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Novel Bradykinin Analogues Modified in the N-Terminal Part of the Molecule with a Variety of Acyl Substituents.
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- International Journal of Peptide Research & Therapeutics, 2012, v. 18, n. 2, p. 117, doi. 10.1007/s10989-011-9285-5
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Design, Synthesis and Structure-Activity Relationship of New Arginine Vasopressin Analogues Containing Proline Derivatives in Position 2.
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- Chemical Biology & Drug Design, 2013, v. 81, n. 3, p. 420, doi. 10.1111/cbdd.12093
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Highly Potent Antidiuretic Antagonists: Conformational Studies of Vasopressin Analogues Modified with 1-Naphthylalanine Enantiomers at Position 2.
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- Chemical Biology & Drug Design, 2012, v. 79, n. 6, p. 1033, doi. 10.1111/j.1747-0285.2012.01358.x
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Understanding the Role of Self-Assembly and Interaction with Biological Membranes of Short Cationic Lipopeptides in the Effective Design of New Antibiotics.
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- Antibiotics (2079-6382), 2022, v. 11, n. 11, p. 1491, doi. 10.3390/antibiotics11111491
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Bradykinin and Neurotensin Analogues as Potential Compounds in Colon Cancer Therapy.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 11, p. 9644, doi. 10.3390/ijms24119644
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Lipidation of Naturally Occurring α-Helical Antimicrobial Peptides as a Promising Strategy for Drug Design.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3951, doi. 10.3390/ijms24043951
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Improving Fmoc Solid Phase Synthesis of Human Beta Defensin 3.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 20, p. 12562, doi. 10.3390/ijms232012562
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Lipidation of Temporin-1CEb Derivatives as a Tool for Activity Improvement, Pros and Cons of the Approach.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 6679, doi. 10.3390/ijms22136679
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Potent antidiuretic agonists, deamino-vasopressin and desmopressin, and their inverso analogs: NMR structure and interactions with micellar and liposomic models of cell membrane.
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- Biopolymers, 2016, v. 106, n. 3, p. 245, doi. 10.1002/bip.22825
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Improvement of derivatized amino acid detection sensitivity in micellar electrokinetic capillary chromatography by means of acid-induced pH-mediated stacking technique.
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- Analytical & Bioanalytical Chemistry, 2014, v. 406, n. 26, p. 6713, doi. 10.1007/s00216-014-8104-1
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- Article
Role of Phe-D<sub>5</sub> isotopically labeled analogues of bradykinin on elucidation of its adsorption mode on Ag, Au, and Cu electrodes. Surface-enhanced Raman spectroscopy studies.
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- Journal of Raman Spectroscopy, 2013, v. 44, n. 8, p. 1096, doi. 10.1002/jrs.4343
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Influence of applied potential on bradykinin adsorption onto Ag, Au, and Cu electrodes Influence of applied potential on bradykinin adsorption onto Ag, Au, and Cu electrodes.
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- Journal of Raman Spectroscopy, 2013, v. 44, n. 5, p. 655, doi. 10.1002/jrs.4246
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- Article
B<sub>2</sub> bradykinin receptor antagonists: adsorption mechanism on electrochemically roughened Ag substrate.
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- Journal of Raman Spectroscopy, 2013, v. 44, n. 2, p. 205, doi. 10.1002/jrs.4182
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Characterization of adsorption mode of new B<sub>2</sub> bradykinin receptor antagonists onto colloidal Ag substrate.
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- Journal of Raman Spectroscopy, 2013, v. 44, n. 2, p. 212, doi. 10.1002/jrs.4193
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Structure and conformation of Arg<sup>8</sup> vasopressin modified analogs.
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- Journal of Raman Spectroscopy, 2012, v. 43, n. 1, p. 51, doi. 10.1002/jrs.2986
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Charakterystyka peptydów przeciwdrobnoustrojowych oraz wpływ modyfikacji chemicznych na modulowanie ich aktywności biologicznej.
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- Advances in Biochemistry / Postepy Biochemii, 2019, v. 65, n. 4, p. 1, doi. 10.18388/pb.2019_280
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Simultaneous Separation of Eight Benzodiazepines in Human Urine Using Field-Amplified Sample Stacking Micellar Electrokinetic Chromatography.
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- Journal of Analytical Toxicology, 2015, v. 39, n. 6, p. 436, doi. 10.1093/jat/bkv042
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Label-Free Electrochemical Test of Protease Interaction with a Peptide Substrate Modified Gold Electrode.
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- Chemosensors, 2021, v. 9, n. 8, p. 199, doi. 10.3390/chemosensors9080199
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Spectroscopic characterization and in vitro studies of biological activity of bradykinin derivatives.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-23448-7
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- Article
Novel analogues of bradykinin conformationally restricted in the C-terminal part of the molecule.
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- Journal of Peptide Science, 2011, v. 17, n. 5, p. 366, doi. 10.1002/psc.1351
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- Article
Novel analogues of arginine vasopressin containing α-2-indanylglycine enantiomers in position 2.
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- Journal of Peptide Science, 2010, v. 16, n. 1, p. 15, doi. 10.1002/psc.1189
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Analogues of AVP modified in the N-terminal part of the molecule with Pip isomers: TFA-catalysed peptide bond hydrolysis.
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- Journal of Peptide Science, 2009, v. 15, n. 3, p. 161, doi. 10.1002/psc.1094
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Modifications in the bradykinin main chain are not necessary for antagonistic activity in rat blood pressure assay.
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- Journal of Peptide Science, 2007, v. 13, n. 3, p. 206, doi. 10.1002/psc.830
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Analogs of arginine vasopressin modified in the N-terminal part of the molecule with a conformationally constrained cis-peptide bond motif.
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- Journal of Peptide Science, 2007, v. 13, n. 2, p. 128, doi. 10.1002/psc.824
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New bradykinin analogues substituted in positions 7 and 8 with sterically restricted 1-aminocyclopentane-1-carboxylic acid.
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- Journal of Peptide Science, 2006, v. 12, n. 12, p. 775, doi. 10.1002/psc.812
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The influence of 1-aminocyclopentane-1-carboxylic acid at position 2 or 3 of AVP and its analogues on their pharmacological properties.
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- Journal of Peptide Science, 2005, v. 11, n. 9, p. 584, doi. 10.1002/psc.656
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New acylated bradykinin analogues: effect on rat blood pressure and rat uterus.
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- Journal of Peptide Science, 2005, v. 11, n. 7, p. 436, doi. 10.1002/psc.646
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Analogues of arginine vasopressin modified in position 2 and 3 with conformationally constrained dipeptide fragments.
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- Journal of Peptide Science, 2005, v. 11, n. 2, p. 91, doi. 10.1002/psc.600
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Evaluation of sample injection precision in respect to sensitivity in capillary electrophoresis using various injection modes.
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- Journal of Separation Science, 2017, v. 40, n. 5, p. 1167, doi. 10.1002/jssc.201601027
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Design, synthesis and biological activity of new neurohypophyseal hormones analogues conformationally restricted in the N-terminal part of the molecule. Highly potent OT receptor antagonists.
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- Amino Acids, 2012, v. 43, n. 2, p. 617, doi. 10.1007/s00726-011-1109-6
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Arginine-, d-arginine-vasopressin, and their inverso analogues in micellar and liposomic models of cell membrane: CD, NMR, and molecular dynamics studies.
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- European Biophysics Journal, 2015, v. 44, n. 8, p. 727, doi. 10.1007/s00249-015-1071-4
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