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Details

Stereochemistry ACHIRAL
Molecular Formula C23H21ClN2O4
Molecular Weight 424.877
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GEDOCARNIL

SMILES

COCC1=C2C(NC3=C2C(OC4=CC=C(Cl)C=C4)=CC=C3)=CN=C1C(=O)OC(C)C

InChI

InChIKey=SLYDYLLJUXFULK-UHFFFAOYSA-N
InChI=1S/C23H21ClN2O4/c1-13(2)29-23(27)22-16(12-28-3)20-18(11-25-22)26-17-5-4-6-19(21(17)20)30-15-9-7-14(24)8-10-15/h4-11,13,26H,12H2,1-3H3

HIDE SMILES / InChI
Molecular Formula C23H21ClN2O4
Molecular Weight 424.877
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Anxiolytic drug, Gedocarnil [SH 530, ZK 113315], was undergoing phase I clinical trials with Schering AG in Germany as a potential nootropic agent. However it`s development for the treatment of cognition disorders was discontinued.

Originator

Approval Year

Unknown
139594
Patents

Patents

WO2011089216A1
1
WO2014052394A1
1
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:58 GMT 2023
Edited
by admin
on Fri Dec 15 15:43:58 GMT 2023
Record UNII
BWP53NPW3F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GEDOCARNIL
INN   WHO-DD  
INN  
Official Name English
gedocarnil [INN]
Common Name English
ISOPROPYL 5-(P-CHLOROPHENOXY)-4-(METHOXYMETHYL)-9H-PYRIDO(3,4-.BETA.)INDOLE-3-CARBOXYLATE
Common Name English
Gedocarnil [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
WHO-VATC QN05BX02
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
WHO-ATC N05BX02
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID20148993
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
PUBCHEM
219095
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
EVMPD
SUB07888MIG
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
CAS
109623-97-4
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105080
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
NCI_THESAURUS
C74183
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
INN
6285
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
FDA UNII
BWP53NPW3F
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
DRUG BANK
DB13534
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
WIKIPEDIA
GEDOCARNIL
Created by admin on Fri Dec 15 15:43:59 GMT 2023 , Edited by admin on Fri Dec 15 15:43:59 GMT 2023
PRIMARY
SMS_ID
100000084538
Created by admin on Fri Dec 15 15:43:58 GMT 2023 , Edited by admin on Fri Dec 15 15:43:58 GMT 2023
PRIMARY
Related Record Type Details
Structure of GEDOCARNIL
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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