Method and apparatus for performing unaligned little endian and big
endian data accesses in a processing system
    22.
    发明授权
    Method and apparatus for performing unaligned little endian and big endian data accesses in a processing system 失效
    用于在处理系统中执行未对齐的小端和大端数据访问的方法和装置

    公开(公告)号:US5519842A

    公开(公告)日:1996-05-21

    申请号:US23560

    申请日:1993-02-26

    IPC分类号: G06F9/34 G06F12/04 G06F13/00

    CPC分类号: G06F12/04 G06F9/34

    摘要: A system which is able to perform unaligned big endian and little endian accesses to memory with little or no added overhead to the system. In the preferred embodiment, the processor operates in little endian data format. The memory, however, can store data in big endian and little endian format in different memory regions. If an unaligned access is to be performed, the access requires translation to corresponding aligned memory accesses. However, if the processor operates in little endian format and accesses are to memory which store according big endian format, special code is required to perform proper translation of accesses. When the address generation unit of the processor detects an unaligned memory access, an unaligned signal is set which causes a microassist to initiate a microflow to execute microcode which performs the necessary translations for unaligned accesses. The address generation unit also sends the address to be access to the memory region table which maintains information regarding each memory region, including whether the region is big endian or little endian. The state bit indicative of the data format is logically combined with the unaligned access signal to generate an output which sets the state of the flag. The flag is then accessed by the microcode to determine the translation routine to process the memory access.

    摘要翻译: 能够对系统执行不重要的大端和小端访问的系统,很少或没有额外的开销。 在优选实施例中,处理器以小的数据格式进行操作。 然而,存储器可以在不同的存储器区域中存储大端和小端格式的数据。 如果要执行未对齐的访问,则访问需要转换为对应的对齐的存储器访问。 然而,如果处理器以小的端格式操作,并且访问是根据大端格式存储的存储器,则需要特殊代码来执行适当的访问转换。 当处理器的地址生成单元检测到未对齐的存储器访问时,设置未对齐的信号,其使微辅助器发起微流以执行对未对齐访问执行必要的转换的微代码。 地址生成单元还将要访问的地址发送到维护关于每个存储区域的信息的存储器区域表,包括该区域是大端还是小端。 指示数据格式的状态位与未对准的访问信号逻辑组合以产生设置标志状态的输出。 然后,该标记由微码访问以确定翻译程序来处理存储器访问。

    Mirror
    23.
    外观设计
    Mirror 有权

    公开(公告)号:USD975453S1

    公开(公告)日:2023-01-17

    申请号:US29720975

    申请日:2020-01-16

    申请人: Yan Xu

    设计人: Yan Xu

    Mirror
    24.
    外观设计
    Mirror 有权

    公开(公告)号:USD964049S1

    公开(公告)日:2022-09-20

    申请号:US29720979

    申请日:2020-01-16

    申请人: Yan Xu

    设计人: Yan Xu

    Methods for improving expression levels of foreign proteins by means of phospholipase fusion expression

    公开(公告)号:US10323247B2

    公开(公告)日:2019-06-18

    申请号:US15995134

    申请日:2018-06-01

    申请人: Xiaowei Yu Yan Xu

    发明人: Xiaowei Yu Yan Xu

    摘要: The invention discloses a method for improving the extracellular expression level of a foreign protein by means of phospholipase fusion expression. Four proteins, PLA2, MBP, CBD and SUMO, are used as a fusion tag to construct a fusion gene. Compared with an original protein MOH without any fusion tag, the extracellular expression level and enzymatic activity of all the four fusion proteins are increased to some degree. Among them, the fusion protein using PLA2 as the fusion tag has the highest expression level, which is 7.4 times higher than that of the original protein. Compared with other fusion tags, PLA2 has a low molecular weight and the fusion protein having PLA2 as the fusion tag has the highest expression level (up to 12 g·L−1 in a 7 L fermentation tank for high-density fermentation). It is shown that the secretory expression of a foreign protein can be effectively increased by using PLA2 as a fusion tag.

    Hetero-oligomers of (S)-carbonyl reductases and their applications in catalyzing reduction of polyphenyl ketones

    公开(公告)号:US10023882B1

    公开(公告)日:2018-07-17

    申请号:US15641268

    申请日:2017-07-04

    摘要: Provided are novel hetero-oligomers of (S)-carbonyl reductases and their application in catalyzing the reduction of polyphenyl ketones. Also provided are recombinant strains expressing hetero-oligomers of SCR/SCR2 or SCR2/SCR3, which can catalyze the reduction of polyphenyl ketones. The hetero-oligomer of SCR/SCR2 is capable of catalyzing 2,4-dichlorobenzophenone, 2-naphthalenone and [(E)-2-[3-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-oxopropyl]benzoic acid methyl ester (Keto Easter M) with a specific activity of 4.55 U/mg, 2.43 U/mg and 0.86 U/mg, respectively. The hetero-oligomer of SCR2/SCR3 is capable of catalyzing 2,4-dichlorobenzophenone and [(E)-2-[3-[3-[2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-oxopropyl]benzoic acid methyl ester (Keto Easter M) with a specific activity of 4.42 U/mg and 1.21 U/mg, respectively. No catalyzing activities for reducing polyphenyl ketones were detected in the naturally existing homo-oligomers of SCR, SCR2 or SCR3, which can catalyze the reduction of monobenzoic cyclic compounds. The invention expands the substrate spectrum of natural (S)-carbonyl reductases (SCR, SCR2 and SCR3) and provides a novel type of oxidoreductases for catalyzing the reduction of polyphenyl ketones.

    SMALL MOLECULE POLYPEPTIDE FOR PREVENTING AND RESTRAINING INFLAMMATION AND APPLICATION OF SAME
    29.
    发明申请
    SMALL MOLECULE POLYPEPTIDE FOR PREVENTING AND RESTRAINING INFLAMMATION AND APPLICATION OF SAME 有权
    用于预防和限制其相容性和应用的小分子聚合物

    公开(公告)号:US20150266926A1

    公开(公告)日:2015-09-24

    申请号:US14412497

    申请日:2011-12-19

    申请人: Xun Xu Yan Xu

    发明人: Xun Xu Yan Xu

    IPC分类号: C07K14/00

    摘要: The present invention provides a polypeptide that is rich in leucine and used for preventing and restraining inflammation, and an application of same. The present invention further provides a method for preparing the polypeptide and a pharmaceutical composition containing the polypeptide. The advantage of the polypeptide comprises: small molecular weight, so as to permeate various eye tissue barriers; high water solubility, so as to have high dissolubility in neutral tears, aqueous humor and vitreous humor; and simple synthesis, so as to have a low preparation cost.

    摘要翻译: 本发明提供富含亮氨酸并用于预防和抑制炎症的多肽及其应用。 本发明还提供了制备多肽的方法和含有多肽的药物组合物。 多肽的优点包括:分子量小,以渗透各种眼组织屏障; 水溶性高,以至于在中性眼泪,房水和玻璃体液中具有高溶解性; 和简单的合成,从而具有较低的制备成本。

    Amide derivatives of benzene-sulfonanilide, pharmaceutical composition thereof and method for cancer treatment using the same
    30.
    发明授权
    Amide derivatives of benzene-sulfonanilide, pharmaceutical composition thereof and method for cancer treatment using the same 有权
    苯 - 磺酰苯胺的酰胺衍生物,其药物组合物和使用其的癌症治疗方法

    公开(公告)号:US08802895B2

    公开(公告)日:2014-08-12

    申请号:US12906315

    申请日:2010-10-18

    申请人: Bin Su Aimin Zhou Yan Xu

    发明人: Bin Su Aimin Zhou Yan Xu

    IPC分类号: C07C303/00

    摘要: The invention provides a compound of formula (I), a pharmaceutical composition thereof, a method of preparing a medicament for the treatment of a cancer, and a method of treating cancers. The invention exhibits merits against cancers such as significantly higher potency and effectiveness over a broader range of cancers. In formula (I), Ra is a benzyl group with alkyl and/or alkoxy; Rb is selected from H and alkyl groups; Rf is an alkyl; and R3 is selected from a substituted phenyl, a heterocyclic group, and wherein Rc is selected from a fused ring, fused rings, and any bivalent cyclic group.

    摘要翻译: 本发明提供式(I)化合物,其药物组合物,制备用于治疗癌症的药物的方法和治疗癌症的方法。 本发明表现出对癌症的优点,例如在更广泛的癌症上显着更高的效力和有效性。 在式(I)中,R a为具有烷基和/或烷氧基的苄基; Rb选自H和烷基; Rf是烷基; 并且R 3选自取代的苯基,杂环基,并且其中R c选自稠环,稠环和任何二价环状基团。