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2-[4-(3-methoxyphenyl)butyl]phenol

中文名称
——
中文别名
——
英文名称
2-[4-(3-methoxyphenyl)butyl]phenol
英文别名
——
2-[4-(3-methoxyphenyl)butyl]phenol化学式
CAS
——
化学式
C17H20O2
mdl
——
分子量
256.345
InChiKey
VTMAOKFGHJPQHN-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):
    4.8
  • 重原子数:
    19
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 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:
    描述:
    2-[4-(3-methoxyphenyl)butyl]phenol 在 lithium aluminium tetrahydride 、 三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 7.0h, 生成 4-{2-[4-(3-methoxyphenyl)butyl]phenoxy}-1-methylpiperidine
    参考文献:
    名称:
    [2-(.OMEGA.-Phenylalkyl)phenoxy]alkylamines: Synthesis and Dual Dopamine2 (D2) and 5-Hydroxytryptamine2 (5-HT2) Receptor Antagonistic Activities.
    摘要:
    一系列[2-(ω-苯基烷基)苯氧基]烷基胺被合成,并在体外检测了它们对5-羟色胺2 (5-HT2)和/或多巴胺2 (D2)受体的拮抗活性。[2-(4-苯基丁基)苯氧基]烷基胺显示出对5-HT2和D2受体的强烈抑制作用。特别是,[2-(4-苯基丁基)苯氧基]甲基哌啶衍生物,10b、10i和10q,表现出了强大的抑制作用。讨论了这一系列化合物的结构-活性关系。
    DOI:
    10.1248/cpb.46.639
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文献信息

  • [EN] COMPOSITIONS AND METHODS THEREOF<br/>[FR] COMPOSITIONS ET PROCÉDÉS ASSOCIÉS
    申请人:EXCIVA UG HAFTUNGSBESCHRAENKT
    公开号:WO2018039642A1
    公开(公告)日:2018-03-01
    Compounds of formula I, (I) or enantiomers thereof, metabolites thereof, derivatives thereof, deuterated derivatives thereof, halogenated derivatives thereof, prodrugs thereof, pharmaceutically acceptable salts thereof, N- oxides thereof, or a combination thereof, processes and intermediates for preparation thereof, compositions thereof, and uses thereof, are provided. Pharmaceutical compositions comprising a compound of formula I and a compound of Formula II: (IIa) (IIb) or enantiomers thereof, metabolites thereof, derivatives thereof, deuterated derivatives thereof, prodrugs thereof, pharmaceutically acceptable salts thereof, N-oxides thereof, or a combination thereof. Compositions and methods for improving the efficacy of DEX, or providing beneficial pharmacokinetic effects to DEX, comprising co-administering a compound of formula I or SARPO, and a compound of Formula II or DEX to a subject in need thereof, and dosage forms, drug delivery systems, methods of treatment thereof.
    提供具有公式I的化合物(I)或其对应异构体、代谢物、衍生物、氘化衍生物、卤化衍生物、前药、药用可接受盐、N-氧化物或其组合,以及它们的制备过程和中间体、组合物和使用方法。包含公式I化合物的药物组合物以及公式II的化合物(IIa) (IIb)或其对应异构体、代谢物、衍生物、氘化衍生物、前药、药用可接受盐、N-氧化物或其组合。包含共给予需要该物质的受试者公式I化合物或SARPO和公式II化合物或DEX的DEX效能改进或提供DEX有益药代动力学效果的组合物和方法,以及剂量形式、药物传递系统、治疗方法。
  • .alpha.-.omega.-diarylalkane compounds serotonin-2 receptor agonists
    申请人:Sankyo Company, Limited
    公开号:US05556864A1
    公开(公告)日:1996-09-17
    Compounds of formula (I): ##STR1## [wherein: R.sup.1 is aryl; R.sup.2 is hydrogen, alkyl, alkoxy, halogen or cyano; R.sup.3 is a group of formula --B--NR.sup.4 R.sup.5, where R.sup.4 and R.sup.5 are independently hydrogen, alkyl or substituted alkyl or R.sup.4 and R.sup.5, together with the nitrogen to which they are attached, form a heterocycle, and B is alkylene or a group of formula --CH.sub.2 CH(OR.sup.6)CH.sub.2 --, where R.sup.6 is hydrogen, alkanoyl, substituted alkanoyl or arylcarbonyl, or a group of formula --D--R.sup.7, where D is a single bond or alkylene and R.sup.7 is a heterocycle; and A is alkylene; and pharmaceutically acceptable salts and esters thereof] are useful for the treatment and prevention of circulatory diseases and psychosis.
    化合物的化学式(I):##STR1## [其中:R.sup.1是芳基;R.sup.2是氢、烷基、烷氧基、卤素或氰基;R.sup.3是化学式--B--NR.sup.4R.sup.5的基团,其中R.sup.4和R.sup.5独立地是氢、烷基或取代烷基或R.sup.4和R.sup.5与它们连接的氮一起形成杂环,B是烷基或化学式--CH.sub.2CH(OR.sup.6)CH.sub.2--的基团,其中R.sup.6是氢、烷酰基、取代烷酰基或芳基甲酰基,或化学式--D--R.sup.7的基团,其中D是单键或烷基且R.sup.7是杂环;A是烷基;以及其药学上可接受的盐和酯] 用于治疗和预防循环系统疾病和精神病。
  • Phenoxyalkylamines, -pyrrolidines and -piperidines for the treatment and prevention of circulatory diseases and psychosis
    申请人:SANKYO COMPANY LIMITED
    公开号:EP0600717A1
    公开(公告)日:1994-06-08
    Compounds of formula (I): [wherein: R¹ is aryl; R² is hydrogen, alkyl, alkoxy, halogen or cyano; R³ is a group of formula -B-NR⁴R⁵, where R⁴ and R⁵ are independently hydrogen, alkyl or substituted alkyl or R⁴ and R⁵, together with the nitrogen to which they are attached, form a heterocycle, and B is alkylene or a group of formula -CH₂CH(OR⁶ )CH₂-, where R⁶ is hydrogen, alkanoyl, substituted alkanoyl or arylcarbonyl, or a group of formula -D-R⁷, where D is a single bond or alkylene and R⁷ is a heterocycle; and A is alkylene; and pharmaceutically acceptable salts and esters thereof] are useful for the treatment and prevention of circulatory diseases and psychosis.
    式(I)的化合物:[其中:R¹为芳基;R²为氢、烷基、烷氧基、卤素或氰基;R³为式-B-NR⁴R⁵的基团,其中R⁴和R⁵独立地为氢、烷基或取代烷基,或者R⁴和R⁵与它们所连接的氮一起形成杂环,B为烷基或式-CH₂CH(OR⁶)CH₂-的基团,其中R⁶为氢、烷酰基、取代烷酰基或芳基羰基,或式-D-R⁷的基团,其中D为单键或烷基烯丙基,R⁷为杂环;且A为烷基;以及其药学上可接受的盐和酯]可用于治疗和预防循环系统疾病和精神病。
  • Use of alpha, omega-diarylalkane derivatives in the treatment and prevention of psychosis
    申请人:SANKYO COMPANY LIMITED
    公开号:EP0844000A1
    公开(公告)日:1998-05-27
    Compounds of formula (I): [wherein: R1 is aryl; R2 is hydrogen, alkyl, alkoxy, halogen or cyano; R3 is a group of formula -B-NR4R5, where R4 and R5 are independently hydrogen, alkyl or substituted alkyl or R4 and R5, together with the nitrogen to which they are attached, form a heterocycle, and B is alkylene or a group of formula -CH2CH(OR6)CH2-, where R6 is hydrogen, alkanoyl, substituted alkanoyl or arylcarbonyl, or a group of formula -D-R7, where D is a single bond or alkylene and R7 is a heterocycle; and A is alkylene; and pharmaceutically acceptable salts and esters thereof] are useful for the treatment and prevention of psychosis.
    式(I)化合物: 其中R1 是芳基;R2 是氢、烷基、烷氧基、卤素或氰基;R3 是式-B-NR4R5 的基团,其中 R4 和 R5 独立地是氢、烷基或取代的烷基,或 R4 和 R5 与它们所连接的氮一起构成杂环,B 是亚烷基或式-CH2CH(OR6)CH2-的基团,其中 R6 是氢、烷酰基、取代的烷酰基或芳羰基,或式-D-R7 的基团,其中 D 是单键或亚烷基,R7 是杂环;和 A 是亚烷基;及其药学上可接受的盐和酯]可用于治疗和预防精神病。
  • COMPOSITIONS AND METHODS THEREOF
    申请人:Exciva UG (Haftungsbeschränkt)
    公开号:EP3503879A1
    公开(公告)日:2019-07-03
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