Zobrazeno 1 - 3
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pro vyhledávání: '"Rainer Martin Lüönd"'
Autor:
Rainer Martin Lüönd, Peter Schürmann, Caroline Jarret, Maurus Marty, Janette Bobalova, Reinhard Neier, Matthias E. Henz, Frédéric Stauffer
Publikováno v:
Chemistry & Biology. 7:185-196
Background: Porphobilinogen synthase is the second enzyme involved in the biosynthesis of natural tetrapyrrolic compounds, and condenses two molecules of 5-aminolevulinic acid (ALA) through a nonsymmetrical pathway to form porphobilinogen. Each subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7669cb24fab328bed33601ed38a80c3
https://doi.org/10.1016/s1074-5521(00)00089-2
https://doi.org/10.1016/s1074-5521(00)00089-2
Autor:
Reinhard Neier, Rainer Martin Lüönd
Publikováno v:
Helvetica Chimica Acta. 74:91-102
To obtain stable derivatives of α-unsubstituted pyrroles, the reaction of the test pyrrole 9 with a series of chalcones 14a–h were studied. Michael adducts 16b–h could be isolated. In order to synthesize coloured derivatives, the reaction of dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe4a6e86833e182f5bed407624ef0ae7
https://doi.org/10.1002/hlca.19910740111
https://doi.org/10.1002/hlca.19910740111
Autor:
Rainer Martin Lüönd, Reinhard Neier
Publikováno v:
Biochimica et biophysica acta. 1289(1)
The enzyme porphobilinogen synthase (PBGS) catalyses the formation of porphobilinogen (PBG) from two molecules of 5-aminolevulinic acid (ALA). It has been claimed that the PBGS from Rhodobacter spheroides is able to form a mixed pyrrole, from one mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b05d63b935df8bf1315d05a4a89f5cfd
https://pubmed.ncbi.nlm.nih.gov/8605237
https://pubmed.ncbi.nlm.nih.gov/8605237