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Details

Stereochemistry ACHIRAL
Molecular Formula C15H19IN4S
Molecular Weight 414.308
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IODOPHENPROPIT

SMILES

IC1=CC=C(CCNC(=N)SCCCC2=CNC=N2)C=C1

InChI

InChIKey=UBHYDQAARZKHEZ-UHFFFAOYSA-N
InChI=1S/C15H19IN4S/c16-13-5-3-12(4-6-13)7-8-19-15(17)21-9-1-2-14-10-18-11-20-14/h3-6,10-11H,1-2,7-9H2,(H2,17,19)(H,18,20)

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
7.9 nM [EC50]
PubMed

PubMed

TitleDatePubMed
Involvement of histamine H3 receptors in scratching behaviour in mast cell-deficient mice.
2003 Jul
Intracerebroventricular administration of histamine H3 receptor antagonists decreases seizures in rat models of epilepsia.
2004 May
Generation of cell lines for drug discovery through random activation of gene expression: application to the human histamine H3 receptor.
2005 Jun
Evaluation of histamine H1-, H2-, and H3-receptor ligands at the human histamine H4 receptor: identification of 4-methylhistamine as the first potent and selective H4 receptor agonist.
2005 Sep
Role of substance P on histamine H(3) antagonist-induced scratching behavior in mice.
2006 Apr
Comparison of the binding distribution of agonist and antagonist ligands for histamine H3 receptors in pig brain by quantitative autoradiography.
2007 Jun 14
Histamine-induced itch and its relationship with pain.
2008 Jul 31
Antagonist affinity measurements at the Gi-coupled human histamine H3 receptor expressed in CHO cells.
2008 Jun 6
Implementation of a fluorescence-based screening assay identifies histamine H3 receptor antagonists clobenpropit and iodophenpropit as subunit-selective N-methyl-D-aspartate receptor antagonists.
2010 Jun
Name Type Language
IODOPHENPROPIT
Common Name English
3-(1H-IMIDAZOL-5-YL)PROPYL N'-(2-(4-IODOPHENYL)ETHYL)IMIDOTHIOCARBAMATE
Systematic Name English
Code System Code Type Description
PUBCHEM
3035746
Created by admin on Sat Dec 16 08:01:59 GMT 2023 , Edited by admin on Sat Dec 16 08:01:59 GMT 2023
PRIMARY
FDA UNII
3SH45L9H3Z
Created by admin on Sat Dec 16 08:01:59 GMT 2023 , Edited by admin on Sat Dec 16 08:01:59 GMT 2023
PRIMARY
CAS
145196-88-9
Created by admin on Sat Dec 16 08:01:59 GMT 2023 , Edited by admin on Sat Dec 16 08:01:59 GMT 2023
PRIMARY
WIKIPEDIA
Iodophenpropit
Created by admin on Sat Dec 16 08:01:59 GMT 2023 , Edited by admin on Sat Dec 16 08:01:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID20273996
Created by admin on Sat Dec 16 08:01:59 GMT 2023 , Edited by admin on Sat Dec 16 08:01:59 GMT 2023
PRIMARY