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伊立替康盐酸盐 /Irinotecan hydrochloride 98%

货号:A309111 同义名: 盐酸伊立替康 / CPT-11 hydrochloride;VAL-413 Ambeed 开学季,买赠积分,赢豪礼

Irinotecan hydrochloride是一种拓扑异构酶I抑制剂,主要用于治疗结肠癌和直肠癌。

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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Irinotecan hydrochloride 化学结构 CAS号:100286-90-6
Irinotecan hydrochloride 化学结构
CAS号:100286-90-6
Irinotecan hydrochloride 3D分子结构
CAS号:100286-90-6
Irinotecan hydrochloride 化学结构 CAS号:100286-90-6
Irinotecan hydrochloride 3D分子结构 CAS号:100286-90-6
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Irinotecan hydrochloride 纯度/质量文件 产品仅供科研

货号:A309111 标准纯度: 98%
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1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
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1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Irinotecan hydrochloride 生物活性

描述 Irinotecan ((+)-Irinotecan) is a topoisomerase I inhibitor by preventing the DNA strand's religation through its binding to the topoisomerase I-DNA complex[1].
体内研究

Administered as Irinotecan (CPT-11, 5 mg/kg) through daily intratumoral injections for five days across two successive weeks in rats, and via continuous intraperitoneal infusion using an osmotic minipump in mice, it notably impedes tumor growth, whereas a dosage of 10 mg/kg exhibits no significant tumor growth inhibition by intraperitoneal injection[1].

Furthermore, Irinotecan (CPT-11, 100-300 mg/kg, i.p.) markedly diminishes tumor growth in HT-29 xenografts within athymic female mice by the 21st day. Combination treatments of Irinotecan (125 mg/kg) with TSP-1 (10 mg/kg per day) and Irinotecan (150 mg/kg) with TSP-1 (20 mg/kg per day) achieve tumor growth inhibition rates of 84% and 89%, respectively, surpassing the efficacy of Irinotecan alone at dosages of 250 and 300 mg/kg[3].

体外研究

As a potent topoisomerase I inhibitor, Irinotecan curtails the proliferation of LoVo and HT-29 cells, presenting IC50 values of 15.8 ± 5.1 and 5.17 ± 1.4 μM, respectively, and similarly induces cleavable complexes in both cell types[2].

Irinotecan also hampers the growth of human umbilical vein endothelial cells (HUVEC), showcasing an IC50 of 1.3 μM[3].

Irinotecan hydrochloride 参考文献

[1]Morales C, et al. Antitumoral effect of irinotecan (CPT-11) on an experimental model of malignant neuroectodermal tumor. J Neurooncol. 2002 Feb;56(3):219-26.

[2]Pavillard V, et al. Determinants of the cytotoxicity of irinotecan in two human colorectal tumor cell lines. Cancer Chemother Pharmacol. 2002 Apr;49(4):329-35. Epub 2002 Jan 30.

[3]Allegrini G, et al. Thrombospondin-1 plus irinotecan: a novel antiangiogenic-chemotherapeutic combination that inhibits the growth of advanced human colon tumor xenografts in mice. Cancer Chemother Pharmacol. 2004 Mar;53(3):261-6. Epub 2003 Dec 5.

Irinotecan hydrochloride 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.60mL

0.32mL

0.16mL

8.02mL

1.60mL

0.80mL

16.05mL

3.21mL

1.60mL

Irinotecan hydrochloride 技术信息

CAS号100286-90-6
分子式C33H39ClN4O6
分子量 623.139
别名 盐酸伊立替康 ;CPT-11 hydrochloride;VAL-413;(+)-Irinotecan hydrochloride
运输蓝冰
存储条件

粉末 Keep in dark place,Inert atmosphere,Room temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 120 mg/mL(192.57 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 3 mg/mL(4.81 mM),配合低频超声助溶

动物实验配方
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