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    • 3. 发明授权
    • Diagnosis of fungal infections with a chitinase
    • 用几丁质酶诊断真菌感染
    • US6093552A
    • 2000-07-25
    • US770826
    • 1996-12-20
    • Roger A. LaineWai C. J. Lo
    • Roger A. LaineWai C. J. Lo
    • C12Q1/34G01N33/569G01N33/53
    • G01N33/56961C12Q1/34
    • Chitinase fungal diagnostic reagents comprising a chitinase conjugate comprising a chitinase enzyme and a label, the label selected from among a flourescent or a radioactive compound, an enzyme and a dye, the said chitinase fungal diagnostic reagent comprises a substantially pure aqueous solution of said chitinase conjugate; kits for detecting a fungal cell wall glucosamine compound in a biological specimen comprising the chitinase fungal diagnostic reagent and a filter capable of collecting the fungal cell wall glucosamine compound; and methods for detecting a fungal cell wall glucosamine compound in a biological specimen.
    • 几丁质酶真菌诊断试剂包含几丁质酶偶联物,其包含几丁质酶和标记,选自荧光素或放射性化合物的标签,酶和染料,所述几丁质酶真菌诊断试剂包含基本上纯的所述几丁质酶缀合物的水溶液 ; 用于检测包含几丁质酶真菌诊断试剂的生物样品中的真菌细胞壁葡糖胺化合物的试剂盒和能够收集真菌细胞壁葡糖胺化合物的过滤器; 以及用于检测生物样本中的真菌细胞壁葡糖胺化合物的方法。
    • 4. 发明申请
    • Naphthalene Derivatives as Termite Repellents and Toxicants
    • 萘衍生物作为白蚁驱虫剂和毒素
    • US20080206294A1
    • 2008-08-28
    • US12024453
    • 2008-02-01
    • Gregg HendersonSanaa A. IbrahimRosemary PattonRoger A. LaineBetty C.R. ZhuFeng Chen
    • Gregg HendersonSanaa A. IbrahimRosemary PattonRoger A. LaineBetty C.R. ZhuFeng Chen
    • A01N31/14A01N25/08A01N31/00A01P17/00A01P7/04
    • A01N31/04A01N27/00A01N31/14A01N35/04Y10S424/11
    • Several derivatives of naphthalene, including 1′-acetonaphthone, 2′-acetonaphthone, 1-methoxynaphthalene, and 2-methoxynaphthalene, were discovered to be effective toxicants and repellents of termites, and resulted in significant reduction in termite feeding activity. For example, 2′-acetonaphthone was found to be an effective repellent and feeding deterrent of termites. Termites exposed to concentrations as low as 8 mg/kg sand exhibited a significant reduction in tunneling and feeding activity. Moreover, some of the dead termites had symptoms indicative of a failure to molt. At concentrations ≧20 μg/cm2, 2′-acetonaphthone was a strong repellent. Interestingly, at 160-fold lower concentration (0.125 μg/cm2), 2′-acetonaphthone stimulated termite feeding activity. As a sand barrier, 2′-acetonaphthone significantly inhibited tunneling and feeding activity in concentrations from 8.33 to 35.0 mg/kg. Molting problems were also identified in termites exposed to 2′-acetonaphthone.
    • 发现了萘的几种衍生物,包括1'-乙酰萘酮,2'-乙酰萘酮,1-甲氧基萘和2-甲氧基萘,是白蚁的有效毒素和驱避剂,导致白蚁进食活性显着降低。 例如,发现2'-乙酰萘酮是有效的驱避剂和抑制白蚁的抑制作用。 暴露于浓度低至8 mg / kg沙粒的白蚁显示隧道和进食活动的显着减少。 此外,一些死亡的白蚁有表现为蜕皮失败的症状。 在浓度≥20mug/ cm 2的情况下,2'-乙酰萘酮是强驱虫剂。 有趣的是,在浓度为160倍(0.125mug / cm 2))的情况下,2'-乙酰萘酮刺激白蚁进食活性。 作为沙屏障,2'-乙酰萘酮显着抑制了浓度为8.33〜35.0mg / kg的隧道和摄食活性。 在暴露于2'-乙酰四氢萘酮的白蚁中也发现了溶解问题。
    • 6. 发明授权
    • Diagnosis of fungal infections, and a chitin-binding lectin useful in
such diagnoses
    • 真菌感染的诊断和可用于这种诊断的几丁质结合凝集素
    • US6121420A
    • 2000-09-19
    • US290836
    • 1999-04-13
    • Roger A. Laine
    • Roger A. Laine
    • C07K14/28G01N33/569
    • C07K14/28G01N33/56961G01N2333/4724
    • A 134 kDa, calcium-independent, chitin-binding lectin called chitovibrin is secreted by marine bacteria of the genus Vibnio. The secretion of chitovibrin is inducible by chitin or chitin-oligomers. Chitovibrin shows no apparent enzymatic activity, but has a strong affinity for chitin and for chito-oligomers dp9 and larger. The protein has an isoelectric pH of 3.6, shows thermal tolerance, binds chitin with an optimum at pH 6 and is active in 0-4 M NaCl. Chitovibrin is useful as a stain for fungi and other chitin-containing organisms. Chitovibrin may be used to detect the presence of chitin, particularly in diagnosing fungal infections in humans, animals, and plant materials. Fungal infections are a particular problem in immunocompromised hosts such as AIDS patients and bone marrow transplant patients, because they can cause opportunistic infections. The chitovibrin diagnostic method allows the convenient, broad spectrum diagnosis of fungal infections in tissue samples or in body fluids. Other, smaller polypeptide fragments of chitovibrin will exhibit similar chitin-binding properties, and could be used in coupling to detection systems.
    • 称为chitovibrin的134 kDa,不依赖钙的几丁质结合凝集素由Vibnio属的海洋细菌分泌。 壳多糖蛋白的分泌可由几丁质或几丁质寡聚体诱导。 Chitovibrin没有显示出明显的酶活性,但对几丁质和chito-oligomers dp9及更大的亲和力。 蛋白质具有3.6的等电点pH,显示耐热性,在pH 6下结合几丁质,最适pH为0-4M NaCl。 Chitovibrin可用作真菌和其他含几丁质的生物体的污渍。 Chitovibrin可用于检测几丁质的存在,特别是在诊断人类,动物和植物材料中的真菌感染时。 免疫功能低下的宿主如艾滋病患者和骨髓移植患者,真菌感染是一个特别的问题,因为它们可能引起机会性感染。 chitovibrin诊断方法可以方便,广谱地诊断组织样本或体液中的真菌感染。 其他较小的chitovibrin多肽片段将显示相似的几丁质结合性质,并可用于与检测系统的偶联。
    • 7. 发明授权
    • Synthesis of anti-inflammatory compounds and novel trisaccharides useful
in the synthesis of anti-inflammatory compounds
    • 抗炎化合物的合成和用于合成抗炎化合物的新型三糖
    • US5618705A
    • 1997-04-08
    • US454740
    • 1995-05-31
    • Roger A. LaineEunsun Yoon
    • Roger A. LaineEunsun Yoon
    • C07H3/06C12P19/18C12P19/04C08B37/00C12P19/00
    • C12P19/18C07H3/06
    • Anti-inflammatory compounds are useful, for example, in treating arthritis and heart attack patients. Novel oligosaccharides useful in the rapid synthesis of certain anti-inflammatory compounds are disclosed, as is a rapid method of synthesizing the oligosaccharides. Low pH can loosen the acceptor specificity of galactosyltransferase (lactose synthase: EC 2.4.1.22), allowing the rapid synthesis of novel oligosaccharides. The disaccharides cellobiose (.beta.1.fwdarw.4), laminaribiose (.beta.1.fwdarw.3), gentiobiose (.beta.1.fwdarw.6) and maltose (.alpha.1.fwdarw.4) acted as acceptors for lactose synthase under low pH conditions. From these four acceptors, the following four novel trisaccharides were synthesized: Gal.sub.p (.beta.1.fwdarw.4)Glc.sub.p (.beta.1.fwdarw.3)-Glc, Gal.sub.p (.beta.1.fwdarw.4)Glc.sub.p (.beta.1.fwdarw.4)-Glc, Gal.sub.p (.beta.1.fwdarw.4)Glc.sub.p (.beta.1.fwdarw.6)-Glc and Gal.sub.p (.beta.1.fwdarw.4)Glc.sub.p (.alpha.1.fwdarw.4) Glc. These trisaccharides, and other oligosaccharides, may be synthesized in a few days with the disclosed technique, as opposed to the several months which would likely have been required with more traditional organic synthetic methods. These trisaccharides may be used as intermediates in the rapid synthesis of anti-inflammatory compounds.
    • 抗炎化合物可用于例如治疗关节炎和心脏病发作患者。 公开了用于快速合成某些抗炎化合物的新型寡糖,以及合成低聚糖的快速方法。 低pH可以松散半乳糖转移酶(乳糖合成酶:EC 2.4.1.22)的受体特异性,可以快速合成新的低聚糖。 在低pH条件下,二糖纤维二糖(β1-> 4),层状二糖(β1-> 3),龙胆二糖(β1-> 6)和麦芽糖(α1-> 4)作为乳糖合成酶的受体。 从这四个受体合成了以下四种新型三糖:Galp(β1-> 4)Glcp(β1-> 3)-Glc,Galp(β1-> 4)Glcp(β1-> 4)-Glc ,Glp1(β1-> 4)Glc1(β1-> 6)-Glc和Galp(β1-> 4)Glcp(α1-4)Glc。 这些三糖和其他寡糖可以在几天内用所公开的技术合成,而不是可能用更传统的有机合成方法需要的几个月。 这些三糖可以用作快速合成抗炎化合物的中间体。