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Fluvastatin

CAS No.
93957-54-1
Chemical Name:
Fluvastatin
Synonyms
Lescol;Lipaxan;Leschol;Primexin;T-Powder;FLUVASTATIN;Molysulfide;Moly Powder B;FLUVASTATIN NA;Fluvastatin-D7
CBNumber:
CB7115046
Molecular Formula:
C24H26FNO4
Molecular Weight:
411.47
MDL Number:
MFCD00869941
MOL File:
93957-54-1.mol
MSDS File:
SDS
Last updated:2023-06-08 09:01:57

Fluvastatin Properties

Melting point 193.9-196.9 °C
Boiling point 681.8±55.0 °C(Predicted)
Density 1.23±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility Water 25 mg/ml DMSO 100 mg/ml Ethanol 25 mg/ml
form Powder
pka 4.27±0.10(Predicted)
CAS DataBase Reference 93957-54-1(CAS DataBase Reference)
FDA UNII 4L066368AS
NCI Drug Dictionary Lescol
ATC code C10AA04
EPA Substance Registry System 6-Heptenoic acid, 7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]- 3,5-dihydroxy-, (3R,5S,6E)-rel- (93957-54-1)

Pharmacokinetic data

Protein binding >98%
Excreted unchanged in urine 6%
Volume of distribution 0.35
Biological half-life 1.4-3.2 / Unchanged

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H412
Precautionary statements  P273-P305+P351+P338
NFPA 704
0
3 0

Fluvastatin price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 10010334 Fluvastatin ≥98% 93957-54-1 10mg $40 2024-03-01 Buy
Cayman Chemical 10010334 Fluvastatin ≥98% 93957-54-1 25mg $89 2024-03-01 Buy
Cayman Chemical 10010334 Fluvastatin ≥98% 93957-54-1 50mg $146 2024-03-01 Buy
Cayman Chemical 10010334 Fluvastatin ≥98% 93957-54-1 100mg $254 2024-03-01 Buy
American Custom Chemicals Corporation API0002749 FLUVASTATIN 95.00% 93957-54-1 10MG $1030.02 2021-12-16 Buy
Product number Packaging Price Buy
10010334 10mg $40 Buy
10010334 25mg $89 Buy
10010334 50mg $146 Buy
10010334 100mg $254 Buy
API0002749 10MG $1030.02 Buy

Fluvastatin Chemical Properties,Uses,Production

Originator

Lipaxan, Italfarmaco spa

Uses

anti-hyperlipoproteinemic, 3-hydroxy-3-methyl glutaryl coenzyme A (HMG-CoA) reductase inhibitor

Uses

antineoplastic, aromatase inhibitor

Uses

A synthetic HMG-CoA reductase inhibitor

Definition

ChEBI: (3R,5S)-fluvastatin is a (6E)-7-[3-(4-fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoic acid diastereoisomer in which the stereocentres beta- and delta- to the carboxy group have R and S configuration, respectively. The drug fluvastatin is an equimolar mixture of this compound and its enantiomer. It is a (6E)-7-[3-(4-fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoic acid and a statin (synthetic). It is a conjugate acid of a (3R,5S)-fluvastatin(1-). It is an enantiomer of a (3S,5R)-fluvastatin.

Manufacturing Process

164 ml (235.1 g, 2.04 moles) of chloroacetyl chloride is added over a 50 min period to a mixture of 400 ml (410 g, 4.22 moles) of fluorobenzene and 300.0 g (2.25 moles) of anhydrous aluminum chloride stirred at 75°C under nitrogen. The reaction mixture is stirred at 80°C under nitrogen for 1 h, cooled to 50°C, 500 ml of fluorobenzene is added, and the reaction mixture is cooled to 0°C and gradually (over a 30 min period) siphoned into 1 L of 6 N hydrochloric acid stirred at 0°C. (The temperature of the aqueous acid is maintained at or below 25°C throughout the addition). The quenched, acidified reaction mixture is stirred for 15 min, and the aqueous phase is separated and extracted with 350 ml of fluorobenzene. The two organicphases are combined and washed twice with 500 ml portions of 3 N hydrochloric acid and once with 500 ml of water. The fluorobenzene is distilled at 30 mm. Hg and 60°C and, upon cooling, the obtained 4-chloroacetyl-1fluorobenzene oily residue solidifies.
562.9 g (4.08 moles) of N-isopropylaniline is rapidly added to a solution of the 4-chloroacetyl-1-fluorobenzene in 500 ml of dimethylformamide stirred at 50°C under nitrogen. The reaction mixture is stirred at 100°C under nitrogen for 10 h and allowed to cool to room temperature overnight. The reaction mixture is heated to 60°C, 2 L of water is added, and the mixture is cooled to 10°C. The obtained solids are collected, washed twice with 500 ml portions of water and dissolved in 550 ml of 95% ethanol at 75°C. The solution is cooled to 0°C, and the obtained solids are collected, washed three times with 100 ml portions of 95% ethanol and vacuum dried at 35°-40°C for 4 h to obtain the 95.3% pure yellow product: N-(4-fluorobenzoylmethyl)-N-(1-methylethyl) aniline (466.0 g, 84.2%, melting point 78° -81°C).
4.5 ml of 1 N sodium hydroxide solution (4.5 mmol) and 2.0 g (4.7 mmol) of N-(4-fluorobenzoylmethyl)-N-(1-methylethyl)aniline are stirred in 150 ml of ethanol at room temperature for 2 h, the solvent is evaporated at reduced pressure, and the residue is dissolved in 50 ml of water. The aqueous solution is gently extracted with diethyl ether, the traces of ether in the aqueous layer are removed at reduced pressure, and the aqueous layer is freeze dried to obtain racemic sodium threo-(+/-)-(E)-3,5-dihydroxy-7-[3'-(4"-fluorophenyl)1'-(1"-methylethyl )indol-2'-yl]hept-6-enoate (1.8 g (88%)), melting point 194°-197°C.
The crude sodium threo-(+/-)-(E)-3,5-dihydroxy-7-[3'-(4"-fluorophenyl)-1'(1"-methylethyl )indol-2'-yl]hept-6-enoate is dissolved in water, and the solution is acidified to pH 2 with 2 N hydrochloric acid and extracted with diethyl ether. The diethyl ether extract is washed three times with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated at reduced pressure to obtain the crude solid racemic erythro-(+/)-(E)-3,5-dihydroxy-7-[3'-(4"-fluorophenyl)-1'-(1"-methylethyl )indol-2'-yl] hept-6-enoic acid (6.9 g).
The racemic erythro-(+/-)-(E)-3,5-dihydroxy-7-[3'-(4"-fluorophenyl)-1'-(1"methylethyl )indol-2'-yl]hept-6-enoic acid may both be resolved into two optically pure enantiomers, the 3R, 5S and 3S, 5R isomers by chromatography on silica gel column using organic solutions as the eluent.

brand name

Lescol (Novartis).

Therapeutic Function

Antihyperlipidemic

General Description

Fluvastatin, [R*,S*-(E)]-(±)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxy-6-heptenoic acid monosodium salt (Lescol), is very similarto pravastatin. It possesses a heptanoic acid side chain thatis superimposable over the lactone ring found in lovastatinand simvastatin. This side chain is recognized by HMGCoAreductase. Also, much like pravastatin, the CNS sideeffects of this lipid-lowering agent are much lower thanthose of the agents that possess a lactone ring as part of theirarchitectural design.

Clinical Use

HMG CoA reductase inhibitor:
Primary hypercholesterolaemia
Slowing progression of atherosclerosis
Secondary prevention of coronary events after percutaneous coronary intervention

Drug interactions

Potentially hazardous interactions with other drugs
Antibacterials: rifampicin increases metabolism; increased risk of myopathy with daptomycin; avoid for 7 days after last dose of fusidic acid.
Anticoagulants: anticoagulant effect enhanced.
Antiepileptics: concentration of either or both drugs may be increased with fosphenytoin and phenytoin.
Antifungals: concentration increased by fluconazole - increased risk of myopathy.
Antivirals: possible increased risk of myopathy with ledipasvir - reduce fluvastatin dose; avoid with paritaprevir.
Ciclosporin: concomitant treatment with ciclosporin may lead to risk of muscle toxicity.
Colchicine: isolated cases of myopathy have been reported.
Lipid-lowering drugs: increased risk of myopathy with gemfibrozil, fibrates and nicotinic acid - avoid with gemfibrozil.

Metabolism

Fluvastatin is rapidly and completely absorbed from the gastrointestinal tract and undergoes extensive firstpass metabolism in the liver. Metabolism is mainly by the cytochrome P450 isoenzyme CYP2C9, with only a small amount metabolised by CYP3A4. The major components circulating in the blood are fluvastatin and the pharmacologically inactive N-desisopropyl-propionic acid metabolite. The hydroxylated metabolites have pharmacological activity but do not circulate systemically. About 93% is excreted in the faeces, mainly as metabolites, with only about 6% being excreted in the urine

Fluvastatin Preparation Products And Raw materials

Global( 201)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Shanxi Naipu Import and Export Co.,Ltd
+86-13734021967 +8613734021967 kaia@neputrading.com China 1011 58
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17367 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hubei Ipure Biology Co., Ltd
+8613367258412 ada@ipurechemical.com China 10326 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9358 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58

