首页> 外国专利> NARROW-SPECTRUM ANTIBACTERIAL ANTIBIOTICS TARGETING SPECIFIC TYPES OF BACTERIA THAT SYNTHESIZES MENAQUINONE THROUGH AN ALTERNATIVE PATHWAY VIA FUTALOSINE OR 6-AMINODEOXYFUTALOSINE AS AN INTERMEDIATE.

NARROW-SPECTRUM ANTIBACTERIAL ANTIBIOTICS TARGETING SPECIFIC TYPES OF BACTERIA THAT SYNTHESIZES MENAQUINONE THROUGH AN ALTERNATIVE PATHWAY VIA FUTALOSINE OR 6-AMINODEOXYFUTALOSINE AS AN INTERMEDIATE.

机译:窄谱抗菌剂以特定形式的细菌为目标,该细菌通过呋喃他辛或6-氨基氧代呋喃他命作为中间体,通过替代途径合成甲萘醌。

摘要

Alternative menaquinone biosynthetic pathway via futalosine or 6-aminodeoxyfutalosine as an intermediate (futalosine pathway) is an attractive target for new narrow-spectrum antimicrobial agents. Siamycin I and fatty acids were provided as selective antimicrobial activity against bacteria such as Helicobacter and Campylobacter, which depend on the futalosine pathway to grow. Specifically, siamycin I and omega-3 polyunsaturated fatty acids inhibited the colonization of H. pylori in vivo and thus siamycin I and omega-3 polyunsaturated fatty acids could be a new narrow-spectrum antibiotic for Helicobacter and Campylobacter
机译:通过氟他洛辛或6-氨基脱氧富他洛因作为中间体的另一种甲萘醌生物合成途径(富他洛因途径)是新型窄谱抗菌剂的有吸引力的目标。唾液酸霉素I和脂肪酸作为对细菌(如幽门螺杆菌和弯曲杆菌)的选择性抗菌活性提供,这些细菌取决于他他洛辛的生长途径。具体而言,siamy I和omega-3多不饱和脂肪酸在体内抑制了幽门螺杆菌的定殖,因此siamycin i和omega-3多不饱和脂肪酸可能是幽门螺杆菌和弯曲杆菌的一种新型窄谱抗生素

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