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1-(6-iodo-3,3-dimethylindolin-1-yl)ethanone | 659731-42-7

中文名称
——
中文别名
——
英文名称
1-(6-iodo-3,3-dimethylindolin-1-yl)ethanone
英文别名
1-acetyl-6-iodo-3,3-dimethyl-2,3-dihydro-1H-indole;1-(6-iodo-3,3-dimethyl-2H-indol-1-yl)ethanone
1-(6-iodo-3,3-dimethylindolin-1-yl)ethanone化学式
CAS
659731-42-7
化学式
C12H14INO
mdl
——
分子量
315.154
InChiKey
LSKMWQNKSSYWRM-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):
    2.8
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Discovery and in Vivo Evaluation of Dual PI3Kβ/δ Inhibitors
    摘要:
    Structure-based rational design led to the synthesis of a novel series of potent PI3K inhibitors. The optimized pyrrolopyridine analogue 63 was a potent and selective PI3K beta/delta dual inhibitor that displayed suitable physicochemical properties and pharmacokinetic profile for animal studies. Analogue 63 was found to be efficacious in animal models of inflammation including a keyhole limpet hemocyanin (KLH) study and a collagen-induced arthritis (CIA) disease model of rheumatoid arthritis. These studies highlight the potential therapeutic value of inhibiting both the PI3K beta and delta isoforms in the treatment of a number of inflammatory diseases.
    DOI:
    10.1021/jm300679u
  • 作为产物:
    描述:
    1-乙酰基-6-