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Details

Stereochemistry RACEMIC
Molecular Formula C25H37NO4
Molecular Weight 415.5656
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SALMETEROL

SMILES

OCC1=CC(=CC=C1O)C(O)CNCCCCCCOCCCCC2=CC=CC=C2

InChI

InChIKey=GIIZNNXWQWCKIB-UHFFFAOYSA-N
InChI=1S/C25H37NO4/c27-20-23-18-22(13-14-24(23)28)25(29)19-26-15-7-1-2-8-16-30-17-9-6-12-21-10-4-3-5-11-21/h3-5,10-11,13-14,18,25-29H,1-2,6-9,12,15-17,19-20H2

HIDE SMILES / InChI
Molecular Formula C25H37NO4
Molecular Weight 415.5656
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
123738
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:36:45 UTC 2023
Edited
by admin
on Fri Dec 15 16:36:45 UTC 2023
Record UNII
2I4BC502BT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SALMETEROL
HSDB   INN   MI   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
SALMETEROL [MI]
Common Name English
SALMETEROL [HSDB]
Common Name English
GR 33343 X
Code English
Salmeterol [WHO-DD]
Common Name English
SALMETEROL [VANDF]
Common Name English
SN408D
Code English
salmeterol [INN]
Common Name English
SALMETEROL [USAN]
Common Name English
GR-33343-X
Code English
Classification Tree Code System Code
WHO-ATC R03AC12
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
NDF-RT N0000009922
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
WHO-VATC QR03AC12
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
WHO-VATC QR03AK06
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
EMA ASSESSMENT REPORTS LABAZENIT (REFUSED: ASTHMA)
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
WHO-ATC R03AK06
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
WHO-ATC R03AK12
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
NDF-RT N0000175779
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
LIVERTOX 869
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
NCI_THESAURUS C319
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
Code System Code Type Description
MESH
C057823
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
IUPHAR
559
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
NCI_THESAURUS
C29443
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
DRUG BANK
DB00938
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
EVMPD
SUB10430MIG
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
CHEBI
9011
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
RXCUI
36117
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
SALMETEROL
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
FDA UNII
2I4BC502BT
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
DRUG CENTRAL
2419
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
CAS
89365-50-4
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
DAILYMED
2I4BC502BT
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
PUBCHEM
5152
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
LACTMED
Salmeterol
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
SMS_ID
100000080527
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
USAN
X-46
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
EPA CompTox
DTXSID6023571
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
INN
5578
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
ChEMBL
CHEMBL1263
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
MERCK INDEX
m9745
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY Merck Index
HSDB
7315
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
Related Record Type Details
BETA-2 ADRENERGIC RECEPTOR
TARGET -> AGONIST
SHORT-ACTING
ALDEHYDE OXIDASE
METABOLIC ENZYME -> INHIBITOR
IC50
Structure of SALMETEROL XINAFOATE
SALT/SOLVATE -> PARENT
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
Related Record Type Details
Structure of .ALPHA.-HYDROXYSALMETEROL
METABOLITE -> PARENT
Related Record Type Details
Structure of SALMETEROL
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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