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Details

Stereochemistry ACHIRAL
Molecular Formula C23H26N2O.ClH
Molecular Weight 382.926
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ROXINDOLE HYDROCHLORIDE

SMILES

Cl.OC1=CC2=C(NC=C2CCCCN3CCC(=CC3)C4=CC=CC=C4)C=C1

InChI

InChIKey=ZCEPVNSWLLJECX-UHFFFAOYSA-N
InChI=1S/C23H26N2O.ClH/c26-21-9-10-23-22(16-21)20(17-24-23)8-4-5-13-25-14-11-19(12-15-25)18-6-2-1-3-7-18;/h1-3,6-7,9-11,16-17,24,26H,4-5,8,12-15H2;1H

HIDE SMILES / InChI
Roxindole (EMD-49,980) is a dopaminergic and serotonergic drug which was originally developed for the treatment of schizophrenia. Roxindole has also been investigated as a therapy for the major depressive disorder, Parkinson's disease, and prolactinoma. Roxindole is dopamine autoreceptor-selective agonistic drug with high affinity to D2-like receptors and with much lower affinities to D1-like, % and ol2, muscarinic and 5HT 2 receptors. Additionally, Roxindole exerts 5HT uptake inhibition and 5HT1A agonistic effects. The bioavailability of Roxindole has been estimated at 5% due to a high first-pass metabolization. On the other hand, in 14C distribution studies, Roxindole has crossed the blood-brain barrier readily and the brain concentrations at all intervals have been much higher than corresponding plasma levels. In clinical trials, Roxindole ‘s antipsychotic efficacy was only modest but it was unexpectedly found to produce potent and rapid antidepressant and anxiolytic effects. However, the clinical development of Roxindole was discontinued.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.8 nM [IC50]
0.37 nM [EC50]
0.4 nM [Ki]
24.0 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Treatment of Parkinson's disease with the partial dopamine agonist EMD 49980.
1993 Apr
Roxindole, a potential antidepressant. I. Effect on the dopamine system.
1996
Actions of roxindole at recombinant human dopamine D2, D3 and D4 and serotonin 5-HT1A, 5-HT1B and 5-HT1D receptors.
1999 Jun
A simple procedure for synthesis of roxindole, a dopamine D2-receptor agonist.
2001 Jul
Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. III. Agonist and antagonist properties at serotonin, 5-HT(1) and 5-HT(2), receptor subtypes.
2002 Nov
Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. II. Agonist and antagonist properties at subtypes of dopamine D(2)-like receptor and alpha(1)/alpha(2)-adrenoceptor.
2002 Nov
Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. I. A multivariate analysis of the binding profiles of 14 drugs at 21 native and cloned human receptor subtypes.
2002 Nov
Opioid and monoamine systems mediate the discriminative stimulus of tramadol in rats.
2004 Sep 13
Indolebutylamines as selective 5-HT(1A) agonists.
2004 Sep 9
Patents

Patents

Sample Use Guides

Roxindole was administered at increasing daily doses from 0.3 to 30 mg for 28 days.
Route of Administration: Oral
Roxindole activity was evaluated in [35S]GTPγS binding assay. Membranes of CHO cells stably expressing recombinant human 5-HT1A receptor were treated with [35S]GTPγS (0.1 nM) in assay buffer (HEPES (20 mM), pH 7.4, NaCl (100 mM), GDP (3 µM), MgCl2 (3 mM)) for 20 min at 22 °C. Efficacy is expressed as the increase in [35S]GTPγS binding observed with the agonist relative to that induced by a maximally effective concentration (10 µM) 5HT.
Name Type Language
ROXINDOLE HYDROCHLORIDE
MI  
Common Name English
ROXINDOLE HYDROCHLORIDE [MI]
Common Name English
1H-INDOL-5-OL, 3-(4-(3,6-DIHYDRO-4-PHENYL-1(2H)-PYRIDINYL)BUTYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
1H-INDOL-5-OL, 3-(4-(3,6-DIHYDRO-4-PHENYL-1(2H)-PYRIDINYL)BUTYL)-, MONOHYDROCHLORIDE
Common Name English
EMD-38362
Code English
Classification Tree Code System Code
NCI_THESAURUS C47794
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
NCI_THESAURUS C66884
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
Code System Code Type Description
CAS
108050-82-4
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
PRIMARY
FDA UNII
NS63HO5457
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
PRIMARY
PUBCHEM
9886286
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID1042605
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
PRIMARY
NCI_THESAURUS
C132144
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
PRIMARY
MERCK INDEX
m9678
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
PRIMARY Merck Index
MESH
C059613
Created by admin on Sat Dec 16 02:04:04 GMT 2023 , Edited by admin on Sat Dec 16 02:04:04 GMT 2023
PRIMARY