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  3. Hispolon

Hispolon 是一种多酚,可从桑黄 (Phellinus linteus) 中分离得到。Hispolon 具有抗癌、抗糖尿病、抗氧化、抗病毒、肝保护活性、抗糖尿病和抗炎活性。

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Hispolon Chemical Structure

Hispolon Chemical Structure

CAS No. : 173933-40-9

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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Hispolon, a polyphenol, can be isolated from Phellinus linteus. Hispolon possesses anticancer, antidiabetic, antioxidant, antiviral, hepatoprotective, anti-diabetic, and anti-inflammatory activities[1].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
A10 IC50
37.05 μg/mL
Compound: 1
Antiproliferative activity against rat A10 cells after 24 hrs by MTT assay
Antiproliferative activity against rat A10 cells after 24 hrs by MTT assay
[PMID: 22967007]
A549 IC50
0.183 μM
Compound: 8
Cytotoxicity against human A549 cells after 96 hrs by MTT assay
Cytotoxicity against human A549 cells after 96 hrs by MTT assay
[PMID: 15165144]
Bel-7402 IC50
0.038 μM
Compound: 8
Cytotoxicity against human Bel7402 cells after 96 hrs by MTT assay
Cytotoxicity against human Bel7402 cells after 96 hrs by MTT assay
[PMID: 15165144]
BGC-823 IC50
0.205 μM
Compound: 8
Cytotoxicity against human BGC823 cells after 96 hrs by MTT assay
Cytotoxicity against human BGC823 cells after 96 hrs by MTT assay
[PMID: 15165144]
DU-145 IC50
28.6 μM
Compound: VA-1
Cytotoxicity against human DU145 cells after 72 hrs by MTT assay
Cytotoxicity against human DU145 cells after 72 hrs by MTT assay
[PMID: 25842364]
HCT-116 IC50
5.2 μM
Compound: VA-1
Cytotoxicity against human HCT116 cells after 72 hrs by MTT assay
Cytotoxicity against human HCT116 cells after 72 hrs by MTT assay
[PMID: 25842364]
HCT-8 IC50
0.199 μM
Compound: 8
Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay
Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay
[PMID: 15165144]
HEK293 IC50
7.3 μM
Compound: VA-1
Cytotoxicity against HEK293 cells expressing pcDNA3.1 after 72 hrs by MTT assay
Cytotoxicity against HEK293 cells expressing pcDNA3.1 after 72 hrs by MTT assay
[PMID: 25842364]
HEK293 IC50
9.6 μM
Compound: VA-1
Cytotoxicity against HEK293 cells expressing ABCB1 after 72 hrs by MTT assay
Cytotoxicity against HEK293 cells expressing ABCB1 after 72 hrs by MTT assay
[PMID: 25842364]
KETR3 IC50
0.206 μM
Compound: 8
Cytotoxicity against human Ketr3 cells after 96 hrs by MTT assay
Cytotoxicity against human Ketr3 cells after 96 hrs by MTT assay
[PMID: 15165144]
MCF7 IC50
0.025 μM
Compound: 8
Cytotoxicity against human MCF7 cells after 96 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 96 hrs by MTT assay
[PMID: 15165144]
MCF7 IC50
7.9 μM
Compound: VA-1
Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
[PMID: 25842364]
MDA-MB-231 IC50
32.2 μM
Compound: VA-1
Cytotoxicity against human MDA-MB-231 cells after 72 hrs by MTT assay
Cytotoxicity against human MDA-MB-231 cells after 72 hrs by MTT assay
[PMID: 25842364]
MDCK IC50
36.2 μM
Compound: VA-1
Cytotoxicity against MDCK cells after 72 hrs by MTT assay
Cytotoxicity against MDCK cells after 72 hrs by MTT assay
[PMID: 25842364]
NIH3T3 IC50
51.2 μM
Compound: VA-1
Cytotoxicity against mouse NIH/3T3 cells after 72 hrs by MTT assay
Cytotoxicity against mouse NIH/3T3 cells after 72 hrs by MTT assay
[PMID: 25842364]
PC-3 IC50
12.9 μM
Compound: VA-1
Cytotoxicity against human PC3 cells after 72 hrs by MTT assay
Cytotoxicity against human PC3 cells after 72 hrs by MTT assay
[PMID: 25842364]
S1 IC50
8.4 μM
Compound: VA-1
Cytotoxicity against human S1 cells after 72 hrs by MTT assay
Cytotoxicity against human S1 cells after 72 hrs by MTT assay
[PMID: 25842364]
体外研究
(In Vitro)

Hispolon (25 and 50 μM, 24-72 h) inhibits cell viability of U87MG cells[2].
Hispolon (25 and 50 μM, 24, 48 h) induces G2/M cell cycle arrest and apoptosis in U87MG cells[2].
Hispolon (25 and 50 μM, 2-8 h) decreases the expression of G1–S transition-related protein cyclin D4 but increases the expression of CDK inhibitor p21[2].
Hispolon (25 and 50 μM, 24 h) inhibits the migration of U87MG cells[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[2]

Cell Line: U87MG cells
Concentration: 25 and 50 μM
Incubation Time: 24, 48, 72 h
Result: Inhibited cell viability in a dose and time dependent way.

Western Blot Analysis[2]

Cell Line: U87MG cells
Concentration: 25 and 50 μM
Incubation Time: 2, 4, 8 h
Result: Decreased cyclin D4 level, and increased p21 level.
体内研究
(In Vivo)

Hispolon (2.5-10 mg/kg, i.p.) attenuates LPS-induced acute lung injury in mice[3].
Hispolon (5 and 10 mg/kg, s.c.) reduces tumor growth in DBTRG xenograft mice[4].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: LPS-induced acute lung injury mice[3]
Dosage: 2.5, 5 and 10 mg/kg
Administration: Intraperitoneal injection (i.p.)
Result: Alleviated the pathological effects in the LPS-challenged mouse.
Reduced the W/D ratio in the lung and MPO activity.
Decreased pro-Inflammatory cytokine production.
Animal Model: DBTRG xenograft mice[4]
Dosage: 5 and 10 mg/kg
Administration: Subcutaneous injection (s.c.)
Result: Reduced tumor volume (RTV).
Inhibited GBM cell proliferation in vivo upon HE and ki-67 staining.
分子量

220.22

Formula

C12H12O4

CAS 号
性状

固体

颜色

Light yellow to yellow

结构分类
初始来源

Phellinus linteus

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
细胞实验: 

DMSO 中的溶解度 : 125 mg/mL (567.61 mM; 超声助溶 (<70°C); 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 4.5409 mL 22.7046 mL 45.4091 mL
5 mM 0.9082 mL 4.5409 mL 9.0818 mL
查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料
参考文献

完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 4.5409 mL 22.7046 mL 45.4091 mL 113.5228 mL
5 mM 0.9082 mL 4.5409 mL 9.0818 mL 22.7046 mL
10 mM 0.4541 mL 2.2705 mL 4.5409 mL 11.3523 mL
15 mM 0.3027 mL 1.5136 mL 3.0273 mL 7.5682 mL
20 mM 0.2270 mL 1.1352 mL 2.2705 mL 5.6761 mL
25 mM 0.1816 mL 0.9082 mL 1.8164 mL 4.5409 mL
30 mM 0.1514 mL 0.7568 mL 1.5136 mL 3.7841 mL
40 mM 0.1135 mL 0.5676 mL 1.1352 mL 2.8381 mL
50 mM 0.0908 mL 0.4541 mL 0.9082 mL 2.2705 mL
60 mM 0.0757 mL 0.3784 mL 0.7568 mL 1.8920 mL
80 mM 0.0568 mL 0.2838 mL 0.5676 mL 1.4190 mL
100 mM 0.0454 mL 0.2270 mL 0.4541 mL 1.1352 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Hispolon
目录号:
HY-150521
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