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Details

Stereochemistry RACEMIC
Molecular Formula C20H24FN3O2
Molecular Weight 357.4219
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NARDETEROL

SMILES

CC(C)(CCN1C=NC2=C1C=CC=C2)NCC(O)C3=C(F)C=C(O)C=C3

InChI

InChIKey=KOTMQCNDGLTIHR-UHFFFAOYSA-N
InChI=1S/C20H24FN3O2/c1-20(2,9-10-24-13-22-17-5-3-4-6-18(17)24)23-12-19(26)15-8-7-14(25)11-16(15)21/h3-8,11,13,19,23,25-26H,9-10,12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C20H24FN3O2
Molecular Weight 357.4219
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Nardeterol (SOM-1122) was found to be a high-affinity, partial agonist for beta adrenergic receptors. SOM-1122 inhibited the binding of [125I]iodopindolol to membranes prepared from rat cerebral cortex and cerebellum. SOM-1122 bound to beta adrenergic receptors in vitro and in vivo, increased levels of cyclic AMP in slices of cerebral cortex in vitro and reduced the density of beta adrenergic receptors after chronic treatment. SOM-1122 also was found to be behaviorally active. It reduced locomotor activity and altered behavior maintained under DRL and multiple FlFR schedules. These behavioral effects of SOM-1122 are similar to those reported previously for other centrally acting beta adrenergic agonists.

Approval Year

PubMed

PubMed

TitleDatePubMed
Psychopharmacological consequences of activation of beta adrenergic receptors by SOM-1122.
1988 Jul
Formation of oedema and accumulation of eosinophils in the guinea pig lung. Inhibition by inhaled beta-stimulants.
1989
Patents

Patents

Sample Use Guides

Groups of 10 rats each were used to determine the effects of SOM-1122 (0.003-3 mg/kg) on behavior maintained under DRL and multiple Fl-FR schedules and to determine the ability of propranolol (1 mg/kg) to antagonize the effects of SOM-1122. For all behavioral experiments, SOM-1122 was dissolved in 0.9% NaCl and administered i.p. at a volume of 1 ml/kg b.w.
Route of Administration: Intraperitoneal
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:40:53 GMT 2023
Edited
by admin
on Fri Dec 15 15:40:53 GMT 2023
Record UNII
70859437W3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NARDETEROL
INN  
INN  
Official Name English
nardeterol [INN]
Common Name English
(±)-.ALPHA.-(((3-(1-BENZIMIDAZOLYL)-1,1-DIMETHYLPROPYL)AMINO)METHYL)-2-FLUORO-4-HYDROXYBENZYL ALCOHOL
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
Code System Code Type Description
CAS
73865-18-6
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105150
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
EVMPD
SUB09165MIG
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
PUBCHEM
68918
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
INN
6513
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
FDA UNII
70859437W3
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
NCI_THESAURUS
C76541
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
SMS_ID
100000080341
Created by admin on Fri Dec 15 15:40:53 GMT 2023 , Edited by admin on Fri Dec 15 15:40:53 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY