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Design, synthesis, and conformational analysis of azacycloalkane amino acids as conformationally constrained probes for mimicry of peptide secondary structures.
Biopolymers. 2000;55(2):101-22. doi: 10.1002/1097-0282(2000)55:2<101::AID-BIP20>3.0.CO;2-O.
Biopolymers. 2000.
PMID: 11074409
Review.
Effect of sequence on peptide geometry in 5-tert-butylprolyl type VI beta-turn mimics.
Halab L, Lubell WD.
Halab L, et al.
J Am Chem Soc. 2002 Mar 20;124(11):2474-84. doi: 10.1021/ja012442w.
J Am Chem Soc. 2002.
PMID: 11890796
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Probing opioid receptor interactions with azacycloalkane amino acids. Synthesis of a potent and selective ORL1 antagonist.
Halab L, Becker JA, Darula Z, Tourwé D, Kieffer BL, Simonin F, Lubell WD.
Halab L, et al.
J Med Chem. 2002 Nov 21;45(24):5353-7. doi: 10.1021/jm020078l.
J Med Chem. 2002.
PMID: 12431062
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Use of Steric Interactions To Control Peptide Turn Geometry. Synthesis of Type VI beta-Turn Mimics with 5-tert-Butylproline.
Halab L, Lubell WD.
Halab L, et al.
J Org Chem. 1999 Apr 30;64(9):3312-3321. doi: 10.1021/jo990294a.
J Org Chem. 1999.
PMID: 11674436
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Influence of N-terminal residue stereochemistry on the prolyl amide geometry and the conformation of 5-tert-butylproline type VI beta-turn mimics.
Halab L, Lubell WD.
Halab L, et al.
J Pept Sci. 2001 Feb;7(2):92-104. doi: 10.1002/psc.297.
J Pept Sci. 2001.
PMID: 11277501
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HCV NS5B polymerase-bound conformation of a soluble sulfonamide inhibitor by 2D transferred NOESY.
Yannopoulos CG, Xu P, Ni F, Chan L, Pereira OZ, Reddy TJ, Das SK, Poisson C, Nguyen-Ba N, Turcotte N, Proulx M, Halab L, Wang W, Bédard J, Morin N, Hamel M, Nicolas O, Bilimoria D, L'Heureux L, Bethell R, Dionne G.
Yannopoulos CG, et al. Among authors: halab l.
Bioorg Med Chem Lett. 2004 Nov 1;14(21):5333-7. doi: 10.1016/j.bmcl.2004.08.018.
Bioorg Med Chem Lett. 2004.
PMID: 15454222
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