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
[H][C@@]12C[C@@]([H])(C=C1)[C@]3([H])C(=O)O[C@@H](OC(=O)NC)[C@]23[H]
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 | 4 / 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
Fri Dec 15 16:09:10 GMT 2023
by
admin
on
Fri Dec 15 16:09:10 GMT 2023
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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
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Official Name | English | ||
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Common 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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admin on Fri Dec 15 16:09:10 GMT 2023 , Edited by admin on Fri Dec 15 16:09:10 GMT 2023
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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
Created by
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4992
Created by
admin on Fri Dec 15 16:09:10 GMT 2023 , Edited by admin on Fri Dec 15 16:09:10 GMT 2023
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C90643
Created by
admin on Fri Dec 15 16:09:10 GMT 2023 , Edited by admin on Fri Dec 15 16:09:10 GMT 2023
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Related Record | Type | Details | ||
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ACTIVE MOIETY |