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Saikosaponin D/柴胡皂苷D {[allProObj[0].p_purity_real_show]}

货号:A191999

Saikosaponin D是从柴胡中分离纯化的天然产物,通过抑制 NF-κB 和 STAT3 信号通路来保护肝脏免受对乙酰氨基酚引起的毒性损伤,是 CCl4 引起的急性肝损伤的有效抑制剂,并对人肝癌细胞具有细胞毒性作用。在 A549 细胞中具有抗增殖作用,可能通过诱导 p53 和激活 Fas/FasL 凋亡系统实现。

Saikosaponin D/柴胡皂苷D 化学结构 CAS号:20874-52-6
Saikosaponin D/柴胡皂苷D 化学结构
CAS号:20874-52-6
Saikosaponin D/柴胡皂苷D 3D分子结构
CAS号:20874-52-6
Saikosaponin D/柴胡皂苷D 化学结构 CAS号:20874-52-6
Saikosaponin D/柴胡皂苷D 3D分子结构 CAS号:20874-52-6
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Saikosaponin D/柴胡皂苷D 纯度/质量文件 产品仅供科研

货号:A191999 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

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产品名称 STAT1 STAT3 STAT5 其他靶点 纯度
Nifuroxazide 98%
Fludarabine 98%
Artesunate 98%
BP-1-102 +++

STAT3, Kd: 504 nM

99%+
Niclosamide ++

STAT3, IC50: 0.7 μM

98%
Napabucasin 98%
Cryptotanshinone ++

STAT3, IC50: 4.6 μM

98%
Stattic +

STAT3, IC50: 5.1 μM

98%
NSC 74859 +

STAT3, IC50: 86 μM

99%+
Ochromycinone 98%
HO-3867 97%
C188-9 ++++

STAT3, Kd: 4.7 nM

99%+
HJC0152 99%
SH5-07 95%
SH-4-54 ++++

STAT3, Kd: 300 nM

+++

STAT5, Kd: 464 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Saikosaponin D/柴胡皂苷D 生物活性

描述 Saikosaponin D, a natural product isolated and purified from the herb of Bupleurum chinense DC., is a SERCA inhibitor by inhibiting NF-κB and STAT3 signaling to protect against acetaminophen-induced hepatotoxicity and a potent inhibitor on acute hepatic injury by CCl4 and a potent cytotoxicity agent for human hepatocellular carcinoma cells, and has the antiproliferative effect in A549 cells that may be the induction of p53 and activity of the Fas/FasL apoptotic system.

Saikosaponin D/柴胡皂苷D 细胞实验

Cell Line
Concentration Treated Time Description References
Hippocampal neural progenitor cells (NPCs) 5.13 µM (EC50) 24 hours SSd inhibited the survival and proliferation of NPCs and induced apoptosis by activating the NRAGE/NADE/NRIF apoptotic signaling pathway. Clin Transl Med. 2020 Dec;10(8):e243
HepG2 cells 7.5-15 µM 24 hours Induced autophagy and apoptosis, detected by GFP-LC3 puncta formation and Annexin V staining. Cell Death Dis. 2013 Jul 11;4(7):e720
HepG2 cells 7.5-15 µM 24 hours Induced autophagy and apoptosis, confirmed by GFP-LC3 puncta formation and Annexin V staining. Cell Death Dis. 2013 Jul 11;4(7):e720
MCF-7 cells 10 µM 4 hours Induced autophagy, detected by GFP-LC3 puncta formation and increased LC3-II protein levels. Cell Death Dis. 2013 Jul 11;4(7):e720
HeLa cells 10 µM 4 hours Induced autophagy, detected by GFP-LC3 puncta formation and increased LC3-II protein levels. Cell Death Dis. 2013 Jul 11;4(7):e720
MCF-7 cells 10 µM 4 hours Induced autophagy, confirmed by GFP-LC3 puncta formation and increased LC3-II protein expression. Cell Death Dis. 2013 Jul 11;4(7):e720
HeLa cells 10 µM 4 hours Induced autophagy, confirmed by GFP-LC3 puncta formation and increased LC3-II protein expression. Cell Death Dis. 2013 Jul 11;4(7):e720
U937 cells 1 µM 48 hours Inhibited cell proliferation, promoted apoptosis and cell-cycle arrest Theranostics. 2021 Mar 31;11(12):5831-5846
MV4-11 cells 1 µM 48 hours Inhibited cell proliferation, promoted apoptosis and cell-cycle arrest Theranostics. 2021 Mar 31;11(12):5831-5846
Kasumi-1 cells 1 µM 48 hours Inhibited cell proliferation, promoted apoptosis and cell-cycle arrest Theranostics. 2021 Mar 31;11(12):5831-5846
NB4 cells 1 µM 48 hours Inhibited cell proliferation, promoted apoptosis and cell-cycle arrest Theranostics. 2021 Mar 31;11(12):5831-5846
HeLa cells 15 µM 6 hours To assess the ability of SsD to modulate autophagy, it was found that SsD significantly inhibited the fusion of autophagosomes and lysosomes, leading to the accumulation of autophagosomes, increased lysosomal pH, and TFEB nuclear translocation. Signal Transduct Target Ther. 2019 Feb 22;4:4

