , EMD-386088 , EMDT , LY-586713 , N-Me-5-HT , ST-1936 , tryptamine )
WAY-181187
WAY-208466
Antagonists: ABT-354
Atypical antipsychotics (e.g., aripiprazole , asenapine , clorotepine , clozapine , fluperlapine , iloperidone , olanzapine , tiospirone )
AVN-101
AVN-211
AVN-322
AVN-397
BGC20-760
BVT-5182
BVT-74316
Cerlapirdine
EGIS-12233
GW-742457
Idalopirdine
Ketanserin
Landipirdine
Latrepirdine (dimebolin)
Masupirdine
Metitepine (methiothepin)
MS-245
PRX-07034
Ritanserin
Ro 04-6790
Ro 63-0563
SB-258585
SB-271046
SB-357134
SB-399885
SB-742457
Tetracyclic antidepressants (e.g., amoxapine , mianserin )
Tricyclic antidepressants (e.g., amitriptyline , clomipramine , doxepin , nortriptyline )
Typical antipsychotics (e.g., chlorpromazine , loxapine )
5-HT7
Antagonists: Atypical antipsychotics (e.g., amisulpride , aripiprazole , asenapine , brexpiprazole , clorotepine , clozapine , fluperlapine , olanzapine , risperidone , sertindole , tiospirone , ziprasidone , zotepine )
Butaclamol
DR-4485
EGIS-12233
Ergolines (e.g., 2-Br-LSD (BOL-148) , amesergide , bromocriptine , cabergoline , dihydroergotamine , ergotamine , LY-53857 , LY-215840 , mesulergine , metergoline , methysergide , sergolexole )
JNJ-18038683
Ketanserin
LY-215840
Metitepine (methiothepin)
Ritanserin
SB-258719
SB-258741
SB-269970
SB-656104
SB-656104A
SB-691673
SLV-313
SLV-314
Spiperone
SSR-181507
Tetracyclic antidepressants (e.g., amoxapine , maprotiline , mianserin , mirtazapine )
Tricyclic antidepressants (e.g., amitriptyline , clomipramine , imipramine )
Typical antipsychotics (e.g., acetophenazine , chlorpromazine , chlorprothixene , fluphenazine , loxapine , pimozide )
Vortioxetine
Negative allosteric modulators: Oleamide
Phenethylamines Amphetamines Phentermines Cathinones Phenylisobutylamines (and further-extended) Catecholamines (and close relatives) Cyclized phenethylamines
Phenylalkylpyrrolidines 2-Benzylpiperidines (phenidates ) Phenylmorpholines (phenmetrazines) Phenyloxazolamines (aminorexes) Isoquinolines andtetrahydroisoquinolines 2-Aminoindanes 2-Aminotetralins Others / unsorted
1-Aminomethylindanes (e.g., 2CB-Ind , AMMI , bromojimscaline , jimscaline )
2-ADN
2-Benzhydrylpyrrolidine
2C-B-5-hemiFLY-α6 (BNAP)
2C-B-PYR
2CBecca
2CJP
2CLisaB
2CLisaH
3-Benzhydrylmorpholine
3-Phenylpiperidines (e.g., 3-phenylpiperidine , 3-PPP , OSU-6162 (PNU-96391) , LPH-5 , LPH-48 , Z3517967757 (Z7757) )
6-AB
AL-1095
Aminochromes (e.g., adrenochrome , adrenolutin )
Benzazepines (e.g., fenoldopam , lorcaserin , SCHEMBL5334361 )
Benzocyclobutenes (e.g., 2CBCB-NBOMe , bromotomscaline , S33005 , TCB-2 , tomscaline )
Benzoxepins (e.g., BBOX , IBOX , TFMBOX )
Butyltolylquinuclidine
Camfetamine
Cypenamine (trans -2-phenylcyclopentylamine)
Diphenidine
Diphenylprolinol
DMBMPP
Ergolines (e.g., LSD )
Fencamfamin
GYKI-52895
HDMP-29
Ivabradine
Methoxphenidine
Methylmorphenate
Milnacipran
MT-45
2-Naphthylamine
Org 6582
Partial ergolines (e.g., NDTDI , RU-27849 , DEIMDHPCA , DEMPDHPCA , DEMPDHPCA-2C-D , RU-27251 )
PF-592,379
Phenylcyclopropylamines (e.g., DMCPA , TMT , tranylcypromine )
Phenylpiracetams (e.g., phenylpiracetam , MRZ-9547 , RGPU-95 )
Pyridopyrroloquinoxalines (e.g., lumateperone , deulumateperone , IHCH-7079 , IHCH-7086 , IHCH-7113 , ITI-1549 )
Tetrahydrobenzopyranylamines (e.g., CT-5126 )
Tolazoline
Tricyclics (e.g., AMDA , AMDH , benzoctamine , dizocilpine , SpAMDA )
ZC-B
Related compounds
2-Furylethylamine
2-Pyrrolylethylamine
3-Pyrrolylethylamine
3-Pyrrolylpropylamine
2-Tetrahydrofurylethylamine
4-Benzylpiperidine
7-AB
Alkylamines (e.g., 1,3-DMBA Tooltip 1,3-dimethylbutylamine , 1,4-DMAA Tooltip 1,4-dimethylamylamine , heptaminol , iproheptine , isometheptene , methylhexanamine/1,3-DMAA , octodrine , oenethyl , tuaminoheptane )
Benzylamines (e.g., benzylamine , α-methylbenzylamine , MDM1EA , ALPHA , M-ALPHA , pargyline )
Benzylpiperazines (e.g., benzylpiperazine , MDBZP , fipexide )
Cyclohexylaminopropanes (e.g., propylhexedrine , norpropylhexedrine )
Cyclopentylaminopropanes (e.g., isocyclamine , cyclopentamine )
Phenoxyethylamines (e.g., 3,4,5-trimethoxyphenoxyethylamine , CT-4719 , ORG-37684 )
Phenylalkenylamines (e.g., phenylbutenamine )
Phenylalkynylamines (e.g., phenylbutynamine )
Phenylpiperazines (e.g., 1-phenylpiperazine , mCPP Tooltip meta-chlorophenylpiperazine , TFMPP Tooltip trifluoromethylphenylpiperazine , oMPP Tooltip ortho-methylphenylpiperazine , pFPP Tooltip para-fluorophenylpiperazine , pMeOPP Tooltip para-methoxyphenylpiperazine )
Phenylpropylamines (e.g., phenylpropylamine , homo-MDA , homo-MDMA )
Thienylaminopropanes (thiopropamines) (e.g., thiopropamine , methiopropamine , thiothinone )