製品番号: HY-N0587

Demethylzeylasteral

6 Cited Publications

カスタマーレビュー

Based on 6 publication(s) in Google Scholar

Demethylzeylasteral is an orally active triterpenoid compound isolated from Tripterygium wilfordii, which has functions such as anti-inflammatory, anti-tumor, anti fertility, estrogen metabolism regulation, immune suppression, and immune system regulation ^[1][2].

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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: 99.92%
CAS 番号: 107316-88-1
分子式: C₂₉H₃₆O₆
分子量:480.59

保管条件:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month

Demethylzeylasteral 構造式

CAS 番号: 107316-88-1

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Amount: USD 0.00

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Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

生物活性
- 製品説明
- Cellular Effect
- 体外実験
- 体内実験
化学情報
Publications (6)
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

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Smad1
Smad3

Estrogen Receptor/ERR アイソフォーム固有の製品をすべて表示 :

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Cellular Effect

Cell Line	Type	Value	Description	References
A2780	IC₅₀	10.11 μM Compound: Demethylzeylasteral	Cytotoxicity against human A2780 cells assessed as cell viability measured after 48 hrs by MTT assay Cytotoxicity against human A2780 cells assessed as cell viability measured after 48 hrs by MTT assay	[PMID: 38964974]

体外実験

Demethylzeylasteral (0-50 μM, 72 h) inhibits cell growth and proliferation by inducing cell cycle arrest in glioma cells^[1].
Demethylzeylasteral (5, 10 μM, 48 h) inhibits matrix degradation, migration and invasion of breast cancer cells^[2].
Demethylzeylasteral (1-20 μM, 48 h) inhibits cell proliferation and induces apoptosis by inhibiting MCL1 in melanoma cells^[3].
Demethylzeylasteral (0-2 μM, 48 h) inhibits the proliferation, migration, and activation of hepatic stellate cells^[6].

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

Cell Proliferation Assay^[1].

Cell Line:

LN-229, U-87, A-172, U-251 and U-118 cells
Concentration:

0-50 μM
Incubation Time:

72 h
Result:

Inhibited the proliferation rate of cells

Cell Migration Assay ^[2].

Cell Line:

MDA-MB-231 cell
Concentration:

5, 10 μM
Incubation Time:

48 h
Result:

Inhibited cell migration of MDA-MB-231 cells

Western Blot Analysis^[3].

Cell Line:

MV3 cell, A375 cell
Concentration:

1-20 μM
Incubation Time:

48 h
Result:

Reduced expression of anti-apoptotic protein MCL1

Western Blot Analysis^[6].

Cell Line:

LX-2 cell, HSC-T6 cell, primary HSC cell
Concentration:

0-2 μM
Incubation Time:

48 h
Result:

Reduced the mRNA and protein expression of COL1A1, MMP2, α-SMA, and TIMP-2

体内実験

Demethylzeylasteral (30 mg/kg, 6 times every 2 days, i.p.) inhibits glioma growth by regulating the miR-30e-5p/MYBL2 axis^[1].
Demethylzeylasteral (4 mg/kg, 5 weeks, i.p.) inhibits the invasion of triple negative breast cancer by blocking classical and non classical TGF - β signaling pathways^[2].
Demethylzeylasteral (30-120 mg/kg, 8 weeks, i.p.) improves inflammation in a unilateral ureteral obstruction rat model by inhibiting the activation of the NF - κ B pathway^[4].
Demethylzeylasteral (10, 40 mg/kg, 30 days, i.g.) can alleviate atherosclerosis in AS rabbits^[5].
Demethylzeylasteral (10, 20 mg/kg, 4 weeks, p.o.) improves CCl4 induced liver fibrosis in mice by inhibiting AGAP2 mediated FAK/AKT signaling^[6].

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

Animal Model:

Female nude mice modeled with glioma LN-229 cells^[1].
Dosage:

30 mg/kg, 6 times every 2 days
Administration:

Intraperitoneal injection (i.p.)
Result:

Reduced tumor volume

Animal Model:

Female BALB/c mice modeled with 4T1 cells^[2].
Dosage:

4 mg/kg, 5 weeks
Administration:

Intraperitoneal injection (i.p.)
Result:

Reduced cancer lung metastasis

Animal Model:

Rat model of unilateral ureteral obstruction^[4].
Dosage:

30-120 mg/kg, 8 weeks
Administration:

Intraperitoneal injection (i.p.)
Result:

Inhibited the increases in serum creatinine, blood urea nitrogen and Up/Ucr ratio

Animal Model:

Atherosclerotic rabbit^[5].
Dosage:

10, 40 mg/kg, 30 days
Administration:

Intragastrical (i.g.)
Result:

Reduced blood lipids triglycerides (TG), total cholesterol (TC), low-density lipoprotein (LDL-C)

Animal Model:

CCl4-induced liver fibrosis model^[6].
Dosage:

10, 20 mg/kg, 4 weeks
Administration:

Oral gavage (p.o.)
Result:

Inhibited the expression of TGF-β1

化学情報

CAS 番号 107316-88-1
性状 Solid
分子量 480.59
分子式 C₂₉H₃₆O₆
Color Light yellow to yellow
SMILES

C[C@](C1=CC2=O)(CC[C@]3(C)[C@@]4([H])C[C@@](C(O)=O)(C)CC3)[C@]4(CC[C@]1(C5=C2C(C=O)=C(O)C(O)=C5)C)C
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	6 months
	-20°C	1 month

Publications (6)

All Histological Imaging/StainingCell Proliferation/Viability AssayWBCell Migration/Invasion AssayOthers

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Journal Impact Factor

Phytomedicine

Demethylzeylasteral ameliorates podocyte damage in murine lupus by inhibiting inflammation and enhancing autophagy. [Abstract]

2024 Aug 15:134:155966. PMID: 39241387
Phytomedicine

Demethylzeylasteral attenuates hepatic stellate cell activation and liver fibrosis by inhibiting AGAP2 mediated signaling. [Abstract]

2022 Oct:105:154349. PMID: 35905567
Cell Rep

Carvedilol sensitizes chemotherapy by targeting STING to boost anti-tumor immunity. [Abstract]

2025 Apr 16;44(5):115572. PMID: 40249703
J Ethnopharmacol

Demethylzeylasteral protects against renal interstitial fibrosis by attenuating mitochondrial complex I-mediated oxidative stress. [Abstract]

2024 Jun 12:327:117986. PMID: 38437887

Demethylzeylasteral purchased from MedChemExpress. Usage Cited in: J Ethnopharmacol. 2024 Jun 12:327:117986. [Abstract]

Demethylzeylasteral (DML: 10/20 mg/kg). Reduced kidney damage and fibrosis in UUO mice. Representative images stained with PAS, Sirius red, and Masson's red.

Demethylzeylasteral purchased from MedChemExpress. Usage Cited in: J Ethnopharmacol. 2024 Jun 12:327:117986. [Abstract]

Demethylzeylasteral (DML: 10/20 mg/kg) inhibited the expression of fibrosis-related proteins in UUO mice. The expression levels of α-SMA, FN, type I collagen, and TGF-β1 were also affected.

Demethylzeylasteral purchased from MedChemExpress. Usage Cited in: J Ethnopharmacol. 2024 Jun 12:327:117986. [Abstract]

Demethylzeylasteral (DML: 10/20 mg/kg) inhibits MitROS production and improves mitochondrial function. Total ROS concentration in kidney tissue.
J Bone Oncol

Demethylzeylasteral inhibits proliferation and metastasis of osteosarcoma cells by modulating the PI3K/AKT/Autophagy pathways. [Abstract]

2025 Jun 20:53:100699. PMID: 40655907

Demethylzeylasteral purchased from MedChemExpress. Usage Cited in: J Bone Oncol. 2025 Jun 20:53:100699. [Abstract]

Viability of MG63 cells treated with varying concentrations of DEM (Demethylzeylasteral: 0, 10, 20, and 40 uM) for 24, 48, and 72 h, assessed using a CCK8 assay.

Demethylzeylasteral purchased from MedChemExpress. Usage Cited in: J Bone Oncol. 2025 Jun 20:53:100699. [Abstract]

Transwell migration assays assessed the migration ability of 143B and MG63 cells after treatment with DMSO or DEM (Demethylzeylasteral: 0, 10, 20, and 40 μM) for 48 hours.
Toxicol Appl Pharmacol

Demethylzeylasteral inhibits osteosarcoma cell proliferation by regulating METTL17-mediated mitochondrial oxidative phosphorylation. [Abstract]

2025 Apr 16:117348. PMID: 40250487

溶剤 & 溶解度

体外:

DMSO : 175 mg/mL (364.14 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

2.0808 mL

10.4039 mL

20.8078 mL

5 mM

0.4162 mL

2.0808 mL

4.1616 mL

10 mM

0.2081 mL

1.0404 mL

2.0808 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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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: ≥ 2.08 mg/mL (4.33 mM); Clear solution

This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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.

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%

データシート (289 KB)
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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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MS (2659 KB)
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IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Zhang K, et al. Demethylzeylasteral inhibits glioma growth by regulating the miR-30e-5p/MYBL2 axis. Cell Death Dis. 2018 Oct 10;9(10):1035. [Content Brief]

[2]. Li L, et al. Demethylzeylasteral (T-96) inhibits triple-negative breast cancer invasion by blocking the canonical and non-canonical TGF-β signaling pathways. Naunyn Schmiedebergs Arch Pharmacol. 2019 May;392(5):593-603. [Content Brief]

[3]. Zhao Y, et al. Demethylzeylasteral inhibits cell proliferation and induces apoptosis through suppressing MCL1 in melanoma cells. Cell Death Dis. 2017 Oct 26;8(10):e3133. [Content Brief]

[4]. Wang Q, et al. Demethylzeylasteral ameliorates inflammation in a rat model of unilateral ureteral obstruction through inhibiting activation of the NF‑κB pathway. Mol Med Rep. 2017 Jul;16(1):373-379. [Content Brief]

[5]. Huang Y, et al. Experimental study of the anti-atherosclerotic effect of demethylzeylasteral. Exp Ther Med. 2017 Jun;13(6):2787-2792. [Content Brief]

[6]. Chen K, et al. Demethylzeylasteral attenuates hepatic stellate cell activation and liver fibrosis by inhibiting AGAP2 mediated signaling. Phytomedicine. 2022 Oct;105:154349. [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, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	2.0808 mL	10.4039 mL	20.8078 mL	52.0194 mL
	5 mM	0.4162 mL	2.0808 mL	4.1616 mL	10.4039 mL
	10 mM	0.2081 mL	1.0404 mL	2.0808 mL	5.2019 mL
	15 mM	0.1387 mL	0.6936 mL	1.3872 mL	3.4680 mL
	20 mM	0.1040 mL	0.5202 mL	1.0404 mL	2.6010 mL
	25 mM	0.0832 mL	0.4162 mL	0.8323 mL	2.0808 mL
	30 mM	0.0694 mL	0.3468 mL	0.6936 mL	1.7340 mL
	40 mM	0.0520 mL	0.2601 mL	0.5202 mL	1.3005 mL
	50 mM	0.0416 mL	0.2081 mL	0.4162 mL	1.0404 mL
	60 mM	0.0347 mL	0.1734 mL	0.3468 mL	0.8670 mL
	80 mM	0.0260 mL	0.1300 mL	0.2601 mL	0.6502 mL
	100 mM	0.0208 mL	0.1040 mL	0.2081 mL	0.5202 mL

Keywords

Demethylzeylasteral

6 Cited Publications

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Demethylzeylasteral

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

TGF-beta/Smad アイソフォーム固有の製品をすべて表示

Estrogen Receptor/ERR アイソフォーム固有の製品をすべて表示

NF-κB 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 (6)

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

Demethylzeylasteral 関連分類

HY-N0587 関連分類