Process and intermediates to a tetrahydro-[1,8]- Naphthyridine
    21.
    发明授权
    Process and intermediates to a tetrahydro-[1,8]- Naphthyridine 失效
    四氢 - [1,8] - 萘啶的方法和中间体

    公开(公告)号:US06423845B1

    公开(公告)日:2002-07-23

    申请号:US09718139

    申请日:2000-11-21

    IPC分类号: C07D47104

    CPC分类号: C07D471/04 C07F9/4006

    摘要: A novel process is provided for the preparation of 3-(5,6,7,8-tetrahydro-[1,8]-naphthyridin-2-yl)-propylamine which is useful in the synthesis of &agr;v integrin receptor antagonists. Also provided are useful intermediates obtained from the process.

    摘要翻译: 提供了一种制备3-(5,6,7,8-四氢 - [1,8] - 萘啶-2-基) - 丙胺的新方法,其可用于合成αphav整联蛋白受体拮抗剂。 还提供了从该方法获得的有用的中间体。

    Material and method for colorimetric detection of small-molecule targets

    公开(公告)号:US10725058B2

    公开(公告)日:2020-07-28

    申请号:US16179336

    申请日:2018-11-02

    IPC分类号: G01N33/94 G01N33/52

    摘要: The subject invention provides methods, assays, and products for visual detection of small-molecule targets in a sample in both clinical and field settings within minutes. The subject invention is based on an aptamer sensor that reports the presence of small-molecule target via a sensitive colorimetric signal for naked-eye detection. The aptamer sensor is a CBSAzyme-based sensor having both target-mediated cooperative behavior of the CBSA and peroxidase-mimicking catalytic activity of DNAzyme. The subject invention also provides methods of using the CBSAzyme-based sensor.

    Highly Conductive Porous Paper-Based Metal Thin Films
    23.
    发明申请
    Highly Conductive Porous Paper-Based Metal Thin Films 审中-公开
    高导电性多孔纸基金属薄膜

    公开(公告)号:US20160329121A1

    公开(公告)日:2016-11-10

    申请号:US15146440

    申请日:2016-05-04

    IPC分类号: H01B1/04 H01B1/02

    CPC分类号: H01B1/04 H01B1/02

    摘要: A porous conductive thin film includes a layer of metal nanoparticles decorated on a layer of conductive carbon nanomaterials. The thin film can be supported by a porous support. The porous support can be a MCE paper upon which a metallic or semi-metallic single-walled carbon nanotube (SWCNT) layer is decorated with gold nanoparticles (AuNPs) or platinum nanoparticles (PtNPs). The thin film can be constructed by filtering a dispersion of SWCNTs onto MCE filter paper followed by the filtration of a citrate stabilized dispersion of AuNPs or PtNPs onto the SWCNT layer.

    摘要翻译: 多孔导电薄膜包括在导电碳纳米材料层上装饰的一层金属纳米颗粒。 薄膜可以由多孔载体支撑。 多孔载体可以是MCE纸,金属或半金属单壁碳纳米管(SWCNT)层用金纳米颗粒(AuNP)或铂纳米颗粒(PtNP)进行装饰。 可以通过将SWCNT的分散体过滤到MCE滤纸上,然后将AuNP或PtNP的柠檬酸盐稳定分散体过滤到SWCNT层上来构建薄膜。

    Signal-on architecture for electronic, oligonucleotide-based detectors
    24.
    发明授权
    Signal-on architecture for electronic, oligonucleotide-based detectors 有权
    基于寡核苷酸的电子探测器的信号架构

    公开(公告)号:US07803542B2

    公开(公告)日:2010-09-28

    申请号:US11564674

    申请日:2006-11-29

    IPC分类号: C12Q1/68 C12M1/34

    摘要: The invention provides a general “signal-on” architecture for oligonucleotide-based detectors that leads to order of magnitude increases in signal gain and sensitivity as compared to prior art detectors. The detectors of the invention rely on base pairing between two oligonucleotide strands, the sensor strand and the blocker strand. In the ‘off’ position of the detector, i.e., in the absence of target, the blocker strand and sensor strand are base-paired. As shown in FIG. 1, the formation of comparatively rigid, duplex DNA prevents the redox moiety from approaching the electrode surface, thereby suppressing Faradaic currents. When target is added to the system, the target displaces the blocker strand, binds to the sensor strand, liberating the end of the redox-labeled oligonucleotide to produce a flexible element. This, in turn, allows the redox moiety to collide with the electrode surface, producing a readily detectable Faradaic current.

    摘要翻译: 本发明提供了一种基于寡核苷酸的检测器的通用“信号启动”架构,与现有技术的检测器相比,信号增益和灵敏度的幅度增加了一个数量级。 本发明的检测器依赖于两个寡核苷酸链之间的碱基配对,传感器链和阻断链。 在检测器的“关闭”位置,即在没有靶的情况下,阻滞链和传感器链是碱基配对的。 如图所示。 1,相对刚性的双链DNA的形成防止氧化还原部分接近电极表面,从而抑制法拉第电流。 当将靶标加入到系统中时,靶标取代阻断链,结合传感器链,释放氧化还原标记的寡核苷酸的末端以产生柔性元件。 这又使得氧化还原部分与电极表面碰撞,产生易于检测的法拉第电流。

    SIGNAL-ON ARCHITECTURE FOR ELECTRONIC, OLIGONUCLEOTIDE-BASED DETECTORS
    26.
    发明申请
    SIGNAL-ON ARCHITECTURE FOR ELECTRONIC, OLIGONUCLEOTIDE-BASED DETECTORS 有权
    用于电子,基于寡核苷酸的检测器的信号建筑

    公开(公告)号:US20070154909A1

    公开(公告)日:2007-07-05

    申请号:US11564674

    申请日:2006-11-29

    IPC分类号: C12Q1/68 C12M1/34

    摘要: The invention provides a general “signal-on” architecture for oligonucleotide-based detectors that leads to order of magnitude increases in signal gain and sensitivity as compared to prior art detectors. The detectors of the invention rely on base pairing between two oligonucleotide strands, the sensor strand and the blocker strand. In the ‘off’ position of the detector, i.e., in the absence of target, the blocker strand and sensor strand are base-paired. As shown in FIG. 1, the formation of comparatively rigid, duplex DNA prevents the redox moiety from approaching the electrode surface, thereby suppressing Faradaic currents. When target is added to the system, the target displaces the blocker strand, binds to the sensor strand, liberating the end of the redox-labeled oligonucleotide to produce a flexible element. This, in turn, allows the redox moiety to collide with the electrode surface, producing a readily detectable Faradaic current.

    摘要翻译: 本发明提供了一种基于寡核苷酸的检测器的通用“信号启动”架构,与现有技术的检测器相比,信号增益和灵敏度的幅度增加了一个数量级。 本发明的检测器依赖于两个寡核苷酸链之间的碱基配对,传感器链和阻断链。 在检测器的“关闭”位置,即在没有靶的情况下,阻滞链和传感器链是碱基配对的。 如图所示。 1,相对刚性的双链DNA的形成防止氧化还原部分接近电极表面,从而抑制法拉第电流。 当将靶标加入到系统中时,靶标取代阻断链,结合传感器链,释放氧化还原标记的寡核苷酸的末端以产生柔性元件。 这又使得氧化还原部分与电极表面碰撞,产生易于检测的法拉第电流。

    Traceable Card Holder
    28.
    发明申请

    公开(公告)号:US20230136219A1

    公开(公告)日:2023-05-04

    申请号:US17512697

    申请日:2021-10-28

    IPC分类号: A45C1/06 A45C11/18 A45C13/18

    摘要: The invention discloses a traceable card holder, comprising a first clamp plate, a second clamp plate, an elastic band, top cover components, bottom cover components, a tracker and an elastic clamp; the first clamp plate is arranged oppositely to the second clamp plate, the elastic band is connected respectively with the first clamp plate and the second clamp plate, and the elastic band is used to drive the first clamp plate and the second clamp plate to move towards each other for clamping; the top cover components are detachably mounted on one side of the first clamp plate which is away from the second clamp plate, and the tracker is detachably mounted on the top cover components.

    Materials and methods for rapid and specific detection of synthetic cathinones

    公开(公告)号:US10683507B2

    公开(公告)日:2020-06-16

    申请号:US15900061

    申请日:2018-02-20

    申请人: Yi Xiao Haixiang Yu

    发明人: Yi Xiao Haixiang Yu

    摘要: The subject invention provides methods, assays, and products for detecting small molecules in a sample, in particular, in both clinical and field settings. The method for detecting a small-molecule target, preferably, a synthetic cathinone in a sample comprises contacting the sample with an aptamer-based sensor selective for the small-molecule target, and detecting the small-molecule target in the sample. Specifically, the method utilizes an aptamer-based sensor comprising a dye binding to a three-way junction binding domain of an aptamer. Binding of small-molecule target to the aptamer displaces the dye, generating a spectroscopic signal that can be used for detection of the small-molecule target and quantitative measurement of the target concentration.

    Materials and methods for rapid and sensitive detection of small-molecule targets

    公开(公告)号:US10550395B2

    公开(公告)日:2020-02-04

    申请号:US15947315

    申请日:2018-04-06

    申请人: Yi Xiao Haixiang Yu

    发明人: Yi Xiao Haixiang Yu

    摘要: The subject invention provides methods, assays and products for detecting small-molecules in a sample, in particular, in both clinical and field settings. The method for detecting a small-molecule target in a sample comprises providing a sample, contacting the sample with an aptamer-based sensor selective for the small-molecule target, and sensitively and rapidly detecting the small-molecule target in the sample. Specifically, the method utilizes EATR-amplified small-molecule sensors based on cooperative binding split aptamers (CBSAs).