Summary
During the last decades (-)-deprenyl has become the golden standard of MAO-B inhibitors. It possesses dopamine potentiating and antioxidant properties; however, its effects cannot be explained solely by the enzyme inhibitory action. (-)-Deprenyl prevents the toxicity of certain selective neurotoxins and recently it was demonstrated to increase cell-cell adhesion as well. The complexity of its pharmacological effects reflects the action of both the parent compound and the active metabolites. (-)-Deprenyl and related propargylamines (DRPs) show neuroprotective features in a variety of in vitro and in vivo models that is dependent on the propargyl moiety. The main presumptive targets to date include glyceraldehyde-3-phosphate dehydrogenase, poly(ADP-ribose) polymerase, some kinase cascades, as well as pro- and antiapoptotic proteins, beside the inhibition of MAO-B. The antiapoptotic activity of DRPs converges upon the maintenance of mitochondrial integrity, due to the initiation of a complex transcriptional program, the details of which are yet to be elucidated.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
References
Abu-Raya S, Tabakman R, Blaugrund E, Trembovler V, Lazarovici P (2002) Neuroprotective and neurotoxic effects of monoamine oxidase-B inhibitors and derived metabolites under ischemia in PC12 cells. Eur J Pharmacol 434: 109–116
Andoh T, Chock PB, Murphy DL, Chiueh CC (2005) Role of the redox protein thioredoxin in cytoprotective mechanism evoked by (-)-deprenyl. Mol Pharmacol 68: 1408–1414
Bach MV, Coutts RT, Baker GB (2000) Metabolism of N,N-dialkylated amphetamines, including deprenyl, by CYP2D6 expressed in human cell line. Xenobiotica 30: 297–306
Bar-Am O, Amit T, Youdim MBH (2004) Contrasting neuroprotective and neurotoxic actions of respective metabolites of anti-Parkinson drugs rasagiline and selegiline. Neurosci Lett 355: 169–172
Barrett JS, Hochadel TJ, Morales RJ, Rohatagi S, DeWitt KE, Watson SK, DiSanto AR (1996b) Pharmacokinetics and safety of a selegiline transdermal system relative to single-dose oral administration in the elderly. Am J Ther 3: 688–698
Barrett JS, Rohatagi S, DeWitt KE, Morales RJ, DiSanto AR (1996a) The effect of dosing regimen and food on the bioavailability of the extensively metabolized, highly variable drug Eldepryl® (selegiline hydrochloride). Am J Ther 3: 298–313
Biagini G, Frasoldati A, Fuxe K, Agnati LF (1994) The concept of astrocyte-kinetic drug in the treatment of neurodegenerative diseases: evidence for L-deprenyl-induced activation of reactive astrocytes. Neurochem Int 25: 17–22
Binda C, Newton-Vinson P, Hubálek F, Edmondson DE, Mattevi A (2002) Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders. Nat Struct Biol 9: 22–26
Birkmayer W, Birkmayer GD (1986) Effect of (-)-deprenyl in long-term treatment of Parkinson’s disease. A 10-years experience. J Neural Transm [Suppl 22]: 219–225
Birkmayer W, Knoll J, Riederer P, Youdim MB, Hars V, Marton J (1985) Increased life expectancy resulting from addition of L-deprenyl to Madopar treatment in Parkinson’s disease: a longterm study. J Neural Transm 64: 113–127
Birkmayer W, Riederer P, Ambrozi L, Youdim MB (1977) Implications of combined treatment with ‘Madopar’ and L-deprenil in Parkinson’s disease. A long-term study. Lancet 309: 439–443
Bouchard VJ, Rouleau M, Poirier GG (2003) PARP-1, a determinant of cell survival in response to DNA damage. Exp Hematol 31: 446–454
