Year |
Citation |
Score |
2020 |
Massarano T, Mazir A, Lavi R, Byk G. Solid-Phase Multicomponent Synthesis of 3-Substituted Isoindolinones Generates New Cell-Penetrating Probes as Drug Carriers. Chemmedchem. 15: 833-838. PMID 32147941 DOI: 10.1002/cmdc.201900656 |
0.647 |
|
2019 |
Turdiev A, Filiutovich O, Mirkin F, Byk G. A peptide from Testudo horsfieldii tortoise spleen as a potential helper for reducing acute radiation syndrome. Journal of Peptide Science : An Official Publication of the European Peptide Society. 25: e3202. PMID 31313444 DOI: 10.1002/psc.3202 |
0.684 |
|
2012 |
Elhawi H, Eini H, Douvdevani A, Byk G. Improved methods for thermal rearrangement of alicyclic α-hydroxyimines to α-aminoketones: synthesis of ketamine analogues as antisepsis candidates. Molecules (Basel, Switzerland). 17: 6784-807. PMID 22664467 DOI: 10.3390/molecules17066784 |
0.616 |
|
2011 |
Khandadash R, Partouche S, Weiss A, Margel S, Byk G. A Fully Synthetic “Phage-Like” System II: Synthesis and Live Cell Screening of Combinatorial Libraries of Peptides on Sub-Cellular Sized Microspheres The Open Optics Journal. 5: 17-27. DOI: 10.2174/1874328501105010017 |
0.307 |
|
2010 |
Byk G, Partouche S, Weiss A, Margel S, Khandadash R. Fully synthetic phage-like system for screening mixtures of small molecules in live cells. Journal of Combinatorial Chemistry. 12: 332-45. PMID 20345088 DOI: 10.1021/cc900156z |
0.715 |
|
2009 |
Mirkin F, Eini H, Douvdevani A, Byk G. New degradable cationic peptides for modulated gene delivery. Advances in Experimental Medicine and Biology. 611: 245-6. PMID 19400179 DOI: 10.1007/978-0-387-73657-0_112 |
0.683 |
|
2006 |
Byk G, Cohen-Ohana M, Raichman D. Fast and versatile microwave-assisted intramolecular Heck reaction in peptide macrocyclization using microwave energy. Biopolymers. 84: 274-82. PMID 16283655 DOI: 10.1002/bip.20411 |
0.337 |
|
2004 |
Byk G, Kabha E. Anomalous regioselective four-member multicomponent Biginelli reaction II: one-pot parallel synthesis of spiro heterobicyclic aliphatic rings. Journal of Combinatorial Chemistry. 6: 596-603. PMID 15244421 DOI: 10.1021/cc049962i |
0.719 |
|
1996 |
Bitan G, Zeltser I, Byk G, Halle D, Mashriki Y, Gluhov EV, Sukhotinsky I, Hanani M, Selinger Z, Gilon C. Backbone cyclization of the C-terminal part of substance P. Part 1: The important role of the sulphur in position 11. Journal of Peptide Science : An Official Publication of the European Peptide Society. 2: 261-9. PMID 9231334 DOI: 10.1002/Psc.76 |
0.66 |
|
1996 |
Byk G, Halle D, Zeltser I, Bitan G, Selinger Z, Gilon C. Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P. Journal of Medicinal Chemistry. 39: 3174-8. PMID 8759639 DOI: 10.1021/Jm960154I |
0.661 |
|
1994 |
Grdadolnik SG, Mierke DF, Byk G, Zeltser I, Gilon C, Kessler H. Comparison of the conformation of active and nonactive backbone cyclic analogs of substance P as a tool to elucidate features of the bioactive conformation: NMR and molecular dynamics in DMSO and water. Journal of Medicinal Chemistry. 37: 2145-52. PMID 7518522 DOI: 10.1021/Jm00040A005 |
0.477 |
|
1992 |
Saulitis J, Mierke DF, Byk G, Gilon C, Kessler H. Conformation of cyclic analogues of substance P: NMR and molecular dynamics in dimethyl sulfoxide Journal of the American Chemical Society. 114: 4818-4827. DOI: 10.1021/Ja00038A054 |
0.45 |
|
1992 |
Byk G, Gilon C. Building units for N-backbone cyclic peptides. 1. Synthesis of protected N-(ω-aminoalkylene)amino acids and their incorporation into dipeptide units Journal of Organic Chemistry. 57: 5687-5692. |
0.529 |
|
1991 |
Gilon C, Halle D, Chorev M, Selinger Z, Byk G. Backbone cyclization: A new method for conferring conformational constraint on peptides. Biopolymers. 31: 745-50. PMID 1718473 DOI: 10.1002/Bip.360310619 |
0.578 |
|
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