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Phenothiazine

From Wikipedia, the free encyclopedia
Heterocyclic compound containing a ring of four carbon, one nitrogen and one sulfur atom
Phenothiazine
Names
Preferred IUPAC name
10H-Phenothiazine[1]
Other names
Thiodiphenylamine
Dibenzothiazine
Dibenzoparathiazine
10H-dibenzo-[b,e]-1,4-thiazine
PTZ
Identifiers
3D model (JSmol)
143237
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.001.997Edit this at Wikidata
EC Number
  • 202-196-5
KEGG
RTECS number
  • SN5075000
UNII
  • InChI=1S/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H checkY
    Key: WJFKNYWRSNBZNX-UHFFFAOYSA-N checkY
  • InChI=1/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H
    Key: WJFKNYWRSNBZNX-UHFFFAOYAI
  • c1ccc2c(c1)Nc3ccccc3S2
Properties
C12H9NS
Molar mass199.27 g/mol
Appearancegreenish-yellow rhombic leaflets or diamond-shaped plates
Melting point185 °C (365 °F; 458 K)
Boiling point371 °C (700 °F; 644 K)
0.00051 g/L (20 °C)[2]
Solubility in other solventsbenzene,ether,petroleum ether,chloroform, hotacetic acid,ethanol (slightly),mineral oil (slightly)
Acidity (pKa)approx 23 in DMSO
−114.8·10−6 cm3/mol
Hazards
GHS labelling:
GHS07: Exclamation markGHS08: Health hazard
Warning
H302,H317,H373,H412
P260,P264,P270,P272,P273,P280,P301+P312,P302+P352,P314,P321,P330,P333+P313,P363,P501
NIOSH (US health exposure limits):
PEL (Permissible)
none[3]
REL (Recommended)
TWA 5 mg/m3 [skin]
IDLH (Immediate danger)
N.D.[3]
Pharmacology
QP52AX03 (WHO)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Phenothiazine, abbreviatedPTZ, is anorganic compound that has the formula S(C6H4)2NH and is related to thethiazine-class ofheterocyclic compounds. Derivatives of phenothiazine are highly bioactive and have widespread use.

The derivativeschlorpromazine andpromethazine revolutionized the fields ofpsychiatry andallergy treatment, respectively. An earlier derivative,methylene blue, was one of the firstantimalarial drugs, and derivatives of phenothiazine are currently under investigation as possible anti-infective drugs. Phenothiazine is a prototypical pharmaceuticallead structure inmedicinal chemistry.

Uses

[edit]

Phenothiazine itself is only of theoretical interest, but derivatives of it revolutionized psychiatry, other fields of medicine, and pest management. Other derivatives have been studied for possible use in advanced batteries and fuel cells.[4]

Phenothiazine-derived drugs

[edit]

In 1876,methylene blue, a derivative of phenothiazine, was synthesized byHeinrich Caro atBASF. The structure was deduced in 1885 by Heinrich August Bernthsen. Bernthsen synthesized phenothiazine in 1883.[4] In the mid 1880s,Paul Ehrlich began to use methylene blue in his cell staining experiments that led to pioneering discoveries about different cell types. He was awarded a Nobel Prize based in part on that work. He became particularly interested in its use to stain bacteria and parasites such asPlasmodiidae – the genus that includes themalaria pathogen – and found that it could be stained with methylene blue. He thought methylene blue could possibly be used in the treatment of malaria, tested it clinically, and by the 1890s methylene blue was being used for that purpose.[4]

For the next several decades, research on derivatives lapsed until phenothiazine itself came to market as an insecticide and deworming drug. In the 1940s, chemists working with Paul Charpentier at Rhone-Poulenc Laboratories in Paris (a precursor company toSanofi), began making derivatives. This work led topromethazine which had no activity against infective organisms, but did have goodantihistamine activity, with a strong sedative effect. It went to market as a drug for allergies and foranesthesia. As of 2012 it was still on the market.[4] At the end of the 1940s the same lab producedchlorpromazine which had an even stronger sedative and soothing effect, andJean Delay andPierre Deniker attempted to use it on their psychiatric patients, publishing their results in the early 1950s. The strong effects they found opened the door of the modern field of psychiatry and led to a proliferation of work on phenothiazine derivatives.[4] The systematic research conducted by chemists to explore phenothiazine derivatives and their activity was a pioneering example ofmedicinal chemistry; phenothiazine is often discussed as a prototypical example of a pharmaceuticallead structure.[4][5]

A number of phenothiazines other than methylene blue have been shown to have antimicrobial effects. In particular,thioridazine has been shown to makeextensively drug-resistant tuberculosis (XDR-TB) drug-susceptible again[6][7] and makemethicillin-resistant Staphylococcus aureus (MRSA) susceptible to beta-lactam antibiotics.[7][8] The major reason why thioridazine has not been utilized as an antimicrobial agent is due to adverse effects on the central nervous system and cardiovascular system (particularly QT interval prolongation).[7]

The term "phenothiazines" describes the largest of the five main classes ofantipsychotic drugs. These drugs have antipsychotic and, often,antiemetic properties, although they may also cause severeside effects such asextrapyramidal symptoms (includingakathisia andtardive dyskinesia),hyperprolactinaemia, and the rare but potentially fatalneuroleptic malignant syndrome, as well as substantial weight gain.[4] Use of phenothiazines has been associated withantiphospholipid syndrome, but no causal relationship has been established.[9]

Phenothiazine antipsychotics are classified into three groups that differ with respect to the substituent on nitrogen: thealiphatic compounds (bearingacyclic groups), the "piperidines" (bearingpiperidine-derived groups), and the piperazine (bearingpiperazine-derived substituents).[5]

GroupAnticholinergicExampleSedationExtrapyramidal side effects
Aliphatic compoundsmoderateChlorpromazine (marketed as Thorazine, Aminazine, Chlor-PZ, Klorazine, Promachlor, Promapar, Sonazine, Chlorprom, Chlor-Promanyl, Largactil)strongmoderate
Promazine (trade name Sparine, Propazine)moderatemoderate
Triflupromazine (trade names Clinazine, Novaflurazine, Pentazine, Terfluzine, Triflurin, Vesprin)strongmoderate/strong
Levomepromazine in Germany, Russia, most American countries (e.g., Brazil) andmethotrimeprazine in USA (trade names Nozinan, Levoprome, Tisercin)extremely stronglow
PiperidinesstrongMesoridazine (trade name Serentil)strongweak
Thioridazine (trade names Mellaril, Novoridazine, Thioril, Sonapax)strongweak
PiperazinesweakFluphenazine (trade names Prolixin, Permitil, Modecate, Moditen)weak/moderatestrong
Perphenazine (sold as Trilafon, Etrafon, Triavil, Phenazine, Etaperazin)weak/moderatestrong
Prochlorperazine (trade names Compazine, Stemetil)
Trifluoperazine (trade name Stelazine, Triphtazine)moderatestrong

Nondrug applications

[edit]

The synthetic dyemethylene blue, containing the structure, was described in 1876. Many water-soluble phenothiazine derivatives, such asmethylene blue,methylene green,thionine, and others, can beelectropolymerized intoconductive polymers used aselectrocatalysts for NADH oxidation in enzymatic biosensors and biofuel cells.[10][11][12]

Phenothiazine is used as an anaerobic inhibitor foracrylic acid polymerization, often used as an in-process inhibitor during the purification of acrylic acid.[13]

Trade names

[edit]

Like many commercially significant compounds, phenothiazine has numerous trade names, including AFI-Tiazin, Agrazine, Antiverm, Biverm, Dibenzothiazine, Orimon, Lethelmin, Souframine, Nemazene, Vermitin, Padophene, Fenoverm, Fentiazine, Contaverm, Fenothiazine, Phenovarm, Ieeno, ENT 38, Helmetina, Helmetine, Penthazine, XL-50, Wurm-thional, Phenegic, Phenovis, Phenoxur, and Reconox.[14]

Former uses

[edit]

Phenothiazine was formerly used as an insecticide and as a drug to treat infections withparasitic worms (anthelminthic) inlivestock and people, but its use for those purposes has been superseded by other chemicals.

