Simvastatin

製品コードS1792 バッチS179208

化学情報

	Synonyms	MK 733	Storage (From the date of receipt)	3 years -20°C powder 1 years -80°C in solvent
	化学式	C₂₅H₃₈O₅
	分子量	418.57	CAS No.	79902-63-9
Solubility (25°C)*	体外	DMSO	84 mg/mL (200.68 mM)
		Ethanol	84 mg/mL (200.68 mM)
		Water	Insoluble
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液（一定の濃度）を調合する

生物活性

製品説明	Simvastatin is a competitive inhibitor of HMG-CoA reductase with K_i of 0.1-0.2 nM in cell-free assays. Simvastatin induces ferroptosis, mitophagy, autophagy and apoptosis.
in vitro	Prior to use in cell assays, Simvastatin needs to be activated by NaOH in EtOH treatment. This compound inhibits cholesterol synthesis in mouse L-M cell (fibroblast), rat H4II E cell (liver), and human Hep G2 cell (liver) with IC50 of 19.3 nM, 13.3 nM and 15.6 nM, respectively. ^[1] This compound treatment leads to a dose-dependent increase in serine 473 phosphorylation of Akt within 30 minutes, with maximal phosphorylation occurring at 1.0 µM. It (1.0 μM) enhances phosphorylation of the endogenous Akt substrate endothelial nitric oxide synthase (eNOS), inhibits serum-free media undergo apoptosis and accelerates vascular structure formation. ^[2] This chemical displays anti-inﬂammatory effects in vitro. It (10 μM) reduces anti-CD3/anti-CD28 antibody-stimulated proliferation of PB-derived mononuclear cells and synovial ﬂuid cells from rheumatoid arthritis blood, as well as IFN-γ release. This compound (10 μM) suppresses cell-mediated macrophage TNF-γ release induced via cognate interactions by ~30%. ^[3]
in vivo	Simvastatin orally administration inhibits the conversion of radiolabeled acetate to cholesterol with IC50 of 0.2 mg/kg. ^[1] This compound (4 mg/day) orally administration for 13 weeks to rabbits fed an atherogenci cholesterol-rich diet, returns the cholesterol-induced increases in total cholesterol, LDL-cholesterol and HDL-cholesterol to normal level. ^[4] This compound (6 mg/kg) produces an increase in LDL receptor-dependent binding and increases the number of hepatic LDL receptors in rabbits fed a diet containing 0.25% cholesterol. ^[5] This compound influences inflammation independent of its effect on plasma cholesterol level. In cynomolgus monkeys consumed an atherogenic diet, this compound (20 mg/kg/day) induces a 1.3-fold less macrophage content in lesions, and 2-fold less vascular cell adhesion molecule-1, interleukin-1beta, and tissue factor expression, companied by a 2.1-fold increases in lesional smooth muscle cell and collagen content. ^[6]

製品説明

Simvastatin is a competitive inhibitor of HMG-CoA reductase with K_i of 0.1-0.2 nM in cell-free assays. Simvastatin induces ferroptosis, mitophagy, autophagy and apoptosis.

in vitro

Prior to use in cell assays, Simvastatin needs to be activated by NaOH in EtOH treatment. This compound inhibits cholesterol synthesis in mouse L-M cell (fibroblast), rat H4II E cell (liver), and human Hep G2 cell (liver) with IC50 of 19.3 nM, 13.3 nM and 15.6 nM, respectively. ^[1]

This compound treatment leads to a dose-dependent increase in serine 473 phosphorylation of Akt within 30 minutes, with maximal phosphorylation occurring at 1.0 µM. It (1.0 μM) enhances phosphorylation of the endogenous Akt substrate endothelial nitric oxide synthase (eNOS), inhibits serum-free media undergo apoptosis and accelerates vascular structure formation. ^[2]

This chemical displays anti-inﬂammatory effects in vitro. It (10 μM) reduces anti-CD3/anti-CD28 antibody-stimulated proliferation of PB-derived mononuclear cells and synovial ﬂuid cells from rheumatoid arthritis blood, as well as IFN-γ release. This compound (10 μM) suppresses cell-mediated macrophage TNF-γ release induced via cognate interactions by ~30%. ^[3]

in vivo

Simvastatin orally administration inhibits the conversion of radiolabeled acetate to cholesterol with IC50 of 0.2 mg/kg. ^[1]

This compound (4 mg/day) orally administration for 13 weeks to rabbits fed an atherogenci cholesterol-rich diet, returns the cholesterol-induced increases in total cholesterol, LDL-cholesterol and HDL-cholesterol to normal level. ^[4]

This compound (6 mg/kg) produces an increase in LDL receptor-dependent binding and increases the number of hepatic LDL receptors in rabbits fed a diet containing 0.25% cholesterol. ^[5]

