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7-[(R)-1-hydroxy-4-methylpentan-2-ylamino]-5-[1-(pyridin-2-yl)ethylthio]thiazolo[4,5-d]pyrimidin-2(3H)-one | 1189040-14-9

中文名称
——
中文别名
——
英文名称
7-[(R)-1-hydroxy-4-methylpentan-2-ylamino]-5-[1-(pyridin-2-yl)ethylthio]thiazolo[4,5-d]pyrimidin-2(3H)-one
英文别名
7-[(R)-1-hydroxy-4-methylpentan-2-ylamino]-5-[(1R/S)-(pyridin-2-yl)ethylthio]thiazolo[4,5-d]pyrimidin-2(3H)-one;7-[(R)-1-hydroxy-4-methylpentan-2-ylamino]-5-[1-(pyridin-2-yl)ethylthio]thiazolo [4,5-d]pyrimidin-2(3H)-one;7-[[(2R)-1-hydroxy-4-methylpentan-2-yl]amino]-5-(1-pyridin-2-ylethylsulfanyl)-3H-[1,3]thiazolo[4,5-d]pyrimidin-2-one
7-[(R)-1-hydroxy-4-methylpentan-2-ylamino]-5-[1-(pyridin-2-yl)ethylthio]thiazolo[4,5-d]pyrimidin-2(3H)-one化学式
CAS
1189040-14-9
化学式
C18H23N5O2S2
mdl
——
分子量
405.545
InChiKey
NOAXPQKSDWDNIE-PIJUOVFKSA-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):
    3.4
  • 重原子数:
    27
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    151
  • 氢给体数:
    3
  • 氢受体数:
    8

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

反应信息

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文献信息

  • Methods of Inhibiting Metastasis from Cancer
    申请人:Salvino Joseph M.
    公开号:US20120141471A1
    公开(公告)日:2012-06-07
    The present invention includes compositions that are useful in preventing or treating metastasis in a subject diagnosed with cancer. The present invention also includes methods of preventing or treating metastasis in a subject diagnosed with cancer, wherein the method comprises administering to the subject in need thereof an effective amount of a pharmaceutical formulation comprising at least one pharmaceutically acceptable carrier and at least one CX 3 CR1 or fractalkine antagonist.
    本发明涉及一种用于预防或治疗被诊断为癌症的患者中的转移的组合物。本发明还包括一种用于预防或治疗被诊断为癌症的患者中的转移的方法,其中该方法包括向需要该药物的患者投与至少一种药用制剂,该制剂包括至少一种药用载体和至少一种CX3CR1或fractalkine拮抗剂的有效量。
  • 5,7-Disubstituted[1,3]Thiazolo[4,5-D]Pyrimidin-2(3H)-One Derivatives 258
    申请人:Dahlstrom Mikael
    公开号:US20090247555A1
    公开(公告)日:2009-10-01
    There are disclosed novel 5,7-disubstituted [1,3]thiazolo[4,5-d]pyrimidin-2(3H)-one derivatives of formula (I) wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , and R 7 are as defined in the specification, and pharmaceutically acceptable salts thereof, together with processes for their preparation, pharmaceutical compositions comprising them and their use in therapy. The compounds of formula (I) are CX 3 CR1 receptor antagonists and are thereby particularly useful in the treatment or prophylaxis of neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, is pulmonary diseases such as COPD, asthma or pain.
    本发明揭示了新型的5,7-二取代[1,3]噻唑并[4,5-d]嘧啶-2(3H)-酮衍生物(I)的公式,其中R1、R2、R3、R4、R5、R6和R7如规范中所定义,以及其药学上可接受的盐,以及它们的制备方法,包括它们在治疗中的药物组合物和使用。公式(I)化合物是CX3CR1受体拮抗剂,因此在治疗或预防神经退行性疾病、脱髓鞘性疾病、心血管和脑血管动脉粥样硬化性疾病、周围动脉疾病、类风湿性关节炎、肺部疾病如COPD、哮喘或疼痛中特别有用。
  • Compounds Useful for Inhibiting Metastasis from Cancer and Methods Using Same
    申请人:Drexel University College of Medicine Philadelphia Health & Education Corporation d/b/a
    公开号:US20130156761A1
    公开(公告)日:2013-06-20
    The present invention includes compositions that are useful in preventing or treating metastasis in a subject diagnosed with cancer. The present invention also includes methods of preventing or treating metastasis in a subject diagnosed with cancer, wherein the method comprises administering to the subject in need thereof an effective amount of a pharmaceutical formulation comprising at least one pharmaceutically acceptable carrier and at least one CX 3 CR1 or fractalkine antagonist.
    本发明涉及一种对已被诊断患有癌症的受试者预防或治疗转移的有用组合物。本发明还涉及一种预防或治疗已被诊断患有癌症的受试者的转移的方法,其中该方法包括向需要该药物的受试者施用至少一种药物制剂,该药物制剂包括至少一种药用载体和至少一种CX3CR1或fractalkine拮抗剂的有效量。
  • Compounds useful for inhibiting metastasis from cancer and methods using same
    申请人:Drexel University
    公开号:US10414771B2
    公开(公告)日:2019-09-17
    The present invention includes compositions that are useful in preventing or treating metastasis in a subject diagnosed with cancer. The present invention also includes methods of preventing or treating metastasis in a subject diagnosed with cancer, wherein the method comprises administering to the subject in need thereof an effective amount of a pharmaceutical formulation comprising at least one pharmaceutically acceptable carrier and at least one CX3CR1 or fractalkine antagonist.
    本发明包括可用于预防或治疗确诊癌症患者转移的组合物。本发明还包括预防或治疗被诊断患有癌症的受试者的转移的方法,其中该方法包括向需要该方法的受试者施用有效量的药物制剂,该药物制剂包含至少一种药学上可接受的载体和至少一种CX3CR1或fractalkine拮抗剂。
  • Phosphate and phosphonate derivatives of 7-amino-5-thio-thiazolo[4,5-d]pyrimidines and their use in treating conditions associated with elevated levels of CX3CR1 and/or CX3CL1
    申请人:KANCERA AB
    公开号:US11339183B2
    公开(公告)日:2022-05-24
    There is provided a compound of formula I, wherein R1, R2, Q1 and are as defined herein, which compounds are useful in the treatment of diseases and disorders associated with elevated levels of CX3CR1 and/or CX3CL1, in particular acute and/or chronic inflammation, eye diseases, lung diseases, skin diseases, joint and/or bone diseases, autoimmune diseases, cardiovascular diseases, metabolic diseases, brain diseases, neurodegenerative diseases, pain, cancer, liver diseases, kidney diseases, gastrointestinal diseases, human immunodeficiency virus and mood disorders.
    本发明提供了一种式 I 的化合物、 其中 R1、R2、Q1 和 如本文所定义,这些化合物可用于治疗与 CX3CR1 和/或 CX3CL1 平升高相关的疾病和失调,尤其是急性和/或慢性炎症、眼部疾病、肺部疾病、皮肤疾病、关节和/或骨骼疾病、自身免疫性疾病、心血管疾病、代谢性疾病、脑部疾病、神经退行性疾病、疼痛、癌症、肝脏疾病、肾脏疾病、胃肠道疾病、人类免疫缺陷病毒和情绪失调。
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