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3-[2-{[3-(diethylamino)propyl]amino}-8-(2,6-difluorophenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-5-fluoro-4-methylbenzoic acid | 911490-45-4

中文名称
——
中文别名
——
英文名称
3-[2-{[3-(diethylamino)propyl]amino}-8-(2,6-difluorophenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-5-fluoro-4-methylbenzoic acid
英文别名
3-[2-[3-(diethylamino)propylamino]-8-(2,6-difluorophenyl)-7-oxopyrido[2,3-d]pyrimidin-4-yl]-5-fluoro-4-methylbenzoic acid
3-[2-{[3-(diethylamino)propyl]amino}-8-(2,6-difluorophenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-5-fluoro-4-methylbenzoic acid化学式
CAS
911490-45-4
化学式
C28H28F3N5O3
mdl
——
分子量
539.557
InChiKey
MBDJVPCLBKVGPO-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):
    2.7
  • 重原子数:
    39
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    98.7
  • 氢给体数:
    2
  • 氢受体数:
    10

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

文献信息

  • Novel compounds
    申请人:Callahan F. James
    公开号:US20060235029A1
    公开(公告)日:2006-10-19
    Novel substituted 2,4,8-trisubstituted 8H-pyrido[2,3-d]pyrimidin-7-one containing compounds and compositions, and their use use in therapy as CSBP/RK/p38 kinase inhibitors.
    小说替代2,4,8-三取代8H-吡啶[2,3-d]嘧啶-7-酮含化合物和组合物,并用于治疗作为CSBP / RK / p38激酶抑制剂。
  • Novel Compounds
    申请人:Callahan James Francis
    公开号:US20090069318A1
    公开(公告)日:2009-03-12
    Novel substituted 2,4,8-trisubstituted 8H-pyrido[2,3-d]pyrimidin-7-one containing compounds and compositions, and their use in therapy as CSBP/RK/p38 kinase inhibitors.
    小说代替了2,4,8-三取代8H-吡啶[2,3-d]嘧啶-7-酮化合物和组合物,并且它们作为CSBP / RK / p38激酶抑制剂在治疗中使用。
  • Compounds
    申请人:Glaxo Group Limited
    公开号:US08207176B2
    公开(公告)日:2012-06-26
    The present invention is directed to novel substituted 2,4,8-trisubstituted 8H-pyrido[2,3-d]pyrimidin-7-one containing compounds, compositions, and use in therapy as CSBP/RK/p38 kinase inhibitors of Formulas (V) and (Va) wherein inter alia, G5 and G6 are nitrogen and CH, provided that only one of G5 or G6 is nitrogen and the other is CH; R1 is C(Z)N(R10′)(CR10R20)vRb, C(Z)O(CR10R20)vRb, N(R10′)C(Z)(CR10R20)vRb, N(R10′)C(Z)N(R10′)(CR10R20)vRb, or N(R10′)OC(Z)(CR10R20)vRb; R1′ is independently selected at each occurrence from halogen, C1-4 alkyl, halo-substituted-C1-4 alkyl, cyano, nitro, (CR10R20)v′NRdRd′, (CR10R20)v′C(O)R12, SR5, S(O)R5, S(O)2R5, or (CR10R20)v′OR13; Rb is hydrogen, C1-10 alkyl, C3-7 cycloalkyl, C3-7 cycloalkyl C1-10 alkyl, aryl, arylC1-10alkyl, heteroaryl, heteroarylC1-10 alkyl, heterocyclic, or heterocyclylC1-10 alkyl moiety, which moieties, excluding hydrogen, may all be optionally substituted; X is R2, OR2′, S(O)mR2′, (CH2)n′N(R10′)S(O)mR2′, (CH2)n′N(R10′)C(O)R2′, (CH2)n′NR4R14, (CH2)n′N(R2′)(R2″), or N(R10′)RhNH—C(═N—CN)NRqRq′; and R3 is a C1-10 alkyl, C3-7 cycloalkyl, C3-7 cycloalkyl C1-10 alkyl, aryl, arylC1-10 alkyl, heteroaryl, heteroarylC1-10 alkyl, heterocyclic or a heterocyclylC1-10 alkyl moiety, and wherein each of these moieties may be optionally substituted.
    本发明涉及一种新型的取代的2,4,8-三取代8H-吡啶[2,3-d]嘧啶-7-酮化合物、组合物和在治疗中用作CSBP/RK/p38激酶抑制剂的化合物,其化学式为(V)和(Va),其中,G5和G6是氮和CH,但只有G5或G6是氮,另一个是CH;R1是C(Z)N(R10′)(CR10R20)vRb,C(Z)O(CR10R20)vRb,N(R10′)C(Z)(CR10R20)vRb,N(R10′)C(Z)N(R10′)(CR10R20)vRb或N(R10′)OC(Z)(CR10R20)vRb;R1′在每次出现时独立选择自卤素、C1-4烷基、卤代C1-4烷基、氰基、硝基、(CR10R20)v′NRdRd′、(CR10R20)v′C(O)R12、SR5、S(O)R5、S(O)2R5或(CR10R20)v′OR13;Rb是氢、C1-10烷基、C3-7环烷基、C3-7环烷基C1-10烷基、芳基、芳基C1-10烷基、杂芳基、杂芳基C1-10烷基、杂环或杂环基C1-10烷基基团,这些基团(不包括氢)都可以选择性地被取代;X是R2、OR2′、S(O)mR2′、(CH2)n′N(R10′)S(O)mR2′、(CH2)n′N(R10′)C(O)R2′、(CH2)n′NR4R14、(CH2)n′N(R2′)(R2″)或N(R10′)RhNH—C(═N—CN)NRqRq′;而R3是C1-10烷基、C3-7环烷基、C3-7环烷基C1-10烷基、芳基、芳基C1-10烷基、杂芳基、杂芳基C1-10烷基、杂环或杂环基C1-10烷基基团,这些基团都可以选择性地被取代。
  • 7,8-dihydropyrido[2,3-d]pyrimidin-4-yl substituted compounds as inhibitors of p38 kinase
    申请人:Callahan James F.
    公开号:US08354416B2
    公开(公告)日:2013-01-15
    Novel substituted 2,4,8-trisubstituted 8H-pyrido[2,3-d]pyrimidin-7-one containing compounds and compositions, and their use in therapy as CSBP/RK/p38 kinase inhibitors.
    小说替代物2,4,8-三取代8H-吡啶[2,3-d]嘧啶-7-酮化合物和组合物,并且它们可以作为CSBP/RK/p38激酶抑制剂在治疗中使用。
  • Pyrimidopyridine compound used as a CSBP/RK/p38 modulator
    申请人:GLAXO GROUP LIMITED
    公开号:EP2447266A1
    公开(公告)日:2012-05-02
    Compound I, and compositions and use in therapy as CSBP/RK/p38 kinase inhibitor.
    作为 CSBP/RK/p38 激酶抑制剂的化合物 I 及其组合物和治疗用途。
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