ChemicalBook--->CAS DataBase List--->2222111-87-5

2222111-87-5

2222111-87-5 Structure

2222111-87-5 Structure
IdentificationBack Directory
[Name]

ARD-2128
[CAS]

2222111-87-5
[Synonyms]

ARD-2128
[Molecular Formula]

C45H50ClN7O6
[MDL Number]

MFCD34567333
[MOL File]

2222111-87-5.mol
[Molecular Weight]

820.37
Chemical PropertiesBack Directory
[Boiling point ]

1000.4±65.0 °C(Predicted)
[density ]

1.39±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[form ]

Solid
[pka]

10.83±0.40(Predicted)
[color ]

Light yellow to green yellow
Spectrum DetailBack Directory
[Spectrum Detail]

ARD-2128(2222111-87-5)1HNMR
Hazard InformationBack Directory
[Biological Activity]

ARD-2128 is a highly potent, orally bioavailable PROTAC androgen receptor (AR) degrader. ARD-2128 effectively reduces AR protein, suppresses AR-regulated genes in tumor tissues, and inhibits growth of tumor without signs of toxicity. ARD-2128 has the potential for the research of the prostate cancer[1]. ARD-2128 is highly potent and effective in the inhibition of cell growth in the VCaP cell line and LNCaP cell line with the IC50 values of 4 nM and 5 nM, respectively[1].ARD-2128 (1, 10, 100, and 1000 nM; 24 hours) effectively reduces the AR protein level by >50% at 1 nM and achieves the AR degradation of >90% at 10, 100, and 1000 nM, respectively, in VCaP cell[1]. ARD-2128 (20 mg/kg; p.o.; once) is effective in reducing the level of AR protein in mice after 24 hours[1].ARD-2128 (10-40 mg/kg; p.o.; daily for 21 days) shows antitumor activity in the VCaP xenograft model in mice[1].ARD-2128 (5mg/kg; p.o.) treatment shows the Cmax, AUC0-t and t1/2 values of 1304 ng/mL, 22361 ng h/mL and 18.8 hours, respectively[1].
[References]

[1]. Han X, et al. Strategies toward Discovery of Potent and Orally Bioavailable Proteolysis Targeting Chimera Degraders of Androgen Receptor for the Treatment of Prostate Cancer [published online ahead of print, 2021 Aug 25]. J Med Chem. 2021;10.1021/acs.jmedchem.1c00882.
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