Etoposide 依托泊苷

Etoposide 依托泊苷

货号:
IE0270

品牌:
Jinpan

Etoposide  依托泊苷

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产品简介
EC EINECS 251-509-1
MDL MFCD00869325
别名 依托泊甘; VP-16-213
CAS 33419-42-0
分子式 C29H32O13
分子量 588.56
纯度 HPLC≥98%
单位
生物活性 Etoposide是用于治疗多种癌症的化疗药物。 Etoposide通过与拓扑异构酶II和DNA形成复合物来抑制DNA合成。[1-3]
In Vitro 依托泊苷通过在RIN-m5F细胞中通过JNK / ERK介导的GSK-3下游触发的线粒体依赖性信号传导途径诱导细胞凋亡, 从而对胰腺β细胞产生细胞毒性[1]。依托泊苷和贝伐单抗显着消除了P1球形成能力, 这是一种与该细胞亚群凋亡相关的作用[2]。
In Vivo 静脉注射到免疫缺陷小鼠中的依托泊苷 (50μM) 和贝伐单抗治疗的缺氧细胞显示诱导肺集落的能力降低, 这也显示具有更长的潜伏期[2]。含有异环磷酰胺和卡铂的依托泊苷 (10 mg / kg /天, 静脉注射) 可降低注射肝母细胞瘤细胞的NMRI裸鼠的肿瘤体积[3]。
激酶实验 在不存在或存在Z-DEVD-FMK (20μM) 的情况下, 接种RIN-m5F细胞并用依托泊苷 (10-50μM) 处理。在处理结束时 (24小时) , 将细胞裂解物在37℃下与10μMAc-DEVD-AMC (半胱天冬酶-3 / CPP32底物) 一起温育1小时。通过分光荧光计测量裂解的基板的荧光, 激发波长为380nm, 发射波长为460nm。使用具有570nm吸收带的二辛可宁酸蛋白质测定试剂盒测定细胞裂解物样品的蛋白质水平, 以使对照和依托泊苷处理组之间的细胞数标准化。
SMILES O=C1OC[C@]2([H])[C@H](O[C@H]3[C@@H]([C@H]([C@@H]4O[C@H](C)OC[C@H]4O3)O)O)C5=C(C=C6OCOC6=C5)[C@@H](C7=CC(OC)=C(O)C(OC)=C7)[C@]21[H]
靶点 Topoisomerase
动物实验 建立了裸鼠HB (NMHB) 的体内模型。只有具有胚胎成分的HB细胞才能在该模型中成功移植和再生。随后将每个NMHB移植到50只小鼠中用于治疗组。当大多数肿瘤达到50-100mm 3的体积时开始治疗。根据肿瘤体积对小鼠进行分层, 随机分配给每组10只动物。注射肿瘤的动物在两个区块中给予异环磷酰胺, 顺铂, 多柔比星, 依托泊苷 (10mg / kg /天, iv) 和卡铂作为单一药剂。每组原始异种移植物的一组10只动物作为对照组。在开始治疗后, 以5天的间隔记录肿瘤生长25-30天, 并计算相对肿瘤体积。在处死动物前24小时, 腹膜内注射溴脱氧尿苷 (BrdU) 用于半定量测定肿瘤细胞的增殖活性 (50μgBrdU/ g体重) 。
细胞实验 RIN-m5F细胞是大鼠胰腺β-细胞系, 在37℃下在含有5%CO 2 -95%空气混合物的加湿室中培养, 并保持在补充有10%胎牛血清 (FBS) 的RPIM 1640培养基中。抗生素 (100 U / mL青霉素和100μg/ mL链霉素) 。将RIN-m5F细胞接种 (2×10 4个细胞/孔) 于96孔板中, 使其粘附并回收过夜。将细胞更换为新鲜培养基, 然后在不存在或存在药理学抑制剂 (氯化锂 (LiCl) -50μM; SP600125-20μM; PD98059-20μM) 的情况下与依托泊苷 (1-100μM) 孵育24小时。
数据来源文献 [1]. Lee KI, et al. Etoposide induces pancreatic β-cells cytotoxicity via the JNK/ERK/GSK-3 signaling-mediated mitochondria-dependent apoptosis pathway. Toxicol In Vitro. 2016 Jul 26. pii: S0887-2333 (16) 30147-3.

