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Lovastatin-d9

Catalog No.GC47578 Copy One-Click Copy Product Info

A neuropeptide with diverse biological activities

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Lovastatin-d9 Chemical Structure

Cas No.: N/A

Taille Prix Stock Qté
1 mg
424,00 $US
En stock

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Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.



Description of Lovastatin-d9

Lovastatin-d9 is intended for use as an internal standard for the quantification of lovastatin by GC- or LC-MS. Lovastatin is an HMG-CoA reductase inhibitor that was originally isolated from A. terreus.1 It is a prodrug of its more potent metabolite, lovastatin hydroxy acid . Both competitively inhibit HMG-CoA reductase with Ki values of 1.4 and 0.6 nM for lovastatin and the open ring, hydroxy acid form, respectively.2 Lovastatin (8 mg/kg per day) reduces plasma cholesterol in dogs by 29% over a three-week period. It also suppresses TNF-induced NF-κB activation (IC50 = ~15 µM), which potentiates apoptosis in human myeloid leukemia cells.3 Formulations containing lovastatin were the first HMG-CoA reductase inhibitors to be used in the treatment of hypercholesterolemia.

1.Endo, A.The discovery and development of HMG-CoA reductase inhibitorsJ. Lipid Res.33(11)1569-1582(1992) 2.Alberts, A.W., Chen, J., Kuron, G., et al.Mevinolin: A highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agentProc. Natl. Acad. Sci. USA77(7)3957-3961(1980) 3.Ahn, K.S., Sethi, G., and Aggarwal, B.B.Reversal of chemoresistance and enhancement of apoptosis by statins through down-regulation of the NF-κB pathwayBiochem. Pharmacol.75(4)907-913(2008)

Chemical Properties of Lovastatin-d9

Cas No. N/A SDF
Canonical SMILES C[C@@H]1C[C@H](OC(C(C([2H])([2H])[2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O)[C@@]2([H])C(C=C[C@H](C)[C@@H]2CC[C@@H]3C[C@@H](O)CC(O3)=O)=C1
Formula C24H27D9O5 M.Wt 413.6
Solubility Chloroform: slightly soluble,Methanol: slightly soluble Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Lovastatin-d9

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1 mg 5 mg 10 mg
1 mM 2.4178 mL 12.089 mL 24.1779 mL
5 mM 483.6 μL 2.4178 mL 4.8356 mL
10 mM 241.8 μL 1.2089 mL 2.4178 mL
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In vivo Formulation Calculator (Clear solution) of Lovastatin-d9

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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 saline, 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.
3. All of the above co-solvents are available for purchase on the GlpBio website.

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Review for Lovastatin-d9

Average Rating: 5 ★★★★★ (Based on Reviews and 12 reference(s) in Google Scholar.)

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