SKLB-23bb
CAS No. 1815580-06-3
SKLB-23bb ( —— )
产品货号. M20404 CAS No. 1815580-06-3
SKLB-23bb 是一种口服生物可利用的 HDAC6 选择性抑制剂,还具有微管破坏能力。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥1256 | 有现货 |
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| 5MG | ¥2535 | 有现货 |
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| 10MG | ¥3702 | 有现货 |
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| 25MG | ¥6099 | 有现货 |
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| 50MG | ¥8586 | 有现货 |
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| 100MG | ¥11583 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称SKLB-23bb
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SKLB-23bb 是一种口服生物可利用的 HDAC6 选择性抑制剂,还具有微管破坏能力。
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产品描述SKLB-23bb is an orally bioavailable HDAC6-selective inhibitor and also has microtubule-disrupting ability.
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体外实验SKLB-23bb (Compound 23bb) presents low nanomolar antiproliferative effects against panel of cancer cell lines. The antiproliferative activity is ton human malignant melanoma A375 cells and cervical cancer HeLa cells, SKLB-23bb shows the most potent activities with IC50 values of 50 and 49 nM on A375 and HeLa cells, respectively. The antiproliferative activities against 11 kinds of hematological tumors (myelomaU266, RPMI8226 cells, human leukemia MV4-11, K562 cells, and human B cell lymphoma Ramos cells) or solid tumors (ovarian cancer A2780s, SKOV-3 cells, breast cancer SKBR3 cells, liver cancer HepG2 cells, lung cancer H460, A549 cells, cervical cancer HeLa cells and colon cancer HCT116, HT29 cells) cell lines of SKLB-23bb are evaluated by MTT, and the SAHA and ACY-1215 are as positive control. SKLB-23bb shows significant antiproliferative potential with the IC50 values ranging from 14 to 104 nM in these tumor cell lines.
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体内实验SKLB-23bb (Compound 23bb) reduces the tumor growth in both the hematological tumor MV4-11 xenograft model and solid tumor HCT116 xenograft model. The significant antitumor activities are observed by intravenous administration of SKLB-23bb at 50 mg/kg on MV4-11 and HCT116 xenograft models. The growth of MV4-11 and HCT116 cancer cell xenografts is suppressed by 55.0% and 76.3% (percent of tumor mass change [TGI] values) after iv administration of SKLB-23bb at 50 mg/kg. The HCT116 xenograft model is also established to investigate the antitumor activity of oral administration of SKLB-23bb. The TGI value of oral administration of SKLB-23bb (25 mg/kg) on HCT116 xenograft model is 60.4%, which is superior to the SAHA group (100 mg/kg, 59.2%). Additionally, the body weight decrease is acceptable and no other adverse effects are observed upon treatment with SKLB-23bb. Low clearance (CL=7.008 L/kg per hour for iv, CL=12.877 L/kg per hour for po) and long terminal half-life (t1/2=7.658 h for iv, t1/2=9.62 h for po) are observed in SKLB-23bb. The oral bioavailability of SKLB-23bb is excellent in rats and the bioavailability is up to 47.0%.
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同义词——
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通路Cell Cycle/DNA Damage
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靶点HDAC
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受体HDAC6
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研究领域——
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适应症——
化学信息
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CAS Number1815580-06-3
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分子量396.44
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分子式C21H24N4O4?
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纯度>98% (HPLC)
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溶解度DMSO:32 mg/mL (80.72 mM)
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SMILESCOc1ccc(cc1OCCCC(=O)NO)N(C)c1nc(C)nc2ccccc12
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化学全称Butanamide N-hydroxy-4-[2-methoxy-5-[methyl(2-methyl-4-quinazolinyl)amino]phenoxy]-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Yang Z Wang T Wang F et al. Discovery of Selective Histone Deacetylase 6 Inhibitors Using the Quinazolin as the Cap for the Treatment of Cancer[J]. Journal of Medicinal Chemistry 2015 59(4):1455-1470.
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