Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Fangchao Bi"'
Publikováno v:
Green Synthesis and Catalysis, Vol 1, Iss 1, Pp 66-69 (2020)
Salicylaldehyde containing biaryls are efficiently synthesized via an unprecedented amine promoted Diels-Alder-retro-Diels-Alder cascade reaction of ynals with 2-pyrones in good yields. The reaction is instrumentally metal-free, operationally simple
Externí odkaz:
https://doaj.org/article/b3cca40277884f839461698ef50819ba
Autor:
Wern Chern Chai, Jonathan J. Whittall, Di Song, Steven W. Polyak, Abiodun D. Ogunniyi, Yinhu Wang, Fangchao Bi, Shutao Ma, Susan J. Semple, Henrietta Venter
Publikováno v:
Antibiotics, Vol 9, Iss 12, p 873 (2020)
The bacterial cell division protein, FtsZ, has been identified as a target for antimicrobial development. Derivatives of 3-methoxybenzamide have shown promising activities as FtsZ inhibitors in Gram-positive bacteria. We sought to characterise the ac
Externí odkaz:
https://doaj.org/article/936c6248e7414aecbd7b9d360c1dfaf6
Publikováno v:
Chemical Science
While strategies involving a 2e− transfer pathway have dictated glycosylation development, the direct glycosylation of readily accessible glycosyl donors as radical precursors is particularly appealing because of high radical anomeric selectivity a
Publikováno v:
Green Synthesis and Catalysis, Vol 1, Iss 1, Pp 66-69 (2020)
Salicylaldehyde containing biaryls are efficiently synthesized via an unprecedented amine promoted Diels-Alder-retro-Diels-Alder cascade reaction of ynals with 2-pyrones in good yields. The reaction is instrumentally metal-free, operationally simple
Publikováno v:
European Journal of Medicinal Chemistry. 180:321-339
Macrolides are widely prescribed in clinic to treat various respiratory tract infections. However, due to their inappropriate use, the prevalence of macrolide-resistant strains among clinical isolates has become a concern for public health. Therefore
Autor:
Di Song, Shutao Ma, Yinhui Qin, Nan Zhang, Panpan Zhang, Yuetai Teng, Na Zhang, Fangchao Bi, Xingbang Liu
Publikováno v:
Bioorganic & Medicinal Chemistry. 27:3179-3193
The spread of infections caused by multidrug-resistant (MDR) pathogens, such as methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant S. aureus (VRSA), has created a need for new antibiotics with novel mechanisms of action. The
Autor:
Dan Luo, George R. Uhl, David O. Johnson, Chamani Perera, Jane Smoake, Fangchao Bi, Fanxun Zeng, Nazmul H. Bhuiyan, Wei Wang, Thomas E. Prisinzano, Ian M. Henderson, Maria Carmen Martinez
Publikováno v:
Biochem Pharmacol
Interest in development of potent, selective inhibitors of the phosphatase from the receptor type protein tyrosine phosphatase PTPRD as antiaddiction agents is supported by human genetics, mouse models and studies of our lead compound PTPRD phosphata
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 43:128110
A novel series of 3-O-descladinosyl-3-keto-clarithromycin derivatives, including 11-O-carbamoyl-3-O-descladinosyl-3-keto-clarithromycin derivatives and 2′,9(S)-diaryl-3-O-descladinosyl-3-keto-clarithromycin derivatives, were designed, synthesized a
Autor:
Abiodun D. Ogunniyi, Susan J. Semple, Henrietta Venter, Fangchao Bi, Wern Chern Chai, Jonathan J. Whittall, Yinhu Wang, Shutao Ma, Di Song, Steven W. Polyak
Publikováno v:
Antibiotics
Volume 9
Issue 12
Antibiotics, Vol 9, Iss 873, p 873 (2020)
Volume 9
Issue 12
Antibiotics, Vol 9, Iss 873, p 873 (2020)
The bacterial cell division protein, FtsZ, has been identified as a target for antimicrobial development. Derivatives of 3-methoxybenzamide have shown promising activities as FtsZ inhibitors in Gram-positive bacteria. We sought to characterise the ac
Publikováno v:
Bioorganic & Medicinal Chemistry. 28:115729
Antibiotic resistance among clinically significant bacterial pathogens, such as methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant S. aureus (VRSA) is becoming a prevalent threat to public health, and new antibacterial agents