Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H33NO4S |
| Molecular Weight | 383.545 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC[C@@H](O)\C=C\[C@H]1[C@H](O)C[C@@H]2N=C(C[C@H]12)SCCCC(=O)OC
InChI
InChIKey=TUOQTRVLPKMMDB-RQGIMTSLSA-N
InChI=1S/C20H33NO4S/c1-3-4-5-7-14(22)9-10-15-16-12-19(21-17(16)13-18(15)23)26-11-6-8-20(24)25-2/h9-10,14-18,22-23H,3-8,11-13H2,1-2H3/b10-9+/t14-,15-,16-,17+,18-/m1/s1
| Molecular Formula | C20H33NO4S |
| Molecular Weight | 383.545 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 1 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/8876659
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8876659
Tilsuprost is an iminoprostacyclin derivative patented by Hoechst A.-G. as stable prostacyclin analog useful cytoprotective agent. In preclinical models, Tilsuprost given just before induction of pancreatitis partly prevented the impairment of mitochondrial oxidative and phosphorylative functions, however, these positive effects were limited in acute pancreatitis preceded by acute ethanol intake.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:31:07 GMT 2025
by
admin
on
Wed Apr 02 08:31:07 GMT 2025
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| Record UNII |
C23W8PF2D4
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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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NCI_THESAURUS |
C78568
Created by
admin on Wed Apr 02 08:31:07 GMT 2025 , Edited by admin on Wed Apr 02 08:31:07 GMT 2025
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| Code System | Code | Type | Description | ||
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SUB11059MIG
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100000077219
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CHEMBL2218857
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5543
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C101919
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80225-28-1
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C23W8PF2D4
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76961691
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C76335
Created by
admin on Wed Apr 02 08:31:07 GMT 2025 , Edited by admin on Wed Apr 02 08:31:07 GMT 2025
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |