1. Metabolic Enzyme/Protease Membrane Transporter/Ion Channel
  2. Endogenous Metabolite P-glycoprotein
  3. Estradiol 17-(β-D-Glucuronide)

Estradiol 17-(β-D-Glucuronide) is a D-ring glucuronide metabolite of natural estrogen formed in the liver. Estradiol 17-(β-D-Glucuronide) is a substrate of the organic anion-transporting polypeptide family (Oatp) and multidrug resistance-associated protein 2 (Mrp2). Estradiol 17-(β-D-Glucuronide) regulates MRP8-mediated transport processes and inhibits MRP8-mediated transport of dehydroepiandrosterone 3-sulfate and taurocholic acid. Estradiol 17-(β-D-Glucuronide) induces immediate, reversible reduction of bile flow and acute intrahepatic cholestasis in female rats without altering the bile acid composition in bile. Estradiol 17-(β-D-Glucuronide) can be used in studies related to intrahepatic cholestasis.

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Estradiol 17-(β-D-Glucuronide)

Estradiol 17-(β-D-Glucuronide) Chemische Struktur

CAS. Nr. : 1806-98-0

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Beschreibung

Estradiol 17-(β-D-Glucuronide) is a D-ring glucuronide metabolite of natural estrogen formed in the liver. Estradiol 17-(β-D-Glucuronide) is a substrate of the organic anion-transporting polypeptide family (Oatp) and multidrug resistance-associated protein 2 (Mrp2). Estradiol 17-(β-D-Glucuronide) regulates MRP8-mediated transport processes and inhibits MRP8-mediated transport of dehydroepiandrosterone 3-sulfate and taurocholic acid. Estradiol 17-(β-D-Glucuronide) induces immediate, reversible reduction of bile flow and acute intrahepatic cholestasis in female rats without altering the bile acid composition in bile. Estradiol 17-(β-D-Glucuronide) can be used in studies related to intrahepatic cholestasis[1][2][3].

Cellular Effect
Cell Line Type Value Description References
Sf9 IC50
13.3 μM
Compound: Estradiol-17beta-D-glucuronide
TP_TRANSPORTER: inhibition of DNP-SG uptake (DNP-SG: 0.05 uM) in membrane vesicles from Mrp2-expressing Sf9 cells
TP_TRANSPORTER: inhibition of DNP-SG uptake (DNP-SG: 0.05 uM) in membrane vesicles from Mrp2-expressing Sf9 cells
[PMID: 11306690]
Sf9 IC50
30 μM
Compound: Estradiol-17beta-D-glucuronide
TP_TRANSPORTER: inhibition of DHEAS in membrane vesicles from MRP4-expressing Sf9 cells
TP_TRANSPORTER: inhibition of DHEAS in membrane vesicles from MRP4-expressing Sf9 cells
[PMID: 12523936]
In Vitro

Estradiol 17-(β-D-Glucuronide) (1-1000 μM; 5-10 min) is a substrate of MRP8 in MRP8-transfected LLC-PK1 cell membrane vesicles, with a Km of 62.9 μM and Vmax of 62.0 pmol/mg/min, and it also acts as a concentration-dependent inhibitor of MRP8-mediated DHEAS and taurocholate transport[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Estradiol 17-(β-D-Glucuronide) (10 μmol/kg (4.5 mg/kg); i.v.; single dose) induces severe, reversible intrahepatic cholestasis in female Sprague-Dawley rats via reduced bile flow, with over 84% of the dose excreted into bile, without altering endogenous biliary bile acid composition[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Sprague-Dawley (female, 160-250 g)[1]
Dosage: 10 μmol/kg
Administration: i.v.; single dose
Result: Caused severe, immediate, reversible reduction in bile flow.
Reached more than 84% of the administered dose in biliary excretion.
Showed no significant change in biliary composition of seven endogenous bile acids relative to intact control rats.
Molekulargewicht

448.51

Formel

C24H32O8

CAS. Nr.
Appearance

Solid

Color

White to off-white

SMILES

C[C@@]12[C@](CC[C@@H]2O[C@@H]3O[C@@H]([C@H]([C@@H]([C@H]3O)O)O)C(O)=O)([H])[C@@]4([H])[C@@](CC1)([H])C5=CC=C(O)C=C5CC4

Structure Classification
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.

Speicherung
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
Lösungsmittel & Löslichkeit
In Vitro: 

DMSO : 4.5 mg/mL (10.03 mM; Need ultrasonic and warming; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.2296 mL 11.1480 mL 22.2960 mL
5 mM 0.4459 mL 2.2296 mL 4.4592 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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Reinheit & Dokumentation

Purity: 99.0%

Verweise

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.2296 mL 11.1480 mL 22.2960 mL 55.7401 mL
5 mM 0.4459 mL 2.2296 mL 4.4592 mL 11.1480 mL
10 mM 0.2230 mL 1.1148 mL 2.2296 mL 5.5740 mL
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Estradiol 17-(β-D-Glucuronide)
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