William D. Lubell
Lubell, William D.
VIAF ID: 86279868 (Personal)
Permalink: http://viaf.org/viaf/86279868
Preferred Forms
-
-
- 100 1 _ ‡a Lubell, William D.
- 100 1 _ ‡a Lubell, William D.
- 100 1 _ ‡a Lubell, William D.
- 100 0 _ ‡a William D. Lubell
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
---|---|
Examination of the potential for adaptive chirality of the nitrogen chiral center in aza-aspartame. | |
Fluorometric assay for tissue transglutaminase-mediated transamidation activity. | |
Functional Selectivity Revealed by N-Methylation Scanning of Human Urotensin II and Related Peptides | |
Heumann Indole Flow Chemistry Process | |
Immunometabolic modulation of retinal inflammation by CD36 ligand | |
Insertion of multiple alpha-amino gamma-lactam (Agl) residues into a peptide sequence by solid-phase synthesis on synphase lanterns. | |
Insight into Transannular Cyclization Reactions To Synthesize Azabicyclo[X.Y.Z]alkanone Amino Acid Derivatives from 8-, 9-, and 10-Membered Macrocyclic Dipeptide Lactams | |
Interleukin-1 and ischemic brain injury in the newborn: development of a small molecule inhibitor of IL-1 receptor. | |
Interleukin-1 Receptor Modulation Using β-Substituted α-Amino-γ-Lactam Peptides From Solid-Phase Synthesis and Diversification | |
Isolated α-turn and incipient γ-helix | |
Large structural modification with conserved conformation: analysis of delta(3)-fused aryl prolines in model beta-turns. | |
Microglia and interleukin-1β in ischemic retinopathy elicit microvascular degeneration through neuronal semaphorin-3A. | |
Microwave-assisted synthesis of rhodamine fluorescent tags | |
Mimics of peptide turn backbone and side-chain geometry by a general approach for modifying azabicyclo[5.3.0]alkanone amino acids | |
Modified peptide monolayer binding His-tagged biomolecules for small ligand screening with SPR biosensors. | |
Multicomponent diversity-oriented synthesis of aza-lysine-peptide mimics. | |
N-(9-(9-phenylfluorenyl))homoserine-derived cyclic sulfamidates: novel chiral educts for the synthesis of enantiopure gamma-substituted alpha-amino acids | |
Novel Noncompetitive IL-1 Receptor-Biased Ligand Prevents Infection- and Inflammation-Induced Preterm Birth | |
De Novo Conception of Small Molecule Modulators Based on Endogenous Peptide Ligands: Pyrrolodiazepin-2-one γ-Turn Mimics That Differentially Modulate Urotensin II Receptor-Mediated Vasoconstriction ex Vivo | |
Paired Utility of Aza-Amino Acyl Proline and Indolizidinone Amino Acid Residues for Peptide Mimicry: Conception of Prostaglandin F2α Receptor Allosteric Modulators That Delay Preterm Birth | |
Peptide scanning for studying structure-activity relationships in drug discovery | |
Peptides for youth, 2009: | |
Peptides in Paris | |
Peptides of life teaching peptide science and art in elementary school. | |
Peptidomimetics | |
Photoacoustic FTIR Spectroscopy, a Nondestructive Method for Sensitive Analysis of Solid-Phase Organic Chemistry | |
Poly-(Prophi[Ch(OAc)CH2]Aib)3 a protected trimer of Pro-Aib hydroxyethylene isosteres. | |
Portraits of the pioneers of the American Peptide Society | |
Positional scanning for peptide secondary structure by systematic solid-phase synthesis of amino lactam peptides. | |
Preface | |
Preparation, characterization, and application of poly(vinyl alcohol)-graft-poly(ethylene glycol) resins: novel polymer matrices for solid-phase synthesis. | |
Probing Anti-inflammatory Properties Independent of NF-κB Through Conformational Constraint of Peptide-Based Interleukin-1 Receptor Biased Ligands | |
Probing opioid receptor interactions with azacycloalkane amino acids. Synthesis of a potent and selective ORL1 antagonist | |
Proceedings of the 20th American Peptide Symposium | |
Pyrrole protection | |
Pyrrolo[3,2-e][1,4]diazepin-2-one synthesis: a head-to-head comparison of soluble versus insoluble supports | |
