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

Details

Stereochemistry RACEMIC
Molecular Formula C13H16N2O3
Molecular Weight 248.2777
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of INDORENATE

SMILES

COC(=O)C(CN)C1=CNC2=CC=C(OC)C=C12

InChI

InChIKey=YFEDJMLMWJSRJJ-UHFFFAOYSA-N
InChI=1S/C13H16N2O3/c1-17-8-3-4-12-9(5-8)11(7-15-12)10(6-14)13(16)18-2/h3-5,7,10,15H,6,14H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C13H16N2O3
Molecular Weight 248.2777
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Indorenate (TR3369, INDO) is a serotonin-like compound with high affinity for 5- HT1A receptors and a lower affinity for 5-HT1C and 5-HT1B receptors. Indorenate possesses antihypertensive and anxiolytic activity in animal behaviour tests. Similar to other serotonin receptor agonists, Indorenate also has anorectic activity; this effect was blocked by the administration of the 5-HT2A/2C receptor antagonists cinanserin, cyproheptadine, metergoline and methysergide. A unpublished clinical trial confirmed its antihypertensive activity in men.

Approval Year

PubMed

PubMed

TitleDatePubMed
Discriminative stimulus properties of indorenate, a 5-HT1A, 5-HT1B and 5-HT2C agonist: a study in rats.
2001 Mar
Patents

Sample Use Guides

rats: 1, 3, 10 mg/kg, i.p.
Route of Administration: Intraperitoneal
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:51:10 GMT 2023
Edited
by admin
on Sat Dec 16 17:51:10 GMT 2023
Record UNII
AV9L041QA4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
INDORENATE
INN  
INN  
Official Name English
1H-INDOLE-3-ACETIC ACID, .ALPHA.-(AMINOMETHYL)-5-METHOXY-, METHYL ESTER
Common Name English
METHYL (±)-.ALPHA.-(AMINOMETHYL)-5-METHOXYINDOLE-3-ACETATE
Systematic Name English
indorenate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47794
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
Code System Code Type Description
MESH
C033600
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
CAS
73758-06-2
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
WIKIPEDIA
INDORENATE
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
FDA UNII
AV9L041QA4
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
INN
4929
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID2048400
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
NCI_THESAURUS
C83802
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
PUBCHEM
71987
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
EVMPD
SUB08185MIG
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
SMS_ID
100000083396
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
ChEMBL
CHEMBL414636
Created by admin on Sat Dec 16 17:51:10 GMT 2023 , Edited by admin on Sat Dec 16 17:51:10 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY