Ursolic acid acetate
Based on 1 Customer Validation
Ursolic acid acetate (Acetylursolic acid) is a triterpenoid compound and an inhibitor of Plasmodium falciparum heat shock protein 90 (PfHsp90) with a KD of 8.16 μM. Ursolic acid acetate is cytotoxic to KB cells, with an IC50 value of 8.4 μM. Ursolic acid acetate can be used in tumor and antimalarial research.
For research use only. We do not sell to patients.
- Purity: 98.0%
- CAS No.: 7372-30-7
- Formula: C32H50O4
- Molecular Weight:498.74
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Storage:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
All Parasite Isoforms
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Biological Activity
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HSP90 |
Plasmodium |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| A549 | GI50 |
48 μM
Compound: 17
|
Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by MTT assay
|
[PMID: 32345458] |
| ASPC1 | IC50 |
71 μM
Compound: 2
|
Cytotoxicity against human AsPC1 cells after 72 hrs by MTT assay
Cytotoxicity against human AsPC1 cells after 72 hrs by MTT assay
|
[PMID: 22959527] |
| BGC-823 | IC50 |
19.36 μM
Compound: UA-3
|
Cytotoxicity against human BGC823 cells by MTT assay
Cytotoxicity against human BGC823 cells by MTT assay
|
[PMID: 21664827] |
| GES1 | IC50 |
92.94 μM
Compound: UA-3
|
Cytotoxicity against human GES-1 cells incubated for 48 hrs by MTT assay
Cytotoxicity against human GES-1 cells incubated for 48 hrs by MTT assay
|
[PMID: 21664827] |
| HCT-116 | GI50 |
21 μM
Compound: 17
|
Cytotoxicity against human HCT116 cells assessed as growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human HCT116 cells assessed as growth inhibition after 72 hrs by MTT assay
|
[PMID: 32345458] |
| HeLa | IC50 |
>10 μM
Compound: 2
|
Antiproliferative activity against human HeLa cells after 96 hrs by MTT assay
Antiproliferative activity against human HeLa cells after 96 hrs by MTT assay
|
[PMID: 19091579] |
| HeLa | IC50 |
>20 μM
Compound: 2a
|
Cytotoxicity against human HeLa cells assessed as inhibition of cell growth incubated for 72 hrs by CCK-8 assay
Cytotoxicity against human HeLa cells assessed as inhibition of cell growth incubated for 72 hrs by CCK-8 assay
|
[PMID: 34688014] |
| HepG2 | CC50 |
>400 μM
Compound: 1a
|
Cytotoxicity against human HepG2 cells after 72 hrs by MTT assay
Cytotoxicity against human HepG2 cells after 72 hrs by MTT assay
|
[PMID: 29326018] |
| HepG2 | IC50 |
37.67 μM
Compound: UA-3
|
Cytotoxicity against human HepG2 cells incubated for 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells incubated for 48 hrs by MTT assay
|
[PMID: 21664827] |
| HT-29 | IC50 |
23.89 μM
Compound: UA-3
|
Cytotoxicity against human HT-29 cells incubated for 48 hrs by MTT assay
Cytotoxicity against human HT-29 cells incubated for 48 hrs by MTT assay
|
[PMID: 21664827] |
| MCF7 | GI50 |
6.5 μM
Compound: 17
|
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability after 72 hrs by MTT assay
|
[PMID: 32345458] |
| NTUB1 | IC50 |
14.27 μM
Compound: 12
|
Cytotoxicity against human NTUB1 cells after 72 hrs by MTT assay
Cytotoxicity against human NTUB1 cells after 72 hrs by MTT assay
|
[PMID: 19758808] |
| Vero | CC50 |
>400 μM
Compound: 1a
|
Cytotoxicity against African green monkey Vero cells after 72 hrs by MTT assay
Cytotoxicity against African green monkey Vero cells after 72 hrs by MTT assay
|
[PMID: 29326018] |
Ursolic acid acetate (1-5 mM; 4.5 h) can reduce the ATPase activity of PfHsp90 in a dose-dependent manner[2].
Ursolic acid acetate has an IC50 of 24.93 μM against the P. falciparum FcB1 strain[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 7372-30-7
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Appearance Solid
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Molecular Weight 498.74
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Formula C32H50O4
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Color White to off-white
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SMILES
[H][C@]12C3=CC[C@]4([C@@](CC[C@]5(C(C)([C@H](CC[C@@]54C)OC(C)=O)C)[H])([C@@]3(CC[C@]1(CC[C@H]([C@@H]2C)C)C(O)=O)C)C)[H]
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Synonyms
Acetylursolic acid; 3-Acetylursolic acid
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Solvent & Solubility
DMSO : 25 mg/mL (50.13 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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 (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
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 (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- 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.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 1.25 mg/mL (2.51 mM); Clear solution
This protocol yields a clear solution of ≥ 1.25 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (12.5 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.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%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
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL. * In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation
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Data Sheet (275 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Chiang YM, et al. Cytotoxic triterpenes from the aerial roots of Ficus microcarpa. Phytochemistry. 2005 Feb;66(4):495-501. [Content Brief]
[2]. Nndwammbi AAT, et al. Ursolic acid acetate and iso-mukaadial acetate bind to Plasmodium falciparum Hsp90, abrogating its chaperone function in vitro. Naunyn Schmiedebergs Arch Pharmacol. 2024 Jul;397(7):5179-5192. [Content Brief]
Complete Stock Solution Preparation Table
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 (protect from light). 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 | 2.0051 mL | 10.0253 mL | 20.0505 mL | 50.1263 mL |
| 5 mM | 0.4010 mL | 2.0051 mL | 4.0101 mL | 10.0253 mL | |
| 10 mM | 0.2005 mL | 1.0025 mL | 2.0051 mL | 5.0126 mL | |
| 15 mM | 0.1337 mL | 0.6684 mL | 1.3367 mL | 3.3418 mL | |
| 20 mM | 0.1003 mL | 0.5013 mL | 1.0025 mL | 2.5063 mL | |
| 25 mM | 0.0802 mL | 0.4010 mL | 0.8020 mL | 2.0051 mL | |
| 30 mM | 0.0668 mL | 0.3342 mL | 0.6684 mL | 1.6709 mL | |
| 40 mM | 0.0501 mL | 0.2506 mL | 0.5013 mL | 1.2532 mL | |
| 50 mM | 0.0401 mL | 0.2005 mL | 0.4010 mL | 1.0025 mL |