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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H24N2O
Molecular Weight 296.4067
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NORIBOGAINE

SMILES

CC[C@H]1C[C@H]2C[C@@H]3[C@H]1N(C2)CCC4=C3NC5=C4C=C(O)C=C5

InChI

InChIKey=RAUCDOKTMDOIPF-ZFRACTKTSA-N
InChI=1S/C19H24N2O/c1-2-12-7-11-8-16-18-14(5-6-21(10-11)19(12)16)15-9-13(22)3-4-17(15)20-18/h3-4,9,11-12,16,19-20,22H,2,5-8,10H2,1H3/t11-,12-,16-,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H24N2O
Molecular Weight 296.4067
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Noribogaine, but not 18-MC, exhibits similar actions as ibogaine on GDNF expression and ethanol self-administration.
2010-10
Indolealkylamines: biotransformations and potential drug-drug interactions.
2008-06
Determination of ibogaine and noribogaine in biological fluids and hair by LC-MS/MS after Tabernanthe iboga abuse Iboga alkaloids distribution in a drowning death case.
2008-03-21
Ibogaine, an anti-addictive drug: pharmacology and time to go further in development. A narrative review.
2008-03
Acute toxicity of ibogaine and noribogaine.
2008
Liquid chromatography-electrospray mass spectrometry determination of ibogaine and noribogaine in human plasma and whole blood. Application to a poisoning involving Tabernanthe iboga root.
2006-11-07
Distribution of ibogaine and noribogaine in a man following a poisoning involving root bark of the Tabernanthe iboga shrub.
2006-09
Quantitation of ibogaine and 12-hydroxyibogamine in human plasma by liquid chromatography with fluorimetric detection.
2005-08-05
Addiction research. Ibogaine therapy: a 'vast, uncontrolled experiment'.
2005-04-15
In vivo neurobiological effects of ibogaine and its O-desmethyl metabolite, 12-hydroxyibogamine (noribogaine), in rats.
2001-05
Comparative neuropharmacology of ibogaine and its O-desmethyl metabolite, noribogaine.
2001
Mechanisms of antiaddictive actions of ibogaine.
1998-05-30
Time-dependent interactions between iboga agents and cocaine.
1997-10-08
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:55:01 GMT 2025
Edited
by admin
on Mon Mar 31 21:55:01 GMT 2025
Record UNII
87T5QTN9SK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
J666.099A
Preferred Name English
NORIBOGAINE
Common Name English
IBOGAINE, O-DEMETHYL-
Common Name English
O-NORIBOGAINE
Common Name English
IBOGAMIN-12-OL
Common Name English
(-)-NORIBOGAINE
Common Name English
12-HYDROXYIBOGAMINE
Common Name English
O-DEMETHYLIBOGAINE
Common Name English
Code System Code Type Description
EVMPD
SUB79173
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
FDA UNII
87T5QTN9SK
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
CAS
481-88-9
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
SMS_ID
100000138840
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID90963998
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
CHEBI
146258
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
WIKIPEDIA
Noribogaine
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
PUBCHEM
12313547
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
CHEBI
146264
Created by admin on Mon Mar 31 21:55:01 GMT 2025 , Edited by admin on Mon Mar 31 21:55:01 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY