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

Details

Stereochemistry RACEMIC
Molecular Formula C15H23NO3.ClH
Molecular Weight 301.809
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHOMOXANE HYDROCHLORIDE

SMILES

Cl.CCCCNCC1COC2=C(O1)C(OCC)=CC=C2

InChI

InChIKey=JAIBEXLQBQFZOW-UHFFFAOYSA-N
InChI=1S/C15H23NO3.ClH/c1-3-5-9-16-10-12-11-18-14-8-6-7-13(17-4-2)15(14)19-12;/h6-8,12,16H,3-5,9-11H2,1-2H3;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 C15H23NO3
Molecular Weight 265.348
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Ethomoxane is antagonist of alpha-adrenoreceptor exerting antihypertensive properties.

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
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:44:42 GMT 2023
Edited
by admin
on Fri Dec 15 16:44:42 GMT 2023
Record UNII
M77KGL2QN0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHOMOXANE HYDROCHLORIDE
WHO-DD  
Common Name English
Ethomoxane hydrochloride [WHO-DD]
Common Name English
1,4-BENZODIOXIN-2-METHANAMINE, N-BUTYL-8-ETHOXY-2,3-DIHYDRO-, HYDROCHLORIDE, (±)-
Systematic Name English
(±)-2-(BUTYLAMINOMETHYL)-8-ETHOXY-1,4-BENZODIOXAN HYDROCHLORIDE
Systematic Name English
1,4-BENZODIOXIN-2-METHANAMINE, N-BUTYL-8-ETHOXY-2,3-DIHYDRO-, HYDROCHLORIDE (1:1)
Systematic Name English
883F-HCL
Code English
ETHOMOXANE HCL
Common Name English
NSC-106903
Code English
DL-8-ETHOXY-2-N-BUTYLAMINOMETHYL-1,4-BENZODIOXANE HYDROCHLORIDE
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
227-924-9
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
EVMPD
SUB02003MIG
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
FDA UNII
M77KGL2QN0
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
CAS
6038-78-4
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID40975788
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
PUBCHEM
22398
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
MESH
C004911
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
SMS_ID
100000087300
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
NSC
106903
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
PRIMARY
CAS
17162-23-1
Created by admin on Fri Dec 15 16:44:42 GMT 2023 , Edited by admin on Fri Dec 15 16:44:42 GMT 2023
SUPERSEDED
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY