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5-phenyl-3,6-dihydro-[1,3,4]thiadiazin-2-one | 64273-23-0

中文名称
——
中文别名
——
英文名称
5-phenyl-3,6-dihydro-[1,3,4]thiadiazin-2-one
英文别名
5-Phenyl-6H-1,3,4-thiadiazin-2(3H)-on;5-Phenyl-3,6-dihydro-2H-1,3,4-thiadiazin-2-one;5-phenyl-3,6-dihydro-1,3,4-thiadiazin-2-one
5-phenyl-3,6-dihydro-[1,3,4]thiadiazin-2-one化学式
CAS
64273-23-0
化学式
C9H8N2OS
mdl
——
分子量
192.241
InChiKey
KSGZAADBLLQLIA-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    66.8
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:d1580be8c34e5d58d85c16499b594ced
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反应信息

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文献信息

  • 2-OXO-3-BENZYLBENZOXAZOL-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS MET KINASE INHIBITORS FOR THE TREATMENT OF TUMOURS
    申请人:Schadt Oliver
    公开号:US20100280030A1
    公开(公告)日:2010-11-04
    Compounds of the formula (I), in which R 1 , R 2 , R 3 , R 3′ , R 4 , R 4′ , E, E′, E″ and E′″ have the meanings indicated in Claim 1 , are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumours.
    式(I)中的化合物,其中R1,R2,R3,R3',R4,R4',E,E',E"和E'"的含义如权利要求书中所示,是酪氨酸激酶的抑制剂,特别是Met激酶的抑制剂,并可用于治疗肿瘤。
  • BENZOTHIAZOLONE DERIVATIVES
    申请人:Stieber Frank
    公开号:US20110269756A1
    公开(公告)日:2011-11-03
    Compounds of the formula I, in which R 1 , R 2 , R 3 , R 3′ , R 4 , R 4′ , E, E′, E″ and E′″ have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumours.
    式I中的化合物,其中R1、R2、R3、R3′、R4、R4′、E、E′、E″和E′″的含义如权利要求书1所示,是酪氨酸激酶的抑制剂,特别是Met激酶,并可用于治疗肿瘤等疾病。
  • Substituted 5-Phenyl-3,6-Dihydro-2-Oxo-6H-1,3,4-Thiadiazines
    申请人:Schadt Oliver
    公开号:US20080318936A1
    公开(公告)日:2008-12-25
    Compounds of the formula (I), in which R 1 , R 2 , m, Q and B have the meanings indicated in claim 1 , are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumours.
    式(I)中的化合物,其中R1、R2、m、Q和B具有权利要求1中指示的含义,是酪氨酸激酶的抑制剂,特别是Met激酶,并可用于治疗肿瘤。
  • Pharmaceutically active phenyl-thia-, oxa- or triazinones
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0080296A1
    公开(公告)日:1983-06-01
    Heterocyclic compounds of the formula wherein either X is -CR1R2and Y is -O-, -S- or-NR3-, wherein R1, R2 and R3, which may be the same of different, each is hydrogen or alkyl of up to 4 carbon atoms; or X is-O-, -S- or -NH- and Y is -CF1R2- wherein R1 and R2 have the meanings stated above; wherein either R4 is hydrogen, fluoro or chloro, or alkyl, alkenyl, halogenoalkyl, aminoalkyl, hydroxyalkyl, alkoxyalkyl or alkoxy each of up to 6 carbon atom, and R5, R6 and R7, which may be the same or different, each is hydrogen, fluoro, chloro, bromo or iodo, or alkyl, alkenyl, halogenoalkyl, aminoalkyl, hydroxyalkyl, alkoxyalkyl or alkoxy each of up to 6 carbon atoms, provided that R4, R5, R6 and R7 are not all hydrogen; or R4 is bromo and R5, R6 and R7 have the meanings stated above, provided that R5, R6and R7 are not all hydrogen; or R4 and R5 together, or R5 and R6 together, or R4 and R7 together, from the-CH=CH-CH=CH-group and the othertwo of R4, R5, R6 and R7 have the meanings stated above; processes for their manufacture and pharmaceutical compositions containing them. The compounds possess cardiotonic and/or antihypertensive activity.
    式中的杂环化合物 其中X为-CR1R2,Y为-O-、-S-或-NR3-,其中R1、R2和R3可以相同或不同,各自为氢或最多4个碳原子的烷基; 或 X 为-O-、-S-或-NH-,Y 为-CF1R2-,其中 R1 和 R2 具有上述含义; 其中,R4 是氢、,或烷基、烯基、卤代烷基、基烷基、羟基烷基、烷氧基烷基或烷氧基,每个烷基最多 6 个碳原子;R5、R6 和 R7(可以相同或不同)各自是氢、,或烷基、烯基、卤代烷基、基烷基、羟基烷基、烷氧基烷基或烷氧基,每个烷基最多 6 个碳原子,条件是 R4、R5、R6 和 R7 不全是氢; 或 R4 为,R5、R6 和 R7 具有上述含义,但 R5、R6 和 R7 并非都是氢; 或 R4 和 R5 一起,或 R5 和 R6 一起,或 R4 和 R7 一起,来自-CH=CH-CH=CH-基团,且 R4、R5、R6 和 R7 中的另外两个具有上述含义;它们的制造工艺和含有它们的药物组合物。这些化合物具有强心和/或抗高血压活性。
  • Thiadiazine, oxadiazine and triazine derivatives and pharmaceutical compositions containing them
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0086301A1
    公开(公告)日:1983-08-24
    Heterocyclic compounds of the formula: wherein either X is -CR1R2- and Y is -0-, -S- or -NHR3-, wherein R1, R2 and R3, which may be the same or different, each is hydrogen or alkyl of up to 4 carbon atoms; or X is -0-, -S- or -NH- and Y is -CR1R2- wherein R1 and R2 have the meanings stated above; wherein R4 and R5, which may be the same or different, each is hydrogen (but provided that R4 and R5 are not both hydrogen), or each is a group defined in claim 1 which is readily convertible into a carboxy group; processes for their manufacture; and pharmaceutical compositions containing them. The compounds possess cardiotonic and/or antihypertensive activity.
    式中X为-CR1R2-,Y为-0-、-S-或-NHR3-,其中R1、R2和R3可以相同或不同,各自为氢或最多4个碳原子的烷基;或X为-0-、-S-或-NH-,Y为-CR1R2-,其中R1和R2具有上述含义;其中R4和R5可以相同或不同,各自为氢(但条件是R4和R5不都是氢),或各自为权利要求1中定义的基团,该基团易于转化为羧基;其制造工艺;以及含有它们的药物组合物。 这些化合物具有强心和/或抗高血压活性。
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