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3-(4-fluorophenyl)-6-methoxy-2-(4-methoxyphenoxy)benzo[b]thiophene 1-oxide | 1607817-01-5

中文名称
——
中文别名
——
英文名称
3-(4-fluorophenyl)-6-methoxy-2-(4-methoxyphenoxy)benzo[b]thiophene 1-oxide
英文别名
3-(4-Fluorophenyl)-6-methoxy-2-(4-methoxyphenoxyl)benzo[b]thiophene 1-oxide;3-(4-fluorophenyl)-6-methoxy-2-(4-methoxyphenoxy)-1-benzothiophene 1-oxide
3-(4-fluorophenyl)-6-methoxy-2-(4-methoxyphenoxy)benzo[b]thiophene 1-oxide化学式
CAS
1607817-01-5
化学式
C22H17FO4S
mdl
——
分子量
396.439
InChiKey
SEXWJMMKNUMPKW-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):
    4.9
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    64
  • 氢给体数:
    0
  • 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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Selective Human Estrogen Receptor Partial Agonists (ShERPAs) for Tamoxifen-Resistant Breast Cancer
    摘要:
    Almost 70% of breast cancers are estrogen receptor alpha (ER alpha) positive. Tamoxifen, a selective estrogen receptor modulator (SERM), represents the standard of care for many patients; however, 30-50% develop resistance, underlining the need for alternative therapeutics. Paradoxically, agonists at ER alpha such as estradiol (E-2) have demonstrated clinical efficacy in patients with heavily treated breast cancer, although side effects in gynecological tissues are unacceptable. A drug that selectively mimics the actions of E-2 in breast cancer therapy but minimizes estrogenic effects in other tissues is a novel, therapeutic alternative. We hypothesized that a selective human estrogen receptor partial agonist (ShERPA) at ER alpha would provide such an agent. Novel benzothiophene derivatives with nanomolar potency in breast cancer cell cultures were designed. Several showed partial agonist activity, with potency of 0.8-76 nM, mimicking E-2 in inhibiting growth of tamoxifen-resistant breast cancer cell lines. Three ShERPAs were tested and validated in xenograft models of endocrine-independent and tamoxifen-resistant breast cancer, and in contrast to E-2, ShERPAs did not cause significant uterine growth.
    DOI:
    10.1021/acs.jmedchem.5b01276
  • 作为产物:
    参考文献:
    名称:
    [EN] COMPOSITIONS AND METHODS FOR TREATING ESTROGEN-RELATED MEDICAL DISORDERS
    [FR] COMPOSITIONS ET PROCÉDÉS DE TRAITEMENT DE TROUBLES MÉDICAUX ASSOCIÉS AUX ŒSTROGÈNES
    摘要:
    本文揭示了治疗与雌激素相关的医学疾病的方法。治疗方法可能包括向需要此类治疗的对象施用含有至少一种化合物的组合物,该化合物符合以下公式(I)或其药用可接受盐的治疗有效量。
    公开号:
    WO2014066692A1
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文献信息

  • Compositions and methods for treating estrogen-related medical disorders
    申请人:THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
    公开号:US09895348B2
    公开(公告)日:2018-02-20
    Disclosed herein are methods for treatment of estrogen-related medical disorders. The methods of treatment may comprise administering to a subject in need of such treatment a composition comprising a therapeutically effective amount of at least one compound of formula (I) or a pharmaceutically acceptable salt thereof.
    本文揭示了治疗与雌激素相关的医疗疾病的方法。治疗方法可能包括向需要此类治疗的受试者施用含有至少一种式(I)化合物或其药学上可接受的盐的治疗有效量的组合物。
  • COMPOSITIONS AND METHODS FOR TREATING ESTROGEN-RELATED MEDICAL DISORDERS
    申请人:THATCHER Gregory R.
    公开号:US20150284357A1
    公开(公告)日:2015-10-08
    Disclosed is a compound of formula (I). or a pharmaceutically acceptable salt thereof. Also disclosed are pharmaceutical compositions including the compound of formula (I) and methods of using the compound of formula (I).
    本发明揭示了一种式(I)的化合物或其药学上可接受的盐。还揭示了包括该式(I)化合物的药物组合物以及使用该式(I)化合物的方法。
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