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- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
64-86-8
- 规格:
10 mM * 1 mL/100 mg/200 mg/500 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥500.0 |
|---|---|---|---|
| 规格: | 100 mg | 产品价格: | ¥220.0 |
| 规格: | 200 mg | 产品价格: | ¥350.0 |
| 规格: | 500 mg | 产品价格: | ¥650.0 |
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Colchicine
CAS No. : 64-86-8
MCE 国际站:Colchicine
产品活性:Colchicine 是微管蛋白 (tubulin) 抑制剂和微管 (microtubule) 干扰剂。 Colchicine 抑制微管聚合的 IC50 为 3 nM。Colchicine 还是 α3 甘氨酸受体 (GlyRs) 的竞争性拮抗剂。
研究领域:Cell Cycle/DNA Damage | Cytoskeleton | Autophagy | Apoptosis
作用靶点:Microtubule/Tubulin | Autophagy | Apoptosis
In Vitro: Exposure to 1μM Colchicine, a microtubule disrupting agent, triggered apoptosis in rat cerebellar granule cells (CGC). Colchicine treatment also causes alterations in Ca2+ responses to chemical depolarization and a moderate, but progressive, increase in the resting intracellular Ca2+ concentration. Colchicine exerts its biological effects through binding to the soluble tubulin heterodimer, the major component of the microtubule. The Colchicine binding abilities of tubulins from a variety of sources are summarized, and the mechanism of Colchicine binding to brain tubulin is explored in depth. The relationship between colchicinoid structure and tubulin binding activity provides insight into the structural features of Colchicine responsible for high affinity binding to tubulin and is reviewed for analogs in the Colchicine series. The thermodynamic and kinetic aspects of the association are described and evaluated in terms of the binding mechanism. Colchicine binding to tubulin results in unusual alterations in the low energy electronic spectra of Colchicine. The spectroscopic features of Colchicine bound to tubulin are discussed in terms of the nature of the Colchicine-tubulin complex. Attempts to locate the high affinity Colchicine binding site on tubulin are presented. Colchicine treatment inhibits indomethacin-induced small intestinal injury by 86% (1 mg/kg) and 94% (3 mg/kg) as indicated by the lesion index 24 h after indomethacin administration. Colchicine inhibits the protein expression of cleaved caspase-1 and mature IL-1β, without affecting the mRNA expression of NLRP3 and IL-1β.
In Vivo: Vehicle or Colchicine (1 mg/kg) is administered orally 30 min prior to indomethacin administration. The lesions stained with Evans blue in the small intestine are smaller in Colchicine-treated mice than those in vehicle-treated mice 24 h after indomethacin administration. In addition, histological examination shows that Colchicine-treated mice have less mucosal inflammation and ulceration and a decrease in the size and numbers of lesions compared with vehicle-treated mice. Colchicine treatment significantly reduces the lesion index at doses of 1 mg/kg and 3 mg/kg (by 86% and 94%, respectively) compared with vehicle treatment. Colchicine treatment significantly inhibits the protein levels of mature IL-1β at doses of 1 mg/kg and 3 mg/kg (by 56% and 69%, respectively) without affecting those of pro-IL-1β. Colchicine treatment also significantly inhibits the protein levels of cleaved caspase-1 at doses of 1 mg/kg and 3 mg/kg (by 26% and 39%, respectively) without affecting those of pro-caspase-1.
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文献和实验从百合科的秋水仙(Colchicine autumnale)的种子、鳞茎中提取出的生物碱。呈淡黄色结晶或粉末状,是七元环化合物(分子量为 399.43)。于 1934年 A. P. Dustin发现该药物可引起染色体增大,从而导致巨核形成。 R. J. Ludford( 1936), L. Havas( 1937), P. Gavandan( 1937), A Levan( 1937)等阐明,染色体的成倍增长是由于秋水仙碱抑制了纺锤体的形成和阻碍了纺锤体的机能诱发起来的。 Levan
全国 3.30 亿多心血管疾病患者的希望?2020 年度心血管领域十大研究盘点
管疾病的极大危害性,有关心血管疾病防治的研究,对于降低心血管病发病率,提高患者生活质量,改善预后有着重要意义。今天,丁香学术为大家盘点了 2020 年十大心血管领域前沿进展,其中囊括了心脏病干细胞治疗、心脏代谢组学、肠道微生物、心脏单细胞图谱、猪心移植、人造血管、高血压定义、秋水仙碱老药新用... 诸多顶级期刊基础与临床研究进展,与读者共飨。 1、Nature:南大鼓楼医院王东进完成「世界首例」心脏病干细胞治疗几十年来,心脏病是世界范围内导致死亡的主要原因,研究人员一直试图用成年干细胞治疗心脏病,但这种
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