U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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

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 Fri Dec 15 16:41:40 GMT 2023
Edited
by admin
on Fri Dec 15 16:41:40 GMT 2023
Record UNII
P021X7VTG0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
NSC-760441
Code English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
Code System Code Type Description
WIKIPEDIA
IPROHEPTINE
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
NCI_THESAURUS
C83836
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
CAS
13946-02-6
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
EVMPD
SUB08282MIG
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
NSC
760441
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
ChEMBL
CHEMBL2103925
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
FDA UNII
P021X7VTG0
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID8046248
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
INN
4090
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
DRUG CENTRAL
3783
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
PUBCHEM
19917
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
MERCK INDEX
m828
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY Merck Index
SMS_ID
100000083144
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
ECHA (EC/EINECS)
237-726-4
Created by admin on Fri Dec 15 16:41:41 GMT 2023 , Edited by admin on Fri Dec 15 16:41:41 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY