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5,5-dimethyl-2-(3-(naphthalen-2-ylmethyl)morpholino)-5,6-dihydrobenzo[d]thiazol-7(4H)-one | 913716-74-2

中文名称
——
中文别名
——
英文名称
5,5-dimethyl-2-(3-(naphthalen-2-ylmethyl)morpholino)-5,6-dihydrobenzo[d]thiazol-7(4H)-one
英文别名
5,5-dimethyl-2-[3-(naphthalen-2-ylmethyl)morpholin-4-yl]-4,6-dihydro-1,3-benzothiazol-7-one
5,5-dimethyl-2-(3-(naphthalen-2-ylmethyl)morpholino)-5,6-dihydrobenzo[d]thiazol-7(4H)-one化学式
CAS
913716-74-2
化学式
C24H26N2O2S
mdl
——
分子量
406.549
InChiKey
VEYMNDZFLDNZST-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):
    5.6
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    70.7
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • 作为产物:
    描述:
    2-溴-5,5-二甲基-5,6-二氢-4H-苯并噻唑-7-酮3-(1-naphthylmethyl)morpholineN,N-二异丙基乙胺 作用下, 以 异丙醇 为溶剂, 以83%的产率得到5,5-dimethyl-2-(3-(naphthalen-2-ylmethyl)morpholino)-5,6-dihydrobenzo[d]thiazol-7(4H)-one
    参考文献:
    名称:
    4-(1,3-Thiazol-2-yl)morpholine derivatives as inhibitors of phosphoinositide 3-kinase
    摘要:
    4-(1,3-Thiazol-2-yl)morpholine derivatives have been identified as potent and selective inhibitors of phosphoinositide 3-kinase. The SAR data of selected examples are presented and the in vivo pro. ling of compound 18 is shown to demonstrate the utility of this class of compounds in xenograft models of tumor growth. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.06.076
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文献信息

  • Fused Thiazole Derivatives as Kinase Inhibitors
    申请人:Alexander Rikki Peter
    公开号:US20080306060A1
    公开(公告)日:2008-12-11
    A series of 5,6-dihydro-1,3-benzothiazol-7(4H)-one derivatives, and analogues thereof, which are substituted in the 2-position by an optionally substituted morpholin-4-yl moiety, being selective inhibitors of PD kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.
    一系列取代在2位位置具有可选取代的morpholin-4-yl基团的5,6-二氢-1,3-苯并噻唑-7(4H)-酮衍生物及其类似物,是选择性PD激酶酶抑制剂,在医学上具有益处,例如在治疗炎症、自身免疫、心血管、神经退行性、代谢、肿瘤、疼痛或眼科疾病方面。
  • FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS
    申请人:UCB Pharma, S.A.
    公开号:EP1881827B1
    公开(公告)日:2011-09-28
  • US7888344B2
    申请人:——
    公开号:US7888344B2
    公开(公告)日:2011-02-15
  • 4-(1,3-Thiazol-2-yl)morpholine derivatives as inhibitors of phosphoinositide 3-kinase
    作者:Rikki Alexander、Ahrani Balasundaram、Mark Batchelor、Daniel Brookings、Karen Crépy、Tom Crabbe、Marie-France Deltent、Frank Driessens、Andrew Gill、Sue Harris、Gillian Hutchinson、Claire Kulisa、Mark Merriman、Prakash Mistry、Ted Parton、James Turner、Ian Whitcombe、Sara Wright
    DOI:10.1016/j.bmcl.2008.06.076
    日期:2008.8
    4-(1,3-Thiazol-2-yl)morpholine derivatives have been identified as potent and selective inhibitors of phosphoinositide 3-kinase. The SAR data of selected examples are presented and the in vivo pro. ling of compound 18 is shown to demonstrate the utility of this class of compounds in xenograft models of tumor growth. (c) 2008 Elsevier Ltd. All rights reserved.
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