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- Loteprednol etabonate
Loteprednol etabonate
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 466.95 |
Cas No. | 82034-46-6 |
Formula | C24H31ClO7 |
Solubility | insoluble in H2O; insoluble in EtOH; ≥16.95 mg/mL in DMSO |
Chemical Name | chloromethyl (8S,9S,10R,11S,13S,14S,17R)-17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene-17-carboxylate |
SDF | Download SDF |
Canonical SMILES | O[C@@H]1[C@H]([C@@](C)(C=C2)C3=CC2=O)[C@@H](CC3)[C@H](CC4)[C@@](C1)(C)[C@]4(C(OCCl)=O)OC(OCC)=O |
Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Animal experiment [1]: | |
Animal models |
Rats |
Dosage form |
0.5~10 mg/kg (i.v.) |
Application |
The results showed that Loteprednol etabonate showed a rapid dose-dependent elimination effect, with a total blood clearance of more than 60 ml/min/kg. Loteprednol etabonate, which is absorbed systemically after topical administration, can be quickly converted into inactive metabolites and is mainly cleared from the body by bile and urine. |
Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
References: [1]. Bodor N, Wu WM, Murakami T, Engel S. Soft drugs. 19. Pharmacokinetics, metabolism and excretion of a novel soft corticosteroid, loteprednol etabonate, in rats. Pharm Res. 1995 Jun;12(6):875-9. PubMed PMID: 7667193. |
Quality Control & MSDS
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