📜Heptylmagnesium Bromide置于吡啶,乙醚,Sodium Acetate,三溴化磷,溶剂黄146体系中,化学反应生成反式-2-癸烯醇 参考文献:Delaby,Bulletin De La Societe Chimique De France,1936,Vol. <5>3,P. 2380 标题:Delaby,Bulletin De La Societe Chimique De France,1936,Vol. <5>3,P. 2380
专利号:US-8865624-B2 优先权日:2010-09-01 标题 :Inhibitor for tobacco axillary bud growth and method for inhibiting tobacco axillary bud growth 发明人:TANAKA MOTOKI; TANAKA KEIJITSU; SHIBUYA TAKESHI; IKUTA EIJI; YOSHINAGA KOTARO; YAMAGUCHI YUKI 权利人:TANAKA MOTOKI; TANAKA KEIJITSU; SHIBUYA TAKESHI; IKUTA EIJI; YOSHINAGA KOTARO; YAMAGUCHI YUKI; SDS BIOTECH CORP 摘要:The present invention relates to an inhibitor for tobacco axillary bud growth, the inhibitor comprising, as an active ingredient, one or more kinds of very-long chain fatty acid synthesis inhibitors such as a chloroacetamide-based herbicide, fentrazamide, cafenstrole or indanofan; an inhibitor for tobacco axillary bud growth, the inhibitor comprising the aforesaid very-long chain fatty acid synthesis inhibitor together with clorthal-dimethyl or an aliphatic alcohol having 6 to 20 carbon atoms; and a method for inhibiting tobacco axillary bud growth which comprises applying the inhibitor for tobacco axillary bud growth. The inhibitor for tobacco axillary bud growth of the present invention shows sustained drug efficacy at a low concentration, induces neither chemical injury nor disease, and can contribute to the improvement in labor productivity.
专利号:US-8859615-B2 优先权日:2008-08-27 标题 :Compounds, compositions and methods for reducing toxicity and treating or preventing diseases 发明人:DANISHEFSKY SAMUEL J; CHOU TING-CHAO; LEI XIAOGUANG; YUN HEEDONG; NG FAY; HARTUNG JOHN; SAMES DALIBOR 权利人:DANISHEFSKY SAMUEL J; CHOU TING-CHAO; LEI XIAOGUANG; YUN HEEDONG; NG FAY; HARTUNG JOHN; SAMES DALIBOR 摘要:The present invention provides compounds of Formula (I), compositions comprising an effective amount of a compound of Formula (I), optionally with chemotherapeutic drugs such as a tubulin-binding drug, and methods of their use for reducing the toxicity of cytotoxic agents, treating or preventing cancer or a neuropathic disorder, inducing a chemoprotective phase II enzyme, DNA, or protein synthesis, enhancing the immune system, treating inflammation, improving and enhancing general health or well-being, and methods for making compounds of Formula (I).
参考标题:Convergent Synthesis Of Calcium-Dependent Antibiotic Cda3A And Analogues With Improved Antibacterial Activity Via Late-Stage Serine Ligation 作者:Delin Chen,Kathy Hiu Laam Po,Pilar Blasco,Sheng Chen,Xuechen Li |发布日期:2020.6.19 摘要:A Convergent Synthesis Via The Late-Stage Serine Ligation Of Naturally Occurring Calcium-Dependent Antibiotic Cda3A And Its Analogues Has Been Developed, Which Allowed Us To Readily Synthesize The Analogues With The Variation On The Lipid Tail. Some Analogues Were Found To Show 100-500-Fold Higher Antimicrobial Activity Than The Natural Compound Cda3A Against Drug Resistant Bacteria. This Study Will
合成参考文献
摘要:Race, N. J.; Patel, H. H.; Sigman, M. S., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 445.