Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Brian M. Gulledge"'
Autor:
Bo Liang, Adam D. Richardson, James J. La Clair, Thomas P. Brady, Matthew D Alexander, Joel S. Sandler, Santosh J. Gharpure, Alexei Polosukhin, Hai Ren Zhang, Xiaobin Ding, Madeleine M. Joullié, A. Richard Chamberlin, Chris M. Ireland, James B. Aggen, Brian M. Gulledge, Mary Kay Harper, Michael D. Burkart, P. Andrew Evans, Binh G. Vong, William Fenical, Padma Portonovo, Emmanuel A. Theodorakis, Michael S. Leonard, Jian Cui
Publikováno v:
Chembiochem : a European journal of chemical biology. 7(3)
A Central Strategy for Converting Natural Products into Fluorescent Probes Matthew D. Alexander, Michael D. Burkart, Michael S. Leonard, Padma Portonovo, Bo Liang, Xiaobin Ding, Madeleine M. Joulli!, Brian M. Gulledge, James B. Aggen, A. Richard Cham
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::049bc9f76b514a0c5296477d75bac41e
https://pubmed.ncbi.nlm.nih.gov/16432909
https://pubmed.ncbi.nlm.nih.gov/16432909
Publikováno v:
Bioorganicmedicinal chemistry letters. 13(17)
A series of greatly simplified microcystin analogues comprised only of Adda (the beta-amino acid common to the microcystins, nodularins, and motuporin,) and a single additional amino acid residue was synthesized and screened for inhibition of the pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e036485a6e846c9bdbf4687eee48680
https://pubmed.ncbi.nlm.nih.gov/14611855
https://pubmed.ncbi.nlm.nih.gov/14611855
Publikováno v:
Bioorganicmedicinal chemistry letters. 13(17)
A series of acyclic, truncated microcystin analogues, comprised of the dienic beta-amino acid (Adda) and up to four additional amino acids characteristic of the parent toxin, was synthesized and screened for activity as inhibitors of PP1 and PP2A. De
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49e826ba8122ef6047baeaccc2d85da6
https://pubmed.ncbi.nlm.nih.gov/14611854
https://pubmed.ncbi.nlm.nih.gov/14611854
Publikováno v:
Current medicinal chemistry. 9(22)
The serine/threonine phosphatases are inhibited by a variety of natural toxins, including the microcystins and nodularins. Progress in understanding the details of the biosynthetic origin and the binding of these compounds is discussed, as is the pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062e3c0b18f675f103c8695a15f09750
https://pubmed.ncbi.nlm.nih.gov/12369867
https://pubmed.ncbi.nlm.nih.gov/12369867
Autor:
A. Richard Chamberlin, James J. La Clair, Brian M. Gulledge, Joel S. Sandler, William Fenical
Publikováno v:
Journal of the American Chemical Society. 127:9320-9321
The identification of natural product producer organisms remains a problem for both isolation and natural product classification. A concise screen is developed through fluorescent modification of a set of natural products that offer a common activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e1c2a0c3a3789bebf937b1b3676d79
https://doi.org/10.1021/ja042756u
https://doi.org/10.1021/ja042756u