IO1290 双醋酚丁 抑制剂/拮抗剂/激动剂 索莱宝

IO1290 双醋酚丁 抑制剂/拮抗剂/激动剂 索莱宝

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  • ¥182 - 2478
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  • 北京
  • IO1290
  • 2025年07月23日
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    • 详细信息
    • 技术资料
    • 保存条件

      Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 保质期

      Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 英文名

      Oxyphenisatin Acetate

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • CAS号

      115-33-3

    • 规格

      25mg/50mg/100mg/5mg/10mg/500mg

    规格:25mg产品价格:¥482.0
    规格:50mg产品价格:¥676.0
    规格:100mg产品价格:¥988.0
    规格:5mg产品价格:¥182.0
    规格:10mg产品价格:¥300.0
    规格:500mg产品价格:¥2478.0

    基本信息
    CASNo.115-33-3
    中文名称双醋酚丁
    英文名称Oxyphenisatin Acetate
    别名双醋酚丁;Izafenin;Diphesatine;Brocatine;
    分子式C24H19NO5
    分子量401.41
    溶解性Soluble in DMSO
    纯度≥98%
    外观(性状)White to off-white Solid
    储存条件Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
    ECEINECS 204-083-6
    MDLMFCD00022793
    SMILESCC(=O)OC1=CC=C(C=C1)C2(C3=CC=CC=C3NC2=O)C4=CC=C(C=C4)OC(=O)C
    InChIKeyPHPUXYRXPHEJDF-UHFFFAOYSA-N
    InChIInChI=1S/C24H19NO5/c1-15(26)29-19-11-7-17(8-12-19)24(18-9-13-20(14-10-18)30-16(2)27)21-5-3-4-6-22(21)25-23(24)28/h3-14H,1-2H3,(H,25,28)
    PubChem CID8269
    靶点Others
    通路Others
    背景说明Oxyphenisatin Acetate是一种具有生物活性或化学活性的化合物。
    生物活性Oxphenisatin Acetate inhibits the growth of breast cancer cells by inhibiting translation, rapid phosphorylation. The pathways involved in apoptosis induction, starvation responses, and RNA/protein metabolism. Oxphenisatin Acetate also results in mitochondrial dysfunction.[1]
    In VitroOxyphenisatin acetate inhibits the growth of the breast cancer cell lines MCF7,T47D,HS578T,and MDA-MB-468. In the estrogen receptor(ER)positive MCF7 and T47D cells,oxyphenisatin acetate induces TNFα expression and TNFR1 degradation,indicating autocrine receptor-mediated apoptosis in these lines. Ten micromoles per liter Oxyphenisatin acetate treatment results in autophagy and mitochondrial dysfunction[1].In the estrogen receptor(ER)positive MCF7 and T47D cells,OXY induced TNFα expression and TNFR1 degradation,indicating autocrine receptor-mediated apoptosis in these lines. Lastly,in an MCF7 xenograft model,OXY delivered intraperitoneally inhibited tumor growth,accompanied by phosphorylation of eIF2α and degradation of TNFR1. OXY induces a multifaceted cell starvation response,which ultimately induces programmed cell death[1].
    细胞实验Oxyphenisatin acetate(300 mg/kg,i.p.)delivers intraperitoneally inhibited tumor growth,accompanied by phosphorylation of eIF2α and degradation of TNFR1 in an MCF7 xenograft model[1].
    细胞实验Total RNA was isolated from MCF7 cells treated with 10 μmol/L OXY for 24 h and the microarray procedure performed as described previously using the GeneChip Human U133 plus 2.0 array . Pairwise analysis was performed on control versus treated arrays using a fivefold change cutoff,<0.01 adjusted P-value,GC-RMA normalization with Benjamini–Hochberg false discovery estimation[1].
    动物实验Assessment in several other tumor models demonstrates tolerability with oxyphenisatin acetate at 300 mg/kg given once daily or 200 mg/kg given twice daily. For the MCF-7 study treatments are administered on an exact body weight basis using dose volumes of 1-2 mL/kg body weight. The vehicle control receives 100% DMSO. The treated group receives 300 mg/kg oxyphenisatin acetate once daily for a total of 10 days,followed by a 3 day rest and an additional 6 days of dosing. The dose solutions are prepared in 100% DMSO,aliquoted and stored frozen until used. The mice are monitored for a total of 52 days with treatment initiation occurring on day 27 posttumor implantation[1].
    数据来源文献[1]. Morrison BL, et al. Oxyphenisatin acetate (NSC 59687) triggers a cell starvation response leading to autophagy, mitochondrial dysfunction, and autocrine TNFα-mediated apoptosis. Cancer Med. 2013 Oct;2(5):687-700.
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    ¥182 - 2478