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Details

Stereochemistry RACEMIC
Molecular Formula C23H29N3O2
Molecular Weight 379.4953
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETOMIDOLINE

SMILES

CCN1C(NC2=CC=C(OCCN3CCCCC3)C=C2)C4=CC=CC=C4C1=O

InChI

InChIKey=ITIONVBQFUNVJV-UHFFFAOYSA-N
InChI=1S/C23H29N3O2/c1-2-26-22(20-8-4-5-9-21(20)23(26)27)24-18-10-12-19(13-11-18)28-17-16-25-14-6-3-7-15-25/h4-5,8-13,22,24H,2-3,6-7,14-17H2,1H3

HIDE SMILES / InChI

Molecular Formula C23H29N3O2
Molecular Weight 379.4953
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Etomidoline is a synthetic antispasmodic that seems to have an action similar to benactyzine.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
[Endoscopic evaluation of the etomidoline effect on gastric motility].
1976 Sep-Oct
[Characteristic effect of etomidoline on contractile activity in the gastrointestinal tract in conscious dogs (author's transl)].
1978 Aug
[Simultaneous observation of gastric acid secretion and antral motility. Comparative study of the action of 2 synthetic anticholinergics].
1979 Nov
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Guinea pig ileum was incubated with different concentrations of etomidoline (from 10(-7) to 10(-4) M) and its effect on ACh contraction curves was studied. 3*10(-4) M of the drug significantly restricted the elevation of cyclic AMP level induced by Ba(II).
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:58:20 GMT 2023
Edited
by admin
on Sat Dec 16 17:58:20 GMT 2023
Record UNII
WFS7G78GYJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETOMIDOLINE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
etomidoline [INN]
Common Name English
ETOMIDOLINE [MI]
Common Name English
AMIDOLINE
Common Name English
ETOMIDOLINE [JAN]
Common Name English
SMEDOLIN
Brand Name English
1H-ISOINDOL-1-ONE, 2-ETHYL-2,3-DIHYDRO-3-((4-(2-(1-PIPERIDINYL)ETHOXY)PHENYL)AMINO)-
Systematic Name English
K-2680
Code English
Etomidoline [WHO-DD]
Common Name English
ETOMIDOLINE [MART.]
Common Name English
NONSPA
Brand Name English
2-ETHYL-3-(.BETA.-PIPERIDINO-P-PHENETIDINO)PHTHALIMIDINE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
Code System Code Type Description
DRUG CENTRAL
3214
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106603
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
NCI_THESAURUS
C65595
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
INN
3353
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
244-463-9
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
EVMPD
SUB07331MIG
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID4048800
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
MERCK INDEX
m1143
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY Merck Index
PUBCHEM
3309
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
CAS
21590-92-1
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
RXCUI
17684
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY RxNorm
SMS_ID
100000082088
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
FDA UNII
WFS7G78GYJ
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
MESH
C002545
Created by admin on Sat Dec 16 17:58:21 GMT 2023 , Edited by admin on Sat Dec 16 17:58:21 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY