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Dimethylcurcumin

🥰Excellent
Catalog No. TQ0214Cas No. 52328-98-0
Alias GO-Y025, ASC-J9

Dimethylcurcumin (ASC-J9) (ASC-J9) is an androgen receptor degradation enhancer. It effectively suppresses castration-resistant prostate cancer cell proliferation and invasion.

Dimethylcurcumin

Dimethylcurcumin

🥰Excellent
Purity: 98.96%
Catalog No. TQ0214Alias GO-Y025, ASC-J9Cas No. 52328-98-0
Dimethylcurcumin (ASC-J9) (ASC-J9) is an androgen receptor degradation enhancer. It effectively suppresses castration-resistant prostate cancer cell proliferation and invasion.
Pack SizePriceAvailabilityQuantity
20 mg$130In Stock
1 mL x 10 mM (in DMSO)$54In Stock
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Purity:98.96%
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Product Introduction

Bioactivity
Description
Dimethylcurcumin (ASC-J9) (ASC-J9) is an androgen receptor degradation enhancer. It effectively suppresses castration-resistant prostate cancer cell proliferation and invasion.
In vitro
Dimethylcurcumin is able to degrade fAR and AR3 in a dose-dependent manner in various human PCa cells. Dimethylcurcumin can also effectively suppress AR-targeted genes in CWR22Rv1-fARKD cells. Dimethylcurcumin (5 or 10 μM) significantly suppresses the DHT-induced cell growth in all three PCa cell lines. Dimethylcurcumin suppresses AR-targeted genes and cell growth by the degradation of fAR and ectopic AR3 in C81 and C4-2 cells [1]. ASC-J9 reduces the AR aggregated AR-112Q in cells. Dimethylcurcumin suppresses the aggregation of AR-112Q in SBMA PC12/AR-112Q cells [2].
In vivo
Dimethylcurcumin (75 mg/kg, i.p.) degrades both fAR and AR3 in the xenografted tumors in vivo and ASC-J9-treated tumors have significantly decreased Ki67-positive cells [1]. Dimethylcurcumin (50 mg/kg every 48 h, i.p.) substantially ameliorates the SBMA symptoms in AR-97Q mice and ameliorates neuromuscular pathological findings [2]. ASC-J9-treated mice show significantly smaller prostate tumor sizes when compared with those receiving classic ADT/castration with little serum androgen [3].
Cell Research
For the cell survival assay, the PC12/AR-112Q and PC12/AR-10Q cells are cultured as described previously and incubated cells in the presence of 10 μg/mL doxycycline for 24 h. Then the cells are treated with a vehicle, 5 μM Dimethylcurcumin or 10 μM Dimethylcurcumin, along with 1 nM DHT, and determined cell viability using Trypan blue staining at specific time intervals [2].
Animal Research
CWR22Rv1 cells (1×10^6 cells per site) are injected into both anterior prostates of the castrated nude mice after 2 weeks of implantation. The mice were randomly divided into two groups (four mice/eight tumors each group) and either receive 75 mg/kg Dimethylcurcumin intraperitoneal injection or vehicle control every other day. After 4 weeks of treatment, all mice are killed to examine the tumor growth. Body weights and mice activity are measured weekly [1].
AliasGO-Y025, ASC-J9
Chemical Properties
Molecular Weight396.43
FormulaC23H24O6
Cas No.52328-98-0
SmilesCOc1ccc(\C=C\C(\O)=C\C(=O)\C=C\c2ccc(OC)c(OC)c2)cc1OC
Relative Density.1.191 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 48 mg/mL (121.08 mM)
H2O: Insoluble
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5225 mL12.6126 mL25.2251 mL126.1257 mL
5 mM0.5045 mL2.5225 mL5.0450 mL25.2251 mL
10 mM0.2523 mL1.2613 mL2.5225 mL12.6126 mL
20 mM0.1261 mL0.6306 mL1.2613 mL6.3063 mL
50 mM0.0505 mL0.2523 mL0.5045 mL2.5225 mL
100 mM0.0252 mL0.1261 mL0.2523 mL1.2613 mL

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