Restoration of renal function by a novel prostaglandin EP4 receptor-derived peptide in models of acute renal failure. | |
Reversible and competitive cinnamoyl triazole inhibitors of tissue transglutaminase. | |
Rho signaling pathway targeted to promote spinal cord repair. | |
Rigid Dipeptide Mimics: Synthesis of Enantiopure 5- and 7-Benzyl and 5,7-Dibenzyl Indolizidinone Amino Acids via Enolization and Alkylation of delta-Oxo alpha,omega-Di-[N-(9-(9-phenylfluorenyl))amino]azelate Esters | |
Selective tert-butyl ester deprotection in the presence of acid labile protecting groups with use of ZnBr2. | |
Serine as chiral educt for the practical synthesis of enantiopure N-protected beta-hydroxyvaline | |
Site-specific protein propargylation using tissue transglutaminase. | |
Small-molecule ligands of GD2 ganglioside, designed from NMR studies, exhibit induced-fit binding and bioactivity | |
Solid-Phase Azopeptide Diels-Alder Chemistry for Aza-pipecolyl Residue Synthesis To Study Peptide Conformation | |
Solid-phase synthesis of 1,3,5-trisubstituted 1,4-diazepin-2-one peptide mimic. | |
Solid-phase synthesis of 3-aminopyrrole-2,5-dicarboxylate analogues | |
SPOCC-194, a new high functional group density PEG-based resin for solid-phase organic synthesis | |
Stereo- and Regiochemical Transannular Cyclization of a Common Hexahydro-1H-azonine to Afford Three Different Indolizidinone Dipeptide Mimetics | |
Structure-activity analysis of the growth hormone secretagogue GHRP-6 by alpha- and beta-amino gamma-lactam positional scanning | |
Structure-activity relationships of GHRP-6 azapeptide ligands of the CD36 scavenger receptor by solid-phase submonomer azapeptide synthesis | |
Structure-activity study of the ORL1 antagonist Ac-Arg-D-Cha-Qaa-D-Arg-D-p-ClPhe-NH2. | |
Surfactant Mediated Cationic and Anionic Suspension Polymerization of PEG-Based Resins in Silicon Oil: Beaded SPOCC 1500 and POEPOP 1500. | |
Synthesis and alkylation of aza-glycinyl dipeptide building blocks. | |
Synthesis and Biomedical Potential of Azapeptide Modulators of the Cluster of Differentiation 36 Receptor (CD36) | |
Synthesis and evaluation of 4-(1-aminoalkyl)-N-(4-pyridyl)cyclohexanecarboxamides as Rho kinase inhibitors and neurite outgrowth promoters. | |
Synthesis and pharmacology of new enantiopure delta(3)-4-arylkainoids. | |
Synthesis of a new pi-deficient phenylalanine derivative from a common 1,4-diketone intermediate and study of the influence of aromatic density on prolyl amide isomer population. | |
Synthesis of enantiopure 7-[3-azidopyl]indolizidin-2-one amino acid. A constrained mimic of the peptide backbone geometry and heteroatomic side-chain functionality of the ala-lys dipeptide. | |
Synthesis of fused heteroarylprolines and pyrrolopyrroles | |
Synthesis of protected 2-pyrrolylalanine for peptide chemistry and examination of its influence on prolyl amide isomer equilibrium | |
Synthesis of pyrrolo[3,2-e] [1,4]diazepin-2-ones as potential gamma-turn mimetics | |
Systematic study of the synthesis of macrocyclic dipeptide beta-turn mimics possessing 8-, 9-, and 10- membered rings by ring-closing metathesis | |
Targeting the prostaglandin F2α receptor for preventing preterm labor with azapeptide tocolytics. | |
THG113: a novel selective FP antagonist that delays preterm labor | |
Thoughts on Meldal and Hirschmann. | |
Unsymmetric electronic push-pull bipyrroles - synthesis, spectroelectrochemical, and photophysical investigation | |
Urotensin core mimics that modulate the biological activity of urotensin-II related peptide but not urotensin-II. | |
Use of Steric Interactions To Control Peptide Turn Geometry. Synthesis of Type VI beta-Turn Mimics with 5-tert-Butylproline. | |
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate | |
মুখবন্ধ |