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3,9-Dimethoxy-5,6-dihydrotetraphen-7-OL | 362689-32-5

中文名称
——
中文别名
——
英文名称
3,9-Dimethoxy-5,6-dihydrotetraphen-7-OL
英文别名
3,9-dimethoxy-5,6-dihydrobenzo[a]anthracen-7-ol
3,9-Dimethoxy-5,6-dihydrotetraphen-7-OL化学式
CAS
362689-32-5
化学式
C20H18O3
mdl
——
分子量
306.4
InChiKey
ONNZDKMXDZGECI-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):
    4.7
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

文献信息

  • Substituted 10-aryl-11h-benzo[b]fluourenes and 7-aryl-5, 6-dihydro-benzo[a]anthracenes for selective effects on estrogen receptors
    申请人:Loozen Hubert, Jan, Jozef
    公开号:US20050159405A1
    公开(公告)日:2005-07-21
    This invention provides a compound, or its possible salt, having the formula, wherein: R e and ′R e are OH, optionally independently etherified or esterified; Z is —CH 2 CH 2 — or —C(R 4 ,R 5 )—, wherein R 4 and R 5 are independently H, (1C-2C)alkyl or form together a spiro(3C-5C)cycloalkyl; R 1 is H, halogen, CF 3 , or (1C-4C)alkyl; R 2 and R 3 are independently H, halogen, —CF 3 , —OCF 3 , (1C-8C)alkyl, hydroxy, (1C-8C)alkyloxy, aryloxy, aryl(1C-8C)alkyl, halo(1C-8C)alkyl, —O(CH 2 ) m X, wherein X is halogen or phenyl and m=2-4; —O(CH 2 ) m NR a R b , —S(CH 2 ) m NR a R b or —(CH 2 ) m NR a R b , wherein m=2-4 and wherein R a , R b are independently (1C-8C)alkyl, (2C-8C)alkenyl, (2C-8C)alkynyl, or aryl, which alkyl, alkenyl and aryl can optionally be substituted with halogen, —CF 3 , —OCF 3 , —CN, —NO 2 , —OH, (1C-8C)alkoxy, aryloxy, carboxyl, (1C-8C)alkylthio, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl or halo(1C-8C)alkyl; or R a and R b form a 3-8 membered ring structure, optionally substituted with halogen, —CF 3 , —OCF 3 , —CN, —NO 2 , hydroxy, hydroxy(1C-4C)alkyl, (1C-8C)alkoxy, aryloxy, (1C-8C)alkylthio, carboxyl, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl, halo(1C-8C)alkyl.
    本发明提供了一种化合物或其可能的盐,其化学式为:其中:Re和′Re分别为OH,可选地独立地醚化或酯化;Z为—CH2CH2—或—C(R4,R5)—,其中R4和R5独立地为H,(1C-2C)烷基或形成一个spiro(3C-5C)环烷基;R1为H,卤素,CF3或(1C-4C)烷基;R2和R3独立地为H,卤素,—CF3,—OCF3,(1C-8C)烷基,羟基,(1C-8C)烷氧基,芳氧基,芳基(1C-8C)烷基,卤代(1C-8C)烷基,—O(CH2)mX,其中X为卤素或苯基,m=2-4;—O(CH2)mNRaRb,—S(CH2)mNRaRb或—(CH2)mNRaRb,其中m=2-4,且Ra,Rb独立地为(1C-8C)烷基,(2C-8C)烯基,(2C-8C)炔基或芳基,所述烷基、烯基和芳基可选地被卤素、—CF3、—OCF3、—CN、—NO2、—OH、(1C-8C)烷氧基、芳氧基、羧基、(1C-8C)烷硫基、羧酸盐、(1C-8C)烷基、芳基、芳基(1C-8C)烷基或卤代(1C-8C)烷基取代;或Ra和Rb形成一个3-8成员环结构,可选地被卤素、—CF3、—OCF3、—CN、—NO2、羟基、羟基(1C-4C)烷基、(1C-8C)烷氧基、芳氧基、(1C-8C)烷硫基、羧基、羧酸盐、(1C-8C)烷基、芳基、芳基(1C-8C)烷基或卤代(1C-8C)烷基取代。
  • 10-ARYL-11H-BENZO[B]FLUORENE DERIVATIVES AND ANALOGS FOR MEDICINAL USE
    申请人:——
    公开号:US20040059004A1
    公开(公告)日:2004-03-25
    The invention provides for a non-steroidal compound having the formula 1 wherein R e and ′R e are OH, optionally independently etherified or esterified; Z is —CH 2 — or —CH 2 CH 2 —; R 1 is H, halogen, CF 3 , or (1C-4C)alkyl; R 2 , R 3 and R 4 are independently H, halogen, —CF 3 , —OCF 3 , (1C-8C)Alkyl, hydroxy, (1C-8C)alkyloxy, aryloxy, aryl(1C-8C)alkyl, halo(1C-8C)alkyl, —O(CH 2 ) m X, wherein X is halogen or phenyl and m=2-4; —O(CH 2 ) m NR a R b , —S(CH 2 ) m NR a R b or —(CH 2 ) m NR a R b , wherein m=2-4 and R a , R b are independently (1C-8C)alkyl, (2C-8C)alkenyl, (2C-8C)alkynyl, or aryl, optionally substituted with halogen, —CF 3 , —OCF 3 , —CN, —NO 2 , —OH, (1C-8C)alkoxy, aryloxy, carboxyl, (1C-8C)alkylthio, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl, halo(1C-8C)alkyl or R a and R b form a 3-8 membered ring structure, optionally substituted with halogen, —CF 3 , —OCF 3 , —CN, —NO 2 , hydroxy, hydroxy(1C-4C)alkyl, (1C-8C)alkoxy, aryloxy, (1C-8C)alkylthio, carboxyl, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl, halo(1C-8C)alkyl. The compounds can be used for the preparation of a medicine, in particular for use in estrogen-receptor-related treatments.
    本发明提供了一种非甾体化合物,其化学式为1,其中Re和′Re为OH,可选独立醚化或酯化;Z为—CH2—或—CH2CH2—;R1为H,卤素,CF3或(1C-4C)烷基;R2、R3和R4独立地为H,卤素,—CF3,—OCF3,(1C-8C)烷基,羟基,(1C-8C)烷氧基,芳氧基,芳基(1C-8C)烷基,卤代(1C-8C)烷基,—O(CH2)mX,其中X为卤素或苯基,m=2-4;—O(CH2)mNRaRb,—S(CH2)mNRaRb或—(CH2)mNRaRb,其中m=2-4,Ra和Rb独立地为(1C-8C)烷基,(2C-8C)烯基,(2C-8C)炔基或芳基,可选用卤素,—CF3,—OCF3,—CN,—NO2,—OH,(1C-8C)烷氧基,芳氧基,羟基(1C-4C)烷基,(1C-8C)烷硫基,羧基,羧酸盐,(1C-8C)烷基,芳基,芳基(1C-8C)烷基,卤代(1C-8C)烷基或Ra和Rb形成3-8成员环结构,可选用卤素,—CF3,—OCF3,—CN,—NO2,羟基,羟基(1C-4C)烷基,(1C-8C)烷氧基,芳氧基,(1C-8C)烷硫基,羧基,羧酸盐,(1C-8C)烷基,芳基,芳基(1C-8C)烷基,卤代(1C-8C)烷基。这些化合物可用于制备药物,特别是用于雌激素受体相关治疗。
  • 10-ARYL-11H-BENZO[B]FLUORENE DERIVATIVES AND ANALOGS AS ESTROGENIC COMPOUNDS
    申请人:Akzo Nobel N.V.
    公开号:EP1313700B1
    公开(公告)日:2005-11-09
  • SUBSTITUTED 10-ARYL-11H-BENZO¬B|FLUORENES FOR SELECTIVE EFFECTS ON ESTROGEN RECEPTORS
    申请人:Akzo Nobel N.V.
    公开号:EP1478613B1
    公开(公告)日:2006-05-24
  • US6756375B2
    申请人:——
    公开号:US6756375B2
    公开(公告)日:2004-06-29
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