Brabeck C, Pfeiffer R, Leake A, Beneke S, Meyer R, Bürkle A (2003) L-Selegiline potentiates the cellular poly(ADP-ribosyl)ation to ionizing radiation. J Pharmacol Exp Ther 306: 973–979
Carlile GW, Chalmers-Redman RME, Tatton NA, Pong A, Borden KE, Tatton WG (2000) Reduced apoptosis after nerve growth factor and serum withdrawal: conversion of tetrameric glyceradehyde-3-phosphate dehydrogenase to a dimer. Mol Pharmacol 57: 2–12
Chen R-W, Saunders PA, Wei H, Li Z, Seth P, Chuang DM (1999) Involvement of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and p53 in neuronal apoptosis: Evidence that GAPDH is upregulated by p53. J Neurosci 19: 9654–9662
De la Cruz CP, Revilla E, Rodriguez-Gomez JA, Vizuete ML, Cano J, Machado A (1997) (-)-Deprenyl treatment restores serum insulin-like growth factor-I (IGF-I) levels in aged rats to young rat level. Eur J Pharmacol 53: 593–604
Ekstedt B, Magyar K, Knoll J (1979) Does the B form selective monoamine oxidase inhibitor lose selectivity by long term treatment? Biochem Pharmacol 28: 919–923
Falsaperla A, Monici Preti PA, Oliani C (1990) Selegiline versus oxiracetam in patients with Alzheimer-type dementia. Clin Ther 12: 376–384
Fowler JS, Volkow ND, Logan J, Franceschi D, Wang GJ, MacGregor R, Shea C, Garza V, Pappas N, Carter P, Netusil N, Bridge P, Liederman D, Elkashef A, Rotrosen J, Hitzemann R (2001) Evidence that L-deprenyl treatment for one week does not inhibit MAO A or the dopamine transporter in the human brain. Life Sci 68: 2759–2768
Frielingsdorf H, Schwarz K, Brundin P, Mohapel P (2004) No evidence for new dopaminergic neurons in the adult mammalian substantia nigra. P Natl Acad Sci USA 101: 10177–10182
Fukuhara Y, Takeshima T, Kashiwaya Y, Shimoda K, Ishitani R, Nakashima K (2001) GAPDH knockdown rescues mesencephalic dopaminergic neurons from MPP+-induced apoptosis. Neuroreport 12: 2049–2052
Garner CC, Zhai RG, Gundelfinger D, Ziv NE (2002) Molecular mechanisms of CNS synaptogenesis. Trends Neurosci 25: 243–250
Grace JM, Kinter MT, Macdonald TL (1994) Atypical metabolism of deprenyl and its enantiomer, (S)-(+)-N-alpha-dimethyl-N-propynylphenethylamine, by cytochrome P450 2D6. Chem Res Toxicol 7: 286–290
Hamada-Kanazawa M, Ishikawa K, Nomoto K, Uozumi T, Kawai Y, Narahara M, Miyake M (2004) Sox6 overexpression causes cellular aggregation and the neuronal differentiation of P19 embryonic carcinoma cells in the absence of retinoic acid. FEBS Lett 560: 192–198
Heinonen EH, Myllyla V, Sotaniemi K, Lammintausta R, Salonen JS, Anttila M, Savijarvi M, Kottila M, Rinne UK (1989) Pharmacokinetics and metabolism of selegiline. Acta Neurol Scand 126: 93–99
Höglinger GU, Rizk P, Muriel MP, Duyckaerts C, Oertel WH, Caille I, Hirsch EC ((2004) Dopamine depletion impairs precursor cell proliferation in Parkinson disease. Nat Neurosci 7: 726–735
Ishitani R, Tanaka M, Sunaga K, Katsube N, Chuang D-M (1998) Nuclear localization of overexpressed glyceraldehyde-3-phosphate dehydrogenase in cultured cerebellar neurons undergoing apoptosis. Mol Pharmacol 53: 701–707
Jayanthi S, Deng X, Bordelon M, McCoy MC, Cadet JL (2001) Methamphetamine causes differential regulation of pro-death and antideath Bcl-2 genes in the mouse neocortex. FASEB J 15: 1745–1752
Jenei V, Zor K, Magyar K, Jakus J (2005) Increased cell-cell adhesion, a novel effect of R-(-)-deprenyl. J Neural Transm 112: 1433–1445
Jenner P, Olanow CW (1996) Oxidative stress and the pathogenesis of Parkinson’s disease. Neurology 47: S161–S170
Jin K, Peel AL, Mao XO, Xie L, Cottrell BA, Henshall DC, Greenberg DA (2004) Increased hippocampal neurogenesis in Alzheimer’s disease. P Natl Acad Sci USA 101: 343–347
Johnston JP (1968) Some observations upon a new inhibitor of monoamine oxidase in brain tissue. Biochem Pharmacol 17: 1285–1297
Katagi M, Tatsuno M, Miki A, Nishikawa M, Nakajima K, Tsuchihashi H (2001) Simultaneous determination of selegiline-N-oxide, a new indicator for selegiline administration, and other metabolites in urine by high-performance liquid chromatography-electrospray ionization mass spectrometry. J Chromatogr B 759: 125–133
Katagi M, Tatsuno M, Tsutsumi H, Miki A, Kamata T, Nishioka H, Nakajima K, Nishikawa M, Tsuchihashi H (2002) Urinary excretion of selegiline N-oxide, a new indicator for selegiline administration in man. Xenobiotica 32: 823–831
Kitani K, Minami C, Isobe K, Maehara K, Kanai S, Ivy GO, Carillo M-C (2002) Why (-)-deprenyl prolongs survival of experimental animals: Increase of anti-oxidant enzymes in brain and other body tissues as well as mobilization of various humoral factors may lead to systemic anti-aging effects. Mech Ageing Dev 123: 1087–1100
Knoll J, Ecseri Z, Kelemen K, Nievel J, Knoll B (1965) Phenylisopropylmethylpropinyl-amine (E-250), and new spectrum psychic energizer. Arch Int Pharmacodyn Ther 155: 154–164
Knoll J, Magyar K (1972) Some puzzling pharmacological effects of monoamine oxidase inhibitors. Adv Biochem Psychopharmacol 5: 393–408
Kragten E, Lalande I, Zimmermann K, Roggo S, Schindler P, Müller D, Van Oostrum J, Waldmeier P, Fürst P (1998) Glyceraldehyde-3-phosphate dehydrogenase, the putative target of the anti-apoptotic compounds CGP 3466 and R-(-)-deprenyl. J Biol Chem 273: 5821–5828
Kraus WL, Lis JT (2003) PARP goes transcription. Cell 113: 677–683
Laine K, Anttila M, Huupponen R, Maki-Ikola O, Heinonen E (2000) Multiple-dose pharmacokinetics of selegiline and desmethylselegiline suggest saturable tissue binding. Clin Neuropharmacology 23: 22–27
Lange KW, Riederer P, Youdim MB (1994) Biochemical actions of ldeprenyl (selegiline). Clin Pharmacol Ther 56: 734–741
Laplante I, Beliveau R, Paquin J (2004) RhoA=ROCK and Cdc42 regulate cell-cell contact and N-cadherin protein level during neurodetermination of P19 embryonal stem cells. J Neurobiol 60: 289–307
Lengyel J, Magyar K, Hollósi I, Bartók T, Báthori M, Kalász H, Fürst S (1997) Urinary excretion of deprenyl metabolites. J Chromatogr A 762: 321–326
Levai F, Fejer E, Szeleczky G, Szabo A, Eros Takacsy T, Hajdu F, Szebeni G, Szatmari I, Hermecz I (2005) In vitro formation of selegiline-Noxide as a metabolite of selegiline in human, hamster, mouse, rat, guinea-pig, rabbit and dog. Eur J Drug Metab Ph 29: 169–178
Lew MF (2005) Selegiline orally disintegrating tablets for the treatment of Parkinson’s disease. Expert Rev Neurother 5: 705–712
Magyar K, Ecseri Z, Bernáth G, Sátory É, Knoll J (1980) Structure-activity relationship of selective inhibitors of MAO-B. In: Magyar K (ed) Monoamines oxidases and their selective inhibition. Third Congress of the Hungarian Pharmacological Society, Pergamon Press, Budapest, pp 11–21
Magyar K, Lengyel J, Szatmari I, Gaal J (1995) The distribution of orally administered (-)-deprenyl-propynyl-14C and (-)-deprenyl-phenyl-3H in rat brain. Prog Brain Res 106: 143–153
Magyar K, Pálfi M, Tábi T, Kalász H, Szende B, Szökő É (2004) Pharmacological aspects of (-)-deprenyl. Curr Med Chem 111: 2017–2031
Magyar K, Szende B (2000) In: Cameron EG, Feuer G (eds) Handbook of experimental pharmacology. Apoptosis and its modulation by drugs. Springer-Verlag, Berlin-Heidelberg, Vol 142, pp 457–472
Magyar K, Szende B (2004) (-)-Deprenyl, a selective MAO-B inhibitor, with apoptotic and antiapoptotic properties. Neurotoxicology 25: 233–242
Magyar K, Szende B, Lengyel J, Tekes K (1996) The pharmacology of B-type selective monoamine oxidase inhibitors; milestones in (-)-deprenyl research. J Neural Transm [Suppl 48]: 29–43
Magyar K, Szende B, Lengyel J, Tarczali J, Szatmary I (1998) The neuroprotective and neuronal rescue effects of (-)-deprenyl. J Neural Transm [Suppl 52]: 109–123
Magyar K, Vízi ES, Ecseri Z, Knoll J (1967) Comparative pharmacological analysis of the optical isomers of phenyl-isopropyl-methyl-propinylamine (E-250). Acta Physiol Hung 32: 377–387
Mahmood I (1997) Clinical pharmacokinetics and pharmacodynamics of selegiline. An update. Clin Pharmacokinet 33: 91–102
Mandel S, Weinreb O, Amit T, Youdim MB (2005) Mechanism of neuroprotective action of the anti-Parkinson drug rasagiline and its derivatives. Brain Res Rev 48: 379–387
Maruyama W, Akao Y, Carillo MC, Kitani K, Youdim MBH, Naoi M (2002) Neuroprotection by propargylamines in Parkinson’s disease. Suppression of apoptosis and induction of prosurvival genes. Neurotoxicol Teratol 24: 675–682
Maruyama W, Nitta A, Shamoto-Nagai M, Hirata Y, Akao Y, Youdim M, Furukawa S, Nabeshima T, Naoi M (2004) N-propargyl-1(R)-aminoindan, rasagiline, increases glial cell line-derived neurotrophic factor (GDNF) in neuroblastoma SH-SY5Y cells through activation of NF-kB transcription factor. Neurochem Int 44: 393–400
Maruyama W, Youdim MBH, Naoi M (2001) Antiapoptotic properties of rasagiline, N-propargylamine-1(R)-aminoindan, and its optical (S)-isomer TV1022. Ann NY Acad Sci 939: 320–329
Mazzola JL, Sirover MA (2002) Alteration of intracellular structure and function of glyceraldehydes-3-phosphate dehydrogenase: a common phenotype of neurodegenerative disorders? Neurotoxicology 23: 603–609
Meyer-Ficca ML, Meyer RG, Jacobson EL, Jacobson MK (2005) Poly(ADP-ribose) polymerases: managing genome stability. Int J Biochem Cell B 37: 920–926
Minton AP, Wilf J (1981) Effect of macromolecular crowding upon the structure and function of an enzyme: glyceraldehyde-3-phosphate dehydrogenase. Biochemistry 20: 4821–4826
Mizuta I, Ohta M, Ohta K, Nishimura M, Mizuta E, Hayashi K, Kuno S (2000) Selegiline and desmethylselegiline stimulate NGF, BDNF, and GDNF synthesis in cultured mouse astrocytes. Biochem Bioph Res Co 279: 751–755
Naoi M, Maruyama W (2001) Future of neuroprotection in Parkinson’s disease. Parkinsonism Relat D 8: 139–145
Naoi M, Maruyama W, Akao Y, Yi H (2002) Mitochondria determine the survival and death in apoptosis by an endogenous neurotoxin, N-methyl(R)salsolinol, and neuroprotection by propargylamines. J Neural Transm 109: 607–621
Qin F, Shite J, Mao W, Liang CS (2003) Selegiline attenuates cardiac oxidative stress and apoptosis in heart failure: association with improvement of cardiac function. Eur J Pharmacol 461: 149–158
Reynolds GP, Elsworth JD, Blau K, Sandler M, Lees AJ, Stern GM (1978) Deprenyl is metabolized to methamphetamine and amphetamine in man. Brit J Clin Pharmaco 6: 542–544
Riederer P, Youdim MB, Rausch WD, Birkmayer W, Jellinger K, Seeman D (1978) On the mode of L-Deprenyl in the human central nervous system. J Neural Transm 43: 217–226
Riva MA, Molteni R, Racagni G (1997) L-deprenyl potentiates cAMP-induced elevation of FGF-2 mRNA levels in rat cortical astrocytes. Neuroreport 8: 2165–2168
Salonen JS, Nyman L, Boobis AR, Edwards RJ, Watts P, Lake BG, Price RJ, Renwick AB, Gómez-Lechón M-J, Castell JV, Ingelman-Sundberg M, Hidestrand M, Guillouzo A, Corcos L, Goldfarb PS, Lewis DFV, Taavitsainen P, Pelkonen O (2003) Comparative studies on the cytochrome P450-associated metabolism and interaction potential of selegiline between human liver-derived in vitro systems. Drug Metab Dispos 31: 1093–1102
Sawa A, Khan AA, Hester LD, Snyder SH (1997) Glyceraldehyde-3-phosphate dehydrogenase: Nuclear translocation participates in neuronal and nonneuronal cell death. P Natl Acad Sci USA 94: 11669–11674
Schlett K, Czirók A, Tárnok K, Vicsek T, Madarász E (2000) Dynamics of cell aggregation during in vitro neurogenesis by immortalized neuroectodermal progenitors. J Neurosci Res 60: 184–194
Semkova I, Wolz P, Schilling M, Krieglstein J (1996) Selegiline enhances NGF synthesis and protects central nervous system neurons from excitotoxic and ischemic damage. Eur J Pharmacol 315: 19–30
Seymour CB, Mothersill C, Mooney R, Moriarty M, Tipton KF (2003) Monoamine oxidase inhibitors l-deprenyl and clorgyline protect nonmalignant human cells from ionizing radiation and chemotherapy toxicity. Brit J Cancer 89: 1979–1986
Shi Y, Shi Y (2004) Metabolic enzymes and coenzymes in transcription — a direct link between metabolism and transcription? Trends Genet 20: 445–452
Shin H-S (1997) Metabolism of selegiline in humans. Identification, excretion, and stereochemistry of urine metabolites. Drug Metab Dispos 25: 657–662
Szebeni G, Lengyel J, Székács G, Magyar K, Gaál J, Szatmári I (1995) Gas chromatographic procedure for simultaneous determination of selegiline metabolites, amphetamine, methamphetamine and desmethyl-deprenyl in pig plasma. Acta Physiol Hung 83: 135–141
Szende B, Bökönyi J, Bocsi J, Kéri Gy, Timár F, Magyar K (2001) Antiapoptotic and apoptotic action of (-)-deprenyl and its metabolites. J Neural Transm 108: 25–33
Szökő É, Kalász H, Magyar K (1999) Biotransformation of deprenyl enantiomers. Eur J Drug Metab Ph 24: 315–319
Szökő É, Magyar K (1996) Enantiomer identification of the major metabolites of (-)-deprenyl in rat urine by capillary electrophoresis. Int J Pharm Adv 1: 320–328
SzÖkő É, Tábi T, Halász AS, Pálfi M, Kalász H, Magyar K (2004a) Chiral characterization and quantification of deprenyl-N-oxide and other deprenyl metabolites in rat urine by capillary electrophoresis. Chromatographia 60: S245–S251
Szökő É, Tábi T, Borbás T, Dalmadi B, Tihanyi K, Magyar K (2004b) Assessment of the N-oxidation of deprenyl, methamphetamine, and amphetamine enantiomers by chiral capillary electrophoresis: an in vitro metabolism study. Electrophoresis 25: 2866–2875
Taavitsainen P, Anttila M, Nyman L, Karnani H, Salonen JS, Pelkonen O (2000) Selegiline metabolism and cytochrome P450 enzymes: in vitro study in human liver microsomes. Pharmacol Toxicol 86: 215–221
Tabakman R, Lecht S, Lazarovici P (2003) Neuroprotection by monoamine oxidase inhibitors: a therapeutic strategy for Parkinson’s disease? Bioessays 26: 80–90
Tábi T, Magyar K, Szökő É (2003) Chiral characterization of deprenyl-Noxide and other deprenyl metabolites by capillary electrophoresis using dual cyclodextrin system in rat urine. Electrophoresis 24: 2665–2673
Tatton WG, Chalmers-Redman RME (1996) Modulation of gene expression rather than monoamine oxidase inhibition: (-)-Deprenyl-related compounds in controlling neurodegeneration. Neurology 47[Suppl 3]: S171–S183
Tatton WG, Chalmers-Redman RME, Ju WJH, Mammen M, Carlile GW, Pong AW, Tatton NA (2002) Propargylamines induce antiapoptotic new protein synthesis in serum-and nerve growth factor (NGF)-withdrawn, NGF-differentiated PC-12 cells. J Pharmacol Exp Ther 301: 753–764