View Lastest Price from Fluvastatin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fluvastatin pictures 2023-08-16 Fluvastatin
93957-54-1
US $80.00 / KG 1KG >99% 20tons Weijer International Trade (Hebei) Co., Ltd
Fluvastatin pictures 2023-03-14 Fluvastatin
93957-54-1
US $20.00 / kg 1kg 99% 5000 Ton Hebei Duling International Trade Co. LTD
Fluvastatin pictures 2022-02-25 Fluvastatin
93957-54-1
US $100.00 / KG 1KG 99 5TONS Shanxi Naipu Import and Export Co.,Ltd
  • Fluvastatin pictures
  • Fluvastatin
    93957-54-1
  • US $80.00 / KG
  • >99%
  • Weijer International Trade (Hebei) Co., Ltd
  • Fluvastatin pictures
  • Fluvastatin
    93957-54-1
  • US $20.00 / kg
  • 99%
  • Hebei Duling International Trade Co. LTD
  • Fluvastatin pictures
  • Fluvastatin
    93957-54-1
  • US $100.00 / KG
  • 99
  • Shanxi Naipu Import and Export Co.,Ltd

Fluvastatin Spectrum

FLUVASTATIN FLUVASTATIN NA FLUVASTATIN SODIUM METHYL-(+/-)-(E)-7-[3'-(4-FLUOROPHENYL)-1'-(1-METHYLETHYL)INDOL-2'-YL]-3,5-DIHYDROXY-6-HEPTENOATE FLUVASTATIN[METHYL-(±)-(E)-7-[3’-(4”-FLUOROPHENYL )-1’-(1”-METHYLETHYL)INDOL-2’-YL]-3,5- DIHYDROXY-6- HEPTENOATE ] FluvastatinC24H26FN04 (3S,5R,E)-7-(3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl)-3,5-dihydroxyhept-6-enoic acid Lipaxan Primexin 7-(3-(4-fluorophenyl)-1-(1-methylethyl)-1h-indol-2-yl)-3,5-dihydroxy-6-heptenoic acid (3R,5S,6E)-3,5-Dihydroxy-7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-6-heptenoic acid sodium salt (3R,5S,6E)-7-[3-(4-Fluorophenyl)-1-isopropyl-1H-indole-2-yl]-3,5-dihydroxy-6-heptenoic acid sodium salt 7-(3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl)-3,5-dihydroxy-6-heptenoic acid Sodium Salt Fluvastatin, >=98% (3R,5S,E)-7-(3-(4-Fluorophenyl)-1-isopropyl-1H-indol-2-yl)-3,5-dihydroxyhept-6-enoic acid Fluvastatin-D7 METHYL-(+/-)-(E)-7-[3'-(4-FLUOROPHENYL)-1'-(1-METHYLETHYL)INDOL-2'-YL]-3,5-DIHYDROXY-6-HEPTENOAT Leschol (r*,s*-(e))-(+-)-ihydroxy 6-heptenoicacid,7-(3-(4-fluorophenyl)-1-(1-methylethyl)-1h-indol-2-yl)-3,5-d Lescol (+/-)-(3R',5S',6E)-7-[3-(4-FLUOROPHENYL)-1-ISOPROPYLINDOL-2-YL]-3,5-DIHYDROXY-6-HEPTENOATE (+/-)-(3R',5S',6E)-7-[3-(4-FLUOROPHENYL)-1-ISOPROPYLINDOL-2-YL]-3,5-DIHYDROXY-6-HEPTENOATE, SODIUM 6-HEPTENOIC ACID,7-[3-(4-FLUOROPHENYL)-1-(1-METHYLETHYL)-1H-INDOL-2-YL]-3,5-DIHYDROXY-,(3R,5S,6E)-REL- 6-Heptenoic acid, 7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxy-, (3R,5S,6E)-rel- Fluvastatin USP/EP/BP FluvastatinQ: What is Fluvastatin Q: What is the CAS Number of Fluvastatin Q: What is the storage condition of Fluvastatin Q: What are the applications of Fluvastatin (3RS,5RS,6E)-7-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoic Acid Moly Powder B Molykote Microsize Powder Molysulfide T-Powder 7-[3-(4-fluorophenyl)-1-propan-2-yl-2-indolyl]-3,5-dihydroxy-6-heptenoate Fhh(Intermediate Of Fluvastatin) FLUVASTATIN SODIUM 25% GRANULES 93957-54-1 C24H25FNaNO4 C24H26FNO4 C24H25FNO4 AROMASIN Isotopically Labeled Pharmaceutical Reference Standard API Fluvastatin Pharmaceuticals (intermediate of fluvastatin) Indoles and derivatives Intermediates & Fine Chemicals