Phenothiazine was introduced byDuPont as aninsecticide in 1935.[15] About 3,500,000 pounds were sold in the US in 1944.[16] However, because it was degraded by sunlight and air, it was difficult to determine how much to use in the field, and its use waned in the 1940s with the arrival of new pesticides likeDDT that were more durable.[17]: 161–162  As of July 2015 it is not registered for pesticide use in the US, Europe,[18] or Australia.[19]

As an anthelminthic

[edit]

It was introduced as anthelminthic in livestock in 1940 and is considered, withthiabendazole, to be the first modern anthelminthic.[20] The first instances of resistance were noted in 1961.[20] Among anthelmintics, Blizzard et al. 1990 found onlyparaherquamide to have similar activity to phenothiazine. It is possible that they share the samemode of action.[21] Uses for this purpose in the US are still described[22] but it has "virtually disappeared from the market."[23]: 369 

In the 1940s it also was introduced as antihelminthic for humans; since it was often given to children, the drug was often sold in chocolate, leading to the popular name, "worm chocolate." Phenothiazine was superseded by other drugs in the 1950s.[4]

Structure and synthesis

[edit]

The central C4SN ring is folded in phenothiazines.[24]

The compound was originally prepared by Bernthsen in 1883 via the reaction ofdiphenylamine with sulfur, but more recent syntheses rely on the cyclization of 2-substituted diphenyl sulfides. Few pharmaceutically significant phenothiazines are prepared from phenothiazine,[25] although some of them are.[26]

Phenothiazines are electron donors, forming charge-transfer salts with many acceptors.

References

[edit]
  1. ^"Front Matter".Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge:The Royal Society of Chemistry. 2014. p. 216.doi:10.1039/9781849733069-FP001.ISBN 978-0-85404-182-4.
  2. ^"Sigma-Aldrich catalog of Phenothiazine". Retrieved2022-02-28.
  3. ^abNIOSH Pocket Guide to Chemical Hazards."#0494".National Institute for Occupational Safety and Health (NIOSH).
  4. ^abcdefghM. J. Ohlow; B. Moosmann (2011). "Phenothiazine: the seven lives of pharmacology's first lead structure".Drug Discov. Today.16 (3–4):119–31.doi:10.1016/j.drudis.2011.01.001.PMID 21237283.
  5. ^abJaszczyszyn, A; et al. (2012)."Chemical structure of phenothiazines and their biological activity"(PDF).Pharmacol. Rep.64 (1):16–23.doi:10.1016/s1734-1140(12)70726-0.PMID 22580516. Archived fromthe original(PDF) on 2020-07-28. Retrieved2015-07-26.
  6. ^Amaral, L; Viveiros, M (May 2012). "Why thioridazine in combination with antibiotics cures extensively drug-resistant Mycobacterium tuberculosis infections".International Journal of Antimicrobial Agents.39 (5):376–380.doi:10.1016/j.ijantimicag.2012.01.012.PMID 22445204.
  7. ^abcThanacoody, HKR (November 2007)."Thioridazine: resurrection as an antimicrobial agent?".British Journal of Clinical Pharmacology.64 (5):566–574.doi:10.1111/j.1365-2125.2007.03021.x.PMC 2203271.PMID 17764469.
  8. ^Thorsing, M; Klitgaard, JK; Atilano, ML; Skov, MN; Kolmos, HJ; Filipe, SR; Kallipolitis, BH (May 2013)."Thioridazine Induces Major Changes in Global Gene Expression and Cell Wall Composition in Methicillin-Resistant Staphylococcus aureus USA300".PLOS ONE.8 (5) e64518.Bibcode:2013PLoSO...864518T.doi:10.1371/journal.pone.0064518.PMC 3656896.PMID 23691239.
  9. ^"Antiphospholipid Syndrome - Doctor's Information | Patient".Patient. Retrieved2015-07-25.
  10. ^Chi, Qijin; Dong, Shaojun (1994-01-20). "Electrocatalytic oxidation of reduced nicotinamide coenzymes at Methylene Green-modified electrodes and fabrication of amperometric alcohol biosensors".Analytica Chimica Acta.285 (1–2):125–133.Bibcode:1994AcAC..285..125C.doi:10.1016/0003-2670(94)85016-X.
  11. ^Karyakin, Arkady A.; Karyakina, Elena E.; Schuhmann, Wolfgang; Schmidt, Hanns-Ludwig (1999). "Electropolymerized Azines: Part II. In a Search of the Best Electrocatalyst of NADH Oxidation".Electroanalysis.11 (8):553–557.doi:10.1002/(SICI)1521-4109(199906)11:8<553::AID-ELAN553>3.0.CO;2-6.
  12. ^Sokic-Lazic, Daria; Minteer, Shelley D. (December 2008). "Citric acid cycle biomimic on a carbon electrode".Biosensors and Bioelectronics.24 (4):939–944.doi:10.1016/j.bios.2008.07.043.PMID 18774285.
  13. ^Levy, Leon B. (1992-03-30). "Inhibition of acrylic acid polymerization by phenothiazine and p-methoxyphenol. II. Catalytic inhibition by phenothiazine".Journal of Polymer Science Part A: Polymer Chemistry.30 (4):569–576.Bibcode:1992JPoSA..30..569L.doi:10.1002/pola.1992.080300407.
  14. ^"U.S. Department of Labor Occupational Safety & Health Administration Chemical Sampling Information Phenothiazine". Archived fromthe original on 2007-08-08. Retrieved2007-07-06.
  15. ^History of Insecticides and Control Equipment Clemson University Pesticide Information Program.
  16. ^Robert Lee Metcalf. The Mode of Action of Organic Insecticides, Issues 1-5. National Academies, 1948,page 44
  17. ^G. Matolcsy, M. Nádasy, V. Andriska. Studies in Environmental Science: Pesticide Chemistry. Elsevier, 1989ISBN 9780080874913
  18. ^ECHAphenothiazine at the European Chemicals AuthorityArchived 2019-01-23 at theWayback Machine Page accessed July 26, 2015. Note - Registered uses are only in manufacturing.
  19. ^Australian Pesticides and Veterinary Medicine AuthorityPhenothiazine Chemical Review Page accessed July 26, 2015
  20. ^abNielsen, MK; et al. (Jul 2014). "Anthelmintic resistance in equine parasites--current evidence and knowledge gaps".Vet Parasitol.204 (1–2):55–63.doi:10.1016/j.vetpar.2013.11.030.PMID 24433852.
  21. ^Monaghan, Richard L.; Tkacz, Jan S. (1990). "Bioactive Microbial Products: Focus upon Mechanism of Action".Annual Review of Microbiology.44 (1).Annual Reviews:271–331.doi:10.1146/annurev.mi.44.100190.001415.ISSN 0066-4227.PMID 2252385.
  22. ^The Texas A&M University System; Texas AgriLife Extension ServiceIntegrated pest management of flies in Texas dairiesArchived 2014-08-11 at theWayback Machine
  23. ^Heinz Mehlhorn, Philip M. Armstrong. Encyclopedic Reference of Parasitology: Diseases, Treatment, Therapy, Volume 2. Springer Science & Business Media, 2001ISBN 9783540668299
  24. ^J. J. H. McDowell (1976). "The crystal and molecular structure of phenothiazine".Acta Crystallographica Section B.32 (1): 5.Bibcode:1976AcCrB..32....5M.doi:10.1107/S0567740876002215.
  25. ^Gérard Taurand, "Phenothiazine and Derivatives" inUllmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.doi:10.1002/14356007.a19_387
  26. ^T. Kahl, K.-W. Schröder, F. R. Lawrence, W. J. Marshall, Hartmut Höke, Rudolf Jäckh, "Aniline" inUllmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH: Weinheim.

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