Umifenovir Explained
Verifiedfields: | changed |
Watchedfields: | changed |
Verifiedrevid: | 457138656 |
Width: | 200 |
Tradename: | Arbidol |
Pregnancy Category: | C |
Routes Of Administration: | By mouth (hard capsules, tablets) |
Atc Prefix: | J05 |
Atc Suffix: | AX13 |
Legal Status: | RU OTC[1] CN Rx-only BY OTC[2] |
Bioavailability: | 40% |
Metabolism: | Hepatic, CYP3A4 |
Elimination Half-Life: | 17–21 hours |
Excretion: | 40% excrete as unchanged umifenovir in feces (38.9%) and urine (0.12%)[3] |
Cas Number: | 131707-25-0 |
Pubchem: | 131411 |
Drugbank: | DB13609 |
Chemspiderid: | 116151 |
Unii: | 93M09WW4RU |
Kegg: | D10558 |
Chebi: | 134730 |
Chembl: | 1214598 |
Pdb Ligand: | 75U |
Synonyms: | AR-1I9514, Russian: Арбидол, . |
Iupac Name: | ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-[(phenylsulfanyl)methyl]-1H-indole-3-carboxylate |
C: | 22 |
H: | 25 |
Br: | 1 |
N: | 2 |
O: | 3 |
S: | 1 |
Smiles: | CCOC(=O)c1c(n(c2c1c(c(c(c2)Br)O)CN(C)C)C)CSc3ccccc3 |
Stdinchi: | 1S/C22H25BrN2O3S/c1-5-28-22(27)20-18(13-29-14-9-7-6-8-10-14)25(4)17-11-16(23)21(26)15(19(17)20)12-24(2)3/h6-11,26H,5,12-13H2,1-4H3 |
Stdinchikey: | KCFYEAOKVJSACF-UHFFFAOYSA-N |
Umifenovir, sold under the brand name Arbidol, is sold and used as an antiviral medication for influenza in Russia and China. The drug is manufactured by Pharmstandard (Russian: Фармстандарт). It is not approved by the U.S. Food and Drug Administration (FDA) for the treatment or prevention of influenza.[4]
Medical use
Testing of umifenovir's efficacy has mainly occurred in China and Russia,[5] [6] and it is well known in these two countries.[7] Some of the Russian tests showed the drug to be effective against influenza A and a direct comparison with oseltamivir showed similar efficiency in vitro and in a clinical setting.[8] In 2010 Arbidol was the drug brand with the highest sales volume in Russia.[9] In the first quarter of 2020 it had a 16 percent share in the Russian antiviral market.[10]
Umifenovir is used primarily as an antiviral treatment for influenza. The drug has also been investigated as a candidate drug for treatment of hepatitis C.[11]
Some preliminary research suggests it could be useful for flavivirus infection like West Nile virus.[12]
Some studies also indicate that umifenovir also has in vitro effectiveness at preventing entry of Zaire ebolavirus (Kikwit strain), Tacaribe arenavirus and Kaposi's sarcoma-associated herpesvirus in mammalian cell cultures, while confirming umifenovir's suppressive effect in vitro on Hepatitis B and poliovirus infection of mammalian cells when introduced either in advance of viral infection or during infection.[13] [14]
Side effects
Side effects in children include sensitization to the drug. No known overdose cases have been reported and allergic reactions are limited to people with hypersensitivity. The is more than 4 g/kg.[15]
Pharmacology
Pharmacodynamics
Umifenovir inhibits membrane fusion of influenza virus in vitro.[16] Fusion between the viral envelope (surrounding the viral capsid) and the cell membrane of the target cell is inhibited.[17] [18] This prevents viral entry to the target cell, and therefore protects it from infection.[19]
Some evidence suggests that the drug's actions are more effective at preventing infections from RNA viruses than infections from DNA viruses.[20]
As well as specific antiviral action against both influenza A and influenza B viruses, umifenovir exhibits modulatory effects on the immune system. The drug stimulates a humoral immune response, induces interferon-production, and stimulates the phagocytic function of macrophages.[21]
Pharmacokinetics
The maximum concentration of umifenovir in blood plasma when taking a dose of 50 mg is achieved after 1.2 hours, with 100 mg the maximum dose is obtained after 1.5 hours.[22] The bioavailability of the drug is about 40% and does not depend on food intake.[22]
The half-life is about 17-21 hours.[22] It is metabolized in the liver primarily by CYP3A4 but also by several other enzymes.[23] About 40% is excreted unchanged, mainly in bile (38.9%) and in small amounts by the kidneys (0.12%). During the first 24 hours, 90% of the administered dose is eliminated.[23]
Chemistry
Chemically, umifenovir features an indole core, functionalized at all but one positions with different substituents. The molecular groups of umifenovir - hydroxy, amino and carboxy - can form different hydrogen-bonded synthons. Umifenovir is characterized by only one polymorphic form but can exist in the form of a large number of crystal solvates, the production of which depends on the medium and conditions of synthesis. Umifenovir is poorly soluble in water. Crystaline solvates and other solid forms may be determined by the spatial structure and conformational equilibria in the saturated solution.[24] [25]
History and criticism
thumb|A Russian packet of Arbidol capsules
In 2006 the American company Good Earth Medicine applied to the FDA for an Emergency Use Authorization of Arbidol during the H5N1 bird flu epidemic, but their application was rejected on the grounds that the lab data provided was not strong enough to justify use.[26] [27]
In 2007, the Russian Academy of Medical Sciences stated that the effects of Arbidol (umifenovir) are not scientifically proven.[28]
In the early 2010s Russian media criticized lobbying attempts by Tatyana Golikova (then-Minister of Healthcare) to promote umifenovir,[29] and the unsubstantiated claim that Arbidol can speed up recovery from flu or cold by 1.3-2.3 days.[30] They also made claims that comparative clinical studies have proven umifenovir to be inefficient.[31] [32]
In January 2020, the Russian drug company OTCPharm (Отисифарм) published advertisements stating that the drug is effective against SARS-CoV-2. Shortly afterwards the Russian Federal Antimonopoly Service fined the company for violation of its advertising rules.[33] In March 2020 a video promoting the drug for COVID-19 went viral on Facebook and circulated heavily on WhatsApp, and around the same time a shortage of the drug ensued in Russia.[34]
Research for COVID-19
See also: COVID-19 drug repurposing research. In early 2020 umifenovir was touted as a potential treatment for COVID-19 in China, where it was sometimes given to patients in combination with other drugs such as the anti-HIV drug Darunavir.[35] [36] [37] [38] [39] A three-arm RCT study published in May 2020 in the Cell Press journal Clinical Advances found that neither Umifenovir or Lopinavir/Ritonavir helped patients with mild to moderate COVID-19.[40] A similar study comparing Umifenovir directly with Lopinavir/Ritonavir found no difference in fever duration between the two groups but found a lower viral load on day 14 in the Umifenovir group.[41] A systemic review and meta-analysis of 16 studies on Umifenovir published in March 2021 concluded that there is "no significant benefit of using Arbidol compared with non‐antiviral treatment or other therapeutic agents against COVID‐19 disease."[42]
External links
- Web site: Umifenovir . U.S. National Library of Medicine . Drug Information Portal .
Notes and References
- Web site: 阿比朵尔抑制新冠,先声药业生产的吗? . 全民健康网 . 17 June 2020 . https://web.archive.org/web/20200617095604/http://www.qm120.com/tags/116282.htm . 17 June 2020 . zh.
- Web site: ИНСТРУКЦИЯ ПО ПРИМЕНЕНИЮ АРПЕТОЛ (ARPETOL) . Vidal . 17 June 2020 . https://web.archive.org/web/20180126132837/https://www.vidal.by/poisk_preparatov/arpetol.html . 26 January 2018 . be.
- Web site: Full Prescribing Information: Arbidol (umifenovir) film-coated tablets 50 and 100 mg: Corrections and Additions. State Register of Medicines. Open joint-stock company "Pharmstandard-Tomskchempharm". 3 June 2015. ru.
- Web site: FDA Approved Drugs for Influenza . U.S. Food and Drug Administration . 8 December 2022 .
- Leneva IA, Fediakina IT, Gus'kova TA, Glushkov RG . [Sensitivity of various influenza virus strains to arbidol. Influence of arbidol combination with different antiviral drugs on reproduction of influenza virus A] ]. Terapevticheskii Arkhiv . 77 . 8 . 84–88 . 2005 . 16206613 . ИЗДАТЕЛЬСТВО "МЕДИЦИНА" (Publishing House "Medicine") . Russian translation .
- Wang MZ, Cai BQ, Li LY, Lin JT, Su N, Yu HX, Gao H, Zhao JZ, Liu L . [Efficacy and safety of arbidol in treatment of naturally acquired influenza] . Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae . 26 . 3 . 289–293 . June 2004 . 15266832 .
- Boriskin YS, Leneva IA, Pécheur EI, Polyak SJ . Arbidol: a broad-spectrum antiviral compound that blocks viral fusion . Current Medicinal Chemistry . 15 . 10 . 997–1005 . 2008 . 18393857 . 10.2174/092986708784049658 .
- Leneva IA, Burtseva EI, Yatsyshina SB, Fedyakina IT, Kirillova ES, Selkova EP, Osipova E, Maleev VV . Virus susceptibility and clinical effectiveness of anti-influenza drugs during the 2010-2011 influenza season in Russia . International Journal of Infectious Diseases . 43 . 77–84 . February 2016 . 26775570 . 10.1016/j.ijid.2016.01.001 . free .
- Web site: Russian Pharmaceutical Market 2010 . DSM Group . 17 June 2020 . https://web.archive.org/web/20181220202655/https://www.dsm.ru/docs/analytics/farmrinok_roccii_itogi_2010_eng.pdf . 20 December 2018.
- Web site: Most popular antiviral medication brands in the Russian pharmaceutical market in 1st quarter 2020 by sales value share . Statista . 17 June 2020.
- Pécheur EI, Lavillette D, Alcaras F, Molle J, Boriskin YS, Roberts M, Cosset FL, Polyak SJ . Biochemical mechanism of hepatitis C virus inhibition by the broad-spectrum antiviral arbidol . Biochemistry . 46 . 20 . 6050–6059 . May 2007 . 17455911 . 2532706 . 10.1021/bi700181j .
- Qian X, Qi Z . Mosquito-Borne Flaviviruses and Current Therapeutic Advances . Viruses . 14 . 6 . 1226 . June 2022 . 35746697 . 9229039 . 10.3390/v14061226 . free .
- Pécheur EI, Borisevich V, Halfmann P, Morrey JD, Smee DF, Prichard M, Mire CE, Kawaoka Y, Geisbert TW, Polyak SJ . The Synthetic Antiviral Drug Arbidol Inhibits Globally Prevalent Pathogenic Viruses . Journal of Virology . 90 . 6 . 3086–3092 . January 2016 . 26739045 . 4810626 . 10.1128/JVI.02077-15 .
- Hulseberg CE, Fénéant L, Szymańska-de Wijs KM, Kessler NP, Nelson EA, Shoemaker CJ, Schmaljohn CS, Polyak SJ, White JM . Arbidol and Other Low-Molecular-Weight Drugs That Inhibit Lassa and Ebola Viruses . Journal of Virology . 93 . 8 . April 2019 . 30700611 . 6450122 . 10.1128/JVI.02185-18 .
- Web site: АРБИДОЛ (ARBIDOL) . https://web.archive.org/web/20090204121605/http://www.vidal.ru/poisk_preparatov/arbidol.htm . 4 February 2009 . dead . Vidal .
