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Noribogainalog

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Noribogainalog
Clinical data
Other namesNor-IBG; 9-Hydroxyibogaminalog
Identifiers
  • 3-methyl-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-9-ol
CAS Number
PubChem CID
ChemSpider
Chemical and physical data
FormulaC13H16N2O
Molar mass216.284 g·mol−1
3D model (JSmol)
  • CN1CCC2=C(CC1)NC3=C2C=C(C=C3)O
  • InChI=1S/C13H16N2O/c1-15-6-4-10-11-8-9(16)2-3-12(11)14-13(10)5-7-15/h2-3,8,14,16H,4-7H2,1H3
  • Key:OOROJSRWMMKEQK-UHFFFAOYSA-N

Noribogainalog (nor-IBG), also known as 9-hydroxyibogaminalog, is a drug of the ibogalog family related to noribogaine.[1][2] It is a simplified analogue of noribogaine.[1][2]

Pharmacology

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The drug acts as a potent serotonin 5-HT2A receptor partial agonist (EC50Tooltip half-maximal effective concentration ≈ 90 nM; EmaxTooltip maximal efficacy = 35%).[2] It also has activity as a dopamine transporter (DAT) chaperone.[3] Noribogainalog does not affect locomotor activity, does not produce the head-twitch response, and does not affect various other physiological and behavioral measures.[2] However, it does produce analgesic effects that can be diminished by the serotonin 5-HT2A receptor antagonist ketanserin.[2] The drug shows relatively low expected blood–brain barrier permeability.[2]

History

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Noribogainalog was first described in the scientific literature by David E. Olson and colleagues by 2021.[1]

See also

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References

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  1. ^ a b c Cameron LP, Tombari RJ, Lu J, Pell AJ, Hurley ZQ, Ehinger Y, et al. (January 2021). "A non-hallucinogenic psychedelic analogue with therapeutic potential". Nature. 589 (7842): 474–479. Bibcode:2021Natur.589..474C. doi:10.1038/s41586-020-3008-z. PMC 7874389. PMID 33299186.
  2. ^ a b c d e f Arias HR, Micheli L, Jensen AA, Galant S, Vandermoere F, Venturi D, et al. (March 2025). "Ibogalogs decrease neuropathic pain in mice through a mechanism involving crosstalk between 5-HT2A and mGlu2 receptors". Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 184 117887: 117887. doi:10.1016/j.biopha.2025.117887. PMID 39938347.
  3. ^ Sutton C, Williams EQ, Homsi H, Beerepoot P, Nazari R, Han D, et al. (2022). "Structure-Activity Relationships of Dopamine Transporter Pharmacological Chaperones". Frontiers in Cellular Neuroscience. 16: 832536. doi:10.3389/fncel.2022.832536. PMC 9124866. PMID 35614973.
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