词条 | Clioquinol | ||||||||||||
释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 443528768 | IUPAC_name = 5-Chloro-7-iodo-quinolin-8-ol | image = Clioquinol.png | width = 140 | alt = Skeletal formula of clioquinol | image2 = Clioquinol 3D ball.png | width2 = 165 | alt2 = Ball-and-stick model of the clioquinol molecule | tradename = Cortin | Drugs.com = {{drugs.com|CONS|clioquinol}} | MedlinePlus = a682367 | pregnancy_US = C | pregnancy_US_comment = [1] | legal_UK = PoM | legal_US = Rx | routes_of_administration = topical only | bioavailability = | metabolism = | excretion = | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 130-26-7 | ATC_prefix = D08 | ATC_suffix = AH30 | ATC_supplemental = {{ATC|D09|AA10}} (dressing) {{ATC|G01|AC02}} {{ATC|P01|AA02}} {{ATC|S02|AA05}} | PubChem = 2788 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = DB04815 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 2686 | ChEBI_Ref = {{ebicite|changed|EBI}} | ChEBI = 74460 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 7BHQ856EJ5 | KEGG_Ref = {{keggcite|correct|kegg}} | KEGG = D03538 | ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL = 497 | C=9 | H=5 | Cl=1 | I=1 | N=1 | O=1 | smiles = Ic1c(O)c2ncccc2c(Cl)c1 | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C9H5ClINO/c10-6-4-7(11)9(13)8-5(6)2-1-3-12-8/h1-4,13H | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = QCDFBFJGMNKBDO-UHFFFAOYSA-N }}Clioquinol (iodochlorhydroxyquin) is an antifungal drug and antiprotozoal drug. It is neurotoxic in large doses. It is a member of a family of drugs called hydroxyquinolines which inhibit certain enzymes related to DNA replication. The drugs have been found to have activity against both viral and protozoal infections.[2] Antiprotozoal useA 1964 report described the use of Clioquinol in both the treatment and prevention of shigella infection and Entamoeba histolytica infection in institutionalized individuals at Sonoma State Hospital in California. The report indicates 4000 individuals were treated over a 4-year period with few side effects.[3] Several recently reported journal articles describing its use as an antiprotozoal include:
Subacute myelo-optic neuropathyClioquinol's use as an antiprotozoal drug has been restricted or discontinued in some countries due to an event in Japan where over 10,000 people developed subacute myelo-optic neuropathy (SMON) between 1957 and 1970. The drug was used widely in many countries before and after the SMON event without similar reports.[7] As yet, no explanation exists as to why it produced this reaction, and some researchers have questioned whether clioquinol was the causative agent in the disease, noting that the drug had been used for 20 years prior to the epidemic without incident, and that the SMON cases began to reduce in number prior to the discontinuation of the drug.[8] Theories suggested have included improper dosing, the permitted use of the drug for extended periods of time,[9] and dosing which did not consider the smaller average stature of Japanese; however a dose dependant relationship between SMON development and clioquinol use was never found, suggesting the interaction of another compound. Researchers have also suggested the SMON epidemic could have been due to a viral infection with an Inoue-Melnick virus.[10] Topical useClioquinol is a constituent of the prescription medicine Vioform, which is a topical antifungal treatment. It is also used in the form of a cream (and in combination with betamethasone or fluocinolone) in the treatment of inflammatory skin disorders. Potential use as a preventative or treatment in prostate cancerIt has long been recognized that normal prostate cells have high zinc content through ZIP1 mediated uptake, and have low respiration (OXPHOS ATP generation is diverted to citrate export for sperm energetics). Prostate cancer cells have downregulated ZIP1 transporters which leads to greater ATP generation which is diverted to cancer proliferation. An example of a normal-like metabolic phenotype instead being malignant (disguised Warburg effect?). The zinc ionophore clioquinol was shown in mice to restore zinc levels and stop the growth of prostate tumors (see Figure 13).[11] Use in neurodegenerative diseasesResearch at UCSF indicates that clioquinol appears to block the genetic action of Huntington's disease in mice and in cell culture.[12] Recent animal studies have shown that clioquinol can reverse the progression of Alzheimer's, Parkinson's and Huntington's diseases.[13] According to Dr. Siegfried Hekimi and colleagues at McGill's Department of Biology, clioquinol acts directly on a protein called Clk-1, often informally called “clock-1,” and might slow down the aging process. They theorize that this may explain the apparent ability of the drug to be effective in the above conditions, but warn against individuals experimenting with this drug.[14] In addition, a study performed in Drosophila [15] by Huang and Wu, two researchers from Tsinghua University and Stanford University, demonstrates that Clioquinol can slower the pathogenesis of Tauopathy model by removing the excessive Zinc in the cell. Continued use and manufacture around the world
