Loteprednol etabonate

This product is for research use only, not for human use. We do not sell to patients.

Loteprednol etabonate
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
500mg$400Check With Us
1g$650Check With Us
5g$1755Check With Us

Cat #: V1700 CAS #: 82034-46-6 Purity ≥ 98%

Description: Loteprednol etabonate (Lotemax; Alrex; HGP-1; Loterox; Locort; P-5604; HGP1; Lenoxin, CDDD-5604), the esther form of Loteprednol, is a potent glucocorticoid receptor agonist approved as a medication used in treatment of inflammation of the eye due to allergies.

References: Noble S, Goa KL. Loteprednol etabonate: clinical potential in the management of ocular inflammation. BioDrugs. 1998 Oct;10(4):329-39

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Molecular Weight (MW)466.95
Molecular FormulaC24H31ClO7
CAS No.82034-46-6
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 93 mg/mL (199.2 mM)r
Water:<1 mg/mLr
Ethanol: 4 mg/mL (8.6 mM)
Solubility In VivoChloromethyl (11β,17α)-17-[(Ethoxycarbonyl)oxy]-11-hydroxy-3-oxoandrosta-1,4-diene-17-carboxylate (11β,17α)-17-[(Ethoxycarbonyl)oxy]-11-hydroxy-3-oxoa
SynonymsLoteprednol Etabonate; Lotemax; Alrex; HGP-1; Loterox; Locort; P 5604; HGP1; Lenoxin, CDDD 5604
ProtocolIn VivoIntravenous administration of Loteprednol etabonate (5 mg/kg) to dogs reveals a terminal half-life of 2.8 h, a volume of distribution of 3.7 L/kg, and a total body clearance of 0.9 L/h/kg. Intact loteprednol etabonate was not detectable in the urine. After oral administration of the drug (5 mg/kg) to dogs, only metabolites, but no intact drug, were found in the plasma, an indication for a high first-pass effect.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM2.1416 mL10.7078 mL21.4156 mL42.8311 mL
5mM0.4283 mL2.1416 mL4.2831 mL8.5662 mL
10mM0.2142 mL1.0708 mL2.1416 mL4.2831 mL
20mM0.1071 mL0.5354 mL1.0708 mL2.1416 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.