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(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE

(E)-2
(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE
CAS号:
130306-02-4
英文名:
(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE
英文别名:
tezaciabine;(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE;2'-deoxy-2'-(fluoromethylene)-(2E)Cytidine;Cytidine, 2'-deoxy-2'-(fluoromethylene)-, (2'E)-
中文名:
(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE
中文别名:
替扎西他滨;化合物 TEZACITABINE
CBNumber:
CB3221204
分子式:
C10H12FN3O4
分子量:
257.22
MOL File:
130306-02-4.mol

(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE化学性质

沸点:
512.5±60.0 °C(Predicted)
密度:
1.71±0.1 g/cm3(Predicted)
储存条件:
-80°C
溶解度:
DMSO : 200 mg/mL (777.54 mM; Need ultrasonic)
酸度系数(pKa):
12.50±0.60(Predicted)
安全信息

(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE性质、用途与生产工艺

生物活性

Tezacitabine 是一种具有细胞生长抑制和细胞毒性的抗代谢药,是一种核苷类似物。Tezacitabine 不可逆地抑制核糖核苷酸还原酶 (ribonucleotide reductase) 并干扰 DNA 复制和修复。Tezacitabine 有效诱导细胞凋亡 (apoptotic),可用于白血病和实体瘤的研究。

靶点

Ribonucleotide reductase

体外研究

Tezacitabine (0.01-10 µM; 24 hours; CCRF-SB, KG-1, Jurkat, COLO-205, MCF-7 and PC-3 cells) treatment induces the G1 and S-phase leaky block of the cell cycle.
Tezacitabine (0.01-10 µM; 24 hours; CCRF-SB, KG-1, Jurkat, COLO-205, MCF-7 and PC-3 cells) treatment apoptotic death of cells by the caspase 3/7 pathway in a concentration-dependent manner.
Tezacitabine has strong cytostatic and cytotoxic properties. Cytotoxic effect of Tezacitabine reveals not only as apoptosis, but also as a change in protein metabolism.

Cell Cycle Analysis

Cell Line: CCRF-SB, KG-1, Jurkat, COLO-205, MCF-7 and PC-3 cells
Concentration: 0.01 µM, 0.1 µM, 1.0 µM, and 10 µM
Incubation Time: 24 hours
Result: Induced the G1 (at concentrations higher than 10 nM) and S-phase (at low concentration) leaky block of the cell cycle.

Apoptosis Analysis

Cell Line: CCRF-SB, KG-1, Jurkat, COLO-205, MCF-7 and PC-3 cells
Concentration: 0.01 µM, 0.1 µM, 1.0 µM, and 10 µM
Incubation Time: 24 hours
Result: Induced apoptotic death of cells by the caspase 3/7 pathway in a concentration-dependent manner.

体内研究

Tezacitabine (100 mg/kg; intraperitoneal injection; daily; female nude mice) treatment inhibits tumor growth in HCT 116 tumor xenografts.

Animal Model: Female nude mice (7-9-week-old) injected with HCT 116 cells
Dosage: 100 mg/kg
Administration: Intraperitoneal injection; daily; 14 days
Result: Inhibited tumor growth in HCT 116 tumor xenografts.

(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE 上下游产品信息

上游原料

下游产品


(E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE 生产厂家

全球有 14家供应商   (E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE国内生产厂家
供应商联系电话电子邮件国家产品数优势度
北京普西唐生物科技有限公司 010-60605840 18892239720 psaitong@jm-bio.com 中国 12308 58
NewCan Biotech Limited +86-0571-86912261 +8613735419629 sales@newcanbio.com 中国 9980 58
BOC Sciences 16314854226; +16314854226 inquiry@bocsci.com 美国 19743 58
天津普西唐生物医药科技有限公司 010-60605840 psaitong@jm-bio.com 中国 29778 58
常州博嘉生物医药科技有限公司 2122619822 czbjpharma@126.com 中国 18488 58
TargetMol中国(陶术生物) 4008200310 marketing@tsbiochem.com 中国 24018 58
銳迪國際科技有限公司 18024082417 market@ubiochem.com 中国 9180 58
 

130306-02-4, (E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE 相关搜索:

  • C10H12FN3O4
  • 化合物 TEZACITABINE
  • 替扎西他滨
  • 130306-02-4
  • 2'-deoxy-2'-(fluoromethylene)-(2E)Cytidine
  • Cytidine, 2'-deoxy-2'-(fluoromethylene)-, (2'E)-
  • tezaciabine
  • (E)-2'-DEOXY-2'-(FLUOROMETHYLENE) CYTIDINE
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