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fimbrolide | 63025-34-3

中文名称
——
中文别名
——
英文名称
fimbrolide
英文别名
(5E)-4-bromo-5-(bromomethylidene)-3-butylfuran-2-one
fimbrolide化学式
CAS
63025-34-3
化学式
C9H10Br2O2
mdl
——
分子量
309.985
InChiKey
UVJAGAXWVHGYRW-FNORWQNLSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] DUAL ACTION NITRIC OXIDE DONORS AND THEIR USE AS ANTIMICROBIAL AGENTS<br/>[FR] DONNEURS D'OXYDE NITRIQUE À DOUBLE ACTION ET LEUR UTILISATION COMME AGENTS ANTIMICROBIENS
    申请人:NEWSOUTH INNOVATIONS PTY LTD
    公开号:WO2014071457A1
    公开(公告)日:2014-05-15
    The present invention relates generally to conjugates comprising a nitric oxide donor and an acyl homoserine lactone, fimbrolide, fimbrolide derivative, dihydropyrrolone or indole, and to the use of such conjugates as antimicrobial agents.
    本发明涉及一般地与一氧化氮供体和酰基同源丁氨酸内酯、菲螺啉、菲螺啉衍生物、二氢吡咯酮或吲哚构成的结合物,以及将这些结合物用作抗微生物剂的用途。
  • NON-AMPHIPHILE-BASED WATER-IN-WATER EMULSION AND USES THEREOF
    申请人:LUK Yan-Yeung
    公开号:US20090269323A1
    公开(公告)日:2009-10-29
    The present invention relates to a non-amphiphile-based water-in-water emulsion composition. The non-amphiphile-based water-in-water emulsion composition includes a water-soluble polymer, a non-amphiphilic lyotropic mesogen encapsulated by the water-soluble polymer; and water. In one embodiment, the non-amphiphilic lyotropic mesogen includes, without limitation, a lyotropic chromonic liquid crystal, and more specifically disodium cromoglycate (DSCG). In another embodiment, the water-soluble polymer can include, without limitation, a polyacrylamide, a polyol, a polyvinylpyrrolidone, a polysaccharide, or a water-soluble fluoride-bearing polymer. The present invention also relates to a porous hydrogel made with the use of the non-amphiphile-based water-in-water emulsion. The present invention further relates to using the emulsion and hydrogel for various applications.
    本发明涉及一种非两亲性基材的水包水乳液组合物。该非两亲性基材的水包水乳液组合物包括水溶性聚合物、被水溶性聚合物封装的非两亲性溶致液晶;和水。在一个实施例中,非两亲性溶致液晶包括但不限于溶致色浆液晶,更具体地是无钠 Cromoglicate (DSCG)。在另一个实施例中,水溶性聚合物可以包括但不限于聚丙烯酰胺、聚醇、聚乙烯吡咯烷酮、多糖或水溶性含氟聚合物。本发明还涉及一种用非两亲性基材的水包水乳液制成的多孔水凝胶。本发明进一步涉及使用该乳液和水凝胶用于各种应用。
  • SYSTEM AND METHOD FOR CONTROLLING GROWTH OF MICROORGANISMS WITH BROMINATED FURANONES
    申请人:Luk Yan-Yeung
    公开号:US20100120905A1
    公开(公告)日:2010-05-13
    A method for inhibiting the growth of a microorganism using an effective amount of one or more of the following synthetic brominated furanones: (i) 4-bromo-5Z-(bromomethylene)-3-methylfuran-2-one; (ii) 3-(dibromomethyl)-5-(dibromomethylene)furan-2-one; (iii) 3-(bromomethyl)-5-(dibromomethylene)furan-2-one; (iv) 4-bromo-3-(bromomethyl)-5Z-(bromomethylene)furan-2-one; or (v) 4-bromo-5-(dibromomethyl)-3-methylfuran-2(5H)-one. The brominated furanones inhibit the growth of both fungi and bacteria, including the fungal species Candida albicans, Gloeophyllum trabeum, Chaetomium globosum , and Trametes versicolor and the bacterial species Pseudomonas aeruginosa . The brominated furanones can be used topically or internally to treat human infections, and can be used to treat other objects, such as wood building supplies, to prevent fungal rot.
    使用以下合成溴化呋喃酮之一或多个有效量,抑制微生物的生长:(i)4-溴-5Z-(溴甲烯基)-3-甲基呋喃-2-酮;(ii)3-(二溴甲基)-5-(二溴甲烯基)呋喃-2-酮;(iii)3-(溴甲基)-5-(二溴甲烯基)呋喃-2-酮;(iv)4-溴-3-(溴甲基)-5Z-(溴甲烯基)呋喃-2-酮;或(v)4-溴-5-(二溴甲基)-3-甲基呋喃-2(5H)-酮。 溴化呋喃酮抑制真菌和细菌的生长,包括真菌物种Candida albicans,Gloeophyllum trabeum,Chaetomium globosum和Trametes versicolor,以及细菌物种Pseudomonas aeruginosa。 溴化呋喃酮可用于局部或内部治疗人类感染,并可用于治疗其他物体,例如木材建筑用品,以预防真菌腐烂。
  • [EN] FURANONE DERIVATIVES AND METHODS OF MAKING SAME<br/>[FR] DERIVES DE FURANONE ET LEURS PROCEDES DE PRODUCTION
    申请人:BIOSIGNAL PTY LTD
    公开号:WO2004016588A1
    公开(公告)日:2004-02-26
    Novel synthesis methods, to the products of such novel methods, and to uses of these products. In particular, the present invention provides methods for the reactions of furanones, in particular fimbrolides, with amines. The invention has particular application in the synthesis of halogenated 1,5-dihydro-pyrrol-2-one, 5-halomethylene substituted 1,5-dihydropyrrol-2-ones (lactam analogues of fimbrolides), 5-amino substituted furanones and 5-aminomethylene-2(5H)-furanones and their synthetic analogues. The invention also relates to novel compounds and uses thereof.
    本发明涉及新颖的合成方法,新方法的产物以及这些产物的用途。特别地,本发明提供了一种将呋喃酮(尤其是fimbrolides)与胺反应的方法。本发明在卤代1,5-二氢吡咯-2-酮,5-卤代亚甲基取代的1,5-二氢吡咯-2-酮(fimbrolides的内酰胺类似物),5-氨基取代呋喃酮和5-氨基亚甲基-2(5H)-呋喃酮及其合成类似物的合成中具有特定应用。本发明还涉及新化合物及其用途。
  • B. anthracis prevention and treatment: mutant B. anthracis lacking luxS activity and furanone inhibition of growth, AI-2 quorum sensing, and toxin production
    申请人:Jones B. Marcus
    公开号:US20050042634A1
    公开(公告)日:2005-02-24
    The present invention pertains to the discovery that B. anthracis possesses a luxS gene that encodes a functional LuxS polypeptide, and that B. anthracis synthesizes a functional AI-2 quorum-sensing molecule. The invention provides mutant B. anthracis bacteria lacking the function of the luxS gene, which do not produce a functional AI-2 molecule and have growth defects compared to wild-type B. anthracis . The invention also concerns methods for inhibiting the growth of B. anthracis , or for preventing or treating B. anthracis infection, by inhibiting the activity of the B. anthracis LuxS polypeptide, or by exposure of the B. anthracis to furanone. In particular, the invention concerns the use of furanone, a compound that inhibits AI-2-mediated quorum-sensing, to inhibit the growth of B. anthracis , to inhibit B. anthracis toxin production, particularly that of protective antigen, and to prevent or treat B. anthracis infection. The invention also provides methods to prevent B. anthracis infection, or enhance an immune response to B. anthracis infection, by administering a vaccine comprising a B. anthracis cell in which the luxS gene is mutated.
    本发明涉及发现B. anthracis具有编码功能性LuxS多肽的luxS基因,以及B. anthracis合成功能性AI-2类群体感应分子。该发明提供了缺乏luxS基因功能、不产生功能性AI-2分子并与野生型B. anthracis相比具有生长缺陷的突变B. anthracis细菌。本发明还涉及通过抑制B. anthracis LuxS多肽的活性或暴露于呋喃酮来抑制B. anthracis的生长,预防或治疗B. anthracis感染的方法。特别是,本发明涉及使用呋喃酮,一种抑制AI-2介导的类群体感应的化合物,来抑制B. anthracis的生长,抑制B. anthracis毒素的产生,特别是保护性抗原的产生,并预防或治疗B. anthracis感染。本发明还提供了通过给予包含luxS基因突变的B. anthracis细胞的疫苗来预防B. anthracis感染或增强对B. anthracis感染的免疫反应的方法。
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同类化合物

(2R)-4-十六烷酰基-3-羟基-2-(羟甲基)-2H-呋喃-5-酮 马来酸酐-丙烯酸共聚物钠盐 马来酸酐-d2 马来酸酐-13C4 马来酸酐-1-13C 马来酸酐 顺丁烯酸酐-2,3-13C2 顺丁烯二酐与2,2-二甲基-1,3-丙二醇和1,2-丙二醇的聚合物 雄甾-3,5,9(11)-三烯-17-酮,3-甲氧基-(8CI,9CI) 阿西弗兰 阻垢分散剂 重氮基烯,二环[2.2.1]庚-1-基(1,1-二甲基乙基)-,(Z)-(9CI) 赤藻糖酸钠 螺甲螨酯代谢物 M01 葫芦巴内酯 苯基顺酐 聚氧乙烯(2-甲基-2-丙烯基)甲基二醚-马来酸酐共聚物 聚(甲基乙烯基醚-ALT-马来酸酐) 聚(异丁烯-马来酸酐) 聚(乙烯-co-丙烯酸乙酯-co-顺丁烯二酐) 聚(乙烯-co-丙烯酸丁酯-co-马来酸酐) 维生素C钠 维生素C磷酸酯钠 维生素C磷酸酯 维生素C杂质 维生素C亚铁盐 维生素C乙基醚 维生素 C 维他命C磷酸镁盐 纯绿青霉酸 粘氯酸酐 粘氯酸酐 粘氯酸酐 粘康酸内酯 粉青霉酸酐 穿心莲丁素 硫酰胺,(3-氰基-5,6,7,8-四氢-4H-环庚三烯并[b]噻吩并-2-基)-(9CI) 白头翁素 甲基7-氧杂双环[2.2.1]庚-2,5-二烯-2-羧酸酯 甲基5-甲基-4,5-二氢-3-呋喃羧酸酯 甲基4-氰基-2,5-二氢-3-呋喃羧酸酯 甲基4,5-二氢-2-呋喃羧酸酯 甲基3-甲基-2,3-二氢-3-呋喃羧酸酯 甲基2-甲基-5-亚甲基-4,5-二氢-3-呋喃羧酸酯 甲基2-甲基-2,5-二氢-2-呋喃羧酸酯 甲基2-氨基-4,5-二氢-3-呋喃羧酸酯 甲基2-乙烯基-4,5-二氢-3-呋喃羧酸酯 特春酸 溴代马来酸酐 氟2-(5-氧代-2H-呋喃-2-基)乙酸酯