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N-(3-morholinopropyl)-N-(8-(3-pyridin-4-ylthioureido)octyl)methanesulfonamide | 1258218-38-0

中文名称
——
中文别名
——
英文名称
N-(3-morholinopropyl)-N-(8-(3-pyridin-4-ylthioureido)octyl)methanesulfonamide
英文别名
1-[8-[Methylsulfonyl(3-morpholin-4-ylpropyl)amino]octyl]-3-pyridin-4-ylthiourea
N-(3-morholinopropyl)-N-(8-(3-pyridin-4-ylthioureido)octyl)methanesulfonamide化学式
CAS
1258218-38-0
化学式
C22H39N5O3S2
mdl
——
分子量
485.715
InChiKey
MGOFRPUXYWEADX-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):
    2.3
  • 重原子数:
    32
  • 可旋转键数:
    15
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    127
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • [EN] PYRIDINYL DERIVATIVES AS INHIBITORS OF ENZYME NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE<br/>[FR] DÉRIVÉS DE PYRIDINYLE UTILISÉS EN TANT QU'INHIBITEURS DE L'ENZYME NICOTINAMIDE PHOSPHORIBOSYLTRANSFÉRASE
    申请人:TOPOTARGET AS
    公开号:WO2010142735A1
    公开(公告)日:2010-12-16
    The present application discloses a compound of the formula (I) wherein Q is optionally substituted pyridyl; p is 0-6; Y is formulae (i), (ii) and (iii) where X is =O, =S and =N-CN, r is 1-12, R is -Z-A, Z is a single bond, -S(=O)2-, >P=O, >C=O, -C(=O)NH-, and -C(=S)NH-; and A is hydrogen, C1-12-alkyl, C3-12-cycloalkyl, - [CH2CH2O]1-10-(C1-6-alkyl), C1-12-alkenyl, aryl, heterocyclyl, and heteroaryl; B is a single bond, -NRN-, -S(=O)2- and -O-; wherein RN is selected from hydrogen, C1-12-alkyl, C3-12-cycloalkyl, -[CH2CH2O]1-10-(C1-6-alkyl), C1-12-alkenyl, aryl, heterocyclyl, and heteroaryl; s is 0-6; and Cy is aryl, cycloalkyl, heterocyclyl, and heteroaryl. The compounds are usefuld for use as a medicament for the treatment of a disease or a condition caused by an elevated level of nicotinamide phosphoribosyltransferase (NAMPRT).
    本申请公开了一种化合物,其化学式为(I),其中Q是可选择取代的吡啶基;p为0-6;Y是式(i)、(ii)和(iii),其中X为=O、=S和=N-CN,r为1-12,R为-Z-A,Z为单键,-S(=O)2-,>P=O,>C=O,-C(=O)NH-和-C(=S)NH-;A为氢、C1-12-烷基、C3-12-环烷基、-[CH2CH2O]1-10-(C1-6-烷基)、C1-12-烯基、芳基、杂环烷基和杂芳基;B为单键,-NRN-,-S(=O)2-和-O-;其中RN从氢、C1-12-烷基、C3-12-环烷基、-[CH2CH2O]1-10-(C1-6-烷基)、C1-12-烯基、芳基、杂环烷基和杂芳基中选择;s为0-6;Cy为芳基、环烷基、杂环烷基和杂芳基。这些化合物可用作治疗由烟酰胺磷酸核糖转移酶(NAMPRT)平升高引起的疾病或症状的药物。
  • PYRIDINYL DERIVATIVES AS INHIBITORS OF ENZYME NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE
    申请人:Christensen Mette K.
    公开号:US20120264755A1
    公开(公告)日:2012-10-18
    The present application discloses a compound of the formula (I) wherein Q is optionally substituted pyridyl; p is 0-6. Y is formulae (i), (ii) and (iii) where X is ═O, ═S and ═N—CN, r is 1-12, R is —Z-A, Z is a single bond, —S(═O) 2 —, >P═O, >C═O, —C(═O)NH—, and —C(═S)NH—; and A is hydrogen, C 1-12 -alkyl, C 3-12 -cycloalkyl, —[CH 2 CH 2 O] 1-10 —(C 1-6 -alkyl), C 1-12 -alkenyl, aryl, heterocyclyl, and heteroaryl; B is a single bond, —NR N —, —S(═O) 2 — and —O—; wherein R N is selected from hydrogen, C 1-12 -alkyl, C 3-12 -cycloalkyl, —[CH 2 CH 2 O] 1-10 —(C 1-6 -alkyl), C 1-12 -alkenyl, aryl, heterocyclyl, and heteroaryl; s is 0-6; and Cy is aryl, cycloalkyl, heterocyclyl, and heteroaryl. The compounds are useful for use as a medicament for the treatment of a disease or a condition caused by an elevated level of nicotinamide phosphoribosyltransferase (NAMPRT).
    本申请公开了一个式子(I)的化合物,其中Q是可选取代的吡啶基;p为0-6。Y为式(i),(ii)和(iii),其中X为═O,═S和═N-CN,r为1-12,R为-Z-A,Z为单键,-S(═O)2-,>P═O,>C═O,-C(═O)NH-和-C(═S)NH-;A为氢,C1-12-烷基,C3-12-环烷基,-[CH2CH2O]1-10-(C1-6-烷基),C1-12-烯基,芳基,杂环基和杂芳基;B为单键,-NRN-,-S(═O)2-和-O-;其中RN选择自氢,C1-12-烷基,C3-12-环烷基,-[CH2CH2O]1-10-(C1-6-烷基),C1-12-烯基,芳基,杂环基和杂芳基;s为0-6;Cy为芳基,环烷基,杂环基和杂芳基。这些化合物可用作治疗由尼克酰胺磷酸核糖转移酶(NAMPRT)平升高引起的疾病或病症的药物。
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