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Caroxazone

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Caroxazone
Clinical data
Pregnancy
category
  • ?
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • BR: Class C1 (Other controlled substances)[1]
  • In general: ℞ (Prescription only)
Identifiers
  • 2-(2-oxo-4H-1,3-benzoxazin-3-yl)acetamide
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.038.481Edit this at Wikidata
Chemical and physical data
FormulaC10H10N2O3
Molar mass206.201 g·mol−1
3D model (JSmol)
  • O=C(N)CN2C(=O)Oc1ccccc1C2

Caroxazone (Surodil,Timostenil) is anantidepressant which was formerly used for the treatment ofdepression but is now no longer marketed.[2][3] It acts as areversiblemonoamine oxidase inhibitor (RIMA) of bothMAO-A andMAO-B subtypes, with five-fold preference for the latter.[4][5][6][7][8]

Synthesis

[edit]
Caroxazone synthesis:[9][10][11][12][13]

Synthesis starts byreductive amination ofsalicylaldehyde andglycinamide to give3. The synthesis is completed by reaction withphosgene andNaHCO3.

See also

[edit]

References

[edit]
  1. ^Anvisa (2023-03-31)."RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-04-04).Archived from the original on 2023-08-03. Retrieved2023-08-16.
  2. ^Dictionary of organic compounds. London: Chapman & Hall. 1996.ISBN 0-412-54090-8.
  3. ^Cecchini S, Petri P, Ardito R, Bareggi SR, Torriti A (1978). "A comparative double-blind trial of the new antidepressant caroxazone and amitriptyline".The Journal of International Medical Research.6 (5):388–94.doi:10.1177/030006057800600507.PMID 359383.S2CID 40464443.
  4. ^Monoamine oxidase inhibitors in neurological diseases. New York: M. Dekker. 1994.ISBN 0-8247-9082-0.
  5. ^Moretti A, Caccia C, Martini A, Bonollo L, Amico A, Sega R, et al. (May 1981)."Effect of caroxazone, a new antidepressant drug, on monoamine oxidases in healthy volunteers".British Journal of Clinical Pharmacology.11 (5):511–5.doi:10.1111/j.1365-2125.1981.tb01158.x.PMC 1401585.PMID 7272163.
  6. ^Moretti A, Caccia C, Calderini G, Menozzi M, Amico A (October 1981). "Studies on the mechanism of action of caroxazone, a new antidepressant drug".Biochemical Pharmacology.30 (19):2728–31.doi:10.1016/0006-2952(81)90549-9.PMID 6170295.
  7. ^Martini A, Bonollo L, Nicolis FB, Sega R, Palermo A (June 1981)."Effects of caroxazone, a reversible monoamine oxidase inhibitor, on the pressor response to oral tyramine in man".British Journal of Clinical Pharmacology.11 (6):611–5.doi:10.1111/j.1365-2125.1981.tb01178.x.PMC 1402186.PMID 7272178.
  8. ^Martini A, Bonollo L, Nicolis FB, Sega R, Palermo A, Braibanti E (June 1981)."Effects of caroxazone, a reversible monoamine oxidase inhibitor, on the pressor response to intravenous tyramine in man".British Journal of Clinical Pharmacology.11 (6):605–10.doi:10.1111/j.1365-2125.1981.tb01177.x.PMC 1402193.PMID 7272177.
  9. ^Bernardi L, Coda S, Nicolella V, Vicario GP, Gioia B, Minghetti A, et al. (1979). "Radioisotopic and synthetic studies related to caroxazone metabolism in man".Arzneimittel-Forschung.29 (9):1412–6.PMID 583252.
  10. ^Bernardi L, Coda S, Pegrassi L, Suchowsky GK (August 1968). "Pharmacological properties of some derivatives of 1,3-benzoxazine".Experientia.24 (8):774–5.doi:10.1007/bf02144859.PMID 5683159.S2CID 30917127.
  11. ^Bernardi L, Coda S, Bonsignori A, Pegrassi L, Suchowsky GK (August 1969). "Central depressant properties of 3,1-benzoxazine derivates".Experientia.25 (8):787–8.doi:10.1007/bf01897874.PMID 5348526.S2CID 5347811.
  12. ^GB 1115759, "Carboxamidoalkyl-1,3-benzoxazines", published 1968-05-29, assigned to Societa Farmaceutici Italia 
  13. ^L. Bernardi et al.,U.S. patent 3,427,313 (1969 to Soc. Farma. Italia).
SSRIsTooltip Selective serotonin reuptake inhibitors
SNRIsTooltip Serotonin–norepinephrine reuptake inhibitors
NRIsTooltip Norepinephrine reuptake inhibitors
NDRIsTooltip Norepinephrine–dopamine reuptake inhibitors
NaSSAsTooltip Noradrenergic and specific serotonergic antidepressants
SARIsTooltip Serotonin antagonist and reuptake inhibitors
SMSTooltip Serotonin modulator and stimulators
Others
TCAsTooltip Tricyclic antidepressants
TeCAsTooltip Tetracyclic antidepressants
Others
Non-selective
MAOATooltip Monoamine oxidase A-selective
MAOBTooltip Monoamine oxidase B-selective
Miscellaneous
5-HT1ARTooltip 5-HT1A receptoragonists
GABAARTooltip GABAA receptorPAMsTooltip positive allosteric modulators
Gabapentinoids
(α2δVDCCblockers)
Antidepressants
Sympatholytics
(Antiadrenergics)
Others
Non-specific
AAADTooltip Aromatic L-amino acid decarboxylase
MAOTooltip Monoamine oxidase
Phenethylamines
(dopamine,epinephrine,
norepinephrine)
PAHTooltip Phenylalanine hydroxylase
THTooltip Tyrosine hydroxylase
DBHTooltip Dopamine beta-hydroxylase
PNMTTooltip Phenylethanolamine N-methyltransferase
COMTTooltip Catechol-O-methyl transferase
Tryptamines
(serotonin,melatonin)
TPHTooltip Tryptophan hydroxylase
AANATTooltip Serotonin N-acetyl transferase
ASMTTooltip Acetylserotonin O-methyltransferase
Histamine
HDCTooltip Histidine decarboxylase
HNMTTooltip Histamine N-methyltransferase
DAOTooltip Diamine oxidase
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