| 词条 | Gemfibrozil |
| 释义 |
| Watchedfields = changed | verifiedrevid = 458774072 | IUPAC_name = 5-(2,5-dimethylphenoxy)-2,2-dimethyl-pentanoic acid | image = Gemfibrozil.svg | tradename = Lopid, Jezil, others | Drugs.com = {{drugs.com|monograph|gemfibrozil}} | MedlinePlus = a686002 | pregnancy_US = C | legal_status = Prescription only | routes_of_administration = By mouth | bioavailability = Close to 100% | protein_bound = 95% | metabolism = Hepatic (CYP3A4) | elimination_half-life = 1.5 hours | excretion = Renal 94% Feces 6% | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 25812-30-0 | ATC_prefix = C10 | ATC_suffix = AB04 | ATC_supplemental = | PubChem = 3463 | IUPHAR_ligand = 3439 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = DB01241 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 3345 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = Q8X02027X3 | KEGG_Ref = {{keggcite|correct|kegg}} | KEGG = D00334 | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI = 5296 | ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL = 457 | C=15 | H=22 | O=3 | molecular_weight = 250.333 g/mol | smiles = O=C(O)C(C)(C)CCCOc1cc(ccc1C)C | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C15H22O3/c1-11-6-7-12(2)13(10-11)18-9-5-8-15(3,4)14(16)17/h6-7,10H,5,8-9H2,1-4H3,(H,16,17) | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = HEMJJKBWTPKOJG-UHFFFAOYSA-N | melting_point = 61 | melting_high = 63 }}Gemfibrozil, sold under the brand name Lopid among others, is a medication used to treat abnormal blood lipid levels.[1] Its is generally less preferred than statins.[1][3] Use is recommended together with dietary changes and exercise.[1] It is unclear if it changes the risk of heart disease.[1] It is taken by mouth.[1] Common side effects include headache, dizziness, feeling tired, and intestinal upset.[1] Serious side effects may include angioedema, gallstones, liver problems, and muscle breakdown.[1] Use in pregnancy and breastfeeding is of unclear safety.[1] It belongs to the fibrates group of medications and works by decreasing the breakdown of lipids in fat cells.[2] Gemfibrozil was patented in 1968 and came into medical medical use in 1982.[3] It is avaliable as a generic medication.[4] A month supply in the United Kingdom costs the NHS about 30 £ as of 2019.[4] In the United States the wholesale cost of this amount is about 6 USD.[5] In 2016 it was the 132nd most prescribed medication in the United States with more than 5 million prescriptions.[6] Medical uses
Side effects
Contraindications
Drug interactions
Mechanism of actionsThe exact mechanism of action of gemfibrozil is unknown; however, several theories exist regarding the very low density lipoprotein (VLDL) effect; it can inhibit lipolysis and decrease subsequent hepatic fatty acid uptake as well as inhibit hepatic secretion of VLDL; together these actions decrease serum VLDL levels and increase HDL-cholesterol; the mechanism behind HDL elevation is currently unknown. Gemfibrozil increases the activity of extrahepatic lipoprotein lipase (LL), thereby increasing lipoprotein triglyceride lipolysis. It does so by activating peroxisome proliferator-activated receptor alpha (PPARα) 'transcription factor ligand', a receptor that is involved in metabolism of carbohydrates and fats, as well as adipose tissue differentiation. This increase in the synthesis of lipoprotein lipase thereby increases the clearance of triglycerides. Chylomicrons are degraded, VLDLs are converted to LDLs, and LDLs are converted to HDL. This is accompanied by a slight increase in secretion of lipids into the bile and ultimately the intestine. Gemfibrozil also inhibits the synthesis and increases the clearance of apolipoprotein B, a carrier molecule for VLDL.[8] HistoryGemfibrozil was selected from a series of related compounds synthesized in the laboratories of the American company Parke-Davis in the late 1970s. It came from research for compounds that lower plasma lipid levels in humans and in animals.[9] Environmental dataGemfibrozil has been detected in biosolids (the solids remaining after sewage treatment) at concentrations up to 2650 ng/g wet weight.[10] This indicates that it survives the wastewater treatment process. It is also detected as environmental persistent micropollutant in aquifers and in groundwaters in karstic areas.[11] References1. ^{{cite web |title=Gemfibrozil Use During Pregnancy |url=https://www.drugs.com/pregnancy/gemfibrozil.html |website=Drugs.com |accessdate=3 March 2019 |language=en}} 2. ^1 2 3 4 5 6 7 {{cite web |title=Gemfibrozil Monograph for Professionals |url=https://www.drugs.com/monograph/gemfibrozil.html |website=Drugs.com |publisher=American Society of Health-System Pharmacists |accessdate=3 March 2019 |language=en}} 3. ^{{cite book |last1=Fischer |first1=Jnos |last2=Ganellin |first2=C. Robin |title=Analogue-based Drug Discovery |date=2006 |publisher=John Wiley & Sons |isbn=9783527607495 |page=474 |url=https://books.google.ca/books?id=FjKfqkaKkAAC&pg=PA474 |language=en}} 4. ^1 2 {{cite book|title=British national formulary : BNF 76|date=2018|publisher=Pharmaceutical Press|isbn=9780857113382|pages=198-199|edition=76}} 5. ^{{cite web |title=NADAC as of 2019-02-27 |url=https://data.medicaid.gov/Drug-Pricing-and-Payment/NADAC-as-of-2019-02-27/s7c9-pfa6 |website=Centers for Medicare and Medicaid Services |accessdate=3 March 2019 |language=en}} 6. ^{{cite web |title=The Top 300 of 2019 |url=https://clincalc.com/DrugStats/Top300Drugs.aspx |website=clincalc.com |accessdate=22 December 2018}} 7. ^"Gemfibrozil." WebMD.com Accessed 14 June 2014. http://www.webmd.com/drugs/drug-11423-gemfibrozil+oral.aspx 8. ^https://pubchem.ncbi.nlm.nih.gov/compound/gemfibrozil#section=Mechanism-of-Action 9. ^{{cite journal |last= Rodney |first=G|date=1976 |title=The Hypolipidemic Effect of Gemfibrozil (CI-719) in Laboratory Animals |journal=Proc. R. Soc. Med.|publisher=|volume=69 (Supplement 2) |issue= |pages=6–9 |pmc=1864017 |pmid=828263|display-authors=etal}} 10. ^http://water.epa.gov/scitech/wastetech/biosolids/tnsss-overview.cfm 11. ^{{Cite journal| doi = 10.1016/j.jconhyd.2018.06.003| issn = 0169-7722| volume = 215| pages = 11–20| last1 = Doummar| first1 = Joanna| last2 = Aoun| first2 = Michel| title = Assessment of the origin and transport of four selected emerging micropollutants sucralose, Acesulfame-K, gemfibrozil, and iohexol in a karst spring during a multi-event spring response| journal = Journal of Contaminant Hydrology| date = 2018-08-01}} External links
4 : RTT|Fibrates|Phenol ethers|Carboxylic acids |
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