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Details

Stereochemistry RACEMIC
Molecular Formula C16H22N2O3
Molecular Weight 290.3575
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROCATEROL

SMILES

CC[C@@H](NC(C)C)[C@@H](O)C1=CC=C(O)C2=C1C=CC(=O)N2

InChI

InChIKey=FKNXQNWAXFXVNW-WBMJQRKESA-N
InChI=1S/C16H22N2O3/c1-4-12(17-9(2)3)16(21)11-5-7-13(19)15-10(11)6-8-14(20)18-15/h5-9,12,16-17,19,21H,4H2,1-3H3,(H,18,20)/t12-,16+/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H22N2O3
Molecular Weight 290.3575
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:36:03 UTC 2023
Edited
by admin
on Fri Dec 15 18:36:03 UTC 2023
Record UNII
X7I3EMM5K0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROCATEROL
INN   MI   WHO-DD  
INN  
Official Name English
procaterol [INN]
Common Name English
(±)-ERYTHRO-8-HYDROXY-5-(1-HYDROXY-2-(ISOPROPYLAMINO)BUTYL)CARBOSTYRIL
Common Name English
2(1H)-QUINOLINONE, 8-HYDROXY-5-(1-HYDROXY-2-((1-METHYLETHYL)AMINO)BUTYL)-, (R*,S*)-
Common Name English
PROCATEROL [MI]
Common Name English
Procaterol [WHO-DD]
Common Name English
PROCATEROL [JAN]
Common Name English
MEPTIN
Brand Name English
Classification Tree Code System Code
WHO-VATC QR03AC16
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
WHO-ATC R03CC08
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
WHO-ATC R03AC16
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
WHO-VATC QR03CC08
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
Code System Code Type Description
EVMPD
SUB10058MIG
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
ChEMBL
CHEMBL160519
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
DRUG CENTRAL
2273
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
ECHA (EC/EINECS)
276-590-0
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
SMS_ID
100000081133
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
MERCK INDEX
m9147
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY Merck Index
IUPHAR
3464
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
INN
4259
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
PUBCHEM
688563
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
CAS
72332-33-3
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
DRUG BANK
DB01366
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
NCI_THESAURUS
C170351
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
RXCUI
34530
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY RxNorm
MESH
D017265
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
EPA CompTox
DTXSID5045673
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
FDA UNII
X7I3EMM5K0
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
WIKIPEDIA
PROCATEROL
Created by admin on Fri Dec 15 18:36:03 UTC 2023 , Edited by admin on Fri Dec 15 18:36:03 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
SHORT-ACTING
Related Record Type Details
ACTIVE MOIETY