Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laura R. Osborn"'
Autor:
Samantha V. Crosby, Izzeldin Y. Ahmed, Laura R. Osborn, Zeyuan Wang, Mary A. Schleiff, William E. Fantegrossi, Swati Nagar, Paul L. Prather, Gunnar Boysen, Grover P. Miller
Publikováno v:
Metabolites, Vol 12, Iss 8, p 773 (2022)
In 2019, synthetic cannabinoids accounted for more than one-third of new drugs of abuse worldwide; however, assessment of associated health risks is not ethical for controlled and often illegal substances, making CD-1 mouse exposure studies the gold
Externí odkaz:
https://doaj.org/article/f7f0a85e7d8646fe8b2ebee2d64b2e53
Autor:
Joseph E. Muller II, Laura R. Osborn, Joseph R. Traver, Patrick C. Hillesheim, Matthias Zeller, Arsalan Mirjafari
Publikováno v:
IUCrData, Vol 5, Iss 2, p x200170 (2020)
The title compound, C21H39NS2, crystallizes with two molecules in the asymmetric unit, both having a linear 18-carbon alkyl chain bound through a thioether group. No π–π stacking or hydrogen bonding is observed. The orientation of the alkyl chain
Externí odkaz:
https://doaj.org/article/553a4eaf561442b796f792edee2f9d88
Autor:
Arsalan Mirjafari, Joseph E. Muller, Laura R. Osborn, Matthias Zeller, Joseph R. Traver, Patrick C. Hillesheim
Publikováno v:
IUCrData, Vol 5, Iss 2, p x200170 (2020)
The title compound, C21H39NS2, crystallizes with two molecules in the asymmetric unit, both having a linear 18-carbon alkyl chain bound through a thioether group. No π–π stacking or hydrogen bonding is observed. The orientation of the alkyl chain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e24cc5c1575e2f59bbf09f2d989fafe
https://doi.org/10.1107/s2414314620001704
https://doi.org/10.1107/s2414314620001704
Autor:
Joseph E, Muller Ii, Laura R, Osborn, Joseph R, Traver, Patrick C, Hillesheim, Matthias, Zeller, Arsalan, Mirjafari
Publikováno v:
IUCrData. 5(Pt 2)
The title compound, C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::463f28369c23f1cb6b0bb06548fc6418
https://pubmed.ncbi.nlm.nih.gov/36340840
https://pubmed.ncbi.nlm.nih.gov/36340840
Autor:
Noah R. Flynn, Grover P. Miller, Laura R. Osborn, Mary A. Schleiff, Dustyn A. Barnette, Matthew K. Matlock, S. Joshua Swamidass
Publikováno v:
Toxicology
Thiazoles are biologically active aromatic heterocyclic rings occurring frequently in natural products and drugs. These molecules undergo typically harmless elimination; however, a hepatotoxic response can occur due to multistep bioactivation of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb5cec6ca84b83b79911e323700a0027
https://doi.org/10.1016/j.tox.2020.152478
https://doi.org/10.1016/j.tox.2020.152478