LISSENCEPHALY THERAPEUTIC AGENT
    11.
    发明申请
    LISSENCEPHALY THERAPEUTIC AGENT 有权
    LISSENCEPHALY治疗剂

    公开(公告)号:US20160250276A1

    公开(公告)日:2016-09-01

    申请号:US15074142

    申请日:2016-03-18

    Inventor: Shinji Hirotsune

    CPC classification number: A61K38/05 A61K9/0019 A61K9/0053 A61K31/00

    Abstract: An object of the present invention is to provide a medicament and method for treating lissencephaly patients. The present invention provides a lissencephaly therapeutic or preventive agent comprising a compound represented by the general formula (I): wherein R1 is lower alkyl substituted with lower alkoxy, lower alkyl substituted with a heterocyclic group, a heterocyclic group, or a group represented by the formula (IIa): wherein R4 is lower alkyl, R3 is lower alkylene, and m is an integer of 1 to 6; R2 is lower alkyl optionally substituted with phenyl; and R3 is lower alkyl optionally substituted with halogen, lower alkoxy, or phenyl; condensed polycyclic hydrocarbon; or hydrogen.

    Abstract translation: 本发明的一个目的是提供一种用于治疗失精症患者的药物和方法。 本发明提供一种包含由通式(I)表示的化合物的解散性治疗剂或预防剂:其中R 1为被低级烷氧基取代的低级烷基,被杂环基取代的低级烷基,杂环基或由 式(IIa):其中R 4为低级烷基,R 3为低级亚烷基,m为1至6的整数; R2是任选被苯基取代的低级烷基; 且R 3为任选被卤素,低级烷氧基或苯基取代的低级烷基; 稠合多环烃; 或氢气。

    THERAPEUTIC AGENT OR PROPHYLACTIC AGENT FOR DEMENTIA
    13.
    发明申请
    THERAPEUTIC AGENT OR PROPHYLACTIC AGENT FOR DEMENTIA 审中-公开
    治疗药物或治疗剂

    公开(公告)号:US20150183854A1

    公开(公告)日:2015-07-02

    申请号:US14403803

    申请日:2013-05-30

    Abstract: [SUMMARY][PURPOSE]The invention provides a novel therapeutic agent or prophylactic agent for cognitive disorders.[SOLUTION MEANS]The invention provides an antibody that participates in antigen-antibody reaction specifically with tau protein that has been phosphorylated in the vicinity of Ser413 of SEQ ID NO: 1, and a therapeutic agent or prophylactic agent for cognitive disorders comprising as an active ingredient a peptide that has been phosphorylated in the vicinity of Ser413.

    Abstract translation: 发明内容本发明提供了一种用于认知障碍的新型治疗剂或预防剂。 [解决方案]本发明提供参与抗体 - 抗体反应的抗体,特异性地与在SEQ ID NO:1的Ser413附近被磷酸化的tau蛋白,以及包含作为活性的认知障碍的治疗剂或预防剂 成分在Ser413附近被磷酸化的肽。

    NUCLEIC ACID MOLECULE FOR INHIBITING ACTIVITY OF RNAI MOLECULE
    14.
    发明申请
    NUCLEIC ACID MOLECULE FOR INHIBITING ACTIVITY OF RNAI MOLECULE 审中-公开
    用于抑制RNAI分子活性的核酸分子

    公开(公告)号:US20150011745A1

    公开(公告)日:2015-01-08

    申请号:US14358509

    申请日:2012-11-14

    Abstract: The purpose of the present invention is to develop and provide a nucleic acid molecule that can specifically and efficiently inhibit the activity of a target RNAi molecule and can be produced safely at a low cost. Provided is a nucleic acid molecule for inhibiting the activity of a target RNAi molecule. The nucleic acid molecule comprises a single-stranded nucleic acid moiety that contains one unmodified DNA region composed of a nucleotide sequence completely or sufficiently complementary to a nucleotide sequence of a functional strand having the activity in the target RNAi molecule and a double-stranded nucleic acid moiety to be linked to at least one of the 5′-end and the 3′-end of the single-stranded nucleic acid moiety.

    Abstract translation: 本发明的目的是开发和提供能够特异性且有效地抑制靶RNAi分子的活性并可以以低成本安全地制备的核酸分子。 提供了用于抑制靶RNAi分子的活性的核酸分子。 核酸分子包含单链核酸部分,其含有由与靶RNAi分子中具有活性的功能链的核苷酸序列完全或充分互补的核苷酸序列构成的一个未修饰的DNA区域和双链核酸 部分连接到单链核酸部分的5'末端和3'末端中的至少一个。

    DOUBLE-STRANDED NUCLEIC ACID MOLECULE FOR GENE EXPRESSION CONTROL
    15.
    发明申请
    DOUBLE-STRANDED NUCLEIC ACID MOLECULE FOR GENE EXPRESSION CONTROL 有权
    用于基因表达控制的双链核酸分子

    公开(公告)号:US20140315982A1

    公开(公告)日:2014-10-23

    申请号:US14355711

    申请日:2012-11-01

    Abstract: Provided are an improved double-stranded nucleic acid molecule involved in gene expression control mediated by a gene silencing mechanism, a method of producing the molecule, and a pharmaceutical composition comprising the double-stranded nucleic acid molecule. The double-stranded nucleic acid molecule for gene expression control comprises an antisense strand having a length of 18 to 28 nucleotides and a sense strand including a complementary moiety composed of a sequence sufficiently complementary to the antisense strand and a protruding single-stranded 5′-end moiety having a length of 2 to 100 nucleotides. The sense strand and the antisense strand form base pairs via the complementary moiety. The method produces such a double-stranded nucleic acid molecule, and the pharmaceutical composition contains such a double-stranded nucleic acid molecule as an active ingredient.

    Abstract translation: 提供涉及由基因沉默机制介导的基因表达控制的改进的双链核酸分子,产生该分子的方法和包含双链核酸分子的药物组合物。 用于基因表达控制的双链核酸分子包含长度为18至28个核苷酸的反义链和包含由与反义链足够互补的序列构成的互补部分的有义链和突出的单链5'- 末端部分具有2至100个核苷酸的长度。 有义链和反义链通过互补部分形成碱基对。 该方法产生这样的双链核酸分子,并且该药物组合物含有作为活性成分的这种双链核酸分子。

    METHOD OF PRODUCING VINYL CHLORIDE-BASED POLYMER
    17.
    发明申请
    METHOD OF PRODUCING VINYL CHLORIDE-BASED POLYMER 审中-公开
    制备基于氯乙烯的聚合物的方法

    公开(公告)号:US20100087608A1

    公开(公告)日:2010-04-08

    申请号:US12555247

    申请日:2009-09-08

    CPC classification number: C08F4/20 C08F4/68 C08F14/06 C08F2/02 C08F2/06

    Abstract: A method that is capable of producing a vinyl chloride-based polymer having excellent thermal stability without sacrificing productivity is provided. The method includes polymerizing a vinyl chloride-based monomer in the presence of a vanadium compound (A) represented by formula: Vi(═O)jZk (wherein i is an integer of 2 to 5, j represents 0 or 1, Z represents a ligand such as is an organic ligand that can bond to the vanadium atom via a hetero atom, and a plurality of ligands Z may be bonded together to form a ring that also includes the vanadium atom as a member of the ring, and k is an integer from 1 to 5), and in the presence of at least one aluminum compound (B).

    Abstract translation: 提供能够生产具有优异的热稳定性而不牺牲生产率的氯乙烯类聚合物的方法。 该方法包括在由式(Ⅵ))ZZ表示的钒化合物(A)存在下聚合氯乙烯基单体:其中i为2至5的整数,j表示0或1,Z表示 配体,例如可以通过杂原子键合到钒原子上的有机配体,并且多个配位体Z可以键合在一起形成还包括钒原子作为环的成员的环,k是 1至5的整数)和至少一种铝化合物(B)的存在下进行。

    Fatigue degree determination device, and fatigue degree determination method

    公开(公告)号:US10750988B2

    公开(公告)日:2020-08-25

    申请号:US16270794

    申请日:2019-02-08

    Abstract: A fatigue degree determination device includes a fatigue degree determination unit. A first biological heart rate is acquired while a user is awake and at rest, based on a biological heart rate measured from the user. A second biological heart rate is acquired while the user is sleeping, based on the biological heart rate measured from the user. The fatigue degree determination unit determines a fatigue degree of the user, based on information read out from a storage medium, the first biological heart rate and the second biological heart rate. The storage medium stores the information in which a degree of change of one biological heart rate relative to the other biological heart rate of a biological heart rate while a person is awake and at rest and a biological heart rate while the person is sleeping and a fatigue degree are associated with each other.

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