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

Details

Stereochemistry RACEMIC
Molecular Formula C20H29NO4
Molecular Weight 347.4486
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FEDRILATE

SMILES

CC(CCN1CCOCC1)OC(=O)C2(CCOCC2)C3=CC=CC=C3

InChI

InChIKey=RDEOYUSTRWNWLX-UHFFFAOYSA-N
InChI=1S/C20H29NO4/c1-17(7-10-21-11-15-24-16-12-21)25-19(22)20(8-13-23-14-9-20)18-5-3-2-4-6-18/h2-6,17H,7-16H2,1H3

HIDE SMILES / InChI
Molecular Formula C20H29NO4
Molecular Weight 347.4486
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description

Fedrilate is a mucolytic drug. It was patented in 1963 and claimed to have a noteworthy anti-tussive activity.

Approval Year

Unknown
139594
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:55:36 GMT 2023
Edited
by admin
on Sat Dec 16 16:55:36 GMT 2023
Record UNII
NT86R8M7J5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEDRILATE
INN   MART.   WHO-DD  
INN  
Official Name English
FEDRILATE [MART.]
Common Name English
UCB 3928
Code English
1-METHYL-3-MORPHOLINOPROPYL TETRAHYDRO-4-PHENYL-2H-PYRAN-4-CARBOXYLATE
Systematic Name English
fedrilate [INN]
Common Name English
2H-PYRAN-4-CARBOXYLIC ACID, TETRAHYDRO-4-PHENYL-, 1-METHYL-3-MORPHOLINOPROPYL ESTER
Common Name English
4-MORPHOLINEPROPANOL, .ALPHA.-METHYL-, TETRAHYDRO-4-PHENYL-2H-PYRAN-4-CARBOXYLATE (ESTER)
Common Name English
2H-PYRAN-4-CARBOXYLIC ACID, TETRAHYDRO-4-PHENYL-, 1-METHYL-3-(4-MORPHOLINYL)PROPYL ESTER
Systematic Name English
Fedrilate [WHO-DD]
Common Name English
GOTAS BINELLI
Brand Name English
UCB-3928
Code English
Classification Tree Code System Code
NCI_THESAURUS C66917
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
WHO-VATC QR05DB14
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
WHO-ATC R05DB14
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
Code System Code Type Description
EVMPD
SUB07525MIG
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID70865087
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
INN
2587
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
SMS_ID
100000081256
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
WIKIPEDIA
FEDRILATE
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
FDA UNII
NT86R8M7J5
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
DRUG BANK
DB13825
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
NCI_THESAURUS
C81597
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
PUBCHEM
31796
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104591
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
RXCUI
235961
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
245-545-7
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
CAS
23271-74-1
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
DRUG CENTRAL
1139
Created by admin on Sat Dec 16 16:55:36 GMT 2023 , Edited by admin on Sat Dec 16 16:55:36 GMT 2023
PRIMARY
Related Record Type Details
Structure of FEDRILATE, (R)-
ENANTIOMER -> RACEMATE
Structure of FEDRILATE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Structure of FEDRILATE, (S)-
ENANTIOMER -> RACEMATE
Structure of FEDRILATE MALEATE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of FEDRILATE
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966