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

DT6P9Y45WD | 63199-66-6

中文名称
——
中文别名
——
英文名称
DT6P9Y45WD
英文别名
4-[(1S,2S)-1-hydroxy-2-(propan-2-ylamino)butyl]benzene-1,2-diol
DT6P9Y45WD化学式
CAS
63199-66-6
化学式
C13H21NO3
mdl
——
分子量
239.31
InChiKey
HUYWAWARQUIQLE-GWCFXTLKSA-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):
    1.7
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    72.7
  • 氢给体数:
    4
  • 氢受体数:
    4

文献信息

  • [EN] NOVEL COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF INFLAMMATORY DISORDERS<br/>[FR] NOUVEAUX COMPOSÉS ET COMPOSITIONS PHARMACEUTIQUES LES COMPRENANT POUR LE TRAITEMENT DE TROUBLES INFLAMMATOIRES
    申请人:GALAPAGOS NV
    公开号:WO2017012647A1
    公开(公告)日:2017-01-26
    The present invention discloses compounds according to Formula (I), wherein R1, R3, R4, R5, L1, and Cy are as defined herein. The present invention also provides compounds, methods for the production of said compounds of the invention, pharmaceutical compositions comprising the same and their use in allergic or inflammatory conditions, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6 and/or interferons. The present invention also methods for the prevention and/or treatment of the aforementioned diseases by administering a compound of the invention.
    本发明公开了根据式(I)的化合物,其中R1、R3、R4、R5、L1和Cy如本文所定义。本发明还提供了该发明的化合物、制备该化合物的方法、包括相同化合物的药物组合物以及它们在过敏或炎症症状、自身免疫疾病、增殖性疾病、移植排斥、涉及软骨周转障碍的疾病、先天软骨畸形和/或与IL6和/或干扰素过度分泌相关的疾病中的使用。本发明还提供了通过给予该发明的化合物来预防和/或治疗上述疾病的方法。
  • Benzoxazinyl-amidocyclopentyl-heterocyclic modulators of chemokine receptors
    申请人:Goble D. Stephen
    公开号:US20070238723A1
    公开(公告)日:2007-10-11
    Cyclopentyl compounds linked to a benzoxazinyl group through an amido moiety utilizing the ring nitrogen of the benzoxazine, and further substituted with a heterocyclic moiety, such compounds represented by formula I: which are used to modulate the CCR-2 chemokine receptor to prevent or treat inflammatory and immunoregulatory disorders and diseases, allergic diseases, atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and asthma, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis; and pharmaceutical compositions comprising these compounds and the use of these compounds and compositions.
    环戊基化合物通过酰胺基团与苯并噁唑基团相连,利用苯并噁唑环的环氮原子,并进一步用杂环基团取代,这些化合物由式I表示: 用于调节CCR-2趋化因子受体,以预防或治疗炎症和免疫调节性疾病和疾病,过敏性疾病,包括过敏性鼻炎,皮炎,结膜炎和哮喘,以及类风湿性关节炎和动脉粥样硬化等自身免疫病理病变;以及包含这些化合物的药物组合物和这些化合物和组合物的使用。
  • [EN] MEDICAMENTS FOR INHALATION COMPRISING BETAMIMETICS AND AN ANTICHOLINERGIC AGENT<br/>[FR] MEDICAMENTS POUR INHALATION COMPORTANT DES AGENTS A ACTIVITE BETAMIMETIQUE ET ANTICHOLINERGIQUE
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2005013992A1
    公开(公告)日:2005-02-17
    The present invention relates to novel pharmaceutical compositions based on beta2 agonists and salts of a new anticholinergic, processes for preparing them and their use in the treatment of respiratory complaints, wherein the anticholinergic agent has the formula (I).
    本发明涉及基于β2激动剂和一种新的抗胆碱药盐的新型药物组合物,以及制备这些药物组合物的方法和它们在治疗呼吸道疾病中的应用,其中抗胆碱药物具有化学式(I)。
  • Medicaments for inhalation comprising a novel anticholinergic and a betamimetic
    申请人:Germeyer Sabine
    公开号:US20050107417A1
    公开(公告)日:2005-05-19
    A pharmaceutical composition comprising a compound of formula 1 wherein X − is an anion with a single negative charge, and a betamimetic, optionally together with a pharmaceutically acceptable excipient, the compound of formula 1 and the betamimetic optionally in the form of their enantiomers, mixtures of their enantiomers, their racemates, their solvates, or their hydrates, processes for preparing them, and their use in the treatment of respiratory tract diseases.
    一种包括式1的化合物的药物组合物,其中X-是带有单负电荷的阴离子,以及一种β-肾上腺素受体激动剂,可选地与药用可接受的赋形剂一起,式1的化合物和β-肾上腺素受体激动剂可选地以其对映体、对映体混合物、消旋体、溶剂化合物或合物的形式存在,以及制备它们的方法,以及它们在治疗呼吸道疾病中的用途。
  • [EN] ASH1L INHIBITORS AND METHODS OF TREATMENT THEREWITH<br/>[FR] INHIBITEURS DE ASH1L ET MÉTHODES DE TRAITEMENT AU MOYEN DE CEUX-CI
    申请人:UNIV MICHIGAN REGENTS
    公开号:WO2017197240A1
    公开(公告)日:2017-11-16
    Provided herein are small molecule inhibitors of ASH1L activity and small molecules that facilitate ASH1L degradation and methods of use thereof for the treatment of disease, including acute leukemia, solid cancers and other diseases dependent on activity of ASH1L.
    本文提供了ASH1L活性的小分子抑制剂,促进ASH1L降解的小分子以及它们的使用方法,用于治疗疾病,包括急性白血病、实体肿瘤和其他依赖于ASH1L活性的疾病。
查看更多