[2]. Calvani M, det al. Etoposide-Bevacizumab a new strategy against human melanoma cells expressing stem-like traits. Oncotarget. 2016 Jun 9. doi: 10.18632/oncotarget.9939.

[3]. Fuchs, J., et al. Comparative activity of cisplatin, ifosfamide, doxorubicin, carboplatin, and etoposide in heterotransplanted hepatoblastoma. Cancer, 1998. 83 (11) : p. 2400-7.

备注 以上数据均来自公开文献, Jinpan暂未进行独立验证, 仅供参考。These protocols are for reference only. Jinpan does not independently validate these methods.
规格 10mg 10mM*1mL (in DMSO) 50mg

通过抑制topoisomerase-II,从而抑制 DNA 复制。可以诱导细胞周期停滞,凋亡和自噬。

Etoposide

EtoposideCAS号: 33419-42-0分子式: C29H32O13分子量: 588.56描述纯度储存/保存方法别名外观可溶性/溶解性靶点In vitro(体外研究)In vivo(体内研究)

产品描述
描述

Etoposide is a semisynthetic derivative of podophyllotoxin, which inhibits DNA synthesis via topoisomerase II inhibition activity.

纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
依托泊苷; VP-16;VP-16-213
外观
White or off white crystalline powder
可溶性/溶解性
DMSO :58.9 mg/mL (100 mM)
生物活性
靶点
Topo II
In vitro(体外研究)
Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA, which induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent entry into the mitotic phase of cell division, and lead to cell death. Etoposide acts primarily in the G2 and S phases of the cell cycle. Etoposide inhibits the growth of murine angiosarcoma cell line (ISOS-1) in a 5 days-period with IC50 of 0.25 μg/mL. Cell growth of normal murine microvascular endothelial cells (mECs) is less sensitive to Etoposide with IC50 of 10 μg/mL). Etoposide treated for 6 hr inhibits colonies of tetraploid variant of the human leukemic lymphoblast line CCRF-CEM with IC50 of 0.6 μM. Etoposide treated for 2 hr inhibits growth of human pancreatic cancer cell line Y1, Y3, Y5, Y19, YM. YS, and YT with IC50s of 300 μg/mL, 300 μg/mL, 300 μg/mL, 91 μg/mL, 0.68 μg/mL, 300 μg/mL, 300 μg/mL, and 260 μg/mL, respectively. Etoposide exposed for 1 hr inhibits growth of human glioma cell lines CL5, G142, G152, G111, and G5 with IC50 of 8, 9, 9.8, 10, and 15.8 μg/mL respectively for 12 days. Under same condition, the IC90 value is attained in cell lines CL5, G152, G142, and G111 at 26, 27, 32, and 33 μg/mL. Etoposide inhibition of topoisomerase II is homogeneous for each cell. The average inhibition rates are 15%, 21.8%, 31.8%, 41.5%, and 49.5% for 1, 2, 4, 8, and 16 μg Etoposide, respectively.
In vivo(体内研究)
Etoposide administrated as a single agent is found to been ineffective in many xenografts growth, such as Heterotransplanted Hepatoblastoma NMHB1, and NMHB 2, human neuroblastoma xenograft, and human gastrointestinal cancer xenograft, while the dose of 10 mg/kg i.p. Etoposide inhibits murine angiosarcoma cell ISOS-1 tumors in 36% of controls. Etoposide induces tumor immunity in Lewis lung cancer. A single administration of 50 mg/kg Etoposide i.p., induces a 60% survival of C57B1/6 mice injected with Lewis lung cancer cell (3LL) over 60 days. About 40% of these surviving mice reject a subsequent challenge with 3LL, while none of control mice survive beyond 30 days. 3LL cells which have survived an 90% lethal concentration of Etoposide in vitro kill 75% of recipient mice, but 60% surviving mice reject challenge with 3LL. Splenocytes harvested from tumor rejecting mice protect naive mice injected with 3LL.

分子结构图

Etoposide