Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C25H36O6 |
| Molecular Weight | 432.5497 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@]12CC[C@H]3[C@@H](CC[C@@H]4CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)COC(=O)CCC(O)=O
InChI
InChIKey=KLRNMIUKAXHHFS-ZILYODKUSA-N
InChI=1S/C25H36O6/c1-24-11-9-16(26)13-15(24)3-4-17-18-5-6-20(25(18,2)12-10-19(17)24)21(27)14-31-23(30)8-7-22(28)29/h15,17-20H,3-14H2,1-2H3,(H,28,29)/t15-,17+,18+,19+,20-,24+,25+/m1/s1
Originator
Approval Year
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13356183 |
Preventing | Viadril Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Studies on the clinical and pathological effects of hydroxydione. | 1961-10 |
|
| Hydroxydione sodium (viadril) for anesthesia; a report of clinical experience. | 1956-09 |
|
| Viadril: a new steroid anaesthetic; preliminary communication. | 1956-07-21 |
|
| Steroid anesthetic agent. | 1955-07-08 |
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5869
Created by
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DTXSID00861577
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6LJJ67GNMV
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201-314-2
Created by
admin on Mon Mar 31 21:41:15 GMT 2025 , Edited by admin on Mon Mar 31 21:41:15 GMT 2025
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80-96-6
Created by
admin on Mon Mar 31 21:41:15 GMT 2025 , Edited by admin on Mon Mar 31 21:41:15 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD