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3-methyl-1,3-octandiol | 853999-97-0

中文名称
——
中文别名
——
英文名称
3-methyl-1,3-octandiol
英文别名
3-methyloctane-1,3-diol
3-methyl-1,3-octandiol化学式
CAS
853999-97-0
化学式
C9H20O2
mdl
——
分子量
160.257
InChiKey
MOAVOADAHLJVLU-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):
    1.8
  • 重原子数:
    11
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    3-methyl-1,3-octandiol四丁基溴化铵间氯过氧苯甲酸 、 sodium hydroxide 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 4.5h, 生成 3-methyl-1-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]octan-3-ol
    参考文献:
    名称:
    Synthesis and evaluation of a potent, well-balanced EP 2 /EP 3 dual agonist
    摘要:
    A highly potent and well-balanced dual agonist for the EP2 and EP3 receptors is described. Optimization of the lead compound was accomplished in consideration of the relative agonist activity against each EP subtype receptor and the pharmacokinetic profile. As the result, 2-[(2-{(1R,2R)-2-[(1E,4S)-5-cyclopentyl-4-hydroxy-4-methyl-1-penten-1-yl]-5-oxocyclopentyl}eth-yl)thio]-1,3-thiazole-4-carboxylic acid (10) showed excellent potency (human EC50 EP2 = 1.1 nM, EP3 = 1.0 nM) with acceptable selectivity over the EP1 and EP4 subtypes (> 2000-fold). Further fine-tuning of compound 10 led to identification of ONO-8055 as a clinical candidate. ONO-8055 was effective at an extremely low dose (0.01 mg/kg, po, bid) in rats, and dose-dependently improved voiding dysfunction in a monkey model of underactive bladder (UAB). ONO-8055 is expected to be a novel and highly promising drug for UAB. (C) 2017 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2017.11.035
  • 作为产物:
    描述:
    3-羟基-3-甲基辛酸乙酯 在 lithium aluminium tetrahydride 、 盐酸 作用下, 以 四氢呋喃乙酸乙酯 为溶剂, 反应 0.58h, 生成 3-methyl-1,3-octandiol
    参考文献:
    名称:
    EP1707208
    摘要:
    公开号:
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文献信息

  • Blood flow promoters for cauda equina tissues
    申请人:Ohmoto Kazuyuki
    公开号:US20070129327A1
    公开(公告)日:2007-06-07
    It is intended to provide highly safe and efficacious blood flow promoters for cauda equina tissues. Among prostaglandin-like compounds having a weak hypotensive effect, compounds having an effect of promoting the blood flow in cauda equina tissues (excluding limaprost) are useful as highly safe blood flow promoters for cauda equina tissues and, therefore, are efficacious in preventing and/or treating lumbar pain, lower limb pain, lower limb palsy, intermittent claudication, vesicorectal failure, hypogonadism, etc. caused by cauda equina injuries.
    旨在为马尾神经组织提供高度安全和有效的血流促进剂。在具有弱降压作用的前列腺素类似化合物中,具有促进马尾神经组织血流的作用的化合物(不包括利马前列素)作为高度安全的马尾神经组织血流促进剂是有用的,并且在预防和/或治疗由马尾神经损伤引起的腰痛、下肢疼痛、下肢麻痹、间歇性跛行、膀胱直肠功能障碍、性腺功能减退等方面具有疗效。
  • BLOOD FLOW PROMOTERS FOR CAUDA EQUINA TISSUES
    申请人:Ohmoto Kazuyuki
    公开号:US20110015238A1
    公开(公告)日:2011-01-20
    It is intended to provide highly safe and efficacious blood flow promoters for cauda equina tissues. Among prostaglandin-like compounds having a weak hypotensive effect, compounds having an effect of promoting the blood flow in cauda equina tissues (excluding limaprost) are useful as highly safe blood flow promoters for cauda equina tissues and, therefore, are efficacious in preventing and/or treating lumbar pain, lower limb pain, lower limb palsy, intermittent claudication, vesicorectal failure, hypogonadism, etc. caused by cauda equina injuries.
    旨在为马尾神经组织提供高度安全和有效的促进血流剂。在具有弱降压作用的前列腺素类化合物中,具有促进马尾神经组织血流的作用的化合物(不包括利马前列素)作为高度安全的促进马尾神经组织血流的剂,因此,在预防和/或治疗由马尾神经损伤引起的腰痛、下肢疼痛、下肢瘫痪、间歇性跛行、膀胱直肠功能障碍、性腺功能减退等方面具有疗效。
  • EP1707208
    申请人:——
    公开号:——
    公开(公告)日:——
  • BIO-BASED POLYESTER LATEX
    申请人:OCE-Technologies B.V.
    公开号:EP2686366B1
    公开(公告)日:2019-12-25
  • US20140273447A1
    申请人:——
    公开号:US20140273447A1
    公开(公告)日:2014-09-18
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