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

Details

Stereochemistry RACEMIC
Molecular Formula C15H23NO3
Molecular Weight 265.348
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHOMOXANE

SMILES

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

InChI

InChIKey=WKRAEDUMAWVCOC-UHFFFAOYSA-N
InChI=1S/C15H23NO3/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

HIDE SMILES / InChI

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 Sat Dec 16 17:11:25 GMT 2023
Edited
by admin
on Sat Dec 16 17:11:25 GMT 2023
Record UNII
5F53O2A6GE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHOMOXANE
INN   WHO-DD  
INN  
Official Name English
F-883
Code English
1,4-BENZODIOXAN, 2-(BUTYLAMINOMETHYL)-8-ETHOXY-
Systematic Name English
1,4-BENZODIOXIN-2-METHANAMINE, N-BUTYL-8-ETHOXY-2,3-DIHYDRO-
Systematic Name English
2-N-BUTYLAMINOMETHYL-8-ETHOXYBENZODIOXAN
Common Name English
Ethomoxane [WHO-DD]
Common Name English
ethomoxane [INN]
Common Name English
(±)-2-(BUTYLAMINOMETHYL)-8-ETHOXY-1,4-BENZODIOXAN
Systematic Name English
1,4-BENZODIOXAN-2-METHYLAMINE, N-BUTYL-8-ETHOXY-
Systematic Name English
(±)-ETHOMOXANE
Common Name English
Code System Code Type Description
PUBCHEM
19127
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
INN
1176
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
MESH
C004911
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
NCI_THESAURUS
C166843
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
SMS_ID
100000082619
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
FDA UNII
5F53O2A6GE
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
EPA CompTox
DTXSID00864684
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
CAS
16509-23-2
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
SUPERSEDED
ChEMBL
CHEMBL2110919
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
EVMPD
SUB07281MIG
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
CAS
3570-46-5
Created by admin on Sat Dec 16 17:11:26 GMT 2023 , Edited by admin on Sat Dec 16 17:11:26 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY