Synthesis of a Maskedp -Quinone Methide ? -Lactam as an active metabolite of nocardicins

التفاصيل البيبلوغرافية
العنوان: Synthesis of a Maskedp -Quinone Methide ? -Lactam as an active metabolite of nocardicins
المؤلفون: Jih Ru Hwu, Shwu-Chen Tsay, Gholam Hossein Hakimelahi
المصدر: Helvetica Chimica Acta. 78:411-420
بيانات النشر: Wiley, 1995.
سنة النشر: 1995
مصطلحات موضوعية: Stereochemistry, Organic Chemistry, Biological activity, Antimicrobial, Biochemistry, Quinone methide, Catalysis, In vitro, Nocardicin A, Inorganic Chemistry, chemistry.chemical_compound, chemistry, Drug Discovery, Lactam, Pyridinium, Physical and Theoretical Chemistry, Active metabolite
الوصف: Nocardicin A analogues 30, 34, and 38 as well as the highly strained quinone methide 43 were synthesized. β -Lactam 34 was found biologically active against several Gram-negative microorganisms in vitro; pyridinium N-oxide derivative 38 possessed activity against Gram-positive S. aureus bacterium. Masked p-quinone methide β -lactam 43 exhibited significant antimicrobial activity in vitro. A mechanism involving an oxidation in vivo is proposed for the unprecedented biological properties of nocardicins.
تدمد: 1522-2675
0018-019X
DOI: 10.1002/hlca.19950780212
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3178d5b2f521786187774f226d0dc80f
https://doi.org/10.1002/hlca.19950780212
Rights: CLOSED
رقم الانضمام: edsair.doi...........3178d5b2f521786187774f226d0dc80f
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15222675
0018019X
DOI:10.1002/hlca.19950780212