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6-ethoxy-4-oxochromene-2-carboxylic acid | 1017325-10-8

中文名称
——
中文别名
——
英文名称
6-ethoxy-4-oxochromene-2-carboxylic acid
英文别名
6-ethoxychromone-2-carboxylic acid
6-ethoxy-4-oxochromene-2-carboxylic acid化学式
CAS
1017325-10-8
化学式
C12H10O5
mdl
——
分子量
234.208
InChiKey
LJYCKJZJQFPDKM-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):
    2
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • [EN] ANTI-INFECTIVE AGENTS<br/>[FR] AGENTS ANTI-INFECTIEUX
    申请人:UNIV DUNDEE
    公开号:WO2017221002A1
    公开(公告)日:2017-12-28
    The present invention relates to a novel class of chromene-2-carboxamide compounds inhibitors of general formula (I) wherein R1, R2, R3, R4, R5, R6, R7, R8 and X are as defined herein, to their use in medicine, and their use as anti-infective agents in particular, to compositions containing them, to processes for their preparation and to intermediates used in such processes.
    本发明涉及一类新型的基于色酮-2-羧酰胺化合物的抑制剂,其通式为(I),其中R1、R2、R3、R4、R5、R6、R7、R8和X如本文所定义,其在医学上的用途,特别是作为抗感染剂的用途,包括含有它们的组合物,其制备过程以及用于这些过程的中间体。
  • [EN] SUBSTITUTED PIPERIDINE AND PIPERAZINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR MODULATORS<br/>[FR] DERIVES A SUBSTITUTION PIPERIDINE ET PIPERAZINE AGISSANT COMME MODULATEURS DU RECEPTEUR DE LA MELANOCORTINE 4
    申请人:MYOCONTRACT LTD
    公开号:WO2004083199A1
    公开(公告)日:2004-09-30
    The present invention relates to novel substituted piperidine and piperazine derivatives as melanocortin-4 receptor (MC-4R) modulators. MC-4R agonists of the invention can be used for the treatment of disorders and diseases such as obesity, diabetes, and sexual dysfunction, whereas the MC-4R antagonists are useful for the treatment of disorders and diseases such as cancer cachexia, muscle wasting, anorexia, anxiety and depression. All diseases and disorders where the regulation of the MC-4R is involved can be treated with the compounds of the invention.
    本发明涉及一种新型的取代哌啶哌嗪生物,作为黑色素皮质素-4受体(MC-4R)调节剂。本发明中的MC-4R激动剂可用于治疗肥胖症、糖尿病和性功能障碍等疾病和疾病,而MC-4R拮抗剂则可用于治疗癌症恶病质、肌肉萎缩、厌食、焦虑和抑郁等疾病和疾病。所有涉及MC-4R调节的疾病和疾病都可以用本发明中的化合物进行治疗。
  • Substituted cyclohexyl and piperidinyl derivates as melanocortin-4 receptor modulators
    申请人:Soeberdt Michael
    公开号:US20070155783A1
    公开(公告)日:2007-07-05
    The present invention relates to novel substituted cyclohexyl and piperidinyl derivatives as melanocortin-4. receptor (MC-4R) modulators. MC-4R agonists of the invention can be used for the treatment of disorders and diseases such as obesity, diabetes and sexual dysfunction, whereas the MC-4R antagonists are useful for the treatment of disorders and diseases such as cancer cachexia, muscle wasting, anorexia, anxiety and depression. All diseases and disorders where the regulation of the MC-4R is involved can be treated with the compounds of the invention.
    本发明涉及一种新型的取代环己基和哌啶基生物,作为黑色素皮质素-4受体(MC-4R)调节剂。本发明中的MC-4R激动剂可用于治疗肥胖症、糖尿病和性功能障碍等疾病和疾病,而MC-4R拮抗剂则可用于治疗癌症消瘦、肌肉消耗、厌食、焦虑和抑郁等疾病和疾病。所有涉及MC-4R调节的疾病和疾病均可使用本发明中的化合物进行治疗。
  • Substituted piperidine and piperazine derivatives as melanocortin-4 receptor modulators
    申请人:Soeberdt Michael
    公开号:US20070037823A1
    公开(公告)日:2007-02-15
    The present invention relates to novel substituted piperidine and piperazine derivatives as melanocortin-4 receptor (MC-4R) modulators. MC-4R agonists of the invention can be used for the treatment of disorders and diseases such as obesity, diabetes and sexual dysfunction, whereas the MC-4R antagonists are useful for the treatment of disorders and diseases such as cancer cachexia, muscle wasting, anorexia, anxiety and depression. All diseases and disorders, where the regulation of the MC-4R is involved, can be treated with the compounds of the invention.
    本发明涉及一种新的取代哌啶哌嗪生物,作为黑色素皮质激素-4受体(MC-4R)调节剂。本发明的MC-4R激动剂可用于治疗肥胖症、糖尿病和性功能障碍等疾病和疾病,而MC-4R拮抗剂则可用于治疗癌症恶病质、肌肉消耗、厌食症、焦虑和抑郁症等疾病和疾病。所有涉及MC-4R调节的疾病和疾病都可以用本发明的化合物治疗。
  • SUBSTITUTED PIPERIDINE AND PIPERAZINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR MODULATORS
    申请人:Santhera Pharmaceuticals (Schweiz) GmbH
    公开号:EP1606281A1
    公开(公告)日:2005-12-21
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