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Cat. No.: HY-182728

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CD564

CD564 (Compound 11b) is a cytochrome P450 CYP26A1 and CYP26B1 inhibitor, with IC₅₀ values of 1.63 μM and 0.52 μM, respectively. Cytochrome P450 CYP26 enzymes clear all-trans retinoic acid (atRA).

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CAS No.: 110952-26-6
Formule: C₂₆H₂₆O₃
Masse moléculaire:386.48

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Please store the product under the recommended conditions in the Certificate of Analysis.

CD564 Chemical Structure

CAS No.: 110952-26-6

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- IC₅₀ & Target
- Cellular Effect
- In Vitro
Chemical Information
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
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Activité biologique

Description

IC₅₀ & Target

^[1]

CYP26A1

1.63 μM (IC₅₀)

CYP26B1

0.52 μM (IC₅₀)

Voir tous les produits spécifiques à Isoform Cytochrome P450 :

Cellular Effect

Cell Line	Type	Value	Description	References
Sf9	IC₅₀	0.52 μM Compound: 11b	Inhibition of microsomal fraction of human CYP26B1 expressed in Sf9 cells using 9-cis-RA as substrate preincubated for 5 mins followed by NADPH addition measured after 5 mins by HPLC analysis in presence of rat P450 reductase Inhibition of microsomal fraction of human CYP26B1 expressed in Sf9 cells using 9-cis-RA as substrate preincubated for 5 mins followed by NADPH addition measured after 5 mins by HPLC analysis in presence of rat P450 reductase	[PMID: 26918322]

In Vitro

CD564 (1 min for CYP26A1, 5 min for CYP26B1) exhibits stronger inhibitory activity against CYP26B1 (IC₅₀ = 0.52 μM) than against CYP26A1 (IC₅₀ = 1.63 μM) in recombinant microsome assays^[1].

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

Chemical Information

CAS No. 110952-26-6
Masse moléculaire 386.48
Formule C₂₆H₂₆O₃
SMILES

O=C(C1=CC2=CC=C(C(C3=CC=C4C(C(C)(CCC4(C)C)C)=C3)=O)C=C2C=C1)O
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Instruction de manipulation (2659 KB)

Références

[1]. Diaz P, et al. Development and Characterization of Novel and Selective Inhibitors of Cytochrome P450 CYP26A1, the Human Liver Retinoic Acid Hydroxylase. J Med Chem. 2016;59(6):2579-2595. [Content Brief]

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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