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7-methoxy-2-benzyl-1-methyl-β-carbolinium bromide | 1229021-13-9

中文名称
——
中文别名
——
英文名称
7-methoxy-2-benzyl-1-methyl-β-carbolinium bromide
英文别名
2-benzyl-7-methoxy-1-methyl-9H-pyrido[3,4-b]indol-2-ium;bromide
7-methoxy-2-benzyl-1-methyl-β-carbolinium bromide化学式
CAS
1229021-13-9
化学式
Br*C20H19N2O
mdl
——
分子量
383.288
InChiKey
LVAQTGYHDALGTF-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):
    0.98
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    28.9
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    7-methoxy-2-benzyl-1-methyl-β-carbolinium bromide 在 sodium tetrahydroborate 、 palladium on activated charcoal 、 氢气 作用下, 以 甲醇2,2,2-三氟乙醇 为溶剂, 反应 15.0h, 生成 四氢骆驼蓬碱
    参考文献:
    名称:
    ß-CARBOLINE, DIHYDRO-ß-CARBOLINE AND TETRAHYDRO-ß-CARBOLINE ALKALOID DERIVATIVES AND PREPARATION METHODS SAME AND USE IN ASPECTS OF PREVENTING AND TREATING PLANT VIRUSES, FUNGICIDES AND INSECTICIDES
    摘要:
    本发明涉及β-咔啉、二氢β-咔啉和四氢β-咔啉生物碱衍生物(I),以及其制备方法和在预防和治疗植物病毒、杀菌剂和杀虫剂方面的用途。本发明中的β-咔啉、二氢β-咔啉和四氢β-咔啉生物碱衍生物显示出特别出色的抗植物病毒活性,同时还具有杀菌和杀虫活性。
    公开号:
    US20160326166A1
  • 作为产物:
    描述:
    肉叶云香碱溴甲苯乙酸乙酯 为溶剂, 反应 12.0h, 以74%的产率得到7-methoxy-2-benzyl-1-methyl-β-carbolinium bromide
    参考文献:
    名称:
    ß-CARBOLINE, DIHYDRO-ß-CARBOLINE AND TETRAHYDRO-ß-CARBOLINE ALKALOID DERIVATIVES AND PREPARATION METHODS SAME AND USE IN ASPECTS OF PREVENTING AND TREATING PLANT VIRUSES, FUNGICIDES AND INSECTICIDES
    摘要:
    本发明涉及β-咔啉、二氢β-咔啉和四氢β-咔啉生物碱衍生物(I),以及其制备方法和在预防和治疗植物病毒、杀菌剂和杀虫剂方面的用途。本发明中的β-咔啉、二氢β-咔啉和四氢β-咔啉生物碱衍生物显示出特别出色的抗植物病毒活性,同时还具有杀菌和杀虫活性。
    公开号:
    US20160326166A1
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文献信息

  • Design, synthesis and 3D-QSAR of β-carboline derivatives as potent antitumor agents
    作者:Rihui Cao、Xiangdong Guan、Buxi Shi、Zhiyong Chen、Zhenhua Ren、Wenlie Peng、Huacan Song
    DOI:10.1016/j.ejmech.2010.02.036
    日期:2010.6
    In a continuing effort to develop novel beta-carbolines endowed with better pharmacological profiles, a series of beta-carboline derivatives were designed and synthesized based on the previously developed SARs. Cytotoxicities in vitro of these compounds against a panel of human tumor cell lines were also investigated. The results demonstrated that the N(2)-benzylated beta-carbolinium bromides 56-60 represented the most potent compounds with IC(50) values lower than 10 mu M. The application of 3D-QSAR to these compounds explored the structural basis for their biological activities. CoMFA (q(2) = 0.513, r(2) = 0.862) and CoMSIA (q(2) = 0.503, r(2) = 0.831) models were developed for a set of 47 beta-carbolines. The results indicated that the antitumor pharmacophore of these molecules were marked at position-1, -2, -3, -7 and -9 of beta-carboline ring.
  • Synthesis and Antiviral and Fungicidal Activity Evaluation of β-Carboline, Dihydro-β-carboline, Tetrahydro-β-carboline Alkaloids, and Their Derivatives
    作者:Hongjian Song、Yongxian Liu、Yuxiu Liu、Lizhong Wang、Qingmin Wang
    DOI:10.1021/jf404840x
    日期:2014.2.5
    Six known beta-carboline, dihydro-beta-carboline, and tetrahydro-beta-carboline alkaloids and a series of their derivatives were designed, synthesized, and evaluated for their anti-tobacco mosaic virus (TMV) and fungicidal activities for the first time. All of the alkaloids and some of their derivatives (compounds 3, 4, 14, and 19) exhibited higher anti-TMV activity than the commercial antiviral agent Ribavirin both in vitro and in vivo. Especially, the inactivation, curative, and protection activities of alkaloids Harmalan (62.3, 55.1, and 60.3% at 500 mu g/mL) and tetrahydroharmane (64.2, 57.2, and 59.5% at 500 mu g/mL) in vivo were much higher than those of Ribavirin (37.4, 36.2, and 38.5% at 500 mu g/mL). A new derivative, 14, with optimized physicochemical properties, obviously exhibited higher activities in vivo (50.4, 43.9, and 47.9% at 500 mu g/mL) than Ribavirin and other derivatives; therefore, 14 can be used as a new lead structure for the development of anti-TMV drugs. Moreover, most of these compounds exhibited good fungicidal activity against 14 kinds of fungi, especially compounds 4, 7, and 11.
  • ß-CARBOLINE, DIHYDRO-ß-CARBOLINE AND TETRAHYDRO-ß-CARBOLINE ALKALOID DERIVATIVES AND PREPARATION METHODS SAME AND USE IN ASPECTS OF PREVENTING AND TREATING PLANT VIRUSES, FUNGICIDES AND INSECTICIDES
    申请人:NANKAI UNIVERSITY
    公开号:US20160326166A1
    公开(公告)日:2016-11-10
    The present invention relates to β-carboline, dihydro-β-carboline and tetrahydro-β-carboline alkaloid derivatives (I) and a method for preparing same and the use in the aspects of preventing and treating plant viruses, fungicides and insecticides. For the meaning of each group in formula (I) see the description. The β-carboline, dihydro-β-carboline and tetrahydro-β-carboline alkaloid derivatives of the present invention show a particularly ourstanding anti-plant virus activity, and also have fungicidal and insecticidal activities.
    本发明涉及β-咔啉、二氢β-咔啉和四氢β-咔啉生物碱衍生物(I),以及其制备方法和在预防和治疗植物病毒、杀菌剂和杀虫剂方面的用途。本发明中的β-咔啉、二氢β-咔啉和四氢β-咔啉生物碱衍生物显示出特别出色的抗植物病毒活性,同时还具有杀菌和杀虫活性。
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