Details
Stereochemistry | RACEMIC |
Molecular Formula | C18H27NO2S |
Molecular Weight | 321.477 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)C1=CC(CC2SCNC2=O)=CC(=C1O)C(C)(C)C
InChI
InChIKey=ILMMRHUILQOQGP-UHFFFAOYSA-N
InChI=1S/C18H27NO2S/c1-17(2,3)12-7-11(9-14-16(21)19-10-22-14)8-13(15(12)20)18(4,5)6/h7-8,14,20H,9-10H2,1-6H3,(H,19,21)
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
In vitro biotransformation and identification of human cytochrome P450 isozyme-dependent metabolism of tazofelone. | 1997 Dec |
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Stereoselective metabolism of tazofelone, an anti-inflammatory bowel disease agent, in rats and dogs and in human liver microsomes. | 1999 |
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Discovery of a solid solution of enantiomers in a racemate-forming system by seeding. | 2006 Sep 13 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://adisinsight.springer.com/drugs/800006634
Unknown
Route of Administration:
Rectal
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C574
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107902-67-0
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GG-34
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CHEMBL132991
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100000082453
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C76695
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C109841
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ACTIVE MOIETY