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MilliporeSigma

SML3413

ASC-J9

≥98% (HPLC)

Synonym(s):

(1E, 4Z, 6E)-5-Hydroxy-1,7-bis(3,4-dimethoxyphenyl)-1,4,6-heptatrien-3-one, Dimethylcurcumin, GO-Y025

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About This Item

Empirical Formula (Hill Notation):
C23H24O6
CAS Number:
Molecular Weight:
396.43
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77

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Quality Level

assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

, White to light orange

solubility

DMSO: 2 mg/mL, clear

storage temp.

−20°C

SMILES string

OC(/C=C/C1=CC(OC)=C(C=C1)OC)=C\C(/C=C/C2=CC(OC)=C(C=C2)OC)=O

InChI

1S/C23H24O6/c1-26-20-11-7-16(13-22(20)28-3)5-9-18(24)15-19(25)10-6-17-8-12-21(27-2)23(14-17)29-4/h5-15,24H,1-4H3/b9-5+,10-6+,18-15-

InChI key

ZMGUKFHHNQMKJI-CIOHCNBKSA-N

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1 of 4

This Item
B6938F9057SMB00370
form

powder

form

solid

form

powder

form

powder

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥96% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

-

Quality Level

200

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

solubility

DMSO: 2 mg/mL, clear

solubility

DMSO: ≥20 mg/mL

solubility

DMSO: ≥10 mg/mL

solubility

-

storage condition

desiccated

storage condition

-

storage condition

-

storage condition

-

Biochem/physiol Actions

ASC-J9 (dimethylcurcumin) is an androgen receptor (AR)-selective degradation promoter that disrupts the interaction between AR and its coregulators. ASC-J9 induces AR degration in cultures (5 µM, LNCaP) and shows in vivo therapeutic efficacy (50 mg/kg i.p. qod) in murine bladder cancer (TCC-SUP and UMUC3 xenografts) and a spinal and bulbar muscular atrophy disease model (AR-polyQ transgenic SBMA mice).
Androgen receptor (AR)-selective degradation promoter in cultures and in vivo.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Hao Tian et al.
Journal of experimental & clinical cancer research : CR, 40(1), 3-3 (2021-01-05)
Early studies indicated that ASC-J9®, an androgen receptor (AR) degradation enhancer, could suppress the prostate cancer (PCa) progression. Here we found ASC-J9® could also suppress the PCa progression via an AR-independent mechanism, which might involve modulating the tumor suppressor ATF3

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