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(2,4-diamino-3H-1,3-thiazol-2-yl)-phenylmethanone

中文名称
——
中文别名
——
英文名称
(2,4-diamino-3H-1,3-thiazol-2-yl)-phenylmethanone
英文别名
——
(2,4-diamino-3H-1,3-thiazol-2-yl)-phenylmethanone化学式
CAS
——
化学式
C10H11N3OS
mdl
——
分子量
221.28
InChiKey
ZCYIWRSJCICYHK-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):
    0.8
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    106
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • [EN] COMBINATIONS AND DOSING REGIMES TO TREAT RB-POSITIVE TUMORS<br/>[FR] COMBINAISONS ET RÉGIMES POSOLOGIQUES POUR TRAITER DES TUMEURS RB-POSITIVES
    申请人:G1 THERAPEUTICS INC
    公开号:WO2016040858A1
    公开(公告)日:2016-03-17
    This invention directed to methods for treating select RB-positive cancers and other Rb- positive abnormal cellular proliferative disorders using CDK4/6 inhibitors in specific dosing and combination or alternation regimes. In one aspect, treatments of select RB-positive cancers are disclosed using specific CDK4/6 inhibitors in combination or alternation with another chemotherapeutic, for example, an additional kinase inhibitor, PD-1 inhibitor, or BCL-2 inhibitor, or combination thereof.
    这项发明涉及使用特定剂量和组合或交替方案中的CDK4/6抑制剂治疗选择性RB阳性癌症和其他RB阳性异常细胞增殖紊乱疾病的方法。在一个方面,揭示了使用特定CDK4/6抑制剂与另一种化疗药物(例如,额外的激酶抑制剂、PD-1抑制剂或BCL-2抑制剂,或其组合)组合或交替治疗选择性RB阳性癌症。
  • [EN] TRANSIENT PROTECTION OF NORMAL CELLS DURING CHEMOTHERAPY<br/>[FR] PROTECTION TRANSITOIRE DE CELLULES NORMALES PENDANT UNE CHIMIOTHÉRAPIE
    申请人:G1 THERAPEUTICS INC
    公开号:WO2014144326A1
    公开(公告)日:2014-09-18
    This invention is in the area of improved compounds, compositions and methods of transiently protecting healthy cells, and in particular hematopoietic stem and progenitor cells (HSPC) as well as renal cells, from damage associated with DNA damaging chemotherapeutic agents. In one aspect, improved protection of healthy cells is disclosed using disclosed compounds that act as highly selective and short, transiently-acting cyclin-dependent kinase 4/6 (CDK 4/6) inhibitors when administered to subjects undergoing DNA damaging chemotherapeutic regimens for the treatment of proliferative disorders.
    该发明涉及改进化合物、组合物和方法的领域,用于短暂保护健康细胞,特别是造血干细胞和祖细胞(HSPC)以及肾细胞,免受与损伤有关的DNA损伤化疗药物。在一个方面,通过使用所述的化合物揭示了对健康细胞的改进保护,这些化合物在接受DNA损伤化疗方案治疗增殖性疾病的受试者时作为高度选择性和短暂作用的细胞周期依赖性激酶4/6(CDK 4/6)抑制剂。
  • [EN] TREATMENT OF RB-NEGATIVE TUMORS USING TOPOISOMERASE INHIBITORS IN COMBINATION WITH CYCLIN DEPENDENT KINASE 4/6 INHIBITORS<br/>[FR] TRAITEMENT DE TUMEURS RB-NÉGATIVES EN UTILISANT DES INHIBITEURS DE LA TOPOISOMÉRASE EN ASSOCIATION AVEC DES INHIBITEURS DES KINASES CYCLINE-DÉPENDANTES 4/6
    申请人:G1 THERAPEUTICS INC
    公开号:WO2016040848A1
    公开(公告)日:2016-03-17
    This invention is in the area of improved therapeutic combinations for and methods of treating selected retinoblastoma (Rb)-negative cancers and Rb-negative abnormal cellular proliferative disorders using particular topoisomerase inhibitors and specific cyclin-dependent kinase 4/6 (CDK4/6) inhibitors. In one aspect, the improved treatment of select Rb-negative cancers is disclosed using specific compounds disclosed herein in combination with a topoisomerase I inhibitor.
    这项发明涉及改进的治疗组合和方法,用于治疗选择性视网膜母细胞瘤(Rb)阴性癌症和Rb阴性异常细胞增殖障碍,使用特定的拓扑异构酶抑制剂和特定的细胞周期依赖性激酶4/6(CDK4/6)抑制剂。在一个方面,使用本文披露的特定化合物与拓扑异构酶I抑制剂结合,披露了对选择性Rb阴性癌症的改进治疗。
  • [EN] TRICYCLIC LACTAMS FOR USE IN THE PROTECTION OF NORMAL CELLS DURING CHEMOTHERAPY<br/>[FR] LACTAMES TRICYCLIQUES POUR UNE UTILISATION DANS LA PROTECTION DE CELLULES NORMALES LORS D'UNE CHIMIOTHÉRAPIE
    申请人:G1 THERAPEUTICS INC
    公开号:WO2015161287A1
    公开(公告)日:2015-10-22
    This invention is in the area of tricyclic lactam compounds, compositions and methods of protecting healthy cells, and in particular hematopoietic stem and progenitor cells (HSPC) as well as renal cells, from damage associated with DNA damaging chemotherapeutic agents. In one aspect, protection of healthy cells is disclosed using compounds that act as cyclin-dependent kinase 4/6 (CDK 4/6) inhibitors when administered to subjects undergoing DNA damaging chemotherapeutic regimens for the treatment of proliferative disorders.
    这项发明涉及三环内酰胺化合物领域,以及保护健康细胞的方法和组合物,特别是造血干细胞和祖细胞(HSPC)以及肾脏细胞,免受与DNA损伤化疗药物相关的损害。在一个方面,揭示了使用作为细胞周期依赖性激酶4/6(CDK 4/6)抑制剂的化合物来保护健康细胞,当这些化合物被用于接受DNA损伤化疗方案治疗增殖性疾病的患者时。
  • Tricyclic Lactams for Use in the Protection of Hematopoietic Stem and Progenitor Cells Against Ionizing Radiation
    申请人:G1 THERAPEUTICS, INC.
    公开号:US20150297606A1
    公开(公告)日:2015-10-22
    This invention is in the area of tricyclic lactam compounds and methods for protecting healthy cells, and in particular hematopoietic stem and progenitor cells (HSPC), from the damage associated with ionizing radiation (IR) exposure using selective radioprotectants.
    这项发明涉及三环内酰胺化合物和保护健康细胞的方法,特别是造血干细胞和祖细胞(HSPC),使用选择性辐射保护剂保护它们免受电离辐射(IR)暴露所带来的损伤。
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