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pro vyhledávání: '"Suć, Josipa"'
Autor:
Suć, Josipa, Jerić, Ivanka
Multicomponent reactions (MCRs) have attracted significant attention in organic chemistry because of their exceptional ability to implement a wide range of components in one-pot reactions, affording numerous, very diverse products. MCRs are usually v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::d9e96e6c73e13bfa0be33472a8ae4cdf
https://www.bib.irb.hr/871953
https://www.bib.irb.hr/871953
Dipeptidyl peptidase III (DPP III) is zinc dependent peptidase which catalyses hydrolysis of the 2nd peptide bond from the N-termini of its substrates. DPP III is characterized by poor substrate specificity. Its fundamental physiological role is yet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::1cf8787ee90fec3088bdc824687175f1
https://www.bib.irb.hr/1093852
https://www.bib.irb.hr/1093852
Autor:
Suć, Josipa
Peptidi i proteini imaju ključnu ulogu u nizu bioloških i fizioloških procesa; međutim, njihova primjena kao terapeutika je ograničena slabom stabilnošću i biodostupnošću. Stoga je razvoj peptidomimetika, spojeva koji oponašaju strukturu i/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3908::1f86d5b4d29d3c2bc7167c63a4aac780
https://repozitorij.pmf.unizg.hr/islandora/object/pmf:160
https://repozitorij.pmf.unizg.hr/islandora/object/pmf:160
N(acyl), S¬-acetals are important structural motifs in many natural products investigated for their sedative, and cell growth and HIV-1 inhibitory properties. They are also present as a key functional group in pharmacologically active compounds, suc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e2697520a40e4f64e250d6b0db4455d8
https://www.bib.irb.hr/870674
https://www.bib.irb.hr/870674
Autor:
Suć, Josipa
Peptidi i proteini imaju ključnu ulogu u nizu bioloških i fizioloških procesa ; međutim, njihova primjena kao terapeutika je ograničena slabom stabilnošću i biodostupnošću. Stoga je razvoj peptidomimetika, spojeva koji oponašaju strukturu i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::c3fcc087fb554ed9f7ab23b1ace4e3dc
https://www.bib.irb.hr/827772
https://www.bib.irb.hr/827772
Organocatalytic asymmetric addition of thiols to N-acyl ketimines, which are generated in situ from 3-hydroxy isoindolinones, is described. The reaction proceeds smoothly with a broad range of ketimines and thiols using a chiral Brønsted acid cataly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::4f4350403289d944cf08dc35cd8af11c
https://www.bib.irb.hr/870670
https://www.bib.irb.hr/870670
Peptidomimetics are compounds able to mimic structure and function of natural peptides or proteins, and also circumvent some of the problems associated with their natural counterparts, like poor stability and bioavailability. By mimicking protein sec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::3f38cf2d1ff3316de45ebca9cb39da95
https://www.bib.irb.hr/775737
https://www.bib.irb.hr/775737
Peptide-inspired drug scaffolds having designable molecular shape and surface chemistry pattern are of particular interest. Biological function of biomolecules ; enzyme- substrate specificity, binding to receptors, protein-protein or protein-nucleic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::5e17a9a948b254a52d8735ca260812f0
https://www.bib.irb.hr/776000
https://www.bib.irb.hr/776000
Autor:
Suć, Josipa, Jerić, Ivanka
Peptidomimetici su spojevi koji imaju sve prednosti kao i prirodni peptidi, ali ne i njihove nedostatke (veća stabilnost, bolja selektivnost). Kao važno svojstvo ističe se oponašanje sekundarne strukture biomolekula te stupanje u interakciju s en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::b2358b800abeab86ffd0c673f82e63c2
https://www.bib.irb.hr/783060
https://www.bib.irb.hr/783060
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