CDDO-Im

Catalog No.: A16308

PPARγ Agonist

CDDO-Im

CDDO-Im Chemical Structure

CAS NO. 443104-02-7

CDDO-Im is a novel synthetic triterpenoid more potent than its parent compound CDDO both in vitro and in vivo; PPARγ Agonist.

Availability: In stock

Package Price Qty
5 mg
$110.00
10 mg
$160.00
50 mg
$620.00
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Biological Activity

CDDO-Im is a novel synthetic triterpenoid more potent than its parent compound CDDO both in vitro and in vivo; PPARγ Agonist.
In vitro DMSO 48 mg/mL (88.6 mM)
Water Insoluble
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 18.46 mL 92.3 mL 184.6 mL
0.5 mM 3.69 mL 18.46 mL 36.92 mL
1 mM 1.85 mL 9.23 mL 18.46 mL
5 mM 0.37 mL 1.85 mL 3.69 mL

*The above data is based on the productmolecular weight 541.72. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Catalog Num A16308
Actions Agonist
CAS No. 443104-02-7
Formula C34H43N3O3
M. Wt 541.72
Solubility DMSO
Purity >98%
Synonyms RTA-403, TP-235, CDDO-Imidazolide
SMILES CC1(CCC2(CCC3(C(C2C1)C(=O)C=C4C3(CCC5C4(C=C(C(=O)C5(C)C)C#N)C)C)C)C(=O)N6C=CN=C6)C
Storage

Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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