货号:A200416
同义名:
桦木酸
/ Lupatic acid; Betulic acid
Betulinic acid 是一种天然的五环三萜类化合物,为真核细胞拓扑异构酶 I (topoisomerase I) 的抑制剂,IC50 值为 5 μM,具有抗炎、抗疟疾、抗艾滋病和抗肿瘤等活性。


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| 产品名称 | NF-κB ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ammonium pyrrolidine-1-carbodithioate | ✔ | 98% | |||||||||||||||||
| QNZ |
++++
NF-κB, IC50: 11 nM |
99%+ | |||||||||||||||||
| Sodium 4-Aminosalicylate Dihydrate | ✔ | 98% | |||||||||||||||||
| Sodium Salicylate | ✔ | 95% | |||||||||||||||||
| Parthenolide | ✔ | p53 | 97% HPLC | ||||||||||||||||
| JSH-23 |
+
NF-κB, IC50: 7.1 μM |
98% | |||||||||||||||||
| Phenethyl caffeate | ✔ | 98% | |||||||||||||||||
| Andrographolide | ✔ | 98+% | |||||||||||||||||
| Curcumin | ✔ | HDAC,Nrf2 | 98% | ||||||||||||||||
| SC75741 |
+++
NF-κB, EC50: 200 nM |
99%+ | |||||||||||||||||
| CBL0137 HCl |
++
NF-κB, EC50: 0.47 μM |
p53 | 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。 | |||||||||||||||||||
| 靶点 |
|
| 描述 | Betulinic Acid is a natural pentacyclic triterpenoid compound and a eukaryotic topoisomerase I inhibitor with IC50 value of 0.5 mM. It has anti-inflammatory, anti malaria, anti AIDS and anti-tumor activities[3]. Betulinic Acid is also a new activator of NF κB[4]. Betulinic Acid (20, 40 µM) causes decrease in Bcl-2 expression of MDA-MB-231 cells[5]. Betulinic Acid has anti HIV activity. EC50 of H9 lymphocytes infected with Betulinic Acid is 1.4 μ M[6]. Moreover, oral administration of Betulinic Acid reduced the bleeding score at 10 and 30 mg/kg and improved the stool consistency at 30 mg/kg[7]. |
| Concentration | Treated Time | Description | References | |
| HT22 cells | 12 µg/mL | BA showed no significant toxicity to HT22 cells | J Nanobiotechnology. 2022 Jan 21;20(1):39. | |
| PANC-1 cells | 5, 10, 20 μM | 12, 24, 48 hours | To assess the direct cytotoxicity of BA, which showed concentration- and time-dependent inhibition of cell proliferation. | Cancer Res. 2011 Aug 1;71(15):5182-93. |
| FG cells | 2.5, 5, 10 μM | 48 hours | To evaluate the cytotoxic effects of BA and MIT alone or in combination, showing inhibition of cell proliferation. | Cancer Res. 2011 Aug 1;71(15):5182-93. |
| BxPC-3 cells | 5, 10, 20 μM | 12, 24, 48 hours | To assess the direct cytotoxicity of BA, which showed concentration- and time-dependent inhibition of cell proliferation. | Cancer Res. 2011 Aug 1;71(15):5182-93. |
| A172 cells | 0, 3, 6, 12, 24, 48 µg/mL | 24 hours | BA NPs significantly inhibited A172 cell proliferation with IC50 of 8.5 µg/mL | J Nanobiotechnology. 2022 Jan 21;20(1):39. |
| U87 cells | 0, 3, 6, 12, 24, 48 µg/mL | 24 hours | BA NPs significantly inhibited U87 cell proliferation with IC50 of 12.1 µg/mL | J Nanobiotechnology. 2022 Jan 21;20(1):39. |
| PANC-1 cells | 50 μM | 48 hours | Gene expression profiles were analyzed by cDNA microarray after BA treatment, revealing significant downregulation of lamin B1. | Clin Cancer Res. 2013 Sep 1;19(17):4651-61. |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT00346502 | Dysplastic Nevus Syndrome | Phase 1 Phase 2 | Suspended(The study has been t... 展开 >>emporarily suspended due to funding issues) 收起 << | December 2015 | United States, Illinois ... 展开 >> University of Illinois at Chicago Medical Center Chicago, Illinois, United States, 60612 收起 << |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.19mL 0.44mL 0.22mL |
10.95mL 2.19mL 1.09mL |
21.90mL 4.38mL 2.19mL |
|
| CAS号 | 472-15-1 |
| 分子式 | C30H48O3 |
| 分子量 | 456.7 |
| SMILES Code | C[C@@]1([C@@]2(CC[C@]3(C(C)([C@H](CC[C@@]3([C@]2(CC[C@@]1([C@]4([C@@H](CC5)C(C)=C)[H])[H])[H])C)O)C)[H])C)CC[C@]45C(O)=O |
| MDL No. | MFCD00009619 |
| 别名 | 桦木酸 ;Lupatic acid; Betulic acid; Mairin; NSC 113090; ALS-357 |
| 运输 | 蓝冰 |
| InChI Key | QGJZLNKBHJESQX-FZFNOLFKSA-N |
| Pubchem ID | 64971 |
| 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: 35 mg/mL(76.64 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 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
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