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N,N-二甲基-6-(甲硫基)-1,3,5-三嗪-2,4-二胺 | 35610-09-4

中文名称
N,N-二甲基-6-(甲硫基)-1,3,5-三嗪-2,4-二胺
中文别名
——
英文名称
N2,N2-dimethyl-6-methylthio-1,3,5-triazine-2,4-diamine
英文别名
N,N-dimethyl-6-methylsulfanyl-[1,3,5]triazine-2,4-diamine;N2,N2-dimethyl-6-(methylthio)-1,3,5-triazine-2,4-diamine;2-N,2-N-dimethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine
N,N-二甲基-6-(甲硫基)-1,3,5-三嗪-2,4-二胺化学式
CAS
35610-09-4
化学式
C6H11N5S
mdl
——
分子量
185.253
InChiKey
BSVZMVMAYPPOBI-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

物化性质

  • 溶解度:
    24.3 [ug/mL]

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    93.2
  • 氢给体数:
    1
  • 氢受体数:
    6

安全信息

  • 海关编码:
    2933699090

SDS

SDS:bc219aa3c42ca98bdb6098f8702500a1
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反应信息

  • 作为反应物:
    描述:
    N,N-二甲基-6-(甲硫基)-1,3,5-三嗪-2,4-二胺间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 生成 N2,N2-dimethyl-6-methylsulfinyl-1,3,5-triazine-2,4-diamine
    参考文献:
    名称:
    [EN] 1,3,5-TRIAZINE-2,4,6-TRIAMINE COMPOUND OR PHARMACEUTICAL ACCEPTABLE SALT THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
    [FR] COMPOSÉ DE 1,3,5-TRIAZINE-2,4,6-TRIAMINE OU SON SEL PHARMACEUTIQUEMENT ACCEPTABLE, ET COMPOSITION PHARMACEUTIQUE LE COMPRENANT
    摘要:
    公开号:
    WO2009028891A3
  • 作为产物:
    描述:
    1,1-二甲基硫酸胍N-氰亚胺基-S,S-二硫代碳酸二甲酯potassium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 8.0h, 以54%的产率得到N,N-二甲基-6-(甲硫基)-1,3,5-三嗪-2,4-二胺
    参考文献:
    名称:
    [EN] 1,3,5-TRIAZINE-2,4,6-TRIAMINE COMPOUND OR PHARMACEUTICAL ACCEPTABLE SALT THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
    [FR] COMPOSÉ DE 1,3,5-TRIAZINE-2,4,6-TRIAMINE OU SON SEL PHARMACEUTIQUEMENT ACCEPTABLE, ET COMPOSITION PHARMACEUTIQUE LE COMPRENANT
    摘要:
    公开号:
    WO2009028891A3
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文献信息

  • [EN] 1,3,5-TRIAZINE-2,4,6-TRIAMINE COMPOUND OR PHARMACEUTICAL ACCEPTABLE SALT THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME<br/>[FR] COMPOSÉ DE 1,3,5-TRIAZINE-2,4,6-TRIAMINE OU SON SEL PHARMACEUTIQUEMENT ACCEPTABLE, ET COMPOSITION PHARMACEUTIQUE LE COMPRENANT
    申请人:HANALL PHARMACEUTICAL CO LTD
    公开号:WO2009028891A3
    公开(公告)日:2009-04-30
  • A novel metformin derivative, HL010183, inhibits proliferation and invasion of triple-negative breast cancer cells
    作者:Minsoo Koh、Jong-Cheol Lee、Changhee Min、Aree Moon
    DOI:10.1016/j.bmc.2013.02.015
    日期:2013.4
    Mounting evidence suggests that metformin (N,N-dimethylbiguanide), a widely prescribed drug for the treatment of type II diabetes, exerts an anti-tumor effect on several cancers including breast cancer. Breast cancer has been estimated as one of the most commonly diagnosed types of cancer among women. In particular, triple-negative breast cancers are associated with poor prognosis and metastatic growth. In the present study, we synthesized a novel metformin derivative 5 (HL010183) and metformin salts, 9a, 9b, and 9c (metformin gamma-aminobutyric acid (GABA) salt, metformin pregabalin salt and metformin gabapentin salt), which exerted more potent inhibitory effects on the proliferation and invasiveness of Hs578T triple-negative breast carcinoma cells than metformin. Importantly, 5 showed approximately 100-fold more potent effects compared to metformin. In a triple-negative breast cancer xenograft model, 5 showed a comparable degree of inhibitory effect on in vivo tumor growth at the 100 mg/kg dose to that of metformin at 500 mg/kg. Our results clearly demonstrate that 5 exerts a potent anti-tumor effect both in vitro and in vivo, paving the way for a strategy for treatment of triple-negative breast cancer. (C) 2013 Elsevier Ltd. All rights reserved.
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