See also
References1. ^{{cite web|title=Clioquinol topical medical facts from Drugs.com|url=https://www.drugs.com/mtm/clioquinol-topical.html|website=drugs.com|publisher=Drugs.com|accessdate=15 May 2015}} {{Antiseptics and disinfectants}}{{Medicated dressings}}{{Gynecological anti-infectives and antiseptics}}{{Otologicals}}{{Agents against amoebozoa}}2. ^{{cite journal |vauthors=Rohde W, Mikelens P, Jackson J, Blackman J, Whitcher J, Levinson W |title=Hydroxyquinolines inhibit ribonucleic acid-dependent deoxyribonucleic acid polymerase and inactivate Rous sarcoma virus and herpes simplex virus |journal=Antimicrob. Agents Chemother. |volume=10 |issue=2 |pages=234–40 |year=1976 |pmid=185949 |doi= 10.1128/aac.10.2.234|pmc=429727}} 3. ^{{cite journal |vauthors=GHOLZ LM, ARONS WL |title=Prophylaxis And Therapy Of Amebiasis And Shigellosis With Iodochlorhydroxyquin |journal=Am. J. Trop. Med. Hyg. |volume=13 |issue= 3|pages=396–401 |year=1964 |pmid=14162901 |doi=10.4269/ajtmh.1964.13.396}} 4. ^{{cite journal |author=Kager PA |title=[Outbreak of amoebiasis in a Dutch family; tropics unexpectedly nearby] |language=Dutch, Flemish |journal=Nederlands Tijdschrift voor Geneeskunde |volume=149 |issue=1 |pages=51–2; author reply 52–3 |year=2005 |pmid=15651505 |doi=}} 5. ^1 {{cite journal |vauthors=Bosman DK, Benninga MA, van de Berg P, Kooijman GC, van Gool T |title=[Dientamoeba fragilis: possibly an important cause of persistent abdominal pain in children] |language=Dutch, Flemish |journal=Nederlands Tijdschrift voor Geneeskunde |volume=148 |issue=12 |pages=575–9 |year=2004 |pmid=15074181 |doi=}} 6. ^{{cite journal |vauthors=Masters DK, Hopkins AD |title=Therapeutic trial of four amoebicide regimes in rural Zaire |journal=The Journal of Tropical Medicine and Hygiene |volume=82 |issue=5 |pages=99–101 |year=1979 |pmid=226725 |doi=}} 7. ^{{cite journal |author=Wadia NH |title=SMON as seen from Bombay |journal=Acta Neurol. Scand. Suppl. |volume=100 |issue= |pages=159–64 |year=1984 |pmid=6091394 |doi=}} 8. ^{{cite journal |author=Meade TW |title=Subacute myelo-optic neuropathy and clioquinol. An epidemiological case-history for diagnosis |journal=British Journal of Preventive & Social Medicine |volume=29 |issue=3 |pages=157–69 |year=1975 |pmid=127638 |doi= 10.1136/jech.29.3.157|pmc=478909}} 9. ^{{cite journal |author=Takasu T |title=[SMON--a model of the iatrogenic disease] |language=Japanese |journal=Rinsho Shinkeigaku |volume=43 |issue=11 |pages=866–9 |year=2003 |pmid=15152488 |doi=}} 10. ^{{cite journal |vauthors=Ito M, Nishibe Y, Inoue YK |title=Isolation of Inoue-Melnick virus from cerebrospinal fluid of patients with epidemic neuropathy in Cuba |journal=Arch. Pathol. Lab. Med. |volume=122 |issue=6 |pages=520–2 |year=1998 |pmid=9625419 |doi=}} 11. ^{{cite journal |vauthors=Costello LC, Franklin RB |title=A comprehensive review of the role of zinc in normal prostate function and metabolism; and its implications in prostate cancer|journal=Arch Biochem Biophys|volume=611 |issue=1 |pages=100–112 |year=2016 |pmid=27132038|doi=10.1016/j.abb.2016.04.014 |pmc=5083243}} 12. ^{{cite journal |vauthors=Nguyen T, Hamby A, Massa SM |title=Clioquinol down-regulates mutant huntingtin expression in vitro and mitigates pathology in a Huntington's disease mouse model |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue=33 |pages=11840–5 |year=2005 |pmid=16087879 |doi=10.1073/pnas.0502177102 |pmc=1187967}} 13. ^[https://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=ShowDetailView&TermToSearch=18614028 Rapid restoration of cognition in Alzheimer's transgenic mice with 8-hydroxy quinoline analogs is associated with decreased interstitial Abeta.] 14. ^[https://www.mcgill.ca/newsroom/news/item/?item_id=103574] 15. ^[https://www.sciencedirect.com/science/article/pii/S2211124714005312] Zinc Binding Directly Regulates Tau Toxicity Independent of Tau Hyperphosphorylation, Cell Reports, Volume 8, Issue 3, 7 August 2014, Pages 831-842 16. ^{{cite web|last=Vinaysagar|first=DNS Fine Chemicals|title=Manufacturers of Clioquinol|url=http://dnsfine.com/|publisher=Dns Fine|accessdate=23 December 2017|date=2016-01-06}} 17. ^{{cite web|last=Herlekar|first=Omkar|title=Clioquinol manufacturers India|url=http://www.lasalabs.com/clioquinol.html|publisher=Lasa labs|accessdate=12 March 2013}} 18. ^{{cite web|title=Dermosupril C 0,1% desonide + 3% clioquinol for topical use |url=http://medihealth.net/prospectos/DermosuprilCCrema_1.pdf|publisher=Medihealth laboratories|accessdate=19 September 2016}} 6 : Antiprotozoal agents|Antifungals|Quinolinols|Iodoarenes|Chloroarenes|Otologicals |
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