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5-<3,5-dimethyl-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>phenyl>-2H-tetrazole | 126225-60-3

中文名称
——
中文别名
——
英文名称
5-<3,5-dimethyl-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>phenyl>-2H-tetrazole
英文别名
5-[3,5-Dimethyl-4-[[5-(3-methyl-5-isoxazolyl)pentyl]oxy]phenyl]-2H-tetrazole;5-[5-[2,6-dimethyl-4-(2H-tetrazol-5-yl)phenoxy]pentyl]-3-methyl-1,2-oxazole
5-<3,5-dimethyl-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>phenyl>-2H-tetrazole化学式
CAS
126225-60-3
化学式
C18H23N5O2
mdl
——
分子量
341.413
InChiKey
KDOYANOOPBXBLD-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):
    3.7
  • 重原子数:
    25
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    89.7
  • 氢给体数:
    1
  • 氢受体数:
    6

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Antipicornavirus activity of tetrazole analogs related to disoxaril
    摘要:
    A series of tetrazole analogues of Win 54954, a broad-spectrum antipicornavirus compound, has been synthesized to address the acid lability of the oxazoline ring of this series of compounds. The results of X-ray crystallography studies of several members of the oxazoline series bound to human rhinovirus type IA and 14 have been used to design compounds in the tetrazole series with a broad spectrum of activity. Compound 16b, which has a three-carbon linkage between the isoxazole and phenyl rings and a propyl chain extending from the isoxazole ring, exhibiting an MIC80 for 15 rhinovirus serotypes of 0.20 muM as compared to 0.40 muM for Win 54954. X-ray studies of 16b bound to human rhinovirus-14 show that the propyl side chain extends into a pore in the binding site with the possibility of hydrophobic interactions with a pocket formed by Leu106 and a portion of Ser107.
    DOI:
    10.1021/jm00074a004
  • 作为产物:
    参考文献:
    名称:
    Antipicornavirus activity of tetrazole analogs related to disoxaril
    摘要:
    A series of tetrazole analogues of Win 54954, a broad-spectrum antipicornavirus compound, has been synthesized to address the acid lability of the oxazoline ring of this series of compounds. The results of X-ray crystallography studies of several members of the oxazoline series bound to human rhinovirus type IA and 14 have been used to design compounds in the tetrazole series with a broad spectrum of activity. Compound 16b, which has a three-carbon linkage between the isoxazole and phenyl rings and a propyl chain extending from the isoxazole ring, exhibiting an MIC80 for 15 rhinovirus serotypes of 0.20 muM as compared to 0.40 muM for Win 54954. X-ray studies of 16b bound to human rhinovirus-14 show that the propyl side chain extends into a pore in the binding site with the possibility of hydrophobic interactions with a pocket formed by Leu106 and a portion of Ser107.
    DOI:
    10.1021/jm00074a004
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文献信息

  • Heterocyclic substituted-phenoxyalkylisoxazoles as antiviral useful
    申请人:Sterling Drug Inc.
    公开号:US04857539A1
    公开(公告)日:1989-08-15
    Compounds of the formula ##STR1## wherein: Y is an alkylene bridge of 3-9 carbon atoms; Z is N or HC; R is hydrogen or lower-alkyl of 1-5 carbon atoms, with the proviso that when Z is N, R is lower-alkyl; R.sub.1 and R.sub.2 are hydrogen, halogen, lower-alkyl, lower-alkoxy, nitro, lower-alkoxycarbonyl or trifluoromethyl; and Het is selected from specified heterocyclic groups, are useful and antiviral agents, particularly against picornaviruses, including numerous strains of rhinovirus.
    化合物的公式为##STR1##其中:Y是3-9个碳原子的烷基桥;Z是N或HC;R是氢或1-5个碳原子的低烷基,但当Z是N时,R是低烷基;R.sub.1和R.sub.2是氢、卤素、低烷基、低烷氧基、硝基、低烷氧羰基或三氟甲基;Het从指定的杂环基团中选择,对抗病毒剂,特别是对抗小RNA病毒,包括多种鼻病毒菌株。
  • Oxadiazolyl-phenoxyalkylisoxazoles and their use as antiviral agents
    申请人:STERLING WINTHROP INC.
    公开号:EP0413289A2
    公开(公告)日:1991-02-20
    Compounds of the formulas wherein: Y is an alkylene bridge of 3-9 carbon atoms; R′ is lower-alkyl or hydroxy-lower-alkyl of 1-5 carbon atoms; R₁ and R₂ are hydrogen, halogen, lower-alkyl, lower-alkoxy, nitro, lower-alkoxycarbonyl or trifluoromethyl; and R₈ is hydrogen or lower-alkyl of 1-5 carbon atoms, with the proviso that when R₈ is hydrogen R′ is hydroxy-­lower-alkyl, are useful as antiviral agents, particularly against picornaviruses, including numerous strains of rhinovirus.
    分子式如下的化合物 其中 Y 是 3-9 个碳原子的烯桥; R′ 是 1-5 个碳原子的低级烷基或羟基低级烷基; R₁ 和 R₂ 是氢、卤素、低级烷基、低级烷氧基、硝基、低级烷氧羰基或三氟甲基;以及 R₈ 是氢或 1-5 个碳原子的低级烷基,但当 R₈ 是氢时,R′ 是羟基-低级烷基、 可用作抗病毒剂,尤其是抗皮卡病毒,包括多种鼻病毒。
  • US4857539A
    申请人:——
    公开号:US4857539A
    公开(公告)日:1989-08-15
  • US5110821A
    申请人:——
    公开号:US5110821A
    公开(公告)日:1992-05-05
  • Antipicornavirus activity of tetrazole analogs related to disoxaril
    作者:Guy D. Diana、David Cutcliffe、Deborah L. Volkots、John P. Mallamo、Thomas R. Bailey、Niranjan Vescio、Richard C. Oglesby、Theodore J. Nitz、Joseph Wetzel
    DOI:10.1021/jm00074a004
    日期:1993.10
    A series of tetrazole analogues of Win 54954, a broad-spectrum antipicornavirus compound, has been synthesized to address the acid lability of the oxazoline ring of this series of compounds. The results of X-ray crystallography studies of several members of the oxazoline series bound to human rhinovirus type IA and 14 have been used to design compounds in the tetrazole series with a broad spectrum of activity. Compound 16b, which has a three-carbon linkage between the isoxazole and phenyl rings and a propyl chain extending from the isoxazole ring, exhibiting an MIC80 for 15 rhinovirus serotypes of 0.20 muM as compared to 0.40 muM for Win 54954. X-ray studies of 16b bound to human rhinovirus-14 show that the propyl side chain extends into a pore in the binding site with the possibility of hydrophobic interactions with a pocket formed by Leu106 and a portion of Ser107.
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