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Details

Stereochemistry RACEMIC
Molecular Formula C20H29NO4.ClH
Molecular Weight 383.91
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FEDRILATE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=BDKUCLCOCUQRBK-UHFFFAOYSA-N
InChI=1S/C20H29NO4.ClH/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;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 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 01:28:17 GMT 2023
Edited
by admin
on Sat Dec 16 01:28:17 GMT 2023
Record UNII
00NL8H35Y3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEDRILATE HYDROCHLORIDE
Common Name English
2H-PYRAN-4-CARBOXYLIC ACID, TETRAHYDRO-4-PHENYL-, 1-METHYL-3-MORPHOLINOPROPYL ESTER HYDROCHLORIDE
Common Name English
4-MORPHOLINEPROPANOL, .ALPHA.-METHYL-, TETRAHYDRO-4-PHENYLPYRAN-4-CARBOXYLATE, HYDROCHLORIDE
Systematic Name English
4-MORPHOLINEPROPANOL, .ALPHA.-METHYL-, TETRAHYDRO-4-PHENYL-2H-PYRAN-4-CARBOXYLATE (ESTER), HYDROCHLORIDE
Common Name English
2H-PYRAN-4-CARBOXYLIC ACID, TETRAHYDRO-4-PHENYL-, 1-METHYL-3-(4-MORPHOLINYL)PROPYL ESTER, HYDROCHLORIDE (1:1)
Systematic Name English
PYRAN-4-CARBOXYLIC ACID, TETRAHYDRO-4-PHENYL-, 1-METHYL-3-MORPHOLINOPROPYL ESTER, HYDROCHLORIDE
Common Name English
Code System Code Type Description
CAS
3648-68-8
Created by admin on Sat Dec 16 01:28:17 GMT 2023 , Edited by admin on Sat Dec 16 01:28:17 GMT 2023
PRIMARY
PUBCHEM
126961345
Created by admin on Sat Dec 16 01:28:17 GMT 2023 , Edited by admin on Sat Dec 16 01:28:17 GMT 2023
PRIMARY
FDA UNII
00NL8H35Y3
Created by admin on Sat Dec 16 01:28:17 GMT 2023 , Edited by admin on Sat Dec 16 01:28:17 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE