Details
| Stereochemistry | EPIMERIC |
| Molecular Formula | C21H19ClN2O8 |
| Molecular Weight | 462.837 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@@H]1[C@@H](O)[C@H](OC2N=C(C3=CC=CC=C3)C4=C(NC2=O)C=CC(Cl)=C4)O[C@@H]([C@H]1O)C(O)=O
InChI
InChIKey=FIKQKGFUBZQEBL-IFBJMGMISA-N
InChI=1S/C21H19ClN2O8/c22-10-6-7-12-11(8-10)13(9-4-2-1-3-5-9)24-19(18(28)23-12)32-21-16(27)14(25)15(26)17(31-21)20(29)30/h1-8,14-17,19,21,25-27H,(H,23,28)(H,29,30)/t14-,15-,16+,17-,19?,21-/m0/s1
| Molecular Formula | C21H19ClN2O8 |
| Molecular Weight | 462.837 |
| Charge | 0 |
| Count |
|
| Stereochemistry | EPIMERIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 6 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| (S)oxazepam glucuronidation is inhibited by ketoprofen and other substrates of UGT2B7. | 1995 Feb |
|
| Stereoselective conjugation of oxazepam by human UDP-glucuronosyltransferases (UGTs): S-oxazepam is glucuronidated by UGT2B15, while R-oxazepam is glucuronidated by UGT2B7 and UGT1A9. | 2002 Nov |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:48:29 GMT 2023
by
admin
on
Sat Dec 16 09:48:29 GMT 2023
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| Record UNII |
26IK2C76NO
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID701028080
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6801-81-6
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26IK2C76NO
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160870
Created by
admin on Sat Dec 16 09:48:29 GMT 2023 , Edited by admin on Sat Dec 16 09:48:29 GMT 2023
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> METABOLITE INACTIVE |
MAJOR
PLASMA; URINE
|
