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Details

Stereochemistry RACEMIC
Molecular Formula C17H21NO4
Molecular Weight 303.3529
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENOTEROL

SMILES

C[C@H](CC1=CC=C(O)C=C1)NC[C@H](O)C2=CC(O)=CC(O)=C2

InChI

InChIKey=LSLYOANBFKQKPT-DIFFPNOSSA-N
InChI=1S/C17H21NO4/c1-11(6-12-2-4-14(19)5-3-12)18-10-17(22)13-7-15(20)9-16(21)8-13/h2-5,7-9,11,17-22H,6,10H2,1H3/t11-,17+/m1/s1

HIDE SMILES / InChI

Molecular Formula C17H21NO4
Molecular Weight 303.3529
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 Sat Dec 16 16:58:52 UTC 2023
Edited
by admin
on Sat Dec 16 16:58:52 UTC 2023
Record UNII
22M9P70OQ9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENOTEROL
INN   MART.   MI   USAN   VANDF   WHO-DD  
INN   USAN  
Official Name English
FENOTEROL [MART.]
Common Name English
FENOTEROL [VANDF]
Common Name English
FENOTEROL HYDROBROMIDE IMPURITY A [EP IMPURITY]
Common Name English
3,5-DIHYDROXY-.ALPHA.-(((P-HYDROXY-.ALPHA.-METHYLPHENETHYL)AMINO)METHYL)BENZYL ALCOHOL
Common Name English
FENOTEROL [USAN]
Common Name English
(1RS)-1-(3,5-DIHYDROXYPHENYL)-2-(((1RS)-2-(4-HYDROXYPHENYL)-1-METHYLETHYL)AMINO)ETHANOL
Systematic Name English
1,3-BENZENEDIOL, 5-((1R)-1-HYDROXY-2-(((1R)-2-(4-HYDROXYPHENYL)-1-METHYLETHYL)AMINO)ETHYL)-, REL-
Systematic Name English
1,3-BENZENEDIOL, 5-(1-HYDROXY-2-((2-(4-HYDROXYPHENYL)-1-METHYLETHYL)AMINO)ETHYL)-, (R*,R*)-(±)-
Systematic Name English
FENOTEROL [MI]
Common Name English
TH-1165
Code English
fenoterol [INN]
Common Name English
5-[(1RS)-2-[(1SR)-2-(4-hydroxyphenyl)-1-methylethyl]amino-1-hydroxyethyl]benzene-1,3-diol
Systematic Name English
Fenoterol [WHO-DD]
Common Name English
NSC-757811
Code English
1,3-BENZENEDIOL, 5-(1-HYDROXY-2-((2-(4-HYDROXYPHENYL)-1-METHYLETHYL)AMINO)ETHYL)-
Systematic Name English
Classification Tree Code System Code
WHO-ATC R03AL01
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
WHO-ATC G02CA03
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
NCI_THESAURUS C48149
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
WHO-VATC QG02CA03
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
WHO-VATC QR03AL01
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
WHO-ATC R03CC04
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
WHO-VATC QR03CC04
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
NCI_THESAURUS C319
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
WHO-VATC QR03AC04
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
WHO-ATC R03AC04
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
Code System Code Type Description
CAS
13392-18-2
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
NSC
757811
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID4023046
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
PUBCHEM
688468
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
IUPHAR
557
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL32800
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
NCI_THESAURUS
C65659
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
MESH
D005280
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
RXCUI
4333
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY RxNorm
EVMPD
SUB07579MIG
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
MERCK INDEX
m5282
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY Merck Index
INN
3073
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
WIKIPEDIA
FENOTEROL
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
CHEBI
149226
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
DRUG BANK
DB01288
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
DRUG CENTRAL
1155
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
FDA UNII
22M9P70OQ9
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
CAS
130156-24-0
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
SMS_ID
100000081282
Created by admin on Sat Dec 16 16:58:53 UTC 2023 , Edited by admin on Sat Dec 16 16:58:53 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE ENANTIOMER->RACEMATE
TARGET -> AGONIST
SHORT-ACTING
Related Record Type Details
ACTIVE MOIETY