[CAS NO. 58479-68-8]  Platycodin D

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PRODUCTS SPECIFICATIONS [58479-68-8]

Catalog
HY-N1411
Brand
MCE
CAS
58479-68-8

DESCRIPTION [58479-68-8]

Overview

MDLMFCD09952590
Molecular Weight1225.32
Molecular FormulaC57H92O28
SMILESO=C([C@]1(CCC(C)(C)C2)[C@]2([H])C3=CC[C@@]4([H])[C@@](C)(CC[C@]5([H])[C@@]4(C[C@H](O)[C@H](O[C@]([C@@H]([C@@H](O)[C@@H]6O)O)([H])O[C@@H]6CO)C5(CO)CO)C)[C@]3(C)C[C@H]1O)O[C@H](OC[C@H](O)[C@@H]7O)[C@@H]7O[C@@](O[C@@H](C)[C@H](O[C@@](OC[C@@H](O)[C@@H]8O[C@@](OC[C@]9(O)CO)([H])[C@@H]9O)([H])[C@@H]8O)[C@H]%10O)([H])[C@@H]%10O

For research use only. We do not sell to patients.

1 Publications Citing Use of MCE


Summary

Platycodin D is a saponin isolated from Platycodon grandiflorus , acts as an activator of AMPKα , with anti-obesity property. WNT/β-catenin pathway mediates the anti-adipogenic effect of platycodin D [1] [2] .


IC50 & Target

AMPKα [1]


In Vitro

Platycodin D (4 μM; 24 h) increases gene expressions of Ucp1, Pgc1a, Sirt3, Cytc, Nrf1 and Prdm16, and suppresses expressions of adipokine genes Fabp4, Adipoq, Lipin1 in 3T3-L1 adipocytes and FABP4, ADIPOQ and RESISTIN in hAMSCs [1] .
Platycodin D (2 and 10 μM) suppresses lipid accumulation in murine and human adipocytes respectively [1] .
Platycodin D suppresses the protein expressions of PPARγ and C/EBPα, and increases protein expressions of UCP1, PGC1α, SIRT3, CIDEA and LIPIN1 [1] .
Platycodin D (10 μM) inhibits lipid droplet formation, and reduces the expression of the FABP4 protein involved in lipid metabolism and the expressions of PPARγ and C/EBPα [2] .
Platycodin D (10 μM; 0-7 d) recoveres CCND1 mRNA level and increases PPARδ level [2] .

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


In Vivo

Platycodin D (5 mg/kg; oral administration, 5 times per week for 5 weeks) decreases the body weight of obese mice [1] .

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

Animal Model: Genetically obese db/db mice [1]
Dosage: 5 mg/kg
Administration: Oral administration; 5 mg/kg, 5 times per week for 5 weeks
Result: Significantly decreased body weight gain without affecting food intake of mice. Decreased the liver tissue weight and increased the weight of brown adipose tissue (BAT).

Appearance

Solid



Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : 50 mg/mL ( 40.81 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 0.8161 mL 4.0806 mL 8.1611 mL
5 mM 0.1632 mL 0.8161 mL 1.6322 mL
10 mM 0.0816 mL 0.4081 mL 0.8161 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2.5 mg/mL (2.04 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (2.04 mM); Clear solution

  • 3.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2.5 mg/mL (2.04 mM); Clear solution

* All of the co-solvents are available by MCE.


Synonyms

Olean-12-en-28-oic acid, 3-(β-D-glucopyranosyloxy)-2,16,23,24-tetrahydroxy-, O-D-apio-β-D-furanosyl-(1→3)-O-β-D-xylopyranosyl-(1→4)-O-6-deoxy-α-L-mannopyranosyl-(1→2)-α-L-arabinopyranosyl ester, (2β,3β,16α)-
Platycodin D