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Tanshinone IIA sulfonate丹参酮IIA

磺酸盐,69659-80-9
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  • ¥312 - 4475
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-N1370
  • 2025年12月05日
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    • 详细信息
    • 技术资料
    • 保存条件

      4°C, sealed storage, away from moisture

    • 英文名

      Sodium Tanshinone IIA sulfonate; Tanshinone IIA sodium sulfonate

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      69659-80-9

    • 规格

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

    规格:5 mg产品价格:¥312.0
    规格:10 mg产品价格:¥500.0
    规格:25 mg产品价格:¥800.0
    规格:50 mg产品价格:¥1215.0
    规格:100 mg产品价格:¥1788.0
    规格:500 mg产品价格:¥4475.0

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    Tanshinone IIA sulfonate sodium

    CAS No. : 69659-80-9

    MCE 国际站:Tanshinone IIA sulfonate sodium

    产品活性:Tanshinone IIA sulfonate sodium 是 tanshinone IIA 的衍生物,为 SOCE 的抑制剂,用于心血管疾病的研究。

    研究领域:Membrane Transporter/Ion Channel

    作用靶点:CRAC Channel

    In Vitro: Sodium Tanshinone IIA sulfonate (12.5 μM) inhibits hypoxia-induced PKG and PPAR-γ downregulation in PASMCs and distal pulmonary arteries of rats. The suppressive effects of Sodium Tanshinone IIA sulfonate on TRPC1 and TRPC6 expression in hypoxic PASMCs can be prevented by specific knockdown PKG or PPAR-γ. The suppressive effects of Sodium Tanshinone IIA sulfonate on basal calcium concentration and SOCE in hypoxic PASMCs can be reversed by specific knockdown of PKG or PPAR-γ. PKG-PPAR-γ signaling axis participates in the suppressive effects of Sodium Tanshinone IIA sulfonate on proliferation in hypoxic PASMCs. PPAR-γ agonist promotes the protective role of Sodium Tanshinone IIA sulfonate on basal [Ca2+]i and SOCE in hypoxic PASMCs. Sodium tanshinone IIA sulfonate inhibits the activity of CYP3A4 in a dose-dependent manner by the HLMs and CYP3A4 isoform. The KM and Vmax values of STS are 54.8±14.6 µM and 0.9±0.1 nmol/mg protein/min, respectively, for the HLMs and 7.5±1.4 µM and 6.8±0.3 nmol/nmol P450/min, respectively, for CYP3A4. CYP1A2, CYP2A6, CYP2C9, CYP2D6, CYP2E1, and CYP2C19 show minimal or no effects on the metabolism of STS. Sodium Tanshinone IIA sulfonate inhibits the activity of CYP3A4 in a dose-dependent manner in the HLMs and CYP3A4 isoform. Sodium Tanshinone IIA sulfonate primarily inhibits the activities of CYP3A4 in vitro, and Sodium Tanshinone IIA sulfonate has the potential to perpetrate drug-drug interactions with other CYP3A4 substrates.

    In Vivo: Sodium Tanshinone IIA sulfonate (10 mg/kg, 20 mg/kg) and Donepezil shorten escape latency, increase crossing times of the original position of the platform, and increase the time spent in the target quadrant. Sodium Tanshinone IIA sulfonate decreases the activity of acetylcholinesterase (AChE) and increases the activity of choline acetyltransferase (ChAT) in the hippocampus and cortex of SCOP-treated mice. Sodium Tanshinone IIA sulfonate increases the activity of superoxide dismutase (SOD) and decreases the levels of malondialdehyde (MDA) and reactive oxygen species (ROS) in hippocampus and cortex. Sodium Tanshinone IIA sulfonate prevention (30 mg/kg/day) alleviates hypoxia-induced characteristic changes in chronic hypoxia PH rat model. Sodium Tanshinone IIA sulfonate (20, 10, and 5 mg/kg, i.p.) effectively prevents peritoneal adhesion without affecting anastomotic healing in the rats. Compared with the adhesion model group, the Sodium Tanshinone IIA sulfonate-treated groups show increased peritoneal lavage fluid tPA activity and tPA/PAI-1 ratio in the ischemic tissues with loared TGF-β1 and collagen I expressions in the ischemic tissues.

    相关产品:Natural Product Library Plus  |  Drug Repurposing Compound Library Plus  |  FDA-Approved Drug Library Plus  |  Bioactive Compound Library Plus  |  YM-58483  |  SKF-96365 hydrochloride  |  Zegocractin  |  Synta66  |  MRS1845  |  RO2959 monohydrochloride  |  CRAC intermediate 2  |  GSK-5498A  |  SOCE inhibitor 1  |  5J-4  |  CRAC intermediate 1  |  GSK-5503A  |  piCRAC-1

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