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AU-15330

رقم الكتالوجGC64271

AU-15330 عبارة عن جهاز تحلل مستهدف للتحلل البروتيني (PROTAC) للوحدات الفرعية SWI / SNF ATPase ، SMARCA2 و SMARCA4AU-15330 يحث على تثبيط قوي لنمو الورم في نماذج طعم أجنبي لسرطان البروستاتا ويتآزر مع مضاد AR إنزالوتاميدAU-15330 يحث على مغفرة المرض في نماذج سرطان البروستاتا المقاومة للإخصاء (CRPC) بدون سمية

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AU-15330 التركيب الكيميائي

Cas No.: 2380274-50-8

الحجم السعر المخزون الكميّة
5mg
378٫00
متوفر
10mg
585٫00
متوفر
25mg
1170٫00
متوفر

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مراجعات العميل

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

AU-15330 is a proteolysis-targeting chimera (PROTAC) degrader of the SWI/SNF ATPase subunits, SMARCA2 and SMARCA4. AU-15330 induces potent inhibition of tumour growth in xenograft models of prostate cancer and synergizes with the AR antagonist enzalutamide. AU-15330 induces disease remission in castration-resistant prostate cancer (CRPC) models without toxicity[1].

AU-15330 (10 and 30 mg/kg; i.v.; 5 days per week for 3 weeks) shows no evident toxicity in immuno-competent mice[1].AU-15330 (60 mg/kg with or without 10 mg/kg enzalutamide; i.v.; 3 days per week; p.o.; 5 days per week for 5 weeks) leads to potent inhibition of tumour growth, triggering disease regression in more than 20% of animals. Combinatorial regimen induced the most potent anti-tumour effect, with regression in all animals[1].AU-15330 (60 mg/kg with or without 10 mg/kg enzalutamide; i.v.; 3 days per week; p.o.; 5 days per week for 5 weeks) strongly inhibits the growth of C4-2B cell line-derived CRPC xenografts in intact mice as a single agent and synergized with enzalutamide[1].AU-15330 (60 mg/kg with or without 10 mg/kg enzalutamide; i.v.; 3 days per week; p.o.; 5 days per week for 5 weeks) combines with enzalutamide induces significant tumour growth inhibition, causing regression in more than 30% of animals in the modle of CRPC variant of the MDA-PCa-146-12 PDX by tumour implantation into castrated mice[1].

[1]. Xiao L, et al. Targeting SWI/SNF ATPases in enhancer-addicted prostate cancer. Nature. 2022;601(7893):434-439.

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