Saikosaponin D/柴胡皂苷D 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6N mice Leukemia model Intraperitoneal injection 0.1 mg/kg or 0.5 mg/kg 3 times per week for 3 weeks Significantly inhibited leukemia progression, including reduced WBC count, decreased leukemic blasts in BM, reduced splenomegaly, inhibited lung metastasis and prolonged survival Theranostics. 2021 Mar 31;11(12):5831-5846
C57BL/6J mice Cognitive dysfunction model Oral gavage 16 mg/kg Once daily for 14 consecutive days SSd inhibited hippocampal neurogenesis and caused cognitive dysfunction by disrupting pro-BDNF/p75NTR and BDNF/TrkB signaling pathways. Clin Transl Med. 2020 Dec;10(8):e243
Mice Experimental autoimmune encephalomyelitis (EAE) model Intragastric administration 40 mg/kg Once daily, starting from the day of immunization To investigate the therapeutic effect of SSD on EAE, results showed that SSD significantly alleviated EAE symptoms Nat Commun. 2021 Oct 27;12(1):6198

Saikosaponin D/柴胡皂苷D 参考文献

[1]Liu RY, Li JP. Saikosaponin-d inhibits proliferation of human undifferentiated thyroid carcinoma cells through induction of apoptosis and cell cycle arrest. Eur Rev Med Pharmacol Sci. 2014;18(17):2435-43.

[2]Liu A, Tanaka N, et al. Saikosaponin d protects against acetaminophen-induced hepatotoxicity by inhibiting NF-κB and STAT3 signaling. Chem Biol Interact. 2014 Nov 5;223:80-6.

Saikosaponin D/柴胡皂苷D 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.28mL

0.26mL

0.13mL

6.40mL

1.28mL

0.64mL

12.80mL

2.56mL

1.28mL

Saikosaponin D/柴胡皂苷D 技术信息

CAS号20874-52-6
分子式C42H68O13
分子量 780.98
SMILES Code CC1(C)CC[C@]2(CO3)[C@H](O)C[C@@]4(C)[C@]([C@]5([H])C=C[C@]43[C@]2([H])C1)(C)CC[C@@]([C@]5(C)CC6)([H])[C@@](CO)(C)[C@H]6O[C@@](O[C@H](C)[C@@H]7O)([H])[C@H](O)[C@H]7O[C@@]8([H])[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O8
MDL No. MFCD09028095
别名
运输蓝冰
InChI Key KYWSCMDFVARMPN-LCSVLAELSA-N
Pubchem ID 107793
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry, 2-8°C

溶解方案

DMSO: 50 mg/mL(64.02 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
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