PLUGGABLE TOKEN PROVIDER MODEL TO IMPLEMENT AUTHENTICATION ACROSS MULTIPLE WEB SERVICES
    41.
    发明申请
    PLUGGABLE TOKEN PROVIDER MODEL TO IMPLEMENT AUTHENTICATION ACROSS MULTIPLE WEB SERVICES 有权
    可扩展的供应商模型,实现跨多个WEB服务的认证

    公开(公告)号:US20110231921A1

    公开(公告)日:2011-09-22

    申请号:US12726779

    申请日:2010-03-18

    IPC分类号: H04L9/32 G06F21/00

    摘要: A pluggable token provider model for message level authentication across multiple web services is provided. Web service and token provider implementations within a client application are separated from an actual component that operates the business logic to formulate and understand a web request. The web service components may request web services to be executed and supply the body for the web service message while a common framework maintains the web services metadata, which includes definitions associated with respective tokens. The framework may further maintain token provider implementations that actually fetch authentication tokens and perform the web requests.

    摘要翻译: 提供了一种用于跨多个Web服务进行消息级认证的可插拔令牌提供者模型。 客户端应用程序中的Web服务和令牌提供程序实现与操作业务逻辑的实际组件分离,以制定和理解Web请求。 Web服务组件可以请求执行web服务,并为Web服务消息提供主体,同时公共框架维护web服务元数据,其中包括与相应令牌相关联的定义。 该框架可以进一步维护实际提取认证令牌并执行web请求的令牌提供者实现。

    Combinatorial library of moenomycin analogs and methods of producing same
    45.
    发明授权
    Combinatorial library of moenomycin analogs and methods of producing same 失效
    霉酚霉素类似物组合库及其生产方法

    公开(公告)号:US06207820B1

    公开(公告)日:2001-03-27

    申请号:US09394045

    申请日:1999-09-13

    IPC分类号: C07H100

    摘要: A combinatorial chemical library of compounds structurally related to the moenomycin class of antibiotics has the formula wherein D is a donor mono- or disaccharide, A is an acceptor monosaccharide, and P—R is a lipophosphoglycerate mimetic group. Members of the library have a glycosidic linkage between the anomeric carbon of D and the C2 carbon of A, and the D—A moiety is in turn covalently linked through the anomeric carbon of A to the P—R group. Members of the library exhibit their greatest structural diversity in terms of substitutions occurring at the C3 position of the A residue, substitutions at the C2 position of the D residue, and different P—R groups used in assembling the compounds. Members of the library are preferably synthesized by solid phase techniques involving stepwise coupling of the respective units to a support, functionalizing the A and/or D saccharides either before or after immobilizing them on the support, and cleaving the assembled compounds from the support. Preferred functionalities attached to the sugar residues are amides, carbamates, ureas, sulfonamides, substituted amines, esters, carbonates, and sulfates. Exemplary P—R groups are derivatives of homoserine, glyceric acid, salicylates and mandelic acid. Members of the library can be screened for anti-microbial activity by contacting them with a culture of microbes and monitoring the growth rate of the microbes.

    摘要翻译: 结构上与霉酚霉素类抗生素有关的化合物的组合化学文库,其中D是供体单糖或二糖,A是受体单糖,P-R是脂磷酸甘油酸酯模拟组。 文库成员在D的异头碳和A的C2碳之间具有糖苷键,D-A部分又通过A的端基异碳共价连接到P-R基团。 关于在A残基的C3位置发生的取代,在D残基的C2位置的取代以及用于组装化合物的不同的P-R基团,图书馆的成员表现出最大的结构多样性。 文库的成员优选通过固相技术合成,其包括将各单元逐步偶联到载体上,在将它们固定在载体上之前或之后将A和/或D糖功能化,并将载体化合物从载体上分离。 附着于糖残基的优选功能是酰胺,氨基甲酸酯,脲,磺酰胺,取代的胺,酯,碳酸酯和硫酸酯。 示例性的P-R基团是高丝氨酸,甘油酸,水杨酸盐和扁桃酸的衍生物。 通过与微生物培养物接触并监测微生物的生长速率,可以筛选图书馆成员的抗菌活性。