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Details

Stereochemistry RACEMIC
Molecular Formula C11H25N
Molecular Weight 171.3229
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IPROHEPTINE

SMILES

CC(C)CCCC(C)NC(C)C

InChI

InChIKey=NKGYBXHAQAKSSG-UHFFFAOYSA-N
InChI=1S/C11H25N/c1-9(2)7-6-8-11(5)12-10(3)4/h9-12H,6-8H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C11H25N
Molecular Weight 171.3229
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Iproheptine (Metron, Susat) is a vasoconstrictor, antihistamine, nasal decongestant marketed in Japan.

CNS Activity

Curator's Comment: First-generation antihistamine - can cause side effect of sedation.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
METRON

Approved Use

Vasoconstrictor, antihistamine, nasal decongestant
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG


OverviewOther

Other InhibitorOther SubstrateOther Inducer


Drug as perpetrator​Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
no
Tox targets

Tox targets

TargetModalityActivityMetaboliteClinical evidence

Sample Use Guides

In Vivo Use Guide
Curator's Comment: A daily combination dosage of iproheptine hydrochloride for an adult is usually between 10 and 225 mg, preferably between 20 and 200 mg, more preferably between 30 and 150 mg. http://www.google.ch/patents/WO2005094832A1
Maximum daily dose - 150mg
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:34:45 GMT 2025
Edited
by admin
on Mon Mar 31 18:34:45 GMT 2025
Record UNII
P021X7VTG0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-760441
Preferred Name English
IPROHEPTINE
INN   WHO-DD  
INN  
Official Name English
Iproheptine [WHO-DD]
Common Name English
METRON S [MI]
Common Name English
N-ISOPROPYL-1,5-DIMETHYLHEXYLAMINE
Systematic Name English
iproheptine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
Code System Code Type Description
WIKIPEDIA
IPROHEPTINE
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
NCI_THESAURUS
C83836
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
CAS
13946-02-6
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
EVMPD
SUB08282MIG
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
NSC
760441
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
ChEMBL
CHEMBL2103925
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
FDA UNII
P021X7VTG0
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID8046248
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
INN
4090
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
DRUG CENTRAL
3783
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
PUBCHEM
19917
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
MERCK INDEX
m828
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY Merck Index
SMS_ID
100000083144
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
ECHA (EC/EINECS)
237-726-4
Created by admin on Mon Mar 31 18:34:45 GMT 2025 , Edited by admin on Mon Mar 31 18:34:45 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY