A-486
A-486 is an inactive analog that serves as an inactive control analog for A-485 (HY-107455).
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- CAS 番号: 2143464-15-5
- 分子式: C25H24F4N4O5
- 分子量:536.48
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
体外実験
A-486 shows very weak inhibitory activity against purified p300-BHC HAT domain in vitro, with an IC50 greater than 10,000 nM[1].
A-486 shows very weak inhibitory activity against purified CBP-BHC HAT domain in vitro, with an IC50 of 9,032 nM[1].
A-486 (dose range) binds very weakly to purified p300 HAT domain in vitro, with a Kd of 20,000 nM and a fast off-rate[1].
A-486 (3 h) is inactive in PC-3 prostate adenocarcinoma cells, failing to reduce H3K27Ac or H3K9Ac levels after 3 hours of treatment[1].
A-486 (10 μM; 7-24 h) does not inhibit DHT-stimulated PSA mRNA expression in LnCaP-FGC prostate cancer cells after 7 or 24 hours of treatment[1].
A-486 (10 μM; 7-24 h) does not inhibit MYC mRNA expression in androgen-depleted 22Rv1 prostate cancer cells after 7 or 24 hours of treatment[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .
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Cell Line:LnCaP-FGC androgen-dependent prostate adenocarcinoma cells
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Concentration:10 μM
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Incubation Time:7 h; 24 h
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Result:Did not inhibit DHT-stimulated PSA mRNA expression, remaining at levels comparable to the DMSO control at both time points.
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Cell Line:androgen-depleted 22Rv1 castration-resistant prostate adenocarcinoma cells
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Concentration:10 μM
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Incubation Time:7 h; 24 h
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Result:Did not reduce MYC mRNA expression, remaining at levels comparable to the DMSO control at both time points.
化学情報
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CAS 番号 2143464-15-5
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分子量 536.48
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分子式 C25H24F4N4O5
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SMILES
O=C1[C@]2(OC(N1CC(N([C@@H](C)C(F)(F)F)CC3=CC=C(C=C3)F)=O)=O)C4=CC(NC(NC)=O)=CC=C4CC2
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)