Zobrazeno 1 - 10
of 97
pro vyhledávání: '"D, Vander Velde"'
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 79:503-512
The thermodynamics of binding of various neutral, cationic and anionic substrates to β-cyclodextrin, a hydroxylpropyl-β-cyclodextrin (HP4M-β-CD) and three sulfobutyl-β-cyclodextrins with varying degrees of total substitution (SBE1M-β-CD, SBE7M-
Autor:
C.R. Middaugh, Elizabeth M. Topp, Teruna J. Siahaan, C.E. Stotz, Ronald T. Borchardt, D. Vander Velde
Publikováno v:
Journal of Peptide Research. 63:371-382
A spontaneously folding beta-hairpin peptide (Lys-Lys-Tyr-Thr-Val-Ser-Ile-Asn-Gly-Lys-Lys-Ile-Thr-Val-Ser-Ile) and related cyclic (cyclo-Gly-Lys-Tyr-Ile-Asn-Gly-Lys-Ile-Ile-Asn) and linear (Ser-Ile-Asn-Gly-Lys) controls were studied to determine the
Publikováno v:
The Journal of Peptide Research. 60:159-168
Leuprolide acetate (pGlu-His-Trp-Ser-Tyr-d-Leu-Leu-Arg-Pro-NHEt), a potent LHRH agonist in wide clinical use, was characterized conformationally by NMR and circular dichroism. It displayed quite different preferred conformations under different solut
Publikováno v:
The Journal of Peptide Research. 59:183-195
The coumarinic acid-based cyclic DADLE (H-Tyr-D-Ala-Gly-Phe-D-Leu-OH) prodrug 1a exhibited more favorable physicochemical properties than did DADLE for permeation across the intestinal mucosa. However, prodrug 1a, whose bioconversion to DADLE was slo
Publikováno v:
The Journal of Peptide Research. 57:361-373
Peptide bond bioisosteres, such as hydroxyethylamine (Hea), have frequently been used to stabilize metabolically labile peptide bonds in peptidomimetic drug design in an effort to increase the oral bioavailability of drug candidates. However, the imp
Autor:
Ronald T. Borchardt, D. Vander Velde, Minli Xie, Elizabeth M. Topp, Richard L. Schowen, Martha D. Morton, Jeffrey Aubé
Publikováno v:
The Journal of Peptide Research. 56:165-171
Mimetics of beta-turn structures in proteins have been used to calibrate the relative reactivities toward deamidation of asparagine residues in the two central positions of a beta-turn and in a random coil. N-Acetyl-Asn-Gly-6-aminocaproic acid, an ac
Autor:
Seetharama D. Jois, Teruna J. Siahaan, O.S. Gudmundsson, Ronald T. Borchardt, A. Bak, D. Vander Velde
Publikováno v:
The Journal of Peptide Research. 53:403-413
In an earlier study using Caco-2 cells, an in vitro cell culture model of the intestinal mucosa, we have shown that the acyloxyalkoxy-based cyclic prodrugs 3 and 4 of the opioid peptides [Leu5]-enkephalin(1, H-Tyr-GLY-Gly-Phe-Leu-OH) and DADLE(2, H-T
Autor:
Seetharama D. Jois, Valentine J. Stella, Teruna J. Siahaan, Ronald T. Borchardt, D. Vander Velde, Sanjeev Gangwar
Publikováno v:
Pharmaceutical Research. 13:1657-1662
Purpose. To determine the different conformations of the acyloxyalkoxy-linked cyclic prodrug 1 of the model hexapeptide 2 in solution and to investigate the relationship between these solution conformations and the cellular permeability characteristi
Autor:
Richard L. Schowen, C. M. Riley, J. Zhou, M. A. Mummert, D. Vander Velde, Milan Slavik, Martha D. Morton
Publikováno v:
Pharmaceutical Research. 12:1361-1370
Purpose. The purposes were to study the kinetics of hydrolysis of 2′,3′,5′-triacetyl-6-azauridine ( 1 ) in aqueous solution (µ = 0.5) and to identify the main intermediates and products of the reaction. Methods. A stability indicating isocrati
Publikováno v:
Inorganic Chemistry. 32:1689-1697
W[sub 2](O-t-Bu)[sub 6] reacts with binaphthol derivatives (H[sub 2]BINO, R = H (1); H[sub 2]Me[sub 2]BINO, R = CH[sub 3] (2)) to produce monosubstituted products of the formula (R[sub 2]BINO)W[sub 2](O-t-Bu)[sub 4]. The presence of a single product