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

Details

Stereochemistry ACHIRAL
Molecular Formula C19H24N2.2ClH
Molecular Weight 353.329
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BAMIPINE DIHYDROCHLORIDE

SMILES

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

InChI

InChIKey=MSCVWXUSXBIBAO-UHFFFAOYSA-N
InChI=1S/C19H24N2.2ClH/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;2*1H

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

Molecular Formula ClH
Molecular Weight 36.461
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
PubMed

PubMed

TitleDatePubMed
Hybrid approach for the design of highly affine and selective dopamine D(3) receptor ligands using privileged scaffolds of biogenic amine GPCR ligands.
2007 Dec 1
Antimycobacterial and H1-antihistaminic activity of 2-substituted piperidine derivatives.
2008 Dec 15
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 Sat Dec 16 04:02:09 GMT 2023
Edited
by admin
on Sat Dec 16 04:02:09 GMT 2023
Record UNII
RG2UZ22FEZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BAMIPINE DIHYDROCHLORIDE
Common Name English
4-PIPERIDINAMINE, 1-METHYL-N-PHENYL-N-(PHENYLMETHYL)-, DIHYDROCHLORIDE
Common Name English
4-PIPERIDINAMINE, 1-METHYL-N-PHENYL-N-(PHENYLMETHYL)-, HYDROCHLORIDE (1:2)
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
262-938-9
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID30977312
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
PRIMARY
NCI_THESAURUS
C103224
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
PRIMARY
MESH
C020867
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
PRIMARY
PUBCHEM
109130
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
PRIMARY
FDA UNII
RG2UZ22FEZ
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
PRIMARY
CAS
61732-85-2
Created by admin on Sat Dec 16 04:02:09 GMT 2023 , Edited by admin on Sat Dec 16 04:02:09 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS