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H-D-Leu-OH

中文名称
——
中文别名
——
英文名称
H-D-Leu-OH
英文别名
(3R)-3-amino-5-methylhexan-2-one
H-D-Leu-OH化学式
CAS
——
化学式
C7H15NO
mdl
——
分子量
129.202
InChiKey
RVCJZAGFTBLSSU-SSDOTTSWSA-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:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    43.1
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    光气H-D-Leu-OH四氢呋喃甲苯 为溶剂, 反应 1.33h, 以79%的产率得到D-Leu NCA
    参考文献:
    名称:
    BLOCK COPOLYMERS FOR STABLE MICELLES
    摘要:
    本发明涉及聚合物化学领域,更具体地说是涉及多区块共聚物以及包含相同的多区块共聚物胶束。本发明的组合物适用于药物输送应用。
    公开号:
    US20130280306A1
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文献信息

  • [EN] ARYL AMIDE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE L'ARYLAMIDE KINASE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2015006100A1
    公开(公告)日:2015-01-15
    The present disclosure is generally directed to compounds which can inhibit AAK1 (adaptor associated kinase 1), compositions comprising such compounds, and methods for inhibiting AAK1.
    本公开涉及一般可抑制AAK1(适配器相关激酶1)的化合物,包括这些化合物的组合物,以及抑制AAK1的方法。
  • DEEP RED FLUORESCENT PROBE
    申请人:The University of Tokyo
    公开号:US20200087326A1
    公开(公告)日:2020-03-19
    A near-infrared fluorescent probe has fluorescence in the near-infrared region. Like CaSiR-1, the probe has rhodamines as the fluorescent mother nucleus and accumulates in the cytoplasm. The probe makes it possible to visualize concentration fluctuations in metal ions, such as calcium ions, within the body. The fluorescent probe includes a compound represented by the following general formula or a salt of the compound:
    一个近红外荧光探针在近红外区域有荧光。像CaSiR-1一样,该探针以罗丹明作为荧光母核,并在细胞质中积累。该探针使得可视化体内金属离子,如钙离子的浓度波动成为可能。荧光探针包括由以下通用公式表示的化合物或该化合物的盐:
  • Aryl Substituted Indoles and Their Use as Blockers of Sodium Channels
    申请人:Kyle Donald J.
    公开号:US20130296281A1
    公开(公告)日:2013-11-07
    The invention relates to aryl and heteroaryl substituted compounds of Formula (I), and pharmaceutically acceptable salts, prodrugs, or solvates thereof, wherein G, R 1 , and Z 1 -Z 5 are defined as set forth in the specification. The invention is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of sodium channels. Compounds of the present invention are especially useful for treating pain.
    本发明涉及具有式(I)的芳基和杂芳基取代化合物,以及其药学上可接受的盐、前药或溶剂化物,其中G、R1和Z1-Z5如规范中所述。本发明还涉及利用式(I)的化合物治疗对钠通道阻滞有响应的疾病。本发明的化合物特别适用于治疗疼痛。
  • [EN] N4-HYDROXYCYTIDINE AND DERIVATIVES AND ANTI-VIRAL USES RELATED THERETO<br/>[FR] N4-HYDROXYCYTIDINE ET SES DÉRIVÉS ET UTILISATIONS ANTIVIRALES ASSOCIÉES
    申请人:UNIV EMORY
    公开号:WO2021159044A1
    公开(公告)日:2021-08-12
    This disclosure relates to certain N4-hydroxycytidine derivatives, pharmaceutical compositions, and methods related thereto. In certain embodiments, the disclosure relates to the treatment or prophylaxis of human coronavirus 2019-nCoV.
    这项披露涉及某些N4-羟基胞苷衍生物、药物组合物以及相关方法。在某些实施方式中,该披露涉及治疗或预防人类冠状病毒2019-nCoV。
  • Tamandarin analogs and fragments thereof and methods of making and using
    申请人:Joullie M. Madeleine
    公开号:US20070149446A1
    公开(公告)日:2007-06-28
    The present invention is directed to a compound of Formula I wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , W, X, Y, and Z are defined herein. The compounds of the present invention are useful as anticancer agents. Specifically, the compounds are useful for treating or preventing cancer and tumor growth. The present invention is also directed to compositions comprising a compound according to the above formula. The present invention is also directed to methods of using a compound according to the above formula.
    本发明涉及公式I中R1、R2、R3、R4、R5、R6、W、X、Y和Z所定义的化合物。本发明的化合物可用作抗癌剂。具体而言,这些化合物可用于治疗或预防癌症和肿瘤生长。本发明还涉及包括上述公式中化合物的组合物。本发明还涉及使用上述公式中化合物的方法。
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