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IA1010 积雪草酸 抑制剂/拮抗剂/激动剂 索莱宝

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  • ¥150 - 740
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  • 北京
  • IA1010
  • 2025年12月26日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 保质期

      Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year

    • 英文名

      Asiatic acid

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • CAS号

      464-92-6

    • 规格

      100mg/50mg/10mM*1mL in DMSO/20mg/10mg/5mg

    规格:100mg产品价格:¥740.0
    规格:50mg产品价格:¥490.0
    规格:10mM*1mL in DMSO产品价格:¥160.0
    规格:20mg产品价格:¥360.0
    规格:10mg产品价格:¥240.0
    规格:5mg产品价格:¥150.0

    是一种五环三萜,可诱导黑色素瘤细胞的凋亡。还具有抗炎活性。

    基本信息
    CASNo.464-92-6
    中文名称积雪草酸
    英文名称Asiatic acid
    别名Dammarolic acid
    分子式C30H48O5
    分子量488.7
    溶解性Soluble in DMSO
    纯度HPLC≥98%
    外观(性状)White to off-white Solid
    储存条件Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
    ECEINECS 482-720-9
    MDLMFCD00238541
    SMILESO=C([C@]12CC[C@@H](C)[C@H](C)[C@@]1([H])C3=CC[C@]4([H])[C@@]5(C)C[C@@H](O)[C@H](O)[C@@](C)(CO)[C@]5([H])CC[C@@]4(C)[C@]3(C)CC2)O
    InChIKeyJXSVIVRDWWRQRT-UYDOISQJSA-N
    InChIInChI=1S/C30H48O5/c1-17-9-12-30(25(34)35)14-13-28(5)19(23(30)18(17)2)7-8-22-26(3)15-20(32)24(33)27(4,16-31)21(26)10-11-29(22,28)6/h7,17-18,20-24,31-33H,8-16H2,1-6H3,(H,34,35)/t17-,18+,20-,21-,22-,23+,24+,26+,27+,28-,29-,30+/m1/s
    PubChem CID119034
    靶点p38MAPK
    通路MAPK
    背景说明是一种五环三萜,可诱导黑色素瘤细胞的凋亡。还具有抗炎活性。
    生物活性Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2].
    In VitroAA decreased viability and induced apoptosis in human melanoma SK-MEL-2 cells in a time- and dose-dependent manner. AA also markedly increased intracellular reactive oxygen species(ROS)level and enhanced the expression of Bax but not Bcl-2 protein in the cells. In addition,AA-induced activation of caspase-3 activity in a dose-dependent manner.[1]
    细胞实验Treatment of male ICR mice with AA significantly inhibited the numbers of acetic acid-induced writhing responses and the formalin-induced pain in the late phase. In the anti-inflammatory test,AA decreased the paw edema at the 4th and 5th h after λ-carrageenan(Carr)administration and increased the activities of catalase(CAT),superoxide dismutase(SOD),and glutathione peroxidase(GPx)in the liver tissue. AA decreased the nitric oxide(NO),tumor necrosis factor-α(TNF-α),and interleukin-1β(IL-1β)levels on serum level at the 5th h after Carr injection. Western blotting revealed that AA decreased Carr-induced inducible nitric oxide synthase(iNOS),cyclooxygenase(COX-2),and nuclear factor-κB(NF-κB)expressions at the 5th h in the edema paw. An intraperitoneal(i.p.)injection treatment with AA also diminished neutrophil infiltration into sites of inflammation as did indomethacin(Indo).[2]
    数据来源文献[1]. Park BC, et al. Asiatic acid induces apoptosis in SK-MEL-2 human melanoma cells. Cancer Lett. 2005 Jan 31;218(1):81-90.
    [2]. Huang SS, et al. Antinociceptive activities and the mechanisms of anti-inflammation of asiatic Acid in mice. Evid Based Complement Alternat Med. 2011;2011:895857.
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    • 【求助】蛋白激酶C的信号通路

      2F+DwTquooTcizAj6Sh40arj1e+iWJ2ispgsbT801bWi9OaaVDQ0u7N9Rf22Q7je3ypEkT/aXtAx/4gHh20RbetchuWXizve3YY/3L0LGHHqt8Cva+97zf/vEfvyYb4imWXpTxLz8m4rvgjodswc3X26Xnn2o3LbjZPv/Fv5GGuGa33/ZzO2n2HD17NAEWeUXwmQh44uy32U+uutL+69e+6jjedfsddvSxx3m8xNNFQ67wipqQKHyESZ35

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