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
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)
| 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.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:44:27 GMT 2025
by
admin
on
Wed Apr 02 08:44:27 GMT 2025
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| Record UNII |
CK4M8AX1LN
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English | ||
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Common Name | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
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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
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DTXSID60158677
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134377-69-8
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C109927
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CK4M8AX1LN
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7018
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SUB10413MIG
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CHEMBL2105464
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100000084372
Created by
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65973
Created by
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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
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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