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Details

Stereochemistry ACHIRAL
Molecular Formula C13H19N3O4
Molecular Weight 281.3077
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LUFIRONIL

SMILES

COCCNC(=O)C1=CC(=NC=C1)C(=O)NCCOC

InChI

InChIKey=JUCNGMPTCXPMNB-UHFFFAOYSA-N
InChI=1S/C13H19N3O4/c1-19-7-5-15-12(17)10-3-4-14-11(9-10)13(18)16-6-8-20-2/h3-4,9H,5-8H2,1-2H3,(H,15,17)(H,16,18)

HIDE SMILES / InChI

Molecular Formula C13H19N3O4
Molecular Weight 281.3077
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Lufironil (HOE 077) is an inhibitor of prolyl 4-hydroxylase. In preclinical studies, it prevented liver fibrosis by inhibiting not only the hydroxylation of proline but also the activation of Ito cells, which are considered the main collagen-producing cells, resulting in reduced expression of procollagen mRNA. Lufironil was being developed for the treatment of chronic liver diseases including alcoholic hepatitis and liver cirrhosis.

Approval Year

PubMed

PubMed

TitleDatePubMed
The prolyl 4-hydroxylase inhibitor HOE 077 prevents activation of Ito cells, reducing procollagen gene expression in rat liver fibrosis induced by choline-deficient L-amino acid-defined diet.
1996-04
New prolyl 4-hydroxylase inhibitor reduces procollagen gene expression and enzyme-altered lesions in rat liver cirrhosis.
1995
Beneficial effects of inhibitors of prolyl 4-hydroxylase in CCl4-induced fibrosis of the liver in rats.
1991
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:15:35 GMT 2025
Edited
by admin
on Mon Mar 31 18:15:35 GMT 2025
Record UNII
8MMU177964
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HOE 077
Preferred Name English
LUFIRONIL
INN   USAN  
INN   USAN  
Official Name English
lufironil [INN]
Common Name English
HOE-077
Code English
2,4-PYRIDINEDICARBOXAMIDE,N,N'-BIS(2-METHOXYETHYL)-
Common Name English
LUFIRONIL [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C471
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
Code System Code Type Description
CAS
128075-79-6
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
SMS_ID
100000082251
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
NCI_THESAURUS
C97361
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
PUBCHEM
60788
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
USAN
FF-24
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
FDA UNII
8MMU177964
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID00155802
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106793
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
INN
6715
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
EVMPD
SUB08616MIG
Created by admin on Mon Mar 31 18:15:35 GMT 2025 , Edited by admin on Mon Mar 31 18:15:35 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY