Home Cart Sign in  
Chemical Structure| 101314-97-0 Chemical Structure| 101314-97-0

Structure of 101314-97-0

Chemical Structure| 101314-97-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Simvastatin hydroxy acid sodium is an effective HMG-CoA reductase (HMGCR) inhibitor that significantly reduces indole sulfate-mediated reactive oxygen species (ROS) generation while regulating OATP3A1 expression in cardiomyocytes and OATP3A1-transfected HEK293 cells, demonstrating cardiovascular protective effects.

Synonyms: SVA; Simvastatin (sodium salt); Simvastatin Impurity A sodium

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Simvastatin hydroxy acid sodium

CAS No. :101314-97-0
Formula : C25H39NaO6
M.W : 458.56
SMILES Code : O=C([O-])C[C@H](O)C[C@H](O)CC[C@H]1[C@@H](C)C=CC2=C[C@H](C)C[C@H](OC(C(C)(C)CC)=O)[C@]12[H].[Na+]
Synonyms :
SVA; Simvastatin (sodium salt); Simvastatin Impurity A sodium
MDL No. :MFCD04974206

Safety of Simvastatin hydroxy acid sodium

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H303-H361
Precautionary Statements:P201-P202-P280-P312-P405-P501

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Recombinant CYP2C8 1–100 µM 10 min CYP2C8 catalyzed SVA metabolism to three products with lower activity. Km and Vmax values were 88 μM and 2.8 nmol min-1 pmol-1 P450, respectively. Br J Clin Pharmacol. 2003 Jul;56(1):120-4
Recombinant CYP3A4 1–100 µM 10 min CYP3A4 catalyzed SVA metabolism to three products with the highest activity. Km and Vmax values were 26 μM and 7.3 nmol min-1 pmol-1 P450, respectively. Br J Clin Pharmacol. 2003 Jul;56(1):120-4
Human liver microsomes 1–100 µM 12 min Studied oxidative metabolism of SVA, generating three major oxidative products (M1, M2, and M3). Km and Vmax values were 50-80 μM and 0.6-1.9 nmol min-1 mg-1 protein, respectively. Br J Clin Pharmacol. 2003 Jul;56(1):120-4
Mouse ependymoma cell line 0.1 µM 72 hours Evaluate the cytotoxic effect of simvastatin hydroxy acid on mouse ependymoma cell line, showing antitumor activity Drug Metab Dispos. 2016 Apr;44(4):591-4

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Sprague-Dawley rats Diet-induced nonalcoholic steatohepatitis (NASH) model Intravenous injection 1 mg/kg Single dose, observed for 120 minutes To assess the metabolism and disposition of SIM in a diet-induced rodent model of NASH. Results showed that NASH caused increased plasma retention and decreased biliary excretion of SIMA due to decreased protein expression of multiple hepatic Oatps. J Pharmacol Exp Ther. 2014 Mar;348(3):452-8
CD1 nude mice Mouse ependymoma model Oral 100 mg/kg Single dose Assess the exposure of simvastatin hydroxy acid in tumor extracellular fluid, showing concentrations below in vitro IC50 values, insufficient to achieve tumor growth inhibition Drug Metab Dispos. 2016 Apr;44(4):591-4

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.18mL

0.44mL

0.22mL

10.90mL

2.18mL

1.09mL

21.81mL

4.36mL

2.18mL

 

Historical Records

Categories