• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Methyl pyropheophorbide-a

CAS No. 6453-67-4

Methyl pyropheophorbide-a ( —— )

产品货号. M34657 CAS No. 6453-67-4

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。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥413 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Methyl pyropheophorbide-a
  • 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
    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。
  • 产品描述
    Methyl pyropheophorbide-a (Pyropheophorbide-a methyl ester), a chlorophyll-a derivative, is a potent photosensitizer that can be used in photodynamic therapy (PDT) of cancer. Methyl pyropheophorbide-a has photodynamic activity and can induce apoptosis and inhibit tumor growth.
  • 体外实验
    Pyropheophorbide-a methyl ester (2 μM; 12 h) inhibits the cell cycle progression from the G0/G1-phases and induces apoptosis at the light dosage of 55.6 kJ/m2 in PC-3M cells.Pyropheophorbide-a methyl ester (0.2-15 μM; 20 h) has no signi?cant dark cytotoxicity in NCI-h446 cells.Pyropheophorbide-a methyl ester (0.1-15 μM; 20 h) mediates a dose-dependent photocytotoxicity in the NCI-h446 cells.Pyropheophorbide-a methyl ester (2-4 μM; 0-24 h) induces apoptosis of NCI-h446 cells in a time-dependent manner.Pyropheophorbide-a methyl ester (0.5-4 μM; 0-20 h) shows a photocytotoxicity in PC-3M cells.Apoptosis Analysis Cell Line:PC-3M cells Concentration:2 μM Incubation Time:12 h Result:Apoptosis rate was about 0.27%, 6.15%, 20.49%, 50.76%, 65.39%, 64.92%, and 64.37% at 1, 3, 6, 12, 18, and 24 h posttreatment, respectively under the conditions of LC75 (2 μM+55.6 kJ/m2).
  • 体内实验
    Pyropheophorbide-a methyl ester (15 mg/kg; tail vein and topical injection) inhibits the growth of PC-3M tumors in mice.Animal Model:Male BALB/c nude mice (6-8 weeks, 16-20 g) bearing PC-3M tumor Dosage:15 mg/kg Administration:Tail vein injection and topical injection Result:The tumor volume and the weight inhibition rate were 46.78%, 41.84% in tail vein injection group and 78.66%, 72.07% in topical injection group, respectively.
  • 同义词
    ——
  • 通路
    Apoptosis
  • 靶点
    Apoptosis
  • 受体
    Apoptosis
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    6453-67-4
  • 分子量
    548.67
  • 分子式
    C34H36N4O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO 中的溶解度 : 2.5 mg/mL (4.56 mM; 超声助溶 (<60°C)
  • SMILES
    CCc1c(C)c2cc3[nH]c(cc4nc([C@@H](CCC(=O)OC)[C@@H]4C)c4CC(=O)c5c(C)c(cc1n2)[nH]c45)c(C)c3C=C
  • 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. Sun X, et, al. Photodynamic therapy with pyropheophorbide-a methyl ester in human lung carcinoma cancer cell: efficacy, localization and apoptosis. Photochem Photobiol. 2002 Jun;75(6):644-51.?
产品手册
关联产品
  • Imipramine

    Imipramine 是一种具有口服活性的叔胺类三环抗抑郁药。Imipramine 是一种具有抗肿瘤活性的 Fascin1 抑制剂。Imipramine 也抑制 5-羟色胺转运体 (serotonin transporter),其 IC50 值为 32 nM。Imipramine 刺激 U-87MG 胶质瘤细胞自噬(autophagy),诱导 HL-60 细胞凋亡(apoptosis)。Imipramine 具有神经保护和免疫调节作用。

  • ZINC69391

    ZINC69391 是一种选择性 Rac1 抑制剂,具有抗增殖和抗转移作用。 ZINC69391 干扰 Rac1 与 Dock180 的相互作用,降低 Rac1-GTP 水平并诱导细胞凋亡。

  • TVB-3166

    TVB-3166 诱导细胞凋亡并抑制体内异种移植肿瘤生长。 TVB-3166 是一种可逆、选择性脂肪酸合酶抑制剂(生化 FASN 和细胞棕榈酸酯合成的 IC50 分别为 42 nM 和 81 nM)。