Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jeanna M. MacLeod"'
Autor:
Brendan T. McKeown, Nicholas J. Relja, Steven R. Hall, Simon Gebremeskel, Jeanna M. MacLeod, Chansey J. Veinotte, Leah G. Bennett, Leanne B. Ohlund, Lekha Sleno, David L. Jakeman, Jason N. Berman, Brent Johnston, Kerry B. Goralski
Publikováno v:
Canadian journal of physiology and pharmacology.
Despite numerous therapeutic options, multidrug resistance (MDR) remains an obstacle to successful breast cancer therapy. Jadomycin B, a natural product derived from Streptomyces venezuelae ISP5230, maintains cytotoxicity in MDR human breast cancer c
Autor:
Brendan T. McKeown, Nicholas J. Relja, Steven R. Hall, Simon Gebremeskel, Jeanna M. MacLeod, Chansey J. Veinotte, Leah G. Bennett, Leanne B. Ohlund, Lekha Sleno, David L. Jakeman, Jason N. Berman, Brent Johnston, Kerry B. Goralski
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 101:214-214
Publikováno v:
Canadian Journal of Chemistry. 96:760-764
The jadomycin family of natural products was first identified and characterized by Vining and co-workers at Dalhousie University in the 1990s. Herein, we report findings from a recently developed co-amino acid supplementation culture method with S. v
Publikováno v:
Canadian Journal of Chemistry. 96:495-501
The jadomycin family of natural products was discovered from Streptomyces venezuelae ISP5230 in the 1990s. Subsequent identification of the biosynthetic gene cluster along with synthetic efforts established that incorporation of an amino acid into th
Autor:
Steven R. Hall, Stephanie M. Forget, Jeanna M. MacLeod, Russell G. Kerr, Andrew W. Robertson, David L. Jakeman, David P. Overy, Kerry B. Goralski
Publikováno v:
The Journal of Antibiotics. 71:722-730
Herein, we report the characterization and antimicrobial activity of a previously unreported jadomycin (1) obtained from a culture of S. venezuelae ISP5230 with l-ornithine (Orn). 1 arises from the rearrangement of a putative five-membered ring conta
Autor:
Leah G. Bennett, David L. Jakeman, Hebelin Correa, Kerry B. Goralski, Jeanna M. MacLeod, Steven R. Hall, Russell G. Kerr, Stephanie M. Forget, Andrew W. Robertson, Logan W. MacIntyre
Publikováno v:
The Journal of Organic Chemistry. 83:1876-1890
Polyketide synthase (PKS) derived natural products are biosynthesized by head-to-tail addition of acetate and malonate extender units resulting in linear extended-polyketide chains. Despite the well-documented structural diversity associated with PKS