摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(1S,3S,4S)-3,4-dihydroxycyclohexane-1-carboxylic acid

中文名称
——
中文别名
——
英文名称
(1S,3S,4S)-3,4-dihydroxycyclohexane-1-carboxylic acid
英文别名
——
(1S,3S,4S)-3,4-dihydroxycyclohexane-1-carboxylic acid化学式
CAS
——
化学式
C7H12O4
mdl
——
分子量
160.17
InChiKey
PTPROPUVXIZJPL-ZLUOBGJFSA-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):
    -0.6
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    77.8
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • PYRROLIDINE ETHER DERIVATIVES AS NK3 RECEPTOR ANTAGONISTS
    申请人:Jablonski Philippe
    公开号:US20090306043A1
    公开(公告)日:2009-12-10
    The present invention relates to compounds of formula I wherein R 1 , R 2 , R 3 , R′, Ar, m, n, and o are as defined herein. The invention also relates to pharmaceutical compositions containing compounds of formula I and methods for the manufacture of such compounds and compositions. Compounds of the invention are high potential NK-3 receptor antagonists for the treatment of depression, pain, psychosis, Parkinson's disease, schizophrenia, anxiety and attention deficit hyperactivity disorder (ADHD).
    本发明涉及式I的化合物,其中R1、R2、R3、R′、Ar、m、n和o如本文所定义。该发明还涉及含有式I化合物的药物组合物,以及制备这种化合物和组合物的方法。本发明的化合物是用于治疗抑郁症、疼痛、精神病、帕森病、精神分裂症、焦虑和注意力缺陷多动障碍(ADHD)的高潜力NK-3受体拮抗剂。
  • Production Of Polyketides And Other Natural Products
    申请人:Gregory Matthew Alan
    公开号:US20090253732A1
    公开(公告)日:2009-10-08
    The present invention relates to production of polyketides and other natural products and to libraries of compounds and individual novel compounds. Therefore in aspect the present invention provides 17-desmethylrapamycin and analogues thereof, methods for their production, including recombinant strains, and isolation and uses of the compounds of the invention. In a further aspect the present invention provides for the use of 17-desmethylrapamycin and analogues thereof in the induction or maintenance of immunosuppression, the stimulation of neuronal regeneration or the treatment of cancer, B-cell malignancies, fungal infections, transplantation rejection, graft vs. host disease, autoimmune disorders, diseases of inflammation vascular disease and fibrotic diseases, and in the regulation of wound healing.
    本发明涉及聚酮类化合物和其他天然产物的生产,以及化合物库和独特新化合物的制备。因此,本发明提供了17-去甲基拉帕霉素及其类似物,包括重组菌株的制备方法,以及本发明化合物的分离和用途。此外,本发明还提供了将17-去甲基拉帕霉素及其类似物用于诱导或维持免疫抑制、促进神经再生或治疗癌症、B细胞恶性肿瘤、真菌感染、移植排斥、移植物抗宿主病、自身免疫性疾病、炎症性血管疾病和纤维化疾病的调节。
  • RAPAMYCIN ANALOGUES AND THEIR PHARMACEUTICAL USE
    申请人:Isomerase Therapeutics Limited
    公开号:US20160176893A1
    公开(公告)日:2016-06-23
    Novel rapamycin analogues and methods for their production with FKBP and/or MIP inhibitory activity with reduced mTOR inhibitory activity with therapeutic potential e.g. as bacterial virulence inhibitors.
    小说雷帕霉素类似物及其生产方法,具有FKBP和/或MIP抑制活性,同时减少mTOR抑制活性,具有治疗潜力,例如作为细菌毒力抑制剂
  • 17-Desmethylrapamycin and analogues thereof, methods for their production and their use as immunosupressants, anticancer agents, antifungal agents etc.
    申请人:Biotica Technology Limited
    公开号:EP2471797A2
    公开(公告)日:2012-07-04
    The present invention relates to production of polyketides and other natural products and to libraries of compounds and individual novel compounds. Therefore in one aspect the present invention provides 17-desmethylrapamycin and analogues thereof, methods for their production, including recombinant strains, and isolation and uses of the compounds of the invention. In a further aspect the present invention provides for the use of 17-desmethylrapamycin and analogues thereof in the induction or maintenance of immunosuppression, the stimulation of neuronal regeneration or the treatment of cancer, B-cell malignancies, fungal infections, transplantation rejection, graft vs. host disease, autoimmune disorders, diseases of inflammation vascular disease and fibrotic diseases, and in the regulation of wound healing.
    本发明涉及多酮类化合物和其他天然产物的生产,以及化合物库和单个新型化合物。因此,在一个方面,本发明提供了 17-去甲基拉帕霉素及其类似物、其生产方法(包括重组菌株)以及本发明化合物的分离和用途。在另一个方面,本发明提供了17-去甲基拉帕霉素及其类似物在诱导或维持免疫抑制、刺激神经元再生或治疗癌症、B细胞恶性肿瘤、真菌感染、移植排斥反应、移植物对宿主疾病、自身免疫性疾病、炎症性血管疾病和纤维化疾病以及调节伤口愈合中的用途。
  • PRODUCTION OF POLYKETIDES
    申请人:Buck Institute for Research on Aging
    公开号:EP1521828B1
    公开(公告)日:2015-07-01
查看更多