Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Justin C. Hammons"'
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 10, Pp m1223-m1223 (2008)
The title compound, [Co(C21H22NO)2], crystallizes with two molecules in the asymmetric unit. The coordination environments of the two CoII ions are distorted tetrahedral. The primary structural difference between the two independent complex molecules
Externí odkaz:
https://doaj.org/article/c459bcf0954f4ce7afd3e8c7e48d369d
Autor:
Justin C. Hammons, Amanda Soares Hirata, Letícia V. Costa-Lotufo, Paula C. Jimenez, William Fenical, Lynnie Trzoss, James J. La Clair
Publikováno v:
ACS medicinal chemistry letters, vol 10, iss 2
[Image: see text] Seriniquinone, a marine natural product, displayed potent cytotoxicity and selectivity against melanoma cancer cells. This selectivity, combined with a novel mode of action (MOA), prompted studies to translate a pharmacologically re
Autor:
Zhe Yu, Brian León, Michael D. Burkart, Justin C. Hammons, Manoj Kumar Kashyap, James J. La Clair, Sachin Dhar, Januario E. Castro
Publikováno v:
Journal of the American Chemical Society. 138:5063-5068
Small-molecule splice modulators have recently been recognized for their clinical potential for diverse cancers. This, combined with their use as tools to study the importance of splice-regulated events and their association with disease, continues t
Autor:
Xiaoyun Xia, Zhi Liu, Menghua Yang, Jun Zhu, Justin C. Hammons, William Fenical, Amanda J. Hay
Vibrio cholerae is the causative bacteria of the diarrheal disease cholera, but it also persists in aquatic environments, where it displays an expression profile that is distinct from that during infection. Upon entry into the host, a tightly regulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e5e9be714abe99d18948c76a02911d2
https://europepmc.org/articles/PMC5203667/
https://europepmc.org/articles/PMC5203667/
Autor:
Stephen C. Pelly, Erick Strauss, Wessel J.A. Moolman, Renier van der Westhuyzen, Victor Nizet, Samira Dahesh, Jordan L. Meier, Justin C. Hammons, Michael D. Burkart
Publikováno v:
Chemistry & Biology. 19(5):559-571
Summary The natural product CJ-15,801 is an inhibitor of Staphylococcus aureus , but not other bacteria. Its close structural resemblance to pantothenic acid, the vitamin precursor of coenzyme A (CoA), and its Michael acceptor moiety suggest that it
Publikováno v:
Fullerenes, Nanotubes and Carbon Nanostructures. 17:349-360
Reactions of C60Cl6, C60Br8 and C60(NO2)6 with arene substrates under mild conditions afford primarily monochlorinated, monobrominated or mononitrated organic products in high yield, often with gre...
Autor:
Michael D. Burkart, MinJin Kang, Wei–Lun Yu, Brian D. Jones, James J. La Clair, Justin C. Hammons
Publikováno v:
Journal of natural products. 76(5)
Spirohexenolides A and B comprise a unique family of spirotetronate natural products. We report on the identification of their binding to and modulation of human macrophage migration inhibitor factor (hMIF). Using an immunoaffinity–fluorescent labe
Publikováno v:
Inorganic chemistry. 49(11)
Two modifications to the doubly concaved host molecules based on well-known nickel tetraazaannulene complexes have resulted in the preparation of the compounds Ni(NapTMTAA).2benzene, 1,6,8,15,17-tetramethyldinapthalene-5,9,14,18-tetraazacyclotetradec
Autor:
Michael D. Burkart, Brian D. Jones, Justin C. Hammons, Antonio G. DiPasquale, Alexander Laurence Mandel, James J. La Clair, Arnold L. Rheingold, MinJin Kang
Publikováno v:
ChemInform. 41
In this report, we describe the discovery of a pair of bioactive spirotetronates, spirohexenolides A (1) and B (2), that arose from the application of mutagenesis, clonal selection techniques, and media optimization to strains of Streptomyces platens
Autor:
Arnold L. Rheingold, MinJin Kang, Brian D. Jones, James J. La Clair, Justin C. Hammons, Antonio G. DiPasquale, Michael D. Burkart, Alexander Laurence Mandel
Publikováno v:
The Journal of organic chemistry. 74(23)
In this report, we describe the discovery of a pair of bioactive spirotetronates, spirohexenolides A (1) and B (2), that arose from the application of mutagenesis, clonal selection techniques, and media optimization to strains of Streptomyces platens