产品封面图

Colchicine秋水仙碱,64-86-8

收藏
  • ¥220 - 650
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-16569
  • 2025年12月05日
    avatar
    品牌商
    14钻石会员
  • 企业认证

    点击 QQ 联系

    • 详细信息
    • 文献和实验
    • 技术资料
    • 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

    MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。

    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.

    相关产品:Natural Product Library Plus  |  Drug Repurposing Compound Library Plus  |  FDA-Approved Drug Library Plus  |  FDA-Approved Drug Library Mini  |  Bioactive Compound Library Plus  |  Apoptosis Compound Library  |  Cell Cycle/DNA Damage Compound Library  |  Natural Product Library  |  FDA-Approved Drug Library  |  Anti-Cancer Compound Library  |  Antiviral Compound Library  |  Autophagy Compound Library  |  Anti-Aging Compound Library  |  Drug Repurposing Compound Library  |  NMPA-Approved Drug Library  |  Medicine Food Homology Compound Library  |  Pyroptosis Compound Library  |  Cytoskeleton Compound Library  |  Orally Active Compound Library  |  Traditional Chinese Medicine Active Compound Library  |  FDA Approved & Pharmacopeial Drug Library  |  Anti-Lung Cancer Compound Library  |  Drug-Induced Liver Injury (DILI) Compound Library  |  Rare Diseases Drug Library  |  Children’s Drug Library  |  Anti-Cancer Natural Product Library  |  Protein-protein Interaction Inhibitor Library  |  Plant-Sourced Natural Product Library  |  FDA-Approved Anticancer Drug Library  |  Human Metabolite Library  |  Anti-Prostate Cancer Compound Library  |  Anti-Pulmonary Fibrosis Compound Library  |  Non-steroidal Anti-Inflammatory Compound Library  |  Pain-Related Compound Library  |  Off-patent Drug Library  |  Mitochondrial Toxicity Compound Library  |  Cell Death Library  |  FDA-Approved Traditional Chinese Medicine Active Compound Library  |  MG-132  |  Doxorubicin hydrochloride  |  Bafilomycin A1  |  LY294002  |  Tamoxifen  |  Paclitaxel  |  Y-27632  |  Acetylcysteine  |  Angiotensin II human  |  2-Deoxy-D-glucose  |  Staurosporine  |  SB-431542  |  Actinomycin D  |  Deferoxamine mesylate  |  Bortezomib  |  5-Fluorouracil  |  Trametinib  |  Sorafenib  |  Oxaliplatin  |  Gemcitabine  |  Temozolomide  |  Rotenone  |  Mdivi-1  |  Elesclomol  |  Ruxolitinib  |  Decitabine  |  SP600125  |  MK-2206 dihydrochloride  |  Etoposide  |  Monomethyl auristatin E

    热门产品线:重组蛋白  |  化合物库  |  天然产物  |  荧光染料  |  PROTAC  |  同位素标记物

    Trending products:Recombinant Proteins  |  Bioactive Screening Libraries  |  Natural Products  |  Dye Reagents  |  PROTAC  |  Isotope-Labeled Compounds

    类药多样性化合物库
    顾客使用MCE产品发表的科研文献
    一站式药筛新体验
    MCE 您身边的生物活性分子大师 | 抑制剂、激动剂、化合物库
    重组蛋白 | 高纯度、高稳定性
    磁珠
    MCE Hotline: 4008203792 | 中国现货 - 全球文献引用 - 高纯度高品质 - 全方位技术支持

    风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。

    图标文献和实验
    相关实验
    • 秋水仙碱 colchicine

      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

    • 化学诱变染色体加倍及其鉴定

      是诱导产生多倍体,常用的 试剂 是秋水仙碱Colchicine);另一类是诱发基因突变或染色体断裂,如甲基磺酸乙酯等烷化剂。前者的应用较多、较广泛。 秋水仙碱是从百合科植物秋水仙中提取出来的植物碱,极毒,易溶于冷水和酒精中。用于园艺植物诱变育种的秋水仙碱的有效浓为0.1%~1%,以0.2%最有效。秋水仙碱诱变是通过阻断纺锤体的正常形成,使染色体不能分离而导致加倍。由于有效诱变只发生在细胞分裂状态活跃的细胞、组织,所以常用萌动或萌发的种子、幼苗或生长旺盛的茎尖

    图标技术资料

    暂无技术资料 索取技术资料

    同类产品报价

    产品名称
    产品价格
    公司名称
    报价日期
    询价
    上海研生实业有限公司
    2025年07月16日询价
    ¥200
    上海研谨生物科技有限公司
    2025年11月11日询价
    询价
    上海北诺生物科技有限公司
    2025年07月10日询价
    询价
    江西江蓝纯生物试剂有限公司
    2025年11月20日询价
    Colchicine秋水仙碱,64-86-8
    ¥220 - 650