Tatton WG, Ju WYL, Holland DP, Tai C, Kwan M (1994) Deprenyl reduces PC12 cell apoptosis by inducing new protein synthesis. J Neurochem 63: 1572–1575
Tekes K, Magyar K (2000) Effect of MAO inhibitors on the hjgh-affinity reuptake of biogenic amines in rat subcortical regions. Neurobiology (Bp.) 8: 257–264
Thomas T, McLendon C, Thomas G (1998) L-deprenyl: nitric oxide production and dilation of cerebral blood vessels. Neuroreport 9: 2595–2600
Toronyi E, Hamar J, Magyar K, Szende B (2002) Antiapoptotic effect of (-)-deprenyl in rat kidney after ischemia reperfusion. Med Sci Monitor 8: BR65–68
Tsutsumi H, Katagi M, Nishikawa M, Tsuchihashi H, Kasuya F, Igarashi K (2004) In vitro confirmation of selegiline N-oxidation by flavin-containing monooxygenase in rat microsome using LC-ESI MS. Biol Pharm Bull 27: 1572–1575
Valoti M, Fusi F, Frosini M, Pessina F, Tipton KF, Sgaragli GP (2000) Eur J Pharmacol 391: 199–206
Wadia JS, Chalmers-Redman RME, Ju WJH, Carlile GW, Phillips JL, Fraser AD, Tatton WG (1998) Mitochondrial membrane potential and nuclear changes in apoptosis caused by serum and nerve growth factor withdrawal: time course and modification by (-)-deprenyl. J Neurosci 18: 932–947
Waldmeier PC, Tatton WG (2004) Interrupting apoptosis in neurodegenerative disease: potential for effective therapy? Drug Discov Today 9: 210–218
Weinreb O, Bar-Am O, Amit T, Chillag-Talmor O, Youdim MBH (2004) Neuroprotection via pro-survival PKC isoforms associated with Bcl-2 family members. FASEB J 18: 2033–2043
Yi H, Maruyama W, Akao Y, Takahashi T, Iwasa K, Youdim MBH, Naoi M (2006) N-Propargylamine protects SH-SY5Y cells from apoptosis induced by an endogenous neurotoxin, N-methyl(R)salsolinol, through stabilization of mitochondrial membrane and induction of anti-apoptotic Bcl-2. J Neural Transm 113: 21–32
Yogev-Falach M, Amit T, Bar-Am O, Youdim MBH (2003) The importance of propargylamine moiety in the anti-Parkinson drug rasagiline and its derivatives for MAPK-dependent amyloid preursor protein processing. FASEB J 17: 2325–2327
Yoshida T, Yamada Y, Yamamoto T, Kuroiwa Y (1986) Metabolism of deprenyl, a selective monoamine oxidase (MAO) B inhibitor in rat: relationship of metabolism to MAO-B inhibitory potency. Xenobiotica 16: 129–136
Yoshimi K, Ren YR, Seki T, Yamada M, Ooizumi H, Onodera M, Saito Y, Murayama S, Okano H, Mizuno Y, Mochizuki H (2005) Possibility for neurogenesis in substantia nigra of parkinsonian brain. Ann Neurol 58: 31–40
Youdim MBH, Finberg JPM (1986) MAO type B inhibitors as adjunct to Ldopa therapy. In: Yahr MD, Bergmann KJ (eds) Advances in Neurology Vol. 45, pp 127–136
Zhao M, Momma S, Delfani K, Carlen M, Cassidy RM, Johansson CB, Brismar H, Shupliakov O, Frisen J, Janson AM (2003) Evidence for neurogenesis in the adult mammalian substantia nigra. P Natl Acad Sci USA 100: 7925–7930
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2006 Springer-Verlag
About this chapter
Cite this chapter
Magyar, K., Pálfi, M., Jenei, V., Szökő, É. (2006). Deprenyl: from chemical synthesis to neuroprotection. In: Parvez, H., Riederer, P. (eds) Oxidative Stress and Neuroprotection. Journal of Neural Transmission. Supplementa, vol 71. Springer, Vienna. https://doi.org/10.1007/978-3-211-33328-0_16
Download citation
DOI: https://doi.org/10.1007/978-3-211-33328-0_16
Publisher Name: Springer, Vienna
Print ISBN: 978-3-211-33327-3
Online ISBN: 978-3-211-33328-0
eBook Packages: MedicineMedicine (R0)