research use only
Cat.No.S3909
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In vitro |
DMSO
: 72 mg/mL
(198.71 mM)
Water : 72 mg/mL Ethanol : 5 mg/mL |
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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.
| Molecular Weight | 362.33 | Formula | C15H22O10 |
Storage (From the date of receipt) | |
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| CAS No. | 2415-24-9 | -- | Storage of Stock Solutions |
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| Synonyms | Catalpinoside, Digitalis purpurea L | Smiles | C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O | ||
| In vitro |
Catalpol is able to inhibit HCT116 cell proliferation. Furthermore, this compound induces apoptosis in HCT116 cells, which depends on the increased activities of caspase-3 and −9. In addition, it reduces the expression of PI3K, p-Akt and Akt in HCT116 cells. In vitro, this chemical inhibits TNF-α, IL-6, IL-4 and IL-1β production and up-regulates IL-10 expression in LPS-stimulated alveolar macrophages.
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| In vivo |
Catalpol decreases peroxynitrite formation and consequently exerts cardioprotective effects through the PI3K/Akt signaling pathway in ischemic/reperfusion rats. This compound inhibits lung W/D ratio, myeloperoxidase activity of lung samples, the amounts of inflammatory cells and TNF-α, IL-6, IL-4 and IL-1β in BALF induced by LPS. The production of IL-10 in BALF is up-regulated by this chemical.
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References |
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