Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C26H44N4O6 |
| Molecular Weight | 508.6508 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCC\C=C\CCCCCCCC(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=NC(=N2)C(N)=O
InChI
InChIKey=HNJWVTLAOZFLEK-OOWZQQDUSA-N
InChI=1S/C26H44N4O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(31)35-18-20-22(32)23(33)26(36-20)30-19-28-25(29-30)24(27)34/h9-10,19-20,22-23,26,32-33H,2-8,11-18H2,1H3,(H2,27,34)/b10-9+/t20-,22-,23-,26-/m1/s1
| Molecular Formula | C26H44N4O6 |
| Molecular Weight | 508.6508 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 1 |
| Optical Activity | UNSPECIFIED |
Ribavirin elaidate (CP-4033; TRX-201), a Lipid Vector Technology derivative of ribavirin. It inhibits elongation factor F4E (elF4E), which stimulates cell growth. Translational Therapeutics Inc. received orphan drug status from the U.S. Food and Drug Administration (FDA) in 2011 for ribavirin elaidate in the treatment of aggressive follicular, medullary and anaplastic thyroid carcinoma.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:07:20 GMT 2025
by
admin
on
Mon Mar 31 21:07:20 GMT 2025
|
| Record UNII |
4LU13X0I13
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
FDA ORPHAN DRUG |
344011
Created by
admin on Mon Mar 31 21:07:20 GMT 2025 , Edited by admin on Mon Mar 31 21:07:20 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
1352921-29-9
Created by
admin on Mon Mar 31 21:07:20 GMT 2025 , Edited by admin on Mon Mar 31 21:07:20 GMT 2025
|
PRIMARY | |||
|
DTXSID00159300
Created by
admin on Mon Mar 31 21:07:20 GMT 2025 , Edited by admin on Mon Mar 31 21:07:20 GMT 2025
|
PRIMARY | |||
|
4LU13X0I13
Created by
admin on Mon Mar 31 21:07:20 GMT 2025 , Edited by admin on Mon Mar 31 21:07:20 GMT 2025
|
PRIMARY | |||
|
49848291
Created by
admin on Mon Mar 31 21:07:20 GMT 2025 , Edited by admin on Mon Mar 31 21:07:20 GMT 2025
|
PRIMARY |