Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H28Cl2O3 |
| Molecular Weight | 411.362 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(Cl)[C@@H](Cl)C[C@]2(C)[C@H]1C(=O)CO
InChI
InChIKey=FKRMBGXNTOTQDI-IIEHVVJPSA-N
InChI=1S/C22H28Cl2O3/c1-12-8-16-15-5-4-13-9-14(26)6-7-21(13,3)22(15,24)18(23)10-20(16,2)19(12)17(27)11-25/h6-7,9,12,15-16,18-19,25H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,18+,19-,20+,21+,22+/m1/s1
| Molecular Formula | C22H28Cl2O3 |
| Molecular Weight | 411.362 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Locicortolone is an anti-inflammatory and antiallergic synthetic glucocorticoid. It has high glucocorticoid cytoplasmic receptor binding affinity in vitro (more than four times higher than dexamethasone) but comparable to dexamethasone relative TAT (tyrosine aminotransferase induction) activity. It has six times lower binding affinity to mineralocorticoid receptor in comparison to dexamethasone.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Binding of steroids to the progestin and glucocorticoid receptors analyzed by correspondence analysis. | 1988-06 |
|
| Ornithine decarboxylase induction by glucocorticoids in brain and liver of adrenalectomized rats. | 1982-05 |
|
| Relations between steroid-cell contact, steroid-binding and induction of tyrosine aminotransferase. | 1981-05 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7062053
Single dose - 1 mg per rat
Route of Administration:
Other
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:04:23 GMT 2025
by
admin
on
Mon Mar 31 20:04:23 GMT 2025
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| Record UNII |
9R09I46GBS
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| Record Status |
Validated (UNII)
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| Record Version |
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12905327
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65049-45-8
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DTXSID70215366
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9R09I46GBS
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Locicortolone
Created by
admin on Mon Mar 31 20:04:23 GMT 2025 , Edited by admin on Mon Mar 31 20:04:23 GMT 2025
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PRIMARY |