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(E)-4-(4-{1-ethyl-1-[3-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl) phenyl] propyl}-2-methylphenyl)-1,1,1-trifluoro-2-trifluoromethyl-3-buten-2-ol | 917022-89-0

中文名称
——
中文别名
——
英文名称
(E)-4-(4-{1-ethyl-1-[3-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl) phenyl] propyl}-2-methylphenyl)-1,1,1-trifluoro-2-trifluoromethyl-3-buten-2-ol
英文别名
(E)-4-(4-{1-ethyl-1-[3-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propyl}-2-methyl-phenyl)-1,1,1-trifluoro-2-trifluoromethyl-3-buten-2-ol;(E)-1,1,1-trifluoro-4-[2-methyl-4-[3-[3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pentan-3-yl]phenyl]-2-(trifluoromethyl)but-3-en-2-ol
(E)-4-(4-{1-ethyl-1-[3-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl) phenyl] propyl}-2-methylphenyl)-1,1,1-trifluoro-2-trifluoromethyl-3-buten-2-ol化学式
CAS
917022-89-0
化学式
C30H37BF6O3
mdl
——
分子量
570.423
InChiKey
CHQFFHSHNNMWQU-FOCLMDBBSA-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):
    7.58
  • 重原子数:
    40
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    9

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

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文献信息

  • VITAMIN-D-LIKE COMPOUNDS
    申请人:TAKAHASHI TADAKATSU
    公开号:US20110060146A1
    公开(公告)日:2011-03-10
    The present invention provides a compound represented by the following general formula (I): or a pharmaceutically acceptable salt thereof, a pharmaceutical composition containing such a compound, and the like. The compound or a pharmaceutically acceptable salt thereof, the pharmaceutical composition containing such a compound, or the like is useful as a medicine or the like for therapy of benign prostatic hyperplasia, cancer, osteoporosis, psoriasis, secondary hyperparathyroidism, chronic glomerulonephritis, lupus nephritis and/or diabetic nephropathy and the like.
    本发明提供了以下一般式(I)所代表的化合物或其药学上可接受的盐,含有这种化合物的制药组合物等。该化合物或其药学上可接受的盐,含有这种化合物的制药组合物等可用作治疗良性前列腺增生、癌症、骨质疏松症、银屑病、继发性甲状旁腺功能亢进症、慢性肾小球肾炎、狼疮性肾炎和/或糖尿病肾病等药物或类似物。
  • Vitamin D-like compound
    申请人:Chugai Seiyaku Kabushiki Kaisha
    公开号:US07935688B2
    公开(公告)日:2011-05-03
    The present invention provides a compound represented by the following general formula (I): or a pharmaceutically acceptable salt thereof, a pharmaceutical composition containing such a compound, and the like. The compound or a pharmaceutically acceptable salt thereof, the pharmaceutical composition containing such a compound, or the like is useful as a medicine or the like for therapy of benign prostatic hyperplasia, cancer, osteoporosis, psoriasis, secondary hyperparathyroidism, chronic glomerulonephritis, lupus nephritis and/or diabetic nephropathy and the like.
    本发明提供了一种由以下通式(I)表示的化合物或其药学上可接受的盐,含有该化合物的药物组合物等。该化合物或其药学上可接受的盐,含有该化合物的药物组合物等可用作治疗良性前列腺增生、癌症、骨质疏松症、银屑病、继发性甲状旁腺功能亢进症、慢性肾小球肾炎、狼疮性肾炎和/或糖尿病肾病等疾病的药物或类似物。
  • A series of nonsecosteroidal vitamin D receptor agonists for osteoporosis therapy
    作者:Hirotaka Kashiwagi、Yoshiyuki Ono、Masateru Ohta、Susumu Itoh、Fumihiko Ichikawa、Suguru Harada、Satoshi Takeda、Nobuo Sekiguchi、Masaki Ishigai、Tadakatsu Takahashi
    DOI:10.1016/j.bmc.2013.01.042
    日期:2013.4
    In an extension of our study on gamma hydroxy carboxylic acid analogs, we explored a series of nonsecosteroidal vitamin D receptor (VDR) agonists in which 1,3-diol of 1,25(OH)(2)D-3 had been replaced by aryl acetic acid. These analogs showed very potent activity in vitro compared with 1,25(OH)(2)D-3. An X-ray analysis of 8d showed that the inserted phenyl ring well mimicked the folded methylene linker of the gamma hydroxy carboxylic acid moiety but the carboxylic acid of 8d interacted with VDR in a different manner from gamma hydroxy carboxylic acids. Through our in vivo screening in an osteoporosis rat model using immature rats, we identified a potent active vitamin D-3 analog, compound 7e. In mature rats of the same model, compound 7e also showed good PK profiling and excellent ability to prevent bone mineral density loss without severe hypercalcemia. Our nonsecosteroidal VDR agonist 7e (CH5036249) could be a possible new drug candidate for treating osteoporosis in human. (C) 2013 Elsevier Ltd. All rights reserved.
  • VITAMIN D-LIKE COMPOUND
    申请人:CHUGAI SEIYAKU KABUSHIKI KAISHA
    公开号:EP1894911A1
    公开(公告)日:2008-03-05
    The present invention provides a compound represented by the following general formula (I): or a pharmaceutically acceptable salt thereof, a pharmaceutical composition containing such a compound, and the like. The compound or a pharmaceutically acceptable salt thereof, the pharmaceutical composition containing such a compound, or the like is useful as a medicine or the like for therapy of benign prostatic hyperplasia, cancer, osteoporosis, psoriasis, secondary hyperparathyroidism, chronic glomerulonephritis, lupus nephritis and/or diabetic nephropathy and the like.
    本发明提供了一种由下列通式(I)表示的化合物: 或其药用的可接受盐,包含该化合物的药物组合物等。该化合物或其药用的可接受盐,包含该化合物的药物组合物等,用作治疗良性前列腺增生、癌症、骨质疏松症、银屑病、继发性甲状旁腺功能亢进、慢性肾小球肾炎、狼疮性肾炎和/或糖尿病性肾病等的药物等。
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