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Lovastatin

Lovastatin Structure
CAS No.
75330-75-5
Chemical Name:
Lovastatin
Synonyms
MONACOLIN K;MEVINOLIN;LOVASTATION;Lovastatin,Monacolin K;mevlor;msd803;MK-803;Sivlor;LOVALIP;MEVACOR
CBNumber:
CB7169342
Molecular Formula:
C24H36O5
Molecular Weight:
404.54
MOL File:
75330-75-5.mol
MSDS File:
SDS
Modify Date:
2024/8/21 22:41:43

Lovastatin Properties

Melting point 175°C
alpha D25 +323° (c = 0.5 g in 100 ml acetonitrile)
Boiling point 559.2±50.0 °C(Predicted)
Density 1.12±0.1 g/cm3(Predicted)
vapor pressure 0Pa at 25℃
refractive index 320 ° (C=0.5, CH3CN)
storage temp. -20°C
solubility ethanol: soluble9.80-10.20mg/mL, clear, colorless to faintly yellow
form White to off-white powder
pka 13.49±0.40(Predicted)
color White
Water Solubility 0.0004 mg/mL at 25 ºC
Merck 14,5586
BCS Class 2
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 2 months.
LogP 4.260
CAS DataBase Reference 75330-75-5(CAS DataBase Reference)
EPA Substance Registry System Lovastatin (75330-75-5)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Warning
Hazard statements  H351-H361f
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-36/37/39-26
RIDADR  3077
WGK Germany  3
RTECS  EK7907000
HazardClass  9
PackingGroup  III
HS Code  29322090
Toxicity LD50 orally in mice: >1000 mg/kg (Endo)
NFPA 704
1
2 1

Lovastatin price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) PHR1285 Lovastatin Pharmaceutical Secondary Standard; Certified Reference Material 75330-75-5 1G ₹8042.98 2022-06-14 Buy
Sigma-Aldrich(India) M2147 Mevinolin from Aspergillus sp. ≥98% (HPLC) 75330-75-5 25MG ₹22440.23 2022-06-14 Buy
Sigma-Aldrich(India) 438185 Lovastatin - CAS 75330-75-5 - Calbiochem Lovastatin, CAS 75330-75-5, is an anti-hypercholesterolemic agent that inhibits the activity of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reduct 75330-75-5 25MG ₹20710 2022-06-14 Buy
TCI Chemicals (India) L0214 Lovastatin 75330-75-5 5G ₹9000 2022-05-26 Buy
TCI Chemicals (India) L0214 Lovastatin 75330-75-5 25G ₹13200 2022-05-26 Buy
Product number Packaging Price Buy
PHR1285 1G ₹8042.98 Buy
M2147 25MG ₹22440.23 Buy
438185 25MG ₹20710 Buy
L0214 5G ₹9000 Buy
L0214 25G ₹13200 Buy

Lovastatin Chemical Properties,Uses,Production

Description

Lovastatin is an orally-active hypocholesterolemic useful in the treatment of familial hypercholesterolemia. The drug acts by inhibiting the HMG-CoA reductase-catalyzed rate limiting step of cholesterol biosynthesis. While treatment with lovastatin leads to significant reductions in total and LDL cholesterol, its effect on atherosclerosis or coronary heart disease has not been established.

Chemical Properties

White Solid

Physical properties

Appearance: White, nonhygroscopic crystalline powder. Solubility: Insoluble in water (0.0004?mg/mL); sparingly soluble in ethanol, methanol, isobutanol, isopropanol, acetonitrile, n-propanol; soluble in acetone, N-dimethylformamide; freely soluble in chloroform. Melting point: 174.5?°C. Specific optical rotation: 25?°C for D (sodium) line, +323° (concentration 0.5? g in 100? ml acetonitrile). Stability: Lovastatin is sensitive to light. Following exposure to extreme light conditions, the drug is stable for 24?h or 1?month when exposed to UV (approximately 3230 lux) or fluorescent (approximately 10,764 lux) light, respectively, at 28?°C in air.

History

Statins are the most extensively used class of lipid-lowering medication. Lovastatin is the second statin discovered by scientists.
Later, the official name lovastatin was established. The activity of lovastatin is much better than compactin.
In July 1982, lovastatin showed dramatic effects on lowering LDL cholesterol in patients with severe hypercholesterolemia who were unresponsive to the existedmedicines, with very few adverse reactions .

Uses

Lovastatin (mevinolin) is a metabolite first isolated from Monascus ruber and later found in several other fungal species. Lovastatin is a potent inhibitor of HMG-CoA. HMG-CoA reductase is the rate-controlling enzyme of the mevalonate pathway, responsible for the biosynthesis of cholesterol. Lovastatin was developed as a drug as a hypolipemic agent.

Indications

Hypercholesterolemia, combined hyperlipidemia.

General Description

Lovastatin, 2-methylbutanoic acid 1,2,3,7,8,8a-hexahydro-3,7-dimethyl-8-[2-(tetrahydro-4-hydroxy6-oxo-2H-pyran-2-yl)ethyl]-1-naphthalenyl ester, mevinolin,MK-803 (Mevacor) (formerly called mevinolin), is a potentinhibitor of HMG-CoA. The drug was obtained originallyfrom the fermentation products of the fungi Aspergillus terreusand Monascus ruber. Lovastatin was one of two originalHMG-CoA reductase inhibitors. The other drug, mevastatin(formerly called compactin), was isolated from cultures ofPenicillium cillium citrum. Mevastatin was withdrawn fromclinical trials because it altered intestinal morphology in dogs.This effect was not observed with lovastatin. For inhibitoryeffects on HMG-CoA reductase, the lactone ring must be hydrolyzedto the open-ring heptanoic acid.

Biological Activity

Potent, competitive inhibitor of HMG-CoA reductase (K i = 0.6 nM) therefore decreases cholesterol biosynthesis, in vitro and in vivo . Decreases CDK2, 4, 6 and cyclin E levels and induces G1 arrest and apoptosis in tumor cell lines in vitro .

Pharmacology

Lovastatin is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), an enzyme that catalyzes the conversion of HMG-CoA to mevalonate , a rate-determining step of cholesterol biosynthesis. Lovastatin is metabolized as a prodrug into an active form, lovastatin acid. Lovastatin acid is a reversible competitive inhibitor for HMG-CoA.
However, the reduction in plasma cholesterol by statins is not only due to reduction in cholesterol biosynthesis. .
In addition to their lipid-lowering properties, statins produce several nonlipidrelated properties, include decreasing levels of high-sensitivity C-reactive protein (hsCRP), improving endothelial function, reducing inflammation at the site of the atherosclerotic plaque, inhibiting platelet aggregation, anticoagulant, etc. .

Clinical Use

The primary uses of lovastatin are the treatment of dyslipidemia and the prevention of cardiovascular disease. It is recommended to be used only when other approaches such as diet, exercise, and weight reduction have not improved the cholesterol profile (“Lovastatin”. The American Society of Health-System Pharmacists. Retrieved 3 April 2011.). Lovastatin is useful in treating hypercholesterolemia and combined hyperlipidemia. However, lovastatin is not effective in treatment of receptornegative homozygous familial hypercholesterolemia .

Side effects

Lovastatin's common side effects are listed in approximately descending order of occurrence frequency: creatine phosphokinase elevation, flatulence, abdominal pain, constipation, diarrhea, muscle aches or pains, nausea, indigestion, weakness, blurred vision, rash, dizziness, and muscle cramps. As with all statin drugs, it can rarely cause myopathy, hepatotoxicity (liver damage), dermatomyositis, or rhabdomyolysis.

Lovastatin Preparation Products And Raw materials

Global( 587)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Concord Biotech Limited +91-2714398200 +91-2714398200 Gujarat, India 22 58 Inquiry
Ebenezer Industries Gujarat, India 96 58 Inquiry
Krebs Biochemicals And Industries Limited +91-4066808040 +91-4066808040 Telangana, India 3 58 Inquiry
Scinva Chemicals and Pharmaceuticals Pvt Ltd +91-7406196725 +91-7406196725 Karnataka, India 71 58 Inquiry
Vishrudh laboratories pvt ltd +91-9666132889 +91-8097369002 Telangana, India 117 58 Inquiry
GLP Pharma Standards +91 9866074638 Hyderabad, India 1644 58 Inquiry
SETV ASRV LLP +91-9731133411 +91-9731133411 Telangana, India 531 58 Inquiry
Allmpus Laboratories Pvt Ltd +91-9518738415 +91-9167862134 Maharashtra, India 657 58 Inquiry
Pacific Agencies 08048372547Ext 801 Mumbai, India 135 58 Inquiry
Krebs Bio Chemical & Industries Limited 09849658924 Hyderabad, India 2 58 Inquiry

Lovastatin Spectrum

SiMvastatin EP IMpurity E Lovastatin,Monacolin K 8-[2-(4-Hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-1-nap 6alpha-Methylcompactin Mevinolin Monacolin K )ethyl]-1-naphthalenylester [1s-[1alpha(r*),3alpha,7beta,8beta(2s*,4s*),8abeta]]-2-methylbutanoicacid1,2, 1,2,6,7,8,8a-hexahydro-beta,delta-dihydroxy-2,6-dimethyl-8-(2-methyl-1-oxobuty 2-methyl-,1,2,3,7,8,8a-hexahydro-3,7-dimethyl-8-(2-(tetrahydro-butanoicaci 3,7,8,8a-hexahydro-3,7-dimethyl-8-[2-(tetrahydro-4-hydroxy-6-oxo-2h-pyran-2-yl 8-[2-(4-Hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethy l]-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-1-naphthal Lovastatin, USP 5-(4-broMophenyl)-1,2-thiazole Lovastatin-d9 (Mixture of stereoisoMers) Lovastatin API Mevinolin 6alpha-Methylcompactin Monacolin K 5-KG TIN Lovastatin USP 23 (1S,3R,7S,8S,8aR)-8-{2-[(2R,4R)-4-Hydroxy-6-oxooxan-2-yl]ethyl}-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl (2S)-2-methylbutanoate (2S)-(1S,3R,7S,8S)-8-(2-((2R,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl)-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl 2-methylbutanoate Lovastatin Solution, 1000ppm Simvastatin Impurity 5(Simvastatin EP Impurity E) Lovastatin, 98%, an inhibitor of HMG-CoA reductase lMevinolin 8-[2-(4-Hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-1-naphth Mevinolin, 6-alpha-Methylcompactin Mevinolin, Monacolin K, L 154803, MB 530B, MSD 803 Lovastatin (Mevacor) Lovastatin for peak identification [8-[2-(4-hydroxy-6-oxooxan-2-yl)ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2-methylbutanoate [8-[2-(4-hydroxy-6-oxo-tetrahydropyran-2-yl)ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2-methylbutanoate 2-methylbutanoic acid [8-[2-(4-hydroxy-6-oxo-2-tetrahydropyranyl)ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl 8-[2-(4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl 2-methylbutanoate (2S)-2-methyl-butanoic acid (1S,3R,7S,8S,8aR)-1,2,3,7,8,8a-hexahydro-3,7-dimethyl-8-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1-naphthalenyl ester 3r,7s,8s,8ar)-1,2,3,7,8,8a-hexahydro-3,7-dimethyl-8-[2-[2r,4r)-tetrahydro-(1 4-hydroxy-6-oxo-2h-pyran-2-yl)ethyl)-1-naphthalenylester,(1s-(1-alpha-(r*),3 4-hydroxy-6-oxo-2h-pyran-2-yl]ethyl]-1-naphthalenyl(s)-2-methyl-butyrate mevlor msd803 oxy)-1-naphthaleneheptanoicaciddelta-lactone LOVASTATION LOVASTIN LOVALIP LOVASTATIN MEVINOLIN MEVACOR MEVINACOR (2S)-(1S,3R,7S,8S,8AR)-1,2,3,7,8,8A-HEXAHYDRO-3,7-DIMETHYL-8-[2-[(2R,4R)-TETRAHYDRO-4-HYDROXY-6-OXO-2H-PYRAN-2-YL]ETHYL]-1-NAPHTHALENYL-2-METHYL BUTANOATE 2BETA,6ALPHA-DIMETHYL-8ALPHA-(2-METHYL-1-OXOBUTOXY)MEVINIC ACID LACTONE 1,2,3,7,8,8a-hexahydro-3,7-dimethyl-8-[2-(tetrahydro-4-hydroxy-6-oxo-2h-pyran-2-yl)ethyl]-1-naphthalenyl 2-methylbutanoate 6-A-METHYLCOMPACTIN 6ALPHA-METHYLCOMPACTIN MONACOLIN K MK-803 (S)-2-METHYL-BUTYRIC ACID (1S,3R,7S,8S,8AR)-8-[2-((2R,4R)-4-HYDROXY-6-OXO-TETRAHYDRO-PYRAN-2-YL)-ETHYL]-3,7-DIMETHYL-1,2,3,7,8,8A-HEXAHYDRO-NAPHTHALEN-1-YL ESTER Lovastatin USP24 LOVASTATIN MM(CRM STANDARD) LOVASTATIN USP(CRM STANDARD) RedYeastRice