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AZD9750

Chemical Structure : AZD9750

CAS No.: 3056515-10-4

AZD9750 (AZD-9750)

Catalog No.: PC-28726Not For Human Use, Lab Use Only.

AZD9750 is a potent, selective and orally bioavailable Androgen Receptor (AR) PROTAC degrader with DC50 of 10 nM and 12 nM for AR WT and AR L702H respectively. showed extensive degradation of AR, including L702H AR (Dmax >100%).

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

AZD9750 is a potent, selective and orally bioavailable Androgen Receptor (AR) PROTAC degrader with DC50 of 10 nM and 12 nM for AR WT and AR L702H respectively. showed extensive degradation of AR, including L702H AR (Dmax >100%).
AZD9750 inhibits tumor growth in vivo in a mouse prostate cancer xenograft model.

Physicochemical Properties

M.Wt 758.37
Formula C43H48ClN9O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(S)-4-Chloro-7-(3-(4-(4-((4-(6-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-1-methyl-1H-indol-2-yl)piperidin-1-yl)methyl)piperidin-1-yl)phenyl)piperidin-1-yl)-1H-indazole-3-carbonitrile

References

1. Scott JS, et al. J Med Chem. 2026 Feb 12;69(3):3209-3232.

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