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

Details

Stereochemistry ACHIRAL
Molecular Formula C15H23N3O4
Molecular Weight 309.3608
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SAFIRONIL

SMILES

COCCCNC(=O)C1=CC=NC(=C1)C(=O)NCCCOC

InChI

InChIKey=HLSXICGBWKECLM-UHFFFAOYSA-N
InChI=1S/C15H23N3O4/c1-21-9-3-6-17-14(19)12-5-8-16-13(11-12)15(20)18-7-4-10-22-2/h5,8,11H,3-4,6-7,9-10H2,1-2H3,(H,17,19)(H,18,20)

HIDE SMILES / InChI

Molecular Formula C15H23N3O4
Molecular Weight 309.3608
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Aventis developed safironil as a competitive inhibitor of collagen protein synthesis for the treatment of liver disorders. This compound participated in phase I clinical trial for the treatment of cirrhosis in Germany. In addition, it was studied for hepatic fibrosis treatment. However, information about the further development of this compound is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Antifibrogenic therapies in chronic HCV infection.
2001-08
Two novel antifibrotics, HOE 077 and Safironil, modulate stellate cell activation in rat liver injury: differential effects in males and females.
1998-01
Substance Class Chemical
Created
by admin
on Wed Apr 02 08:44:27 GMT 2025
Edited
by admin
on Wed Apr 02 08:44:27 GMT 2025
Record UNII
CK4M8AX1LN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HOE-277
Preferred Name English
SAFIRONIL
INN  
INN  
Official Name English
safironil [INN]
Common Name English
HOE277
Code English
Classification Tree Code System Code
NCI_THESAURUS C471
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID60158677
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
CAS
134377-69-8
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
MESH
C109927
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
FDA UNII
CK4M8AX1LN
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
INN
7018
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
EVMPD
SUB10413MIG
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105464
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
SMS_ID
100000084372
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
PUBCHEM
65973
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
NCI_THESAURUS
C74278
Created by admin on Wed Apr 02 08:44:27 GMT 2025 , Edited by admin on Wed Apr 02 08:44:27 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY