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Aclacinomycin A hydrochloride

Aclacinomycin A hydrochloride

产品编号 T10238   CAS 75443-99-1
别名: 盐酸阿柔比星, Aclarubicin hydrochloride

Aclacinomycin A (Aclarubicin) hydrochloride is a fluorescent molecule and the first described non-peptidic inhibitor showing discrete specificity for the CTRL (chymotrypsin-like) activity of the 20S proteasome. Aclacinomycin A hydrochloride is also a dual inhibitor of topoisomerase I and II.

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Aclacinomycin A hydrochloride Chemical Structure
Aclacinomycin A hydrochloride, CAS 75443-99-1
规格 价格/CNY 货期 数量
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千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: Aclacinomycin A hydrochloride (T10238)
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参考文献
产品描述 Aclacinomycin A (Aclarubicin) hydrochloride is a fluorescent molecule and the first described non-peptidic inhibitor showing discrete specificity for the CTRL (chymotrypsin-like) activity of the 20S proteasome. Aclacinomycin A hydrochloride is also a dual inhibitor of topoisomerase I and II.
体外活性 Aclacinomycin A could efficiently enter living cells and emit fluorescence in situ. Aclacinomycin A (10 μM for 15 min) is sufficient for clear detection of fluorescence in most of the cultured cells. Aclacinomycin A treatment (10 μM for 15 min) results in approximately 20% dead (or nearly dead) cells [1]. Aclacinomycin A effectively induces incorporation of exon 7 into SMN2 transcripts from the endogenous gene in type I SMA fibroblasts as well as into transcripts from an SMN2 minigene in the motor neuron cell line NSC34 [2].
体内活性 Aclacinomycin A is very well absorbed in mice, rats, and dogs after its oral administration. The oral LD50 (76.5 mg/kg) is about twice the iv LD50 (35.6 mg/kg) in mice. Aclacinomycin A (0.75-6 mg/kg, i.p daily) dose-dependently exhibits tumor growth in mice-based Leukemia P-388 model [4].
动物实验 Animal Model: DBA/2, CDF1 (BALB/c×DBA/2) mice with Leukemia P-388. Dosage: 0.75 mg/kg, 1.5 mg/kg, 3 mg/kg, 6 mg/kg. Administration: Intraperitoneal administration daily for 10 days starting 3 hr after transplantation. Result: Inhibited tumor growth [4].
别名 盐酸阿柔比星, Aclarubicin hydrochloride
分子量 848.33
分子式 C42H54ClNO15
CAS No. 75443-99-1

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 125 mg/mL (147.35 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.1788 mL 5.8939 mL 11.7879 mL 29.4697 mL
5 mM 0.2358 mL 1.1788 mL 2.3576 mL 5.8939 mL
10 mM 0.1179 mL 0.5894 mL 1.1788 mL 2.947 mL
20 mM 0.0589 mL 0.2947 mL 0.5894 mL 1.4735 mL
50 mM 0.0236 mL 0.1179 mL 0.2358 mL 0.5894 mL
100 mM 0.0118 mL 0.0589 mL 0.1179 mL 0.2947 mL

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TargetMol Library Books参考文献

1. Isoe T, et al. Inhibition of different steps of the ubiquitin system by CDDP and aclarubicin. Biochim Biophys Acta. 1992 Sep 15;1117(2):131-5. 2. Hajji N, et al. Induction of genotoxic and cytotoxic damage by aclarubicin, a dual topoisomerase inhibitor. Mutat Res. 2005 May 2;583(1):26-35. 3. Iihoshi H, et al. Aclarubicin, an anthracycline anti-cancer drug, fluorescently contrasts mitochondria and reduces the oxygen consumption rate in living human cells. Toxicol Lett. 2017 Aug 5;277:109-114. 4. Hori S, et al. Antitumor activity of new anthracycline antibiotics, aclacinomycin-A and its analogs, and their toxicity. Gan. 1977 Oct;68(5):685-90.
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Keywords

Aclacinomycin A hydrochloride 75443-99-1 Proteases/Proteasome Ubiquitination Proteasome Aclacinomycin A Hydrochloride Aclarubicin Hydrochloride 盐酸阿柔比星 Aclarubicin hydrochloride Inhibitor inhibitor inhibit

 

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