Mevastatin
Synonym(s):Compactin;Mevastatin - CAS 73573-88-3 - Calbiochem;ML-236B
- CAS NO.:73573-88-3
- Empirical Formula: C23H34O5
- Molecular Weight: 390.51
- MDL number: MFCD05662341
- EINECS: 700-442-0
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-09 19:38:33
What is Mevastatin?
Chemical properties
Off-White Solid
The Uses of Mevastatin
Mevastatin (compactin) is a diterpene produced by several species of the genera Penicillium and Monascus, first reported in 1976. Mevastatin, the prtotype of the statin class, is a potent competitive inhibitor of HMG-CoA reductase, a regulatory enzyme for cholesterol biosynthesis. Mevastatin has also been shown to induce apoptosis by inhibiting post-translational prenylation of proteins such as Ras, increasing eNOS mRNA and protein levels by blocking the geranylgeranylation of Rho, and inhibiting myoblast fusion. It induces cell cycle arrest in late G1 phase and may induce bone morphogenic protein-2 (BMP-2).
The Uses of Mevastatin
A fungal metabolite which is a potent inhibitor of HMG-CoA reductase.
The Uses of Mevastatin
antihyperlipidemic, HMGCoA reductase inhibitor
The Uses of Mevastatin
anti-hyperlipoproteinemic, 3-hydroxy-3-methyl glutaryl coenzyme A (HMG-CoA) reductase inhibitor
What are the applications of Application
Mevastatin (Compactin) is an HMGCR (HMG-CoA reductase) inhibitor
Definition
ChEBI: A carboxylic ester that is pravastatin that is lacking the allylic hydroxy group and in which the lactone moiety has been hydrolysed to the corresponding delta-hydroxy-carboxylic acid. A hydroxymethylglutaryl-CoA reductase inhibitor (stati ) isolated from Penicillium citrinum and from Penicillium brevicompactum, its clinical use as a lipid-regulating drug ceased following reports of toxicity in animals.
General Description
Chemical structure: statin
Biological Activity
Inhibitor of HMG-CoA reductase; decreases cholesterol biosynthesis, in vitro and in vivo . Induces apoptosis, arrests cancer cells in G1 phase and downregulates cdk 2, 4, and 6, cyclin D1 and E1, p21 and p27.
Biochem/physiol Actions
Mevastatin is a selective inhibitor of 3-hydroxy 3-methyl glutaryl coenzyme(A) reductase (HMG-CoA reductase), a major enzyme involved in cholesterol synthesis. It acts as a cholesterol-lowering agent. Mevastatin is obtained from various species of fungi. It acts as an antiresorptive?agent and has therapeutic effects to treat osteoporosis. Mevastatin inhibits bone resorption by triggering osteoclast apoptosis. It is also involved in the inhibition of prenylation of proteins such as Ras. Mevastatin increases endothelial nitric oxide synthase (eNOS) mRNA and protein levels by blocking the geranylgeranylation of transcription factor Rho.
storage
Store at RT
Purification Methods
Purify compactin by recrystallisation from aqueous EtOH. UV (EtOH): max 230, 237 and 246nm (log 4.28, 4.30 and 4.11); IR (KBr): 3520, 1750 (lactone CO) and 1710 (CO ester) cm-1. [Clive et al. J Am Chem Soc 110 6914 1988, Review: Rosen & Heathcock Tetrahedron 42 4909 1986, IR, NMR, MS: Brown et al. J Chem Soc Perkin Trans 1 1165 1976.] It is a potent inhibitor of 3-hydroxy-3-methylglutaryl-CoA reductase (HMG-CoA reductase), an enzyme in cholesterol biosynthesis, and lowers cholesterol levels [Brown et al. J Biol Chem 253 1121 1978, Nakamura & Ableles Biochemistry 24 1364 1985, Beilstein 18/3 V 145].
References
[1] endo a. the discovery and development of hmg-coa reductase inhibitors. journal of lipid research, 1992, 33(11): 1569-1582.
Properties of Mevastatin
Melting point: | 151-153 °C |
Boiling point: | 555.0±50.0 °C(Predicted) |
alpha | D22 +283° (c = 0.48 in acetone) |
Density | 1.13±0.1 g/cm3(Predicted) |
vapor pressure | 0Pa at 25℃ |
storage temp. | 2-8°C |
solubility | DMSO: 20 mg/mL |
form | powder |
pka | 13.49±0.40(Predicted) |
color | white |
λmax | 246nm(MeOH)(lit.) |
Merck | 14,6164 |
BRN | 1269441 |
CAS DataBase Reference | 73573-88-3(CAS DataBase Reference) |
Safety information for Mevastatin
Signal word | Danger |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P271:Use only outdoors or in a well-ventilated area. P280:Wear protective gloves/protective clothing/eye protection/face protection. P312:Call a POISON CENTER or doctor/physician if you feel unwell. P302+P352:IF ON SKIN: wash with plenty of soap and water. P304+P340:IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P403+P233:Store in a well-ventilated place. Keep container tightly closed. |
Computed Descriptors for Mevastatin
InChIKey | AJLFOPYRIVGYMJ-INTXDZFKSA-N |
New Products
ALUMINIUM IODIDE 100 GM BUFFER CAPSULE PH 7.0 - 10 CAP BUFFER SOLUTION PH 9.5 (BORATE) EZEE BLUE GEL STAINER BORAX CARMINE (GRENACHERS ALCOHOLIC) POTASSIUM IODATE - IODIDE SOLN 0.1 N Dabigatran Acyl-O3-D-Glucuronide Trifluoroacetic Acid Salt Isofolic Acid Dabigatran 2-O-acylglucuronide metabolite Dabigatran Acyl-?-D- glucuronide Trifluroacetic Acid Erythromycin EP Impurity A Desloratidine Related Compound ARelated products of tetrahydrofuran
You may like
-
Mevastatin 95% CAS 73573-88-3View Details
73573-88-3 -
Mevastatin CAS 73573-88-3View Details
73573-88-3 -
Mevastatin CAS 73573-88-3View Details
73573-88-3 -
Mevastatin/Lovastatin Impurity A CAS 73573-88-3View Details
73573-88-3 -
Mevastatin CAS 73573-88-3View Details
73573-88-3 -
Edoxaban Impurity 57View Details
2089454-69-1 -
Empagliflozin Bromo ImpurityView Details
-
Ipratropium EP Impurity BView Details
58073-59-9