APPARATUSES, METHODS, AND SYSTEMS FOR HARDWARE-ASSISTED LOCKSTEP OF PROCESSOR CORES

    公开(公告)号:US20210303372A1

    公开(公告)日:2021-09-30

    申请号:US16833454

    申请日:2020-03-27

    IPC分类号: G06F9/52 G06F9/30 G06F9/38

    摘要: Systems, methods, and apparatuses relating to circuitry to implement lockstep of processor cores are described. In one embodiment, a hardware processor comprises a first processor core comprising a first control flow signature register and a first execution circuit, a second processor core comprising a second control flow signature register and a second execution circuit, and at least one signature circuit to perform a first state history compression operation on a first instruction that executes on the first execution circuit of the first processor core to produce a first result, store the first result in the first control flow signature register, perform a second state history compression operation on a second instruction that executes on the second execution circuit of the second processor core to produce a second result, and store the second result in the second control flow signature register.

    Removable anchoring system and uses thereof
    2.
    发明授权
    Removable anchoring system and uses thereof 有权
    可移动锚固系统及其用途

    公开(公告)号:US09464397B1

    公开(公告)日:2016-10-11

    申请号:US14832757

    申请日:2015-08-21

    申请人: Philip Abraham

    发明人: Philip Abraham

    IPC分类号: E04H12/22 E02D5/80

    摘要: In various implementations, an anchoring system may include one or more anchors. An anchor may include a first coupling member, a second coupling member, and a plate. The anchor may be coupleable to other anchors and/or objects. The anchoring system may be used to secure an object to a location.

    摘要翻译: 在各种实现中,锚定系统可以包括一个或多个锚。 锚可以包括第一联接构件,第二联接构件和板。 锚可以与其他锚和/或物体相连。 锚定系统可用于将物体固定到位置。

    Methods, systems, and computer program products for silence insertion descriptor (SID) conversion
    4.
    发明授权
    Methods, systems, and computer program products for silence insertion descriptor (SID) conversion 有权
    用于静音插入描述符(SID)转换的方法,系统和计算机程序产品

    公开(公告)号:US08346239B2

    公开(公告)日:2013-01-01

    申请号:US11965994

    申请日:2007-12-28

    IPC分类号: H04Q7/20

    CPC分类号: H04W88/181

    摘要: Methods, systems, and computer program products for silence insertion descriptor (SID) conversion are disclosed. According to one aspect, the subject matter described herein includes a method for silence insertion descriptor (SID) conversion. The method includes receiving a wireless frame, the frame identifying a first node as a frame source and a second node as a frame destination; determining whether tandem-free operation (TFO) is applicable; responsive to a determination that TFO is applicable, determining whether the frame is a SID frame; responsive to a determination that the frame is a SID frame, determining whether the SID format used by the first node is incompatible with the SID format used by the second node; and responsive to a determination that the SID format used by the first node is incompatible with the SID format used by the second node, converting the SID frame from the SID format used by the first node to the SID format used by the second node.

    摘要翻译: 公开了用于静音插入描述符(SID)转换的方法,系统和计算机程序产品。 根据一个方面,本文描述的主题包括用于静音插入描述符(SID)转换的方法。 所述方法包括接收无线帧,将所述帧识别为第一节点作为帧源,将所述第二节点标识为帧目的地; 确定无串联运行(TFO)是否适用; 响应于TFO可适用的确定,确定该帧是否是SID帧; 响应于所述帧是SID帧的确定,确定由所述第一节点使用的SID格式是否与由所述第二节点使用的SID格式不兼容; 并且响应于第一节点使用的SID格式与第二节点使用的SID格式不兼容的确定,将SID帧从第一节点使用的SID格式转换为第二节点使用的SID格式。

    Ligands for &agr;-7 nicotinic acetylcholine receptors based on methyllcaconitine
    7.
    发明授权
    Ligands for &agr;-7 nicotinic acetylcholine receptors based on methyllcaconitine 失效
    用于基于甲基赖氨酸的α-7烟碱乙酰胆碱受体的配体

    公开(公告)号:US06416735B1

    公开(公告)日:2002-07-09

    申请号:US09435614

    申请日:1999-11-08

    IPC分类号: A61K5100

    CPC分类号: C07D221/24 A61K51/0455

    摘要: Ligands for nAChRs are provided based on various derivatives of methyllycaconitine (MLA) such as radiolabeled MLA, and MLA containing a fluorimetric marker group and their use in imaging for detection of Alzheimer's and other CNS diseases, and combinatorial assays for detection of compounds having affinity for nAChRs, as well as injectable compositions containing the same and kits for performing the imaging studies.

    摘要翻译: 用于nAChRs的配体是基于甲基绞肉碱(MLA)的各种衍生物(例如放射性标记的MLA)和含有荧光标记物组的MLA及其在成像中用于检测阿尔茨海默氏症和其他CNS疾病的组合提供的,以及用于检测具有亲和力的化合物的组合测定 nAChRs,以及含有其的可注射组合物和用于进行成像研究的试剂盒。

    Cocaine receptor binding ligands
    8.
    发明授权
    Cocaine receptor binding ligands 失效
    可卡因受体结合配体

    公开(公告)号:US5496953A

    公开(公告)日:1996-03-05

    申请号:US164576

    申请日:1993-12-10

    摘要: Novel compounds show high affinity for specific cocaine receptors in the brain, particularly dopamine transporter sites, and have the formula ##STR1## Wherein Y=CONRR.sub.2, R.sub.1 =hydrogen, C.sub.1-5 alkyl,X=H, C.sub.1-6 alkyl, C.sub.3-8 cycloalkyl, C.sub.1-4 alkoxy, C.sub.1-6 alkynyl, halogen, amino, acylamido,R and R.sup.2 may be saturated or unsaturated substituents of 1-6 carbon atoms, aromatic, or combine to form pyrrolidinyl, morpholinyl or piperidinyl moieties, andZ=H, I, Br, Cl, F, CN, CF.sub.3 NO.sub.2, N.sub.3, OR.sub.1, CO.sub.2 NH.sub.2, CO.sub.2 R.sub.1, C.sub.1-6 alkyl, NR.sub.4 R.sub.5, NHCOF.sub.5, NHCO.sub.2 R.sub.6,wherein R.sub.4 -R.sub.6 are each C.sub.1-6 alkyl.

    摘要翻译: 新型化合物对脑中特定的可卡因受体,特别是多巴胺转运蛋白位点表现出高亲和力,并且具有下式:其中Y = CONRR2,R1 =氢,C1-5烷基,X = H,C1-6烷基,C3- 8环烷基,C 1-4烷氧基,C 1-6炔基,卤素,氨基,酰基酰氨基,R和R 2可以是1-6个碳原子的饱和或不饱和取代基,芳族或结合形成吡咯烷基,吗啉基或哌啶基部分,Z = H,I,Br,Cl,F,CN,CF 3 NO 2,N 3,OR 1,CO 2 NH 2,CO 2 R 1,C 1-6烷基,NR 4 R 5,NHCOF 5,NHCO 2 R 6,其中R 4 -R 6各自为C 1-6烷基。

    Cocaine receptor binding ligands
    9.
    发明授权
    Cocaine receptor binding ligands 失效
    可卡因受体结合配体

    公开(公告)号:US5380848A

    公开(公告)日:1995-01-10

    申请号:US233723

    申请日:1994-04-26

    IPC分类号: A61K51/04 C07D451/02 C07F7/22

    摘要: Novel compounds show high affinity for specific cocaine receptors in the brain, particularly dopamine transporter sites, and have the formula ##STR1## Wherein Y=CH.sub.2 R.sub.3, CO.sub.2 R.sub.2 or ##STR2## R.sub.1 =hydrogen, C.sub.1-5 alkyl, R.sub.2 =hydrogen, C.sub.1-6 alkyl, C.sub.3-8 cycloalkyl, C.sub.1-4 alkoxy, C.sub.1-6 alkynyl, halogen or amine,R.sub.3 =OH, hydrogen, C.sub.1-6 alkyl, C.sub.3-8 cycloalkyl, C.sub.1-4 alkoxy, Cl Br, I, CN, NH.sub.2, NHC.sub.1-6 alkyl, NC.sub.1-6 alkyl, OCOC.sub.1-6 alkyl, OCOC.sub.1-3 alkylaryl,A=S, 0 or NHX=H, C.sub.1-6 alkyl, C.sub.3-8 cycloalkyl, C.sub.1-4 alkoxy, C.sub.1-6 alkynyl, halogen, amino, acylamido, andZ=H, I, Br, Cl, F, CN, CF.sub.3 NO.sub.2, N.sub.3, OR.sub.1, CO.sub.2 NH.sub.2, CO.sub.2 R.sub.1, C.sub.1-6 alkyl , NR.sub.4 R.sub.5, NHCOR.sub.5, NHCO.sub.2 R.sub.6,wherein R.sub.4 -R.sub.6 are each C.sub.1-6 alkyl.

    摘要翻译: 新型化合物对脑中特定的可卡因受体,特别是多巴胺转运蛋白位点表现出高亲和力,并且具有下式:其中Y = CH 2 R 3,CO 2 R 2或R 1 =氢,C 1-5烷基,R 2 =氢, C6烷基,C3-8环烷基,C1-4烷氧基,C1-6炔基,卤素或胺,R3 = OH,氢,C1-6烷基,C3-8环烷基,C1-4烷氧基,C1 Br,I,CN, NH 2,NHC 1-6烷基,NC 1-6烷基,OCOC 1-6烷基,OCOC 1-3烷基芳基,A = S,O或NH X = H,C 1-6烷基,C 3-8环烷基,C 1-4烷氧基, 6炔基,卤素,氨基,酰氨基和Z = H,I,Br,Cl,F,CN,CF 3 NO 2,N 3,OR 1,CO 2 NH 2,CO 2 R 1,C 1-6烷基,NR 4 R 5,NHCOR 5,NHCO 2 R 6, 各自为C 1-6烷基。

    Azabicyloalkane phenyl substituted alkane carboxylates, their
preparation and use as anticholinergic agents
    10.
    发明授权
    Azabicyloalkane phenyl substituted alkane carboxylates, their preparation and use as anticholinergic agents 失效
    氮杂环烷基苯基取代的烷烃羧酸盐,它们的制备和用作抗胆碱剂

    公开(公告)号:US4713391A

    公开(公告)日:1987-12-15

    申请号:US855857

    申请日:1986-04-17

    IPC分类号: C07D209/02

    CPC分类号: C07D209/02

    摘要: This invention relates to novel compositions, their preparation and the use thereof as anticholinergic agents in the treatment or prophylaxis of organophosphate or nerve gas poisoning in animals. These compositions and pharmaceutical preparations containing them in their free base form and acid addition salts thereof are represented by the formula ##STR1## wherein R represents lower alkyl groups containing 1 to 7 carbon atoms; R.sup.1 represents hydrogen, phenyl, cyclohexyl, and cyclopentyl; and R.sup.2 represents lower alkyl groups containing 1 to 7 carbon atoms, hydroxymethyl, and hydroxyl.

    摘要翻译: 本发明涉及新型组合物,其制备方法及其作为抗胆碱能药物用于治疗或预防动物中的有机磷酸盐或神经气体中毒的用途。 含有它们游离碱形式的这些组合物和药物制剂及其酸加成盐由下式表示:其中R代表含有1至7个碳原子的低级烷基; R1代表氢,苯基,环己基和环戊基; 并且R 2表示含有1至7个碳原子的低级烷基,羟甲基和羟基。