品牌	貨號(hào)	產(chǎn)品規(guī)格	價(jià)格(RMB)	庫存（上海）	北京	武漢	南京
源葉(MedMol)	S80020-2mg	97%	￥255.00元	5	-	-	-
源葉(MedMol)	S80020-5mg	97%	￥335.00元	6	-	-	-
源葉(MedMol)	S80020-10mg	97%	￥425.00元	4	-	-	-
源葉(MedMol)	S80020-50mg	97%	￥1540.00元	4	-	-	-
源葉(MedMol)	S80020-100mg	97%	￥2450.00元	2	-	-	-

產(chǎn)品介紹

CUDC-101 is a potent inhibitor of HDAC, EGFR, and HER2 with IC50s of 4.4, 2.4, and 15.7 nM, respectively.

產(chǎn)品描述： CUDC-101 is a potent inhibitor of HDAC, EGFR, and HER2 with IC50s of 4.4, 2.4, and 15.7 nM, respectively.

靶點(diǎn)： EGFR:2.4 nM (IC50);HER2:15.7 nM (IC50);HDAC:4.4 nM (IC50);HDAC1:4.5 nM (IC50);HDAC2:12.6 nM (IC50);HDAC3:9.1 nM (IC50);HDAC4:13.2 nM (IC50);HDAC6:5.1 nM (IC50);HDAC5:11.4 nM (IC50);HDAC9:67.2 nM (IC50);HDAC10:26.1 nM (IC50);HDAC8:79.8 nM (IC50);HDAC7:373 nM (IC50);EGFR;HER;HDAC

體內(nèi)研究：
CUDC-101 (120 mg/kg, iv, daily) induces tumor regression in the Hep-G2 liver cancer model and is more efficacious than erlotinib at its maximum tolerated dose (MTD). In the erlotinib-resistant A549 NSCLC xenograft model, CUDC-101 (120 mg/kg) shows potent inhibition of tumor growth. In the erlotinib-sensitive H358 NSCLC models, CUDC-101 (15, 30, 60 mg/kg, i.v.) inhibits tumor growth in a dose-dependent manner. CUDC-101 (120 mg/kg) causes significant tumor regression in the lapatinib-resistant, HER2-negative, EGFR-overexpressing MDA-MB-468 breast cancer model and the EGFR-overexpressing CAL-27 head and neck squamous cell carcinoma (HNSCC) model. CUDC-101 (120 mg/kg) also inhibits tumor growth in the K-ras mutant HCT116 colorectal and EGFR/HER2 (neu)-expressing HPAC pancreatic cancer models. In an in vivo mouse model of metastatic ATC, CUDC-101 inhibits tumor growth and metastases, and significantly prolongs survival. CUDC-101 (120 mg/kg) is effective against a broad range of tumor types in xenograft models

參考文獻(xiàn)：
1. Xiong Cai et al Discovery of 7-(4-(3-Ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDC-101) as a Potent Multi-Acting HDAC, EGFR, and HER2 Inhibitor for the Treatment of Cancer J. Med. Chem., 2010, 53 (5), pp 2000–2009 2. Lai CJ, et al. CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity.Cancer Res. 2010 May 1;70(9):3647-56. Epub 2010 Apr 13. 3. Sun H, et al. CUDC-101, a Novel Inhibitor of Full-Length Androgen Receptor (flAR) and Androgen Receptor Variant 7 (AR-V7) Activity: Mechanism of Action and In Vivo Efficacy. Horm Cancer. 2016 Jun;7(3):196-210. 4. Zhang L, et al. Dual inhibition of HDAC and EGFR signaling with CUDC-101 induces potent suppression of tumor growth and metastasis in anaplastic thyroid cancer. Oncotarget. 2015 Apr 20;6(11):9073-85.

溶解性： Soluble in DMSO

保存條件： -20℃

配置溶液濃度參考：

	1mg	5mg	10mg
1 mM	2.302 ml	11.508 ml	23.015 ml
5 mM	0.46 ml	2.302 ml	4.603 ml
10 mM	0.23 ml	1.151 ml	2.302 ml
50 mM	0.046 ml	0.23 ml	0.46 ml

注意：

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參考文獻(xiàn)

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