Fenclonine

Chemical compound
  • None
Identifiers
  • (S)-2-Amino-3-(4-chlorophenyl)propanoic acid
CAS Number
  • 7424-00-2 checkY
PubChem CID
  • 4652
IUPHAR/BPS
  • 5240
ChemSpider
  • 4491 checkY
UNII
  • R5J7E3L9SP
KEGG
  • D04143 checkY
CompTox Dashboard (EPA)
  • DTXSID4045139 Edit this at Wikidata
ECHA InfoCard100.028.229 Edit this at WikidataChemical and physical dataFormulaC9H10ClNO2Molar mass199.63 g·mol−13D model (JSmol)
  • Interactive image
Density1.336 g/cm3Melting point240 °C (464 °F)Boiling point339.5 °C (643.1 °F)
  • Clc1ccc(cc1)CC(C(=O)O)N
InChI
  • InChI=1S/C9H10ClNO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13) checkY
  • Key:NIGWMJHCCYYCSF-UHFFFAOYSA-N checkY
  (verify)

Fenclonine, also known as para-chlorophenylalanine (PCPA), acts as a selective and irreversible inhibitor of tryptophan hydroxylase, which is a rate-limiting enzyme in the biosynthesis of serotonin.[2]

It has been used experimentally to treat carcinoid syndrome, but the side effects, mostly hypersensitivity reactions and psychiatric disturbances, have prevented development for this use.[3]

The effects of serotonin depletion from fenclonine are so drastic that serotonin cannot even be detected immunohistochemically within the first day after administration of a control dose. Tryptophan hydroxylase activity can be detected neither in cell bodies or nerve terminals. After one week 10% of control values (the baseline extrapolated for the study) had replenished in the raphe nucleus, and after two weeks from initial treatment as much was again detected in the hypothalamus region. Aromatic L-amino acid decarboxylase (AADC) levels were at no time affected.[4]

It is used in scientific research in humans[5] and animals[2] to investigate the effects of serotonin depletion.

See also

References

  1. ^ "Fenclonine" entry in Martindale – The Complete Drug Reference. Maintained in Martindale purely for archival purposes, and is no longer subject to revision and update. (Last reviewed: 2008-08-01; last modified: 2011-09-12). The Royal Pharmaceutical Society of Great Britain 2014
  2. ^ a b Jouvet M (August 1999). "Sleep and serotonin: an unfinished story". Neuropsychopharmacology. 21 (2 Suppl): 24S–27S. doi:10.1016/S0893-133X(99)00009-3. PMID 10432485.
  3. ^ Kvols LK (December 1986). "Metastatic carcinoid tumors and the carcinoid syndrome. A selective review of chemotherapy and hormonal therapy". The American Journal of Medicine. 81 (6B): 49–55. doi:10.1016/0002-9343(86)90584-x. PMID 2432781.
  4. ^ Park DH, Stone DM, Baker H, Kim KS, Joh TH (March 1994). "Early induction of rat brain tryptophan hydroxylase (TPH) mRNA following parachlorophenylalanine (PCPA) treatment". Brain Research. Molecular Brain Research. 22 (1–4): 20–8. doi:10.1016/0169-328x(94)90028-0. PMID 8015380.
  5. ^ Ruhé HG, Mason NS, Schene AH (April 2007). "Mood is indirectly related to serotonin, norepinephrine and dopamine levels in humans: a meta-analysis of monoamine depletion studies". Molecular Psychiatry. 12 (4): 331–59. doi:10.1038/sj.mp.4001949. PMID 17389902.
  • v
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Non-specific
AAADTooltip Aromatic L-amino acid decarboxylase
MAOTooltip Monoamine oxidase
Phenethylamines
(dopamine, epinephrine,
norepinephrine)
PAHTooltip Phenylalanine hydroxylase
THTooltip Tyrosine hydroxylase
DBHTooltip Dopamine beta-monooxygenase
PNMTTooltip Phenylethanolamine N-methyltransferase
  • Inhibitors: CGS-19281A
  • SKF-64139
  • SKF-7698
COMTTooltip Catechol-O-methyl transferase
Tryptamines
(serotonin, melatonin)
TPHTooltip Tryptophan hydroxylase
AANATTooltip Serotonin N-acetyl transferase
ASMTTooltip Acetylserotonin O-methyltransferase
Histamine
HDCTooltip Histidine decarboxylase
  • Substrates→Products: L-Histidine→Histamine
HNMTTooltip Histamine N-methyltransferase
  • Substrates→Products: Histamine→N-Methylhistamine
DAOTooltip Diamine oxidase
  • Substrates→Products: Histamine→Imidazole acetic acid
See also: Receptor/signaling modulators • Adrenergics • Dopaminergics • Melatonergics • Serotonergics • Monoamine reuptake inhibitors • Monoamine releasing agents • Monoamine neurotoxins
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Phenethylamines


Stimulants: Phenylethanolamine

Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
Phenylalkylpyrrolidines
Catecholamines
(and close relatives)
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