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Ophiopogonin D'

Catalog No. TN1071   CAS 65604-80-0

Ophiopogonin D' can activate SIRT1 in a dose-dependent manner. Ophiopogonin D' also noncompetitively inhibits UGT1A6 and UGT1A10.

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Ophiopogonin D' Chemical Structure
Ophiopogonin D', CAS 65604-80-0
Pack Size Availability Price/USD Quantity
1 mg In stock $ 196.00
5 mg In stock $ 425.00
10 mg In stock $ 618.00
25 mg In stock $ 962.00
50 mg In stock $ 1,290.00
100 mg In stock $ 1,750.00
1 mL * 10 mM (in DMSO) In stock $ 786.00
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Purity: 99.13%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Ophiopogonin D' can activate SIRT1 in a dose-dependent manner. Ophiopogonin D' also noncompetitively inhibits UGT1A6 and UGT1A10.
In vitro In vitro incubation system to model UGT reaction was used. Recombinant UGT isoforms-catalyzed 4-methylumbelliferone (4-MU) glucuronidation and UGT1A4-catalyzed trifluoperazine (TFP) glucuronidation reactions were employed to phenotype the inhibition profile of maidong's components towards the activity of UGT isoforms. Different inhibition potential of maidong's components towards various UGT isoforms was observed. Based on the inhibition kinetic investigation results, ophiopogonin D (OD) noncompetitively inhibited UGT1A6 and competitively inhibited UGT1A8, Ophiopogonin D' (OD') noncompetitively inhibited UGT1A6 and UGT1A10, and ruscorectal (RU) exhibited competitive inhibition towards UGT1A4. The inhibition kinetic parameters were calculated to be 20.6, 40.1, 5.3, 9.0, and 0.02 μM, respectively[1].
Source
Molecular Weight 855.02
Formula C44H70O16
CAS No. 65604-80-0

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 8.55 mg/mL (10 mM)

TargetMolReferences and Literature

1. The Inhibition of the Components from Shengmai Injection towards UDP-Glucuronosyltransferase.Evid Based Complement Alternat Med. 2014;2014:594354. 2. Wang L , et al. Homo-aro-cholestane, furostane and spirostane saponins from the tubers of Ophiopogonjaponicus. Phytochemistry. 2017 Apr;136:125-132. 3. Wang Y, et al. Specific Turn-On Fluorescent Probe with Aggregation-Induced EmissionCharacteristics for SIRT1 Modulator Screening and Living-Cell Imaging. Anal Chem. 2015;87(10):5046-9.

Related compound libraries

This product is contained In the following compound libraries:
Natural Product Library for HTS Bioactive Compounds Library Max Natural Product Library Anti-Aging Compound Library Epigenetics Compound Library Bioactive Compound Library Metabolism Compound Library Traditional Chinese Medicine Monomer Library Anti-COVID-19 Traditional Chinese Medicine Compound Library Anti-Cancer Compound Library

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Related compounds with same targets
Dihydrocoumarin SRT1720 hydrochloride Z26395438 SIRT1 activator 1 Thiomyristoyl SIRT6-IN-3 MC3482 AGK7

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Keywords

Ophiopogonin D' 65604-80-0 Chromatin/Epigenetic DNA Damage/DNA Repair Metabolism Sirtuin UGT inhibit Inhibitor inhibitor

 

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