製品番号: HY-N0853

アリソールA

(別名: Alisol A; Alisol-A)

5 Cited Publications

カスタマーレビュー

Based on 5 publication(s) in Google Scholar

Alisol A is an orally active tetracyclic triterpenoid compound of the prototerpane type. Alisol A can be extracted from the rhizome of Alisma orientale. Alisol A activates AMPK/ACC/SREBP-1c, SIRT1, PPARα, inhibits MMP-2/-9, decreases inflammatory cytokine expression (IL-1β, IL-6, IL-8). Alisol A has anti-tumor activity against breast cancer and colorectal cancer. Alisol A has anti-obesity and anti-atherosclerotic activities. Alisol A can be used in the research of hepatitis B, breast cancer, colorectal cancer, atherosclerosis, and obesity.

商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。

純度: 99.59%
CAS 番号: 19885-10-0
分子式: C₃₀H₅₀O₅
分子量:490.72

保管条件:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year

Alisol A 構造式

CAS 番号: 19885-10-0

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Amount: USD 0.00

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生物活性
- 製品説明
- IC₅₀ & Target
- Cellular Effect
- 体外実験
- 体内実験
化学情報
Publications (5)
溶剤 & 溶解度
- 体外
- 体内
純度とドキュメンテーション
参考文献
Help & FAQs
関連分類
Bioz

生物活性

製品説明

IC₅₀ & Target^[1]^[2]^[3]^[4]^[5]^[6]^[7]

MMP-9

MMP-2

PPARα

IL-6

IL-1β

IL-8

AMPK アイソフォーム固有の製品をすべて表示 :

PPAR アイソフォーム固有の製品をすべて表示 :

MMP アイソフォーム固有の製品をすべて表示 :

Interleukin Related アイソフォーム固有の製品をすべて表示 :

Cellular Effect

Cell Line	Type	Value	Description	References
Erythrocyte	IC₅₀	13.8 μM Compound: 57a	Antiplasmodial activity against Plasmodium falciparum K1 infected in human erythrocyte assessed as inhibition of parasite growth incubated for 72 hrs by [3H]-hypoxanthine incorporation based liquid scintillation counting method Antiplasmodial activity against Plasmodium falciparum K1 infected in human erythrocyte assessed as inhibition of parasite growth incubated for 72 hrs by [3H]-hypoxanthine incorporation based liquid scintillation counting method	[PMID: 35985254]
HepG2	EC₅₀	10.16 μM Compound: 23	Transactivation of FXR (unknown origin) transfected in HepG2 cells co-expressing pBSEP/pGL4.74 incubated for 24 hrs by luciferase reporter gene assay Transactivation of FXR (unknown origin) transfected in HepG2 cells co-expressing pBSEP/pGL4.74 incubated for 24 hrs by luciferase reporter gene assay	[PMID: 31494470]
HepG2 2.2.15	CC₅₀	0.062 mM Compound: 1	Cytotoxicity against human HepG2.2.15 cells Cytotoxicity against human HepG2.2.15 cells	[PMID: 18644720]
HepG2 2.2.15	IC₅₀	>2.4 mM Compound: 1	Antiviral activity against hepatitis B virus-infected human HepG2.2.15 cells assessed as inhibition of HBV e antigen secretion Antiviral activity against hepatitis B virus-infected human HepG2.2.15 cells assessed as inhibition of HBV e antigen secretion	[PMID: 18644720]
HepG2 2.2.15	IC₅₀	0.039 mM Compound: 1	Antiviral activity against hepatitis B virus-infected human HepG2.2.15 cells assessed as inhibition of HBV surface antigen secretion Antiviral activity against hepatitis B virus-infected human HepG2.2.15 cells assessed as inhibition of HBV surface antigen secretion	[PMID: 18644720]

体外実験

Alisol A (2.5-40 μM; 24 h) suppresses proliferation, migration, and invasion in human breast cancer MDA-MB-231 cells^[3].
Alisol A (1-5 μM) concentration-dependently restores the levels of p-AMPK and p-ACC in HepG2 cells treated with free fatty acids (FFA)^[4].
Alisol A (40 μM; 24-72 h) inhibits the proliferation of human aortic endothelial cells (HAECs)^[5].
Alisol A (5-160 µM; 24 h) inhibits the proliferation of HCT-116 and HT-29 cells in a dose-dependent manner^[6].

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

Western Blot Analysis^[3]

Cell Line:

MDA-MB-231
Concentration:

0, 5 μM
Incubation Time:

24 h
Result:

Downregulated MMP-2/-9.

体内実験

Alisol A (100 mg/kg; i.p.; once daily; 4 weeks) significantly attenuates body weight and abdominal fat weight and activates the AMPK/ACC/SREBP-1c pathway in high-fat diet-induced obese mice^[4].
Alisol A (150 ppm; p.o.; in diet; 16 weeks) significantly reduces the aortic plaque area in ApoE^-/- mice with atherosclerosis, without obvious effect on blood lipid levels^[5].
Alisol A (25-100 mg/kg; i.g.; twice daily; 12 weeks) alleviates arterial plaque by activating AMPK/SIRT1 signaling pathway in apoE-deficient mice^[7].

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

Animal Model:

Male C57BL/6 mice (6 weeks old) with high-fat diet-induced obesity^[4]
Dosage:

100 mg/kg
Administration:

Intraperitoneal injection, once daily, for 4 weeks
Result:

Reduced body weight and abdominal fat mass, improved plasma lipid profiles (decreased TC, TG, LDL-C, NEFA, FABP4).
Enhanced glucose tolerance and insulin sensitivity, alleviated hepatic steatosis (reduced fat vacuoles and lipid deposition).
Decreased inflammatory cytokine expression (TNF-α, IL-1β, IL-6, IL-8) in adipose tissue, and activated the AMPK/ACC/SREBP-1c pathway (increased p-AMPK, p-ACC, decreased SREBP-1c) in liver, skeletal muscle, and adipose tissue.

Animal Model:

Male C57BL/6 background ApoE^-/- mice (6-week-old), high-fat diet-induced atherosclerosis model^[7]
Dosage:

25 mg/kg, 100 mg/kg
Administration:

Intragastric administration, twice daily, 12 weeks
Result:

Attenuated high-fat diet-induced body weight gain, reduced aortic plaque area, widened the inner diameter of the aortic arch.
Inhibited the expression of ICAM-1, IL-6, and MMP-9 in aortic plaques, and increased the expression of PPARα, PPARδ, p-AMPK, SIRT1, and IkBa in the liver.

化学情報

CAS 番号 19885-10-0
性状 Solid
分子量 490.72
分子式 C₃₀H₅₀O₅
Color White to light yellow
SMILES

C[C@]([C@@]1(C2=C([C@H](C)C[C@H](O)[C@@H](O)C(C)(O)C)CC1)C)(CC[C@@]3([H])C4(C)C)[C@]([C@H](C2)O)([H])[C@]3(CCC4=O)C
別名

Alisol A; Alisol-A
Structure Classification
- Terpenoids
- Triterpenes
Initial Source
輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	2 years
	-20°C	1 year

Publications (5)

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Molecules

Alisol A Suppresses Proliferation, Migration, and Invasion in Human Breast Cancer MDA-MB-231 Cells. [Abstract]

2019 Oct 10;24(20):3651. PMID: 31658635
Vet Microbiol

Identification and evaluation of Nordihydroguaiaretic acid (NDGA) as an active traditional Chinese medicine compound inhibiting the 3C-like protease of feline infectious peritonitis virus. [Abstract]

2025 Sep 15:310:110730. PMID: 40976146
Nephrology (Carlton)

Alisol A inhibits the circ_0001831/miR-346/LIN28B pathway to ameliorate high glucose-induced injury of human renal mesangial cells. [Abstract]

2024 Mar;29(3):154-163. PMID: 38013222
Biomed Pharmacother

A novel Alisma orientale extract alleviates non-alcoholic steatohepatitis in mice via modulation of PPARα signaling pathway. [Abstract]

2024 Jun 7:176:116908. PMID: 38850668
Research Square Preprint

2021 Feb.

溶剤 & 溶解度

体外:

DMSO : 100 mg/mL (203.78 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

2.0378 mL

10.1891 mL

20.3782 mL

5 mM

0.4076 mL

2.0378 mL

4.0756 mL

10 mM

0.2038 mL

1.0189 mL

2.0378 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

モル濃度計算機

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

Mass Mass

濃度濃度

体積体積

分子量分子量

希釈計算機

濃度 _(開始) × 体積 _(開始) = 濃度 _(終了) × 体積 _(終了)

濃度 _(開始) 濃度 _(開始)

体積 _(開始) 体積 _(開始)

濃度 _(終了) 濃度 _(終了)

体積 _(終了) 体積 _(終了)

体内:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

Solubility: ≥ 2.5 mg/mL (5.09 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)

Solubility: ≥ 2.5 mg/mL (5.09 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

Protocol 3

Add each solvent one by one: 10% DMSO 90% Corn Oil

Solubility: ≥ 2.5 mg/mL (5.09 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage Dosage
mg/kg
Animal Weight (Per Animal) Animal Weight (Per Animal)
g
Dosing Volume (Per Animal) Dosing Volume (Per Animal)
μL
Number of Animals Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

%
DMSO +

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
%
+
+
%
Tween-80 + +
%
Saline +

The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Working solution concentration: 0.22 mg/mL

純度とドキュメンテーション

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

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COA (2659 KB)
元素分析報告書 (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
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IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
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Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Matsuda H, et al. Studies on Alismatis Rhizoma. II. Anti-complementary activities of methanol extract and terpene components from Alismatis Rhizoma (dried rhizome of Alisma orientale). Biol Pharm Bull. 1998 Dec;21(12):1317-21. [Content Brief]

[2]. Zhang Q, et al. Anti-HBV agents. Part 1: Synthesis of alisol A derivatives: a new class of hepatitis B virus inhibitors. Bioorg Med Chem Lett. 2008 Aug 15;18(16):4647-50. [Content Brief]

[3]. Lou C, et al. Alisol A Suppresses Proliferation, Migration, and Invasion in Human Breast Cancer MDA-MB-231 Cells. Molecules. 2019 Oct 10;24(20):3651. [Content Brief]

[4]. Ho C, et al. Alisol A attenuates high-fat-diet-induced obesity and metabolic disorders via the AMPK/ACC/SREBP-1c pathway. J Cell Mol Med. 2019 Aug;23(8):5108-5118. [Content Brief]

[5]. Ma Y, et al. Alisol A inhibits and stabilizes atherosclerotic plaques by protecting vascular endothelial cells. Front Pharmacol. 2024 Oct 25;15:1493948. [Content Brief]

[6]. Han W, et al. Alisol A attenuates malignant phenotypes of colorectal cancer cells by inactivating PI3K/Akt signaling. Oncol Lett. 2022 Jun 7;24(2):249. [Content Brief]

[7]. Wang K, et al. Alisol A Alleviates Arterial Plaque by Activating AMPK/SIRT1 Signaling Pathway in apoE-Deficient Mice. Front Pharmacol. 2020 Nov 2;11:580073. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	2.0378 mL	10.1891 mL	20.3782 mL	50.9455 mL
	5 mM	0.4076 mL	2.0378 mL	4.0756 mL	10.1891 mL
	10 mM	0.2038 mL	1.0189 mL	2.0378 mL	5.0946 mL
	15 mM	0.1359 mL	0.6793 mL	1.3585 mL	3.3964 mL
	20 mM	0.1019 mL	0.5095 mL	1.0189 mL	2.5473 mL
	25 mM	0.0815 mL	0.4076 mL	0.8151 mL	2.0378 mL
	30 mM	0.0679 mL	0.3396 mL	0.6793 mL	1.6982 mL
	40 mM	0.0509 mL	0.2547 mL	0.5095 mL	1.2736 mL
	50 mM	0.0408 mL	0.2038 mL	0.4076 mL	1.0189 mL
	60 mM	0.0340 mL	0.1698 mL	0.3396 mL	0.8491 mL
	80 mM	0.0255 mL	0.1274 mL	0.2547 mL	0.6368 mL
	100 mM	0.0204 mL	0.1019 mL	0.2038 mL	0.5095 mL

Keywords

Alisol A

5 Cited Publications

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アリソールA

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MedChemExpress（MCE）の使用を引用している文献 Alisol A

AMPK アイソフォーム固有の製品をすべて表示

PPAR アイソフォーム固有の製品をすべて表示

MMP アイソフォーム固有の製品をすべて表示

Interleukin Related アイソフォーム固有の製品をすべて表示

生物活性

化学情報

Publications (5)

溶剤 & 溶解度

純度とドキュメンテーション

参考文献

Help & FAQs

Complete Stock Solution Preparation Table

Alisol A 関連分類

HY-N0853 関連分類