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Journal Abstract Search


331 related items for PubMed ID: 9914649

  • 1. Preparation and configuration of racemic and optically active analgesic cycloaminoalkylnaphthalenes.
    Ghislandi V, Collina S, Azzolina O, Barbieri A, Lanza E, Tadini C.
    Chirality; 1999; 11(1):21-8. PubMed ID: 9914649
    [Abstract] [Full Text] [Related]

  • 2. Preparation and configuration of racemic and optically active analgesic dialkylaminoalkylnaphthalenes.
    Ghislandi V, Azzolina O, Collina S, Paroli E, Antonilli L, Giuseppetti G, Tadini C.
    Chirality; 1994; 6(5):389-99. PubMed ID: 8068498
    [Abstract] [Full Text] [Related]

  • 3. Evaluation of the antiallodynic, teratogenic and pharmacokinetic profile of stereoisomers of valnoctamide, an amide derivative of a chiral isomer of valproic acid.
    Kaufmann D, Yagen B, Minert A, Wlodarczyk B, Finnell RH, Schurig V, Devor M, Bialer M.
    Neuropharmacology; 2010 Jun; 58(8):1228-36. PubMed ID: 20230843
    [Abstract] [Full Text] [Related]

  • 4. Breaking the mirror: pH-controlled chirality generation from a meso ligand to a racemic ligand.
    Zhang L, Zhang J, Li ZJ, Qin YY, Lin QP, Yao YG.
    Chemistry; 2009 Jun; 15(4):989-1000. PubMed ID: 19086049
    [Abstract] [Full Text] [Related]

  • 5. Lipase-catalyzed resolution of (2R*,3S*)- and (2R*,3R*)-3-methyl-3-phenyl-2-aziridinemethanol at low temperatures and determination of the absolute configurations of the four stereoisomers.
    Sakai T, Liu Y, Ohta H, Korenaga T, Ema T.
    J Org Chem; 2005 Feb 18; 70(4):1369-75. PubMed ID: 15704972
    [Abstract] [Full Text] [Related]

  • 6. Synthesis and antinociceptive activity of pyrrolidinylnaphthalenes.
    Collina S, Azzolina O, Vercesi D, Sbacchi M, Scheideler MA, Barbieri A, Lanza E, Ghislandi V.
    Bioorg Med Chem; 2000 Aug 18; 8(8):1925-30. PubMed ID: 11003137
    [Abstract] [Full Text] [Related]

  • 7. Novel diastereomeric opioid tetrapeptides exhibit differing pharmacological activity profiles.
    Ioja E, Tourwé D, Kertész I, Tóth G, Borsodi A, Benyhe S.
    Brain Res Bull; 2007 Sep 14; 74(1-3):119-29. PubMed ID: 17683797
    [Abstract] [Full Text] [Related]

  • 8. Chiral inversion and stereoselective glutathione conjugation of the four 2-bromo-3-methylvaleric acid stereoisomers in the rat in vivo and in vitro.
    Polhuijs M, Tergau AC, Mulder GJ.
    J Pharmacol Exp Ther; 1992 Mar 14; 260(3):1349-54. PubMed ID: 1545397
    [Abstract] [Full Text] [Related]

  • 9. The Synthesis and Absolute Configuration of Enantiomeric Pure (R)- and (S)-3-(piperidin-3-yl)-1H-Indole Derivatives.
    Król M, Ślifirski G, Kleps J, Podsadni P, Materek I, Kozioł AE, Herold F.
    Int J Mol Sci; 2022 Dec 28; 24(1):. PubMed ID: 36613958
    [Abstract] [Full Text] [Related]

  • 10. Diastereoselective synthesis of all four isomers of 3-(4-chlorophenyl) glutamic acid: identification of the isomers responsible for the potentiation of L-homocysteic acid-evoked depolarizations in neonatal rat motoneurons.
    Jane DE, Chalmers DJ, Howard JA, Kilpatrick IC, Sunter DC, Thompson GA, Udvarhelyi PM, Wilson C, Watkins JC.
    J Med Chem; 1996 Nov 22; 39(24):4738-43. PubMed ID: 8941386
    [Abstract] [Full Text] [Related]

  • 11. Preparation of optically active (2RS,3SR)-2-amino-3-hydroxy-3-phenylpropanoic acid (threo-beta-phenylserine) via optical resolutions by replacing and preferential crystallization.
    Shiraiwa T, Kawashima Y, Ikaritani A, Suganuma Y, Saijoh R.
    Chem Pharm Bull (Tokyo); 2006 Aug 22; 54(8):1170-4. PubMed ID: 16880663
    [Abstract] [Full Text] [Related]

  • 12. Enantiomers of diastereomeric cis-N-[1-(2-hydroxy-2-phenylethyl)- 3-methyl-4-piperidyl]-N-phenylpropanamides: synthesis, X-ray analysis, and biological activities.
    Brine GA, Stark PA, Liu Y, Carroll FI, Singh P, Xu H, Rothman RB.
    J Med Chem; 1995 Apr 28; 38(9):1547-57. PubMed ID: 7739013
    [Abstract] [Full Text] [Related]

  • 13. Assessment of stereoselectivity of trimethylphenylalanine analogues of delta-opioid [D-Pen(2),D-Pen(5)]-enkephalin.
    Witt KA, Slate CA, Egleton RD, Huber JD, Yamamura HI, Hruby VJ, Davis TP.
    J Neurochem; 2000 Jul 28; 75(1):424-35. PubMed ID: 10854288
    [Abstract] [Full Text] [Related]

  • 14. Synthesis of eupomatilone-6 and assignment of its absolute configuration.
    Gurjar MK, Karumudi B, Ramana CV.
    J Org Chem; 2005 Nov 11; 70(23):9658-61. PubMed ID: 16268656
    [Abstract] [Full Text] [Related]

  • 15. (2S,3R) beta-methyl-2',6'-dimethyltyrosine-L-tetrahydroisoquinoline-3-carboxylic acid [(2S,3R)TMT-L-Tic-OH] is a potent, selective delta-opioid receptor antagonist in mouse brain.
    Hosohata K, Varga EV, Alfaro-Lopez J, Tang X, Vanderah TW, Porreca F, Hruby VJ, Roeske WR, Yamamura HI.
    J Pharmacol Exp Ther; 2003 Feb 11; 304(2):683-8. PubMed ID: 12538822
    [Abstract] [Full Text] [Related]

  • 16. Synthesis and polymerization of benzyl (3R,4R)-3-methylmalolactonate via enzymatic preparation of the chiral precursor.
    Bear MM, Monne C, Robic D, Campion G, Langlois V, Rimbault A, Bourbouze R, Guerin P.
    Chirality; 1998 Feb 11; 10(8):727-33. PubMed ID: 9803528
    [Abstract] [Full Text] [Related]

  • 17. Absolute configuration of (+)-alpha-dihydrotetrabenazine, an active metabolite of tetrabenazine.
    Kilbourn MR, Lee LC, Heeg MJ, Jewett DM.
    Chirality; 1997 Feb 11; 9(1):59-62. PubMed ID: 9094204
    [Abstract] [Full Text] [Related]

  • 18. Stereospecific formation of dinuclear vanadium(V) tartrato complexes.
    Gáliková J, Schwendt P, Tatiersky J, Tracey AS, Zák Z.
    Inorg Chem; 2009 Sep 07; 48(17):8423-30. PubMed ID: 19673502
    [Abstract] [Full Text] [Related]

  • 19. [Stereochemistry of proton catalyzed dimerization of 3-alkyl-indoles].
    Lów M.
    Acta Pharm Hung; 1999 Jan 07; 69(1):20-3. PubMed ID: 10513408
    [Abstract] [Full Text] [Related]

  • 20. Stereoisomers of N-substituted soft anticholinergics and their zwitterionic metabolite based on glycopyrrolate--syntheses and pharmacological evaluations.
    Wu WM, Wu J, Mori N, Buchwald P, Bodor N.
    Pharmazie; 2008 Mar 07; 63(3):200-9. PubMed ID: 18444508
    [Abstract] [Full Text] [Related]


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