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

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H19NO3
Molecular Weight 225.2842
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRENALTEROL

SMILES

CC(C)NC[C@H](O)COC1=CC=C(O)C=C1

InChI

InChIKey=ADUKCCWBEDSMEB-NSHDSACASA-N
InChI=1S/C12H19NO3/c1-9(2)13-7-11(15)8-16-12-5-3-10(14)4-6-12/h3-6,9,11,13-15H,7-8H2,1-2H3/t11-/m0/s1

HIDE SMILES / InChI
PubMed

PubMed

TitleDatePubMed
Role of selective alpha and beta adrenergic receptor mechanisms in rat jejunal longitudinal muscle contractility.
2008 Jun
Towards a thermodynamic definition of efficacy in partial agonism: The thermodynamics of efficacy and ligand proton transfer in a G protein-coupled receptor of the rhodopsin class.
2010 Nov 15
Patents

Sample Use Guides

The eight patients were given prenalterol (PNL) orally, 30 to 200 mg/day, versus placebo for 6 days
Route of Administration: Oral
Name Type Language
PRENALTEROL
INN   MI   WHO-DD  
INN  
Official Name English
prenalterol [INN]
Common Name English
Prenalterol [WHO-DD]
Common Name English
(-)-(S)-1-(P-HYDROXYPHENOXY)-3-(ISOPROPYLAMINO)-2-PROPANOL
Common Name English
PRENALTEROL [MI]
Common Name English
PHENOL, 4-(2-HYDROXY-3-((1-METHYLETHYL)AMINO)PROPOXY)-
Systematic Name English
Classification Tree Code System Code
WHO-VATC QC01CA13
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
WHO-ATC C01CA13
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
Code System Code Type Description
INN
4121
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
MESH
D011294
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
FDA UNII
M4G34404CX
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
SMS_ID
100000081428
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
PUBCHEM
42396
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
DRUG BANK
DB13777
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
NCI_THESAURUS
C174691
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
EPA CompTox
DTXSID8023507
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
ECHA (EC/EINECS)
260-791-5
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
WIKIPEDIA
Prenalterol
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
EVMPD
SUB10027MIG
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
CAS
57526-81-5
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
DRUG CENTRAL
2258
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
ChEMBL
CHEMBL1160714
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY
MERCK INDEX
m9123
Created by admin on Fri Dec 15 17:59:01 GMT 2023 , Edited by admin on Fri Dec 15 17:59:01 GMT 2023
PRIMARY Merck Index