Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C11H13NO4 |
| Molecular Weight | 223.2252 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)O[C@@H]1OC(=O)[C@H]2[C@H]3C[C@H](C=C3)[C@@H]12
InChI
InChIKey=ZMXUEEVRCMPQPF-UTABRTIASA-N
InChI=1S/C11H13NO4/c1-12-11(14)16-10-8-6-3-2-5(4-6)7(8)9(13)15-10/h2-3,5-8,10H,4H2,1H3,(H,12,14)/t5-,6+,7+,8-,10+/m1/s1
| Molecular Formula | C11H13NO4 |
| Molecular Weight | 223.2252 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Moxadolen is tricyclo-[5.2.1.0.2.6endo]decenone derivative. Moxadolen pharmacokinetics were investigated after oral application in male Wistar rats. The compound is extensively absorbed and mainly renally eliminated. Within 60 h, 63% of the activity is recovered in urine and feces. After 12 h 27% of the activity is eliminated (application in polyethylene glycol). The highest total concentration of the activity in the plasma is found after 2 h, the highest of the unchanged drug is found after 1 h. The half-life is 2.9 h.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:20:20 GMT 2025
by
admin
on
Mon Mar 31 18:20:20 GMT 2025
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| Record UNII |
3AII0O976N
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| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C241
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| Code System | Code | Type | Description | ||
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3AII0O976N
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75992-53-9
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DTXSID401024558
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SUB09079MIG
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100000080595
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71995
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CHEMBL2106637
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4992
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C90643
Created by
admin on Mon Mar 31 18:20:20 GMT 2025 , Edited by admin on Mon Mar 31 18:20:20 GMT 2025
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |