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Simvastatin (CAS: 79902-63-9)
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| SKU-Pack Size | Availability | Size | Price | |
| EBC51095-1ML | In Stock | 1mL(10mM in DMSO) | ¥490.00 | |
| EBC51095-10MG | In Stock | 10mg | ¥490.00 | |
| EBC51095-50MG | In Stock | 50mg | ¥790.00 | |
| EBC51095-100MG | In Stock | 100mg | ¥1390.00 | |
| EBC51095-200MG | In Stock | 200mg | ¥2390.00 |
| Please Select The Country You Are In To Find Your Local Distributor. |
| 北京美瑞克生物科技有限公司 | Phone: +86 010-62890160 / 13691184142(微信同号) | |
| 2 / F, 128 malianwa North Road, Haidian District, | E-mail: mrkbio@163.com | |
| China | Beijing China | Website: www.mrkbio.com |
| Product Information | |||||||||||||||||||||
| Synonym(s) | MK 733, MK-0733,MK733 | ||||||||||||||||||||
| Application | Simvastatin is a HMGCR inhibitor and anti-proliferative agent | ||||||||||||||||||||
| CAS Number | 79902-63-9 | ||||||||||||||||||||
| Purity | ≥98.0% | ||||||||||||||||||||
| Molecular Weight | 418.57 | ||||||||||||||||||||
| Molecular Formula | C₂₅H₃₈O₅ | ||||||||||||||||||||
| SMILES | CCC(C)(C)C(O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(O3)=O)[C@@]12[H])=O | ||||||||||||||||||||
| Target & IC50 | HES: IC50 = 6.5 nM HMG-CoA reductase: IC50 = 3 nM |
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| Solubility | DMSO: 20.9 mg/mL (50 mM) Ethanol: 20.9 mg/mL (50 mM) |
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| Preparing Stock Solutions |
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| Shipping | Gel Pack | ||||||||||||||||||||
| Storage | Store at -20°C | ||||||||||||||||||||
| Research Use | For Research Use Only. Not Intended for Diagnostic Or Therapeutic Use. | ||||||||||||||||||||
| Product Description | |
Simvastatin is an HMGCR (HMG-CoA reductase) inhibitor with anti-proliferative properties. This compound has been shown to modulate purified bovine pituitary 20 S proteasome via mild stimulation of chymotrypsin-like activity and inhibition of peptidylglutamylpeptide hydrolyzing activity. Mechanistic studies suggest that Simvastatin decreases CDK4 and CDK2 kinase activities and represses high glucose-induced Rho A (Rho GTPase)/p21 signaling in mesangial cells. Simvastatin also potentiates apoptosis in human myeloid leukemia cells via the suppression of TNF-induced NF-κB activation (IC50 ~ 13 µM). |
| Specific Protocols | |