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1-(3,5-dimethoxyphenyl)-2-propylaminoethanol | 547770-09-2

中文名称
——
中文别名
——
英文名称
1-(3,5-dimethoxyphenyl)-2-propylaminoethanol
英文别名
1-(3,5-Dimethoxyphenyl)-2-(propylamino)ethanol
1-(3,5-dimethoxyphenyl)-2-propylaminoethanol化学式
CAS
547770-09-2
化学式
C13H21NO3
mdl
MFCD17533511
分子量
239.315
InChiKey
HCECSCMCDGLYFU-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):
    1.5
  • 重原子数:
    17
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.538
  • 拓扑面积:
    50.7
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • [EN] MORPHOLINE DERIVATIVES FOR USE AS DOPAMINE AGONISTS IN THE TREATMENT OF I.A. SEXUAL DYSFUNCTION<br/>[FR] DERIVES DE MORPHOLINE DESTINES A ETRE UTILISES COMME AGONISTES DE LA DOPAMINE DANS LE TRAITEMENT DE LA DYSFONCTION SEXUELLE I.A.
    申请人:PFIZER LTD
    公开号:WO2004052372A1
    公开(公告)日:2004-06-24
    The present invention provides for compounds of formula (I), (la) and (lb) Wherein: A is selected from C-X and N, B is selected from C-Y and N, R1 is selected from H and (C1-C6)alkyl R2 is selected from H and (C1-C6)alkyl, X is selected from H, HO, C(O)NH2, NH2 Y is selected from H HO,, NH2, Br, Cl and F Z is selected from H, HO, F, CONH2 and CN; And pharmaceutically acceptable salts, solvates and prodrugs thereof; With the provisos that: for a compound of formula (I), (la) or (lb), when A is C-X, B is C-Y, at least one of X, Y and Z must be OH; for a compound of formula (I), when A is C-X and B is C-Y, Y is H, Z is H, R1 is H and R2 is H, then X cannot be OH; these compounds are useful as dopamine agonists for the treatment of i.a. secual dysfunction.
    本发明提供了化合物的结构式(I)、(Ia)和(Ib),其中:A选自C-X和N,B选自C-Y和N,R1选自H和(C1-C6)烷基,R2选自H和(C1-C6)烷基,X选自H、HO、C(O)NH2、NH2,Y选自H、HO、NH2、Br、Cl和F,Z选自H、HO、F、CONH2和CN;以及其药学上可接受的盐、溶剂合物和前药;但是:对于结构式(I)、(Ia)或(Ib)的化合物,当A为C-X时,B为C-Y时,X、Y和Z中至少一个必须是OH;对于结构式(I)的化合物,当A为C-X且B为C-Y时,Y为H,Z为H,R1为H,R2为H,则X不能是OH;这些化合物可用作多巴胺激动剂,用于治疗性功能障碍等。
  • [EN] SELECTIVE DOPAMIN D3 RECEPTOR AGONISTS FOR THE TREATMENT OF SEXUAL DYSFUNCTION<br/>[FR] AGONISTES SELECTIFS DU RECEPTEUR DE LA DOPAMINE D3 POUR TRAITER LES TROUBLES D'ORDRE SEXUEL
    申请人:PFIZER LTD
    公开号:WO2003051370A1
    公开(公告)日:2003-06-26
    The use of a composition comprising a selective dopamine D3 receptor agonist, wherein said dopamine D3 receptor agonist is at least about 15-times more functionally selective for a dopamine D3 receptor as compared with a dopamine D2 receptor when measured using the same functional assay, in the preparation of a medicament for the treatment and/or prevention of sexual dysfunction.
    使用一种包含选择性多巴胺D3受体激动剂的组合物,其中所述的多巴胺D3受体激动剂在使用相同的功能性测定时,与多巴胺D2受体相比至少具有15倍的功能选择性,用于制备治疗和/或预防性功能障碍的药物。
  • Morpholine dopamine agonists
    申请人:Pfizer Inc.
    公开号:US20040259874A1
    公开(公告)日:2004-12-23
    The present invention provides for compounds of formula (I), (Ia) and (Ib) 1 Wherein: A is selected from C—X and N, B is selected from C—Y and N, R 1 is selected from H and (C 1 -C 6 )alkyl, R 2 is selected from H and (C 1 -C 6 )alkyl, X is selected from H, HO, C(O)NH 2 , NH 2 Y is selected from H, HO, NH 2 , Br, Cl and F Z is selected from H, HO, F, CONH 2 and CN; And pharmaceutically acceptable salts, solvates and prodrugs thereof; With the provisos that: for a compound of formula (I), (Ia) or (Ib), when A is C—X, B is C—Y, R 1 is H or (C 1 -C 6 )alkyl and R 2 is H or (C 1 -C 6 )alkyl at least one of X, Y and Z must be OH; for a compound of formula (I), when A is C—X and B is C—Y, Y is H, Z is H, R 1 is H and R 2 is H, then X cannot be OH; these compounds are useful as a medicament.
    本发明提供了式(I)、(Ia)和(Ib)的化合物,其中:A选择自C—X和N,B选择自C—Y和N,R1选择自H和(C1-C6)烷基,R2选择自H和(C1-C6)烷基,X选择自H、HO、C(O)NH2和NH2,Y选择自H、HO、NH2、Br、Cl和F,Z选择自H、HO、F、CONH2和CN;以及其药学上可接受的盐、溶剂和前药;但必须满足以下条件:对于式(I)、(Ia)或(Ib)的化合物,当A为C—X,B为C—Y,R1为H或(C1-C6)烷基,R2为H或(C1-C6)烷基时,X、Y和Z中至少有一个必须为OH;对于式(I)的化合物,当A为C—X,B为C—Y,Y为H,Z为H,R1为H,R2为H时,X不能为OH;这些化合物在药物方面有用。
  • Selective dopamin d3 receptor agonists for the treatment of sexual dysfunction
    申请人:Van der Graaf Hadewijn Pieter
    公开号:US20060052435A1
    公开(公告)日:2006-03-09
    The use of a composition comprising a selective dopamine D3 receptor agonist, wherein said dopamine D3 receptor agonist is at least about 15-times more functionally selective for a dopamine D3 receptor as compared with a dopamine D2 receptor when measured using the same functional assay, in the preparation of a medicament for the treatment and/or prevention of sexual dysfunction.
    使用包含选择性多巴胺D3受体激动剂的组合物,其中所述的多巴胺D3受体激动剂在使用相同的功能测定时,与多巴胺D2受体相比至少具有15倍的功能选择性,在制备治疗和/或预防性功能障碍的药物时使用。
  • Morpholine Dopamine Agonists
    申请人:Allerton Moria Norfor Charlotte
    公开号:US20060235016A1
    公开(公告)日:2006-10-19
    The present invention provides for compounds of formula (I), (Ia) and (Ib) Wherein: A is selected from C—X and N, B is selected from C—Y and N, R 1 is selected from H and (C 1 -C 6 )alkyl, R 2 is selected from H and (C 1 -C 6 )alkyl, X is selected from H, HO, C(O)NH 2 , NH 2 Y is selected from H, HO, NH 2 , Br, Cl and F Z is selected from H, HO F, CONH 2 and CN; And pharmaceutically acceptable salts, solvates and prodrugs thereof; With the provisos that: for a compound of formula (I), (Ia) or (Ib), when A is C—X, B is C—Y, R 1 is H or (C 1 -C 6 )alkyl and R 2 is H or (C 1 -C 6 )alkyl at least one of X, Y and Z must be OH; for a compound of formula (I), when A is C—X and B is C—Y, Y is H, Z is H, R 1 is H and R 2 is H, then X cannot be OH; these compounds are useful as a medicament.
    本发明提供了式(I)、(Ia)和(Ib)的化合物,其中:A选自C-X和N,B选自C-Y和N,R1选自H和(C1-C6)烷基,R2选自H和(C1-C6)烷基,X选自H、HO、C(O)NH2、NH2,Y选自H、HO、NH2、Br、Cl和F,Z选自H、HO、F、CONH2和CN;以及其药学上可接受的盐、溶剂和前药;但须注意:对于式(I)、(Ia)或(Ib)的化合物,当A为C-X,B为C-Y,R1为H或(C1-C6)烷基,R2为H或(C1-C6)烷基时,X、Y和Z中至少有一个必须为OH;对于式(I)的化合物,当A为C-X,B为C-Y,Y为H,Z为H,R1为H,R2为H时,X不能为OH。这些化合物有药用价值。
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