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

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H23NO3
Molecular Weight 301.3801
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVDOBUTAMINE

SMILES

C[C@@H](CCC1=CC=C(O)C=C1)NCCC2=CC(O)=C(O)C=C2

InChI

InChIKey=JRWZLRBJNMZMFE-ZDUSSCGKSA-N
InChI=1S/C18H23NO3/c1-13(2-3-14-4-7-16(20)8-5-14)19-11-10-15-6-9-17(21)18(22)12-15/h4-9,12-13,19-22H,2-3,10-11H2,1H3/t13-/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H23NO3
Molecular Weight 301.3801
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Levdobutamine is a beta-adrenoceptor agonist selective for the beta1-subtype. Levdobutamine was derived from dopamine. It is the active (S)-isomer of dobutamine. It is the cardiotonic agent.

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:47:12 GMT 2023
Edited
by admin
on Sat Dec 16 17:47:12 GMT 2023
Record UNII
0PE6UXH3WG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVDOBUTAMINE
INN  
INN  
Official Name English
levdobutamine [INN]
Common Name English
LY206243
Code English
4-(2-(((S)-3-(P-HYDROXYPHENYL)-1-METHYLPROPYL)AMINO)ETHYL)PYROCATECHOL
Common Name English
LY-206243
Code English
Code System Code Type Description
DRUG CENTRAL
13
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
EPA CompTox
DTXSID90210671
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
CAS
61661-06-1
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
SMS_ID
100000082803
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
FDA UNII
0PE6UXH3WG
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
NCI_THESAURUS
C166431
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
EVMPD
SUB08457MIG
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
PUBCHEM
688441
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
INN
6820
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
ChEMBL
CHEMBL1367478
Created by admin on Sat Dec 16 17:47:13 GMT 2023 , Edited by admin on Sat Dec 16 17:47:13 GMT 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY