Batabulin
CAS No. 195533-53-0
Batabulin ( T138067 )
产品货号. M23886 CAS No. 195533-53-0
Batabulin 是一种抗肿瘤化合物,它与 β-微管蛋白同种型的子集共价且选择性结合,从而破坏微管聚合。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1169 | 有现货 |
|
| 10MG | ¥1739 | 有现货 |
|
| 25MG | ¥2939 | 有现货 |
|
| 50MG | ¥4334 | 有现货 |
|
| 100MG | ¥5841 | 有现货 |
|
| 500MG | ¥11520 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥941 | 有现货 |
|
生物学信息
-
产品名称Batabulin
-
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
-
产品简述Batabulin 是一种抗肿瘤化合物,它与 β-微管蛋白同种型的子集共价且选择性结合,从而破坏微管聚合。
-
产品描述Batabulin is an antitumor compound, which binds covalently and selectively to a subset of the β-tubulin isotypes, thereby disrupting microtubule polymerization. Batabulin affects cell morphology and leads to cell-cycle arrest ultimately induce apoptotic cell death.
-
体外实验Cell Cycle Analysis Cell Line:MCF7 cells Concentration:30 nM, 100 nM and 300 nM Incubation Time:24 hours Result:Showed an arrest at the G2/M cell-cycle boundary.Apoptosis Analysis Cell Line:MCF7 cells Concentration:30 nM, 100 nM and 300 nM Incubation Time:24 hours or 48 hours Result:25-30% of cells showed the reduced DNA content characteristic of apoptotic cells.
-
体内实验Animal Model:Male athymic nude mice (nu/nu) (6-8 week-old, 20-25 g) injected with CCRF-CEM cells Dosage:40 mg/kg Administration:Intraperitoneal injection; once per week; on days 5, 12, and 19 Result:Impaired the growth of the drug-sensitive CCRF-CEM tumors.
-
同义词T138067
-
通路Apoptosis
-
靶点Apoptosis
-
受体Apoptosis|Tubulin β
-
研究领域——
-
适应症——
化学信息
-
CAS Number195533-53-0
-
分子量371.26
-
分子式C13H7F6NO3S
-
纯度>98% (HPLC)
-
溶解度DMSO:100 mg/mL (269.35 mM; Need ultrasonic)
-
SMILESO=S(C1=C(F)C(F)=C(F)C(F)=C1F)(NC2=CC=C(OC)C(F)=C2)=O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Shan B, et al. Selective, covalent modification of beta-tubulin residue Cys-239 by T138067, an antitumor agent with in vivo efficacy against multidrug-resistant tumors. Proc Natl Acad Sci U S A. 1999 May 11;96(10):5686-91.
产品手册
关联产品
-
Methyl pyropheophorb...
Methyl pyropheophorbide-a (Pyropheophorbide-a methyl ester),叶绿素 a 的衍生物,是一种有效的光敏剂,可用于癌症的光动力疗法 (PDT)。Methyl pyropheophorbide-a 具有光动力学活性,可以诱导细胞凋亡并抑制肿瘤的生长。
-
Taurodeoxycholic aci...
Taurodeoxycholic acid 是一种胆汁酸,可稳定线粒体膜,减少自由基形成。Taurodeoxycholic acid 通过阻断钙介导的凋亡通路以及 Caspase-12 激活来抑制凋亡 (apoptosis)。Taurodeoxycholic acid 对 3-硝基丙酸诱导或稳定遗传的亨廷顿舞蹈病 (HD) 小鼠模型具有神经保护作用。
-
TD52
TD52 是 PP2A (CIP2A) 癌抑制剂的口服活性抑制剂。 TD52 是厄洛替尼衍生物,通过干扰 Elk1 与 CIP2A 启动子的结合来间接降低 CIP2A。
021-51111890
购物车()
sales@molnova.cn