This compound influences inflammation independent of its effect on plasma cholesterol level. In cynomolgus monkeys consumed an atherogenic diet, this compound (20 mg/kg/day) induces a 1.3-fold less macrophage content in lesions, and 2-fold less vascular cell adhesion molecule-1, interleukin-1beta, and tissue factor expression, companied by a 2.1-fold increases in lesional smooth muscle cell and collagen content. ^[6]

プロトコル(参考用のみ)

キナーゼアッセイ	HMG-CoA reductase activity assay
キナーゼアッセイ	The total volume of each assay is 95 μL and the reaction mixture contained 10 μL of the inhibiting compound to be tested and 85 μL of the incubating buffer containing 2 mg/mL liver microsomes, 0.1 M KH₂PO₄, pH 7.2, 5.7 mM dithiothreitol, 10 mM glucose-6-phosphate, 2 U/mL glucose-6-phosphate dehydrogenase, 1 mM NADP, 10 μM miconazole. Control experiments are done without NADPH generating system. All samples are incubated 10 min at 37 ℃ before addition of 5μL of substrate (unlabelled and 14C-HMG-3-hydroxy-3-methyl glutaryl CoA, final concentration 50 μM, 2.5 nCi/nmole). After 30 min at 37 ℃, the reaction is stopped by adding 27 μL 1N HCl and 20 μL of unlabelled mevalonolactone (200 μg/assay). The conversion of mevalonic acid to lactone is performed at room temperature for 60 min.
細胞アッセイ	細胞株	HUVECs
	濃度	1 μM
	反応時間	30 minutes
	実験の流れ	HUVECs were treated with simvastatin for 30 minutes.
動物実験	動物モデル	Male Japanese white rabbits
	投薬量	2.5, 5, & 10 mg/kg
	投与方法	Oral

参考

https://pubmed.ncbi.nlm.nih.gov/3076125/
https://pubmed.ncbi.nlm.nih.gov/10973320/
https://pubmed.ncbi.nlm.nih.gov/12538717/

https://pubmed.ncbi.nlm.nih.gov/2724674/
https://pubmed.ncbi.nlm.nih.gov/2106347/
https://pubmed.ncbi.nlm.nih.gov/12231565/
https://pubmed.ncbi.nlm.nih.gov/10965989/

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カスタマーフィードバック

: , , JAMA Oncol, 2015, 1(4):495-504.

: Data from [Data independently produced by , , Haematologica, 2018, doi: 10.3324/haematol.2018.204701]

: Data from [Data independently produced by , , Cell Physiol Biochem, 2018, 46(2):618-632]

Selleckの高級品が、幾つかの出版された研究調査結果（以下を含む）で使われた：

Fructose and glucose from sugary drinks enhance colorectal cancer metastasis via SORD [ Nat Metab, 2025, 7(10):2018-2032]	PubMed: 40973819
Simvastatin overcomes the pPCK1-pLDHA-SPRINGlac axis-mediated ferroptosis and chemo-immunotherapy resistance in AKT-hyperactivated intrahepatic cholangiocarcinoma [ Cancer Commun (Lond), 2025, 10.1002/cac2.70036]	PubMed: 40443016
Coenzyme A protects against ferroptosis via CoAlation of mitochondrial thioredoxin reductase [ J Clin Invest, 2025, e190215]	PubMed: 40694424
Commonly prescribed multi-medication therapies exert sex-specific effects on Alzheimer's disease pathology and metabolomic profiles in AppNL-G-F mice: Implications for personalized therapeutics in aging [ Alzheimers Dement, 2025, 21(3):e70081]	PubMed: 40145346
Macrophages form dendrite-like pseudopods to enhance bacterial ingestion [ EMBO J, 2025, 10.1038/s44318-025-00515-z]	PubMed: 40721684
CRISPR/Cas9-mediated SHP-1-knockout T cells combined with simvastatin enhances anti-tumor activity in humanized-PDX HCC model [ iScience, 2025, 28(4):112266]	PubMed: 40241752
Ferroptosis as a therapeutic vulnerability in MDM2 inhibition in dedifferentiated liposarcoma [ Oncol Lett, 2025, 29(6):269]	PubMed: 40247991
Epstein-Barr Virus-Driven B-Cell Transformation under Germinal Center Hypoxia Requires External Unsaturated Fatty Acids [ Res Sq, 2025, rs.3.rs-6506954]	PubMed: 40313738
The mevalonate pathway couples lipid metabolism to amino acid synthesis via ubiquinone-dependent redox control [ bioRxiv, 2025, 2025.08.10.669191]	PubMed: 40832310
ETS1 Orchestrates a Hybrid EMT Program Driving in vivo Metastasis and Immune Evasion [ bioRxiv, 2025, 2025.07.17.665404]	PubMed: 40777467

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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