research use only
Cat.No.S2370
| Molecular Weight | 456.7 | Formula | C30H48O3 |
Storage (From the date of receipt) | |
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| CAS No. | 77-52-1 | Download SDF | Storage of Stock Solutions |
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| Synonyms | NSC 167406, NSC-4060, Prunol, Urson, Malol | Smiles | CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O | ||
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In vitro |
DMSO
: 91 mg/mL
(199.25 mM)
Water : Insoluble Ethanol : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
| In vitro |
Ursolic acid (Malol) is a pentacyclic triterpene acid, used in cosmetics, that is also capable of inhibiting various types of cancer cells by inhibiting the STAT3 activation pathway and human fibrosarcoma cells by reducing the expression of matrix metalloproteinase-9 by acting through the glucocorticoid receptor. As medicine, it is well tolerated and can be used topically and orally. Ursolic acid can also serve as a starting material for synthesis of more potent bioactive derivatives, such as anti-tumour agents.
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References |
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| Methods | Biomarkers | Images | PMID |
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| Western blot | p-AKT / MDM2 / TOPK / p-TOPK p21 KRAS(G12V) / p-B-Raf / B-Raf / p-MEK / MEK / p-ERK / ERK p-IKKα / IKKα / p-IκBα / IκBα / p-p65 / p65 p-NF-κB / NF-κB E-cadherin / Vimentin / N-cadherin / Twist / β-catenin / p-GSK3β / Cyclin D1 |
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26582056 |
| Growth inhibition assay | Cell viability |
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27472952 |
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