- Leneva IA, Russell RJ, Boriskin YS, Hay AJ . Characteristics of arbidol-resistant mutants of influenza virus: implications for the mechanism of anti-influenza action of arbidol . Antiviral Research . 81 . 2 . 132–140 . February 2009 . 19028526 . 10.1016/j.antiviral.2008.10.009 .
- Kadam RU, Wilson IA . Structural basis of influenza virus fusion inhibition by the antiviral drug Arbidol . Proceedings of the National Academy of Sciences of the United States of America . 114 . 2 . 206–214 . January 2017 . 28003465 . 5240704 . 10.1073/pnas.1617020114 . free . 2017PNAS..114..206K .
- Haviernik J, Štefánik M, Fojtíková M, Kali S, Tordo N, Rudolf I, Hubálek Z, Eyer L, Ruzek D . Arbidol (Umifenovir): A Broad-Spectrum Antiviral Drug That Inhibits Medically Important Arthropod-Borne Flaviviruses . Viruses . 10 . 4 . 184 . April 2018 . 29642580 . 5923478 . 10.3390/v10040184 . free .
- Boriskin YS, Pécheur EI, Polyak SJ . Arbidol: a broad-spectrum antiviral that inhibits acute and chronic HCV infection . Virology Journal . 3 . 56 . July 2006 . 16854226 . 1559594 . 10.1186/1743-422X-3-56 . free .
- Shi L, Xiong H, He J, Deng H, Li Q, Zhong Q, Hou W, Cheng L, Xiao H, Yang Z . Antiviral activity of arbidol against influenza A virus, respiratory syncytial virus, rhinovirus, coxsackie virus and adenovirus in vitro and in vivo . Archives of Virology . 152 . 8 . 1447–1455 . 2007 . 17497238 . 10.1007/s00705-007-0974-5 . 13595688 .
- Glushkov RG, Gus'kova TA, Krylova LI, Nikolaeva IS . [Mechanisms of arbidole's immunomodulating action] . ru . Vestnik Rossiiskoi Akademii Meditsinskikh Nauk . 3 . 36–40 . 1999 . 10222830 .
- Liu MY, Wang S, Yao WF, Wu HZ, Meng SN, Wei MJ . Pharmacokinetic properties and bioequivalence of two formulations of arbidol: an open-label, single-dose, randomized-sequence, two-period crossover study in healthy Chinese male volunteers . Clinical Therapeutics . 31 . 4 . 784–792 . April 2009 . 19446151 . 10.1016/j.clinthera.2009.04.016 . 7133634 .
- Deng P, Zhong D, Yu K, Zhang Y, Wang T, Chen X . Pharmacokinetics, metabolism, and excretion of the antiviral drug arbidol in humans . Antimicrobial Agents and Chemotherapy . 57 . 4 . 1743–1755 . April 2013 . 23357765 . 10.1128/aac.02282-12 . 3623363 .
- Eventova VA, Belov KV, Efimov SV, Khodov IA . Conformational Screening of Arbidol Solvates: Investigation via 2D NOESY . Pharmaceutics . 15 . 1 . 226 . January 2023 . 36678855 . 9865235 . 10.3390/pharmaceutics15010226 . free .
- Belov KV, Dyshin AA, Khodov IA . March 2024 . Conformational analysis of arbidol in supercritical carbon Dioxide: Insights into 'opened' and 'closed' conformer groups . Journal of Molecular Liquids . en . 397 . 124074 . 10.1016/j.molliq.2024.124074. 267232952 .
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- Li Y, Xie Z, Lin W, Cai W, Wen C, Guan Y, Mo X, Wang J, Wang Y, Peng P, Chen X, Hong W, Xiao G, Liu J, Zhang L, Hu F, Li F, Zhang F, Deng X, Li L . Efficacy and Safety of Lopinavir/Ritonavir or Arbidol in Adult Patients with Mild/Moderate COVID-19: An Exploratory Randomized Controlled Trial . Med . 1 . 1 . 105–113.e4 . December 2020 . 32838353 . 7235585 . 10.1016/j.medj.2020.04.001 .
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