IBE-2254

Details

Stereochemistry	RACEMIC
Molecular Formula	C19H20INO2
Molecular Weight	421.2721
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC1=CC=C(CCNCC2CCC3=CC=CC=C3C2=O)C=C1I

InChI

InChIKey=DUOOAUBZMQZYLO-UHFFFAOYSA-N

InChI=1S/C19H20INO2/c20-17-11-13(5-8-18(17)22)9-10-21-12-15-7-6-14-3-1-2-4-16(14)19(15)23/h1-5,8,11,15,21-22H,6-7,9-10,12H2

HIDE SMILES / InChI

Molecular Formula	C19H20INO2
Molecular Weight	421.2721
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

PubMed

Title	Date	PubMed
1-Arylpiperazinyl-4-cyclohexylamine derived isoindole-1,3-diones as potent and selective alpha-1a/1d adrenergic receptor ligands.	2007-03-15	17254786
Compensatory changes in the noradrenergic nervous system in the locus ceruleus and hippocampus of postmortem subjects with Alzheimer's disease and dementia with Lewy bodies.	2006-01-11	16407544
Differential antagonism by conotoxin rho-TIA of contractions mediated by distinct alpha1-adrenoceptor subtypes in rat vas deferens, spleen and aorta.	2005-01-31	15680270
Vascular alpha1-adrenoceptor subtype selectivity and alpha1-blocker-induced orthostatic hypotension.	1998-05	9639061
Effects of quinidine and verapamil on human cardiovascular alpha1-adrenoceptors.	1998-04-07	9570190

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:36:49 GMT 2025` Edited by `admin` on `Mon Mar 31 18:36:49 GMT 2025`
Record UNII	3EGK3ZND2L
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

IBE-2254

Common Name

English

2-(P-(4-HYDROXY-3-(125I)IODOPHENYL)ETHYLAMINOMETHYL)-TETRALONE

Preferred Name

English

M-IODO-HEAT

Common Name

English

2-((2-(4-HYDROXY-3-IODANYLPHENYL)ETHYLAMINO)METHYL)-3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE

Systematic Name

English

1(2H)-NAPHTHALENONE, 3,4-DIHYDRO-2-(((2-(4-HYDROXY-3-IODOPHENYL)ETHYL)AMINO)METHYL)-

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID40915164

Created by admin on Mon Mar 31 18:36:49 GMT 2025 , Edited by admin on Mon Mar 31 18:36:49 GMT 2025

PRIMARY

CAS

95034-25-6

Created by admin on Mon Mar 31 18:36:49 GMT 2025 , Edited by admin on Mon Mar 31 18:36:49 GMT 2025

PRIMARY

PUBCHEM

10093628

Created by admin on Mon Mar 31 18:36:49 GMT 2025 , Edited by admin on Mon Mar 31 18:36:49 GMT 2025

PRIMARY

FDA UNII

3EGK3ZND2L

Created by admin on Mon Mar 31 18:36:49 GMT 2025 , Edited by admin on Mon Mar 31 18:36:49 GMT 2025

PRIMARY