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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 ( + / - )

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

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:55:36 UTC 2023
Edited
by admin
on Sat Dec 16 16:55:36 UTC 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 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
WHO-VATC QR05DB14
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
WHO-ATC R05DB14
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
Code System Code Type Description
EVMPD
SUB07525MIG
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
EPA CompTox
DTXSID70865087
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
INN
2587
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
SMS_ID
100000081256
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
WIKIPEDIA
FEDRILATE
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
FDA UNII
NT86R8M7J5
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
DRUG BANK
DB13825
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
NCI_THESAURUS
C81597
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
PUBCHEM
31796
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
ChEMBL
CHEMBL2104591
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
RXCUI
235961
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
245-545-7
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
CAS
23271-74-1
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
DRUG CENTRAL
1139
Created by admin on Sat Dec 16 16:55:36 UTC 2023 , Edited by admin on Sat Dec 16 16:55:36 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY