Open Access Articles- Top Results for L-733,060


Systematic (IUPAC) name
Clinical data
148700-85-0 7pxY
PubChem CID 132846
ChemSpider 117244 7pxN
Chemical data
Formula C20H19F6NO
403.361 g/mol
 14pxN (what is this?)  (verify)

L-733,060 is a drug developed by Merck, Sharpe & Dohme which acts as an orally active, non-peptide, selective antagonist for the NK1 receptor, binding with a Ki of 0.08nM.[1] Only one enantiomer is active which has made it the subject of several asymmetric synthesis efforts.[2][3][4]

L-733,060 has antidepressant[5][6] and anxiolytic effects in animal studies,[7] and reduces both the dopamine release and neurotoxicity produced by methamphetamine and cocaine.[8][9][10][11][12] It shows antiinflammatory and anti-hepatotoxic effects in animals,[13][14] and counteracts the development of hyperalgesia following nerve injury.[15][16] It also has anticancer effects in a variety of in vitro models.[17][18][19]

See also


  1. ^ Seabrook, GR; Shepheard, SL; Williamson, DJ; Tyrer, P; Rigby, M; Cascieri, MA; Harrison, T; Hargreaves, RJ; Hill, RG (1996). "L-733,060, a novel tachykinin NK1 receptor antagonist; effects in Ca2+i mobilisation, cardiovascular and dural extravasation assays". European Journal of Pharmacology 317 (1): 129–35. PMID 8982729. doi:10.1016/S0014-2999(96)00706-6. 
  2. ^ Liu, LX; Ruan, YP; Guo, ZQ; Huang, PQ (2004). "A general approach to (5S,6R)-6-alkyl-5-benzyloxy-2-piperidinones: application to the asymmetric syntheses of neurokinin substance P receptor antagonist (−)-L-733,061 and (−)-deoxocassine". The Journal of Organic Chemistry 69 (18): 6001–9. PMID 15373484. doi:10.1021/jo049166z. 
  3. ^ Tsai, MR; Chen, BF; Cheng, CC; Chang, NC (2005). "A novel and highly regioselective approach to 5-methoxy-6-substituted-3-sulfonyl-delta-enlactams from 5-methoxy-3-sulfonyl glutarimide: synthesis of cis-2-substituted-3-piperidinols". The Journal of Organic Chemistry 70 (5): 1780–5. PMID 15730301. doi:10.1021/jo048073e. 
  4. ^ Liu, RH; Fang, K; Wang, B; Xu, MH; Lin, GQ (2008). "Concise asymmetric synthesis of (+)-CP-99,994 and (+)-L-733,060 via efficient construction of homochiral syn-1,2-diamines and syn-1,2-amino alcohols". The Journal of Organic Chemistry 73 (8): 3307–10. PMID 18331063. doi:10.1021/jo8002979. 
  5. ^ Varty, GB; Cohen-Williams, ME; Hunter, JC (2003). "The antidepressant-like effects of neurokinin NK1 receptor antagonists in a gerbil tail suspension test". Behavioural Pharmacology 14 (1): 87–95. PMID 12576885. doi:10.1097/01.fbp.0000055962.09493.e9 (inactive 2015-01-14). 
  6. ^ Wallace-Boone, TL; Newton, AE; Wright, RN; Lodge, NJ; McElroy, JF (2008). "Behavioral and pharmacological validation of the gerbil forced-swim test: effects of neurokinin-1 receptor antagonists". Neuropsychopharmacology 33 (8): 1919–28. PMID 17912250. doi:10.1038/sj.npp.1301586. 
  7. ^ Varty, GB; Cohen-Williams, ME; Morgan, CA; Pylak, U; Duffy, RA; Lachowicz, JE; Carey, GJ; Coffin, VL (2002). "The gerbil elevated plus-maze II: anxiolytic-like effects of selective neurokinin NK1 receptor antagonists". Neuropsychopharmacology 27 (3): 371–9. PMID 12225694. doi:10.1016/S0893-133X(02)00313-5. 
  8. ^ Kraft, M; Noailles, P; Angulo, JA (2001). "Substance P modulates cocaine-evoked dopamine overflow in the striatum of the rat brain". Annals of the New York Academy of Sciences 937: 121–31. Bibcode:2001NYASA.937..121K. PMID 11458533. doi:10.1111/j.1749-6632.2001.tb03561.x. 
  9. ^ Yu, J; Allison, S; Ibrahim, D; Cadet, JL; Angulo, JA (2002). "Ontogeny of neurokinin-1 receptor mediation of methamphetamine neurotoxicity in the striatum of the mouse brain". Annals of the New York Academy of Sciences 965: 247–53. Bibcode:2002NYASA.965..247Y. PMID 12105100. doi:10.1111/j.1749-6632.2002.tb04166.x. 
  10. ^ Noailles, PA; Angulo, JA (2002). "Neurokinin receptors modulate the neurochemical actions of cocaine". Annals of the New York Academy of Sciences 965: 267–73. Bibcode:2002NYASA.965..267N. PMID 12105102. doi:10.1111/j.1749-6632.2002.tb04168.x. 
  11. ^ Yu, J; Cadet, JL; Angulo, JA (2002). "Neurokinin-1 (NK-1) receptor antagonists abrogate methamphetamine-induced striatal dopaminergic neurotoxicity in the murine brain". Journal of Neurochemistry 83 (3): 613–22. PMID 12390523. doi:10.1046/j.1471-4159.2002.01155.x. 
  12. ^ Loonam, TM; Noailles, PA; Yu, J; Zhu, JP; Angulo, JA (2003). "Substance P and cholecystokinin regulate neurochemical responses to cocaine and methamphetamine in the striatum". Life Sciences 73 (6): 727–39. PMID 12801594. doi:10.1016/S0024-3205(03)00393-X. 
  13. ^ Bang, R; Sass, G; Kiemer, AK; Vollmar, AM; Neuhuber, WL; Tiegs, G (2003). "Neurokinin-1 receptor antagonists CP-96,345 and L-733,060 protect mice from cytokine-mediated liver injury". The Journal of Pharmacology and Experimental Therapeutics 305 (1): 31–9. PMID 12649350. doi:10.1124/jpet.102.043539. 
  14. ^ Bang, R; Biburger, M; Neuhuber, WL; Tiegs, G (2004). "Neurokinin-1 receptor antagonists protect mice from CD95- and tumor necrosis factor-alpha-mediated apoptotic liver damage". The Journal of Pharmacology and Experimental Therapeutics 308 (3): 1174–80. PMID 14617692. doi:10.1124/jpet.103.059329. 
  15. ^ Jang, JH; Nam, TS; Paik, KS; Leem, JW (2004). "Involvement of peripherally released substance P and calcitonin gene-related peptide in mediating mechanical hyperalgesia in a traumatic neuropathy model of the rat". Neuroscience letters 360 (3): 129–32. PMID 15082150. doi:10.1016/j.neulet.2004.02.043. 
  16. ^ Rittner, HL; Lux, C; Labuz, D; Mousa, SA; Schäfer, M; Stein, C; Brack, A (2007). "Neurokinin-1 receptor antagonists inhibit the recruitment of opioid-containing leukocytes and impair peripheral antinociception". Anesthesiology 107 (6): 1009–17. PMID 18043070. doi:10.1097/ 
  17. ^ Muñoz, M; Rosso, M; Coveñas, R; Montero, I; González-Moles, MA; Robles, MJ (2007). "Neurokinin-1 receptors located in human retinoblastoma cell lines: antitumor action of its antagonist, L-732,138". Investigative Ophthalmology & Visual Science 48 (6): 2775–81. PMID 17525212. doi:10.1167/iovs.05-1591. 
  18. ^ Muñoz, M; Rosso, M; Aguilar, FJ; González-Moles, MA; Redondo, M; Esteban, F (2008). "NK-1 receptor antagonists induce apoptosis and counteract substance P-related mitogenesis in human laryngeal cancer cell line HEp-2". Investigational new drugs 26 (2): 111–8. PMID 17906845. doi:10.1007/s10637-007-9087-y. 
  19. ^ Rosso, M; Robles-Frías, MJ; Coveñas, R; Salinas-Martín, MV; Muñoz, M (2008). "The NK-1 receptor is expressed in human primary gastric and colon adenocarcinomas and is involved in the antitumor action of L-733,060 and the mitogenic action of substance P on human gastrointestinal cancer cell lines". Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 29 (4): 245–54. PMID 18781096. doi:10.1159/000152942. 

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