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

Details

Stereochemistry ACHIRAL
Molecular Formula C16H18ClN.ClH
Molecular Weight 296.235
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBENAMINE HYDROCHLORIDE

SMILES

Cl.ClCCN(CC1=CC=CC=C1)CC2=CC=CC=C2

InChI

InChIKey=LZXCEBPGNFLHEQ-UHFFFAOYSA-N
InChI=1S/C16H18ClN.ClH/c17-11-12-18(13-15-7-3-1-4-8-15)14-16-9-5-2-6-10-16;/h1-10H,11-14H2;1H

HIDE SMILES / InChI

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

Molecular Formula C16H18ClN
Molecular Weight 259.774
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Furter investigations on the interaction between alpha-adrenoceptor antagonists and the central hypotensive effect of clonidine in rats, rabbits and dogs.
1980 Jul
[Relationship between arsenic-induced hypothermia and brain monoamines. (2). The roles of noradrenaline and dopamine].
1982 Aug
Discrimination by SZL49 between contractions evoked by noradrenaline in longitudinal and circular muscle of human vas deferens.
2002 May
Contractile actions of imidazoline alpha-adrenoceptor agonists and effects of noncompetitive alpha1-adrenoceptor antagonists in human vas deferens.
2003 Feb 21
Expression of alpha 4 and alpha 7 nicotinic receptors in the brainstem of female rabbits after coitus.
2004 Jun 25
A novel model of pain sensation using superfused gastrosplenic omentum preparation of anesthetized rats.
2008 Feb
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:08:39 GMT 2023
Edited
by admin
on Fri Dec 15 15:08:39 GMT 2023
Record UNII
W65S0F7870
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBENAMINE HYDROCHLORIDE
MI   WHO-DD  
Common Name English
SYMPATHOLYTIN
Brand Name English
(2-CHLOROETHYL)DIBENZYLAMINE HYDROCHLORIDE
Systematic Name English
NSC-11491
Code English
2-(DIBENZYLAMINO)ETHYL CHLORIDE HYDROCHLORIDE
Systematic Name English
(.BETA.-CHLOROETHYL)DIBENZYLAMINE HYDROCHLORIDE
Systematic Name English
DIBENZYLCHLORETHAMINE HYDROCHLORIDE
Common Name English
N,N-DIBENZYL-.BETA.-CHLOROETHYLAMINE HYDROCHLORIDE
Systematic Name English
(N,N-DIBENZYLAMINO)ETHYL CHLORIDE HYDROCHLORIDE
Systematic Name English
BENZENEMETHANAMINE, N-(2-CHLOROETHYL)-N-(PHENYLMETHYL)-, HYDROCHLORIDE
Systematic Name English
DIBENZYLAMINE, N-(2-CHLOROETHYL)-, HYDROCHLORIDE
Systematic Name English
DIBENAMINE HYDROCHLORIDE [MI]
Common Name English
Dibenamine hydrochloride [WHO-DD]
Common Name English
Code System Code Type Description
SMS_ID
100000079529
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
PUBCHEM
5925
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID3075337
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-234-5
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
CAS
55-43-6
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
NSC
11491
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
FDA UNII
W65S0F7870
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
MERCK INDEX
m4279
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY Merck Index
EVMPD
SUB13560MIG
Created by admin on Fri Dec 15 15:08:39 GMT 2023 , Edited by admin on Fri Dec 15 15:08:39 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE