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4-(3-methyl-butyl)-piperazin-1-ylamine | 56964-25-1

中文名称
——
中文别名
——
英文名称
4-(3-methyl-butyl)-piperazin-1-ylamine
英文别名
N-(3-methylbutyl)-N'-amino-piperazine;4-(3-Methylbutyl)piperazin-1-amine
4-(3-methyl-butyl)-piperazin-1-ylamine化学式
CAS
56964-25-1
化学式
C9H21N3
mdl
MFCD18810826
分子量
171.286
InChiKey
RYGFOOLIPWKURO-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):
    1
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    32.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • 作为反应物:
    描述:
    4-(3-methyl-butyl)-piperazin-1-ylamine 、 3-Formyl Rifamycin 以 四氢呋喃 为溶剂, 反应 0.25h, 生成
    参考文献:
    名称:
    Cricchio; Arioli; Lancini, Farmaco, Edizione Scientifica, 1975, vol. 30, # 8, p. 605 - 619
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    Benzamide derivatives
    摘要:
    一种具有以下结构的化合物及其药用盐:其中:R.sub.1是C.sub.1-6烷氧基;R.sub.2和R.sub.3相同或不同,可以是氢、卤素、CF.sub.3、羟基、C.sub.1-6烷氧基、C.sub.2-7酰基、氨基、氨基,氨基上取代一个或两个C.sub.1-6烷基、C.sub.2-10酰胺基、氨基磺酰基、氨基磺酰基上取代一个或两个C.sub.1-6烷基、C.sub.1-6烷基磺酰基或硝基;A是C.sub.2-4烷基基团;R.sub.5和R.sub.6连接在一起,与它们连接的--N--A--N--基团形成6、7或8元杂环环;R.sub.7是C.sub.1-6烷基,或芳基--C.sub.1-6烷基,其中烷基部分可选择地被C.sub.1-6烷基或芳基取代;具有有用的药理活性,例如调节胃肠功能和治疗呕吐。
    公开号:
    US04267175A1
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文献信息

  • [EN] USE OF PYRIDYLOXYPYRIMIDINES FOR TREATING INFECTIOUS DISEASES<br/>[FR] UTILISATION DE PYRIDYLOXYPYRIMIDINES DANS LE TRAITEMENT DE MALADIES INFECTIEUSES
    申请人:BP ASSET V INC
    公开号:WO2021097002A1
    公开(公告)日:2021-05-20
    Provided herein are methods of treating a viral infection in a subject in need thereof, comprising administering to the subject a compound of Formula (I), or a pharmaceutical composition comprising Formula (I). Further provided herein are methods for inhibiting the replication of a virus (e.g., a togaviridae family virus (e.g., an alphavirus (e.g., Chikungunya virus, eastern equine encephalitis, mayaro virus, Venezuelan equine encephalitis virus, western equine encephalitis)), a filoviradae family virus (e.g., a Marburgvirus (e.g., Marburg virus, Ravn virus)), human respiratory syncytial virus (i.e., human orthopneumo virus ), a flavivirus (e.g., dengue virus, Usutu virus, Japanese encephalitis virus, Powassan virus, yellow fever), a paramyxoviridae family virus (e.g., an orthoparamyxovirinae virus (e.g., a henipavims (e.g., Nipah virus), a morbillivims (e.g., measles morbillivirus))) in a subject in need thereof. Also provided herein are methods for treating and/or preventing a disorder due to a microbial toxin (e.g., due to P. aeruginosa exotoxin A, Clostridium septicum alpha-toxin, diphtheria toxin(s), shiga toxin(s)) in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of Formula (I), or a pharmaceutical composition comprising a compound of Formula (I) as described herein. Also provided are pharmaceutical compositions and kits including a compound of Formula (I) for use in the treatment and/or prevention of a viral infection in a subject in need thereof.
    在此提供了治疗需要的受试者病毒感染的方法,包括向受试者给予式(I)的化合物或包含式(I)的药物组合物。此外,在此提供了抑制病毒复制的方法(例如togaviridae家族病毒(例如alphavirus(例如Chikungunya病毒,东部马脑炎,Mayaro病毒,委内瑞拉马脑炎病毒,西部马脑炎) ,filoviradae家族病毒(例如Marburgvirus(例如Marburg病毒,Ravn病毒)),人类呼吸道合胞病毒(即人类正式肺炎病毒),黄病毒等),以及需要的受试者中的微生物毒素引起的疾病的治疗和/或预防方法(例如由P. aeruginosa外毒素A,Clostridium septicum alpha-toxin,白喉毒素,志贺毒素引起的疾病),包括向受试者给予式(I)的化合物的治疗有效量或包含此处所述的式(I)的药物组合物。还提供了用于治疗和/或预防需要的受试者病毒感染的式(I)的化合物的药物组合物和工具包。
  • US4267175A
    申请人:——
    公开号:US4267175A
    公开(公告)日:1981-05-12
  • [EN] FURIN INHIBITORS FOR TREATING CORONAVIRUS INFECTIONS<br/>[FR] INHIBITEURS DE FURINE POUR TRAITER DES INFECTIONS À CORONAVIRUS
    申请人:BP ASSET V INC
    公开号:WO2021202874A1
    公开(公告)日:2021-10-07
    Provided herein are methods, pharmaceutical compositions, and kits for treating and/or preventing a viral infection resulting from a coronaviridae family virus in a subject in need thereof, comprising administering to the subject a compound of Formula (I), or a pharmaceutical composition comprising a compound of Formula (I). Further provided herein are methods for inhibiting the viral entry into a cell of a coronaviridae family virus (e.g., alphacoronavirus (e.g., HCoV-NL63, HCoV-229E), betacoronavirus (e.g., SARS-CoV, SARS-CoV-2, MERS-CoV, HCoV-OC43, HCoV-HKUl)) in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising a compound of Formula (I) as described herein. Also provided are pharmaceutical compositions and kits comprising a compound of Formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment and/or prevention of a viral infection resulting from a coronaviridae family virus in a subject in need thereof.
  • Cricchio; Arioli; Lancini, Farmaco, Edizione Scientifica, 1975, vol. 30, # 8, p. 605 - 619
    作者:Cricchio、Arioli、Lancini
    DOI:——
    日期:——
  • Benzamide derivatives
    申请人:Beecham Group Limited
    公开号:US04267175A1
    公开(公告)日:1981-05-12
    A compound of the formula (I), and pharmaceutically acceptable salts thereof: ##STR1## wherein: R.sub.1 is a C.sub.1-6 alkoxy group; R.sub.2 and R.sub.3 are the same or different and are hydrogen, halogen, CF.sub.3, hydroxy, C.sub.1-6 alkoxy, C.sub.2-7 acyl, amino, amino substituted by one or two C.sub.1-6 alkyl groups, C.sub.2-10 acyl amino, aminosulphone, aminosulphone substituted by one or two C.sub.1-6 alkyl groups, C.sub.1-6 alkyl sulphone or nitro groups; and A is a C.sub.2-4 alkylene group; R.sub.5 and R.sub.6 are joined so that they form with the --N--A--N-- group to which they are attached, a 6, 7 or 8 membered heterocyclic ring; R.sub.7 is a C.sub.1-6 alkyl group, or an aryl --C.sub.1-6 akyl group in which the alkyl moiety is optionally substituted by a C.sub.1-6 alkyl or aryl group; have useful pharmacological activity, such as the ability to regulate the gastrointestinal function and to treat emesis.
    一种具有以下结构的化合物及其药用盐:其中:R.sub.1是C.sub.1-6烷氧基;R.sub.2和R.sub.3相同或不同,可以是氢、卤素、CF.sub.3、羟基、C.sub.1-6烷氧基、C.sub.2-7酰基、氨基、氨基,氨基上取代一个或两个C.sub.1-6烷基、C.sub.2-10酰胺基、氨基磺酰基、氨基磺酰基上取代一个或两个C.sub.1-6烷基、C.sub.1-6烷基磺酰基或硝基;A是C.sub.2-4烷基基团;R.sub.5和R.sub.6连接在一起,与它们连接的--N--A--N--基团形成6、7或8元杂环环;R.sub.7是C.sub.1-6烷基,或芳基--C.sub.1-6烷基,其中烷基部分可选择地被C.sub.1-6烷基或芳基取代;具有有用的药理活性,例如调节胃肠功能和治疗呕吐。
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