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Phemerazole

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Pharmaceutical compound
Phemerazole
Clinical data
Other namesPhemerazol; Femerazol; Femerazole; Phenylmethylpyrazole; 3-Methyl-5-phenylpyrazole
Drug classSedative;Hypnotic;Anticonvulsant;Muscle relaxant;Mammary stimulant
ATC code
  • None
Identifiers
  • 5-methyl-3-phenyl-1H-pyrazole
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.020.091Edit this at Wikidata
Chemical and physical data
FormulaC10H10N2
Molar mass158.204 g·mol−1
3D model (JSmol)
  • CC1=CC(=NN1)C2=CC=CC=C2
  • InChI=1S/C10H10N2/c1-8-7-10(12-11-8)9-5-3-2-4-6-9/h2-7H,1H3,(H,11,12)
  • Key:QHRSESMSOJZMCO-UHFFFAOYSA-N

Phemerazole, orfemerazol, also known as5-phenyl-3-methylpyrazole, is asedativedrug andarylpyrazolederivative.[1][2][3][4][5] It produces sedative,hypnotic,hypolocomotive,antiaggressive,anticonvulsant,muscle relaxant, andhypothermic effects in animals.[1][2][6][7] In addition to itscentral nervous system effects, the drug has been found to potentiate the effects ofdiethylstilbestrol on themammary glands in animals, including producingductal andalveolarhyperplasia,stromalhyperemia, andlactogenesis.[1][4][5] Its effects in this regard were said to resemble those of the sedativeprolactin releaserschlorpromazine andreserpine.[4][5] The exactmechanisms of action of phemerazole in terms of its various effects do not appear to be known.[4][5] Phemerazole was first described in thescientific literature by 1960.[2][6][7] Various activeanalogues andderivatives of phemerazole are known.[1]

See also

[edit]

References

[edit]
  1. ^abcdOrth RE (April 1968). "Biologically active pyrazoles".Journal of Pharmaceutical Sciences.57 (4):537–556.Bibcode:1968JPhmS..57..537O.doi:10.1002/jps.2600570401.PMID 4385101.Phemerazole,3-methyl-5-phenylpyrazole (XL), was one of a group of pyrazoles which evoked sharply pronounced sedative, soporific, anticonvulsant, and hypothermic responses. [...] Phemerazole potentiated the action of diethylstilbestrol on mammary glands (250-254). [...] The versatility of action of even the simplest pyrazoles was noteworthy, and pyrazole, itself, was mentioned on several occasions. [...] The simple histamine isomer, betazole, manifested greater specificity on gastric secretions than histamine, while 3-methyl-5-phenylpyrazole, phemerazole, was an excellent central spasmolytic anticonvulsant.
  2. ^abcStanford Research Institute, Psychopharmacology Service Center (U.S.) (1960)."Phemerazole".Psychopharmacology Handbook: Animal Research in Psychopharmacology. Public Health Service publication. U.S. Department of Health, Education and Welfare, Public Health Service, National Institutes of Health. pp. 325–326.
  3. ^Jablonski S (1967).Russian Drug Index. U.S. Department of Health, Education, and Welfare, Public Health Service. p. 224.
  4. ^abcdPershin GN, Novitskaya NA, Grushina AA (October 1961). "Adjuvant effect of 5-phenyl-3-methylpyrazole (phemerazole) on the action of diethylstilstrol on the mammary glands of rabbits".Biulleten' Eksperimental'noi Biologii I Meditsiny.51 (5):584–586.doi:10.1007/BF00788451.PMID 14038299.
  5. ^abcdPershin GN, Novitskaia NA, Grushina AA (May 1961). "[Potentiation of the effect of diethylstilbestrol on the mammary gland in rabbits under the influence of 3-methyl-5-phenylpyrazole (phemerazole)]".Biulleten' Eksperimental'noi Biologii I Meditsiny (in Russian).51:74–76.PMID 13734605.
  6. ^abPershin GN, Novitskaia NA (1960). "[Sedative and hypothermic properties of 3-methyl-5-phenylpyrazole (Phemerazole)]".Farmakologiia i Toksikologiia (in Russian).23:216–220.PMID 13734606.
  7. ^abNovitskaia NA, Pershin GN (1960). "[Effect of 3-methyl-5-phenylpyrazole (phemerazole) on the action of substances stimulating the central nervous system]".Farmakologiia i Toksikologiia (in Russian).23:488–493.PMID 13729785.
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