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Details

Stereochemistry ACHIRAL
Molecular Formula C17H20INO3.ClH
Molecular Weight 449.711
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENOL, 2-(((2-(4-IODO-2,5-DIMETHOXYPHENYL)ETHYL)AMINO)METHYL)-, HYDROCHLORIDE (1:1)

SMILES

Cl.COC1=CC(CCNCC2=C(O)C=CC=C2)=C(OC)C=C1I

InChI

InChIKey=PXODWOUSZUTKOZ-UHFFFAOYSA-N
InChI=1S/C17H20INO3.ClH/c1-21-16-10-14(18)17(22-2)9-12(16)7-8-19-11-13-5-3-4-6-15(13)20;/h3-6,9-10,19-20H,7-8,11H2,1-2H3;1H

HIDE SMILES / InChI

Approval Year

Targets
PubMed

PubMed

TitleDatePubMed
Electroanalytical identification of 25I-NBOH and 2C-I via differential pulse voltammetry: a rapid and sensitive screening method to avoid misidentification.
2019-05-07
Neurochemical pharmacology of psychoactive substituted N-benzylphenethylamines: High potency agonists at 5-HT2A receptors.
2018-12
EASI-IMS an expedite and secure technique to screen for 25I-NBOH in blotter papers.
2017-10
Bad trip due to 25I-NBOMe: a case report from the EU project SPICE II plus.
2017-09
Characterization of the hepatic cytochrome P450 enzymes involved in the metabolism of 25I-NBOMe and 25I-NBOH.
2017-05
25I-NBOH: a new potent serotonin 5-HT2A receptor agonist identified in blotter paper seizures in Brazil.
2017
Synthesis and structure-activity relationships of N-benzyl phenethylamines as 5-HT2A/2C agonists.
2014-03-19
Radiosynthesis and in vivo evaluation of a series of substituted 11C-phenethylamines as 5-HT (2A) agonist PET tracers.
2011-04
Theoretical studies on the interaction of partial agonists with the 5-HT2A receptor.
2011-01
Name Type Language
PHENOL, 2-(((2-(4-IODO-2,5-DIMETHOXYPHENYL)ETHYL)AMINO)METHYL)-, HYDROCHLORIDE (1:1)
Preferred Name English
Code System Code Type Description
FDA UNII
WK4U8JDX2H
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
PUBCHEM
137699643
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY PUBCHEM
CAS
1539266-12-0
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
EPA CompTox
DTXSID301342539
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY