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

Details

Stereochemistry ACHIRAL
Molecular Formula C19H24N2
Molecular Weight 280.4073
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BAMIPINE

SMILES

CN1CCC(CC1)N(CC2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=VZSXTYKGYWISGQ-UHFFFAOYSA-N
InChI=1S/C19H24N2/c1-20-14-12-19(13-15-20)21(18-10-6-3-7-11-18)16-17-8-4-2-5-9-17/h2-11,19H,12-16H2,1H3

HIDE SMILES / InChI

Molecular Formula C19H24N2
Molecular Weight 280.4073
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Bamipine (trade name Soventol) is a sedating antihistamine with pronounced sedative effects. Bamipine is a pharmaceutical drug acting as an H1 antihistamine with anticholinergic properties. It is used as an antipruritic ointment. Bamipine hydrochloride has been given by mouth. Bamipine, bamipine lactate, and bamipine salicylate have all been applied topically.

CNS Activity

Curator's Comment: Bamipine is an antihistamine with pronounced sedative effects.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Soventol

Approved Use

Allergic conditions
Doses

Doses

DosePopulationAdverse events​
100 mg 4 times / day multiple, oral
Recommended
Dose: 100 mg, 4 times / day
Route: oral
Route: multiple
Dose: 100 mg, 4 times / day
Sources:
unhealthy, CHILD|ADOLESCENT|ADULT
Health Status: unhealthy
Age Group: CHILD|ADOLESCENT|ADULT
Food Status: UNKNOWN
Sources:
Other AEs: Drowsiness, Drowsiness...
AEs

AEs

AESignificanceDosePopulation
Drowsiness
100 mg 4 times / day multiple, oral
Recommended
Dose: 100 mg, 4 times / day
Route: oral
Route: multiple
Dose: 100 mg, 4 times / day
Sources:
unhealthy, CHILD|ADOLESCENT|ADULT
Health Status: unhealthy
Age Group: CHILD|ADOLESCENT|ADULT
Food Status: UNKNOWN
Sources:
Drowsiness
100 mg 4 times / day multiple, oral
Recommended
Dose: 100 mg, 4 times / day
Route: oral
Route: multiple
Dose: 100 mg, 4 times / day
Sources:
unhealthy, CHILD|ADOLESCENT|ADULT
Health Status: unhealthy
Age Group: CHILD|ADOLESCENT|ADULT
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Antimycobacterial and H1-antihistaminic activity of 2-substituted piperidine derivatives.
2008-12-15
Hybrid approach for the design of highly affine and selective dopamine D(3) receptor ligands using privileged scaffolds of biogenic amine GPCR ligands.
2007-12-01
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Can be used topically: A thin layer applied on the surface of the skin. Re-application is possible in 30 min. Duration of treatment depends on allergic process. http://www.druginfosys.com/drug.aspx?drugcode=1567&type=1
The recommended dose is 50-100 mg 3-4 times/day.
Route of Administration: Oral
Bamipine treatment resulted in 29% of inhibition of Mycobacterium tuberculosis H37Rv (after 4 days by microplate alamar blue assay) at 6.25 ug/mL.
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:38:28 GMT 2025
Edited
by admin
on Wed Apr 02 09:38:28 GMT 2025
Record UNII
Y6BHZ28O92
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BAMIPINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
BAMIPINE [MI]
Preferred Name English
bamipine [INN]
Common Name English
4-(N-BENZYLANILINO)-1-METHYLPIPERIDINE
Systematic Name English
Bamipine [WHO-DD]
Common Name English
BAMIPINE [MART.]
Common Name English
Classification Tree Code System Code
WHO-VATC QR06AX01
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
WHO-ATC D04AA15
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
WHO-VATC QD04AA15
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
NCI_THESAURUS C29578
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
WHO-ATC R06AX01
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
Code System Code Type Description
EVMPD
SUB06098MIG
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
PUBCHEM
72075
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
DRUG CENTRAL
288
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID5057751
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
ChEMBL
CHEMBL520400
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
MERCK INDEX
m2219
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
225-587-2
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
SMS_ID
100000088409
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
NCI_THESAURUS
C76058
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
INN
1285
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
DRUG BANK
DB13489
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
FDA UNII
Y6BHZ28O92
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
RXCUI
18753
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY RxNorm
WIKIPEDIA
BAMIPINE
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
CAS
4945-47-5
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
MESH
C020867
Created by admin on Wed Apr 02 09:38:28 GMT 2025 , Edited by admin on Wed Apr 02 09:38:28 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY