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Details

Stereochemistry ACHIRAL
Molecular Formula C14H15N3O2
Molecular Weight 257.2878
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of INDOLIDAN

SMILES

CC1(C)C(=O)NC2=C1C=C(C=C2)C3=NNC(=O)CC3

InChI

InChIKey=LZCQFJKUAIWHRW-UHFFFAOYSA-N
InChI=1S/C14H15N3O2/c1-14(2)9-7-8(3-4-11(9)15-13(14)19)10-5-6-12(18)17-16-10/h3-4,7H,5-6H2,1-2H3,(H,15,19)(H,17,18)

HIDE SMILES / InChI

Molecular Formula C14H15N3O2
Molecular Weight 257.2878
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Indolidan is 2-indolinone derivative patented by American pharmaceutical company Eli Lilly and Co as inotropic agents useful for the treatment of heart failure. Indolidan acts as a phosphodiesterase III inhibitor and decreased the thrombin-induced increase endothelial permeability.

Approval Year

PubMed

PubMed

TitleDatePubMed
Cardiovascular effects of NSP-804 and NSP-805, novel cardiotonic agents with vasodilator properties.
1993-06
Patents

Patents

Sample Use Guides

15 micrograms/kg
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:39:28 GMT 2025
Edited
by admin
on Mon Mar 31 18:39:28 GMT 2025
Record UNII
0751ZOW7OR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LY 195115
Preferred Name English
INDOLIDAN
INN   USAN  
INN   USAN  
Official Name English
3,3-Dimethyl-5-(1,4,5,6-tetrahydro-6-oxo-3-pyridazinyl)-2-indolinone
Systematic Name English
LY-195115
Code English
INDOLIDAN [USAN]
Common Name English
2H-INDOL-2-ONE, 1,3-DIHYDRO-3,3-DIMETHYL-5-(1,4,5,6-TETRAHYDRO-6-OXO-3-PYRIDAZINYL)-
Systematic Name English
indolidan [INN]
Common Name English
Code System Code Type Description
ChEMBL
CHEMBL38224
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
INN
6116
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
MESH
C050325
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
NCI_THESAURUS
C175087
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
CAS
100643-96-7
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
SMS_ID
100000083413
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
USAN
Y-55
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
EVMPD
SUB08179MIG
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
FDA UNII
0751ZOW7OR
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID0020739
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
PUBCHEM
5284402
Created by admin on Mon Mar 31 18:39:28 GMT 2025 , Edited by admin on Mon Mar 31 18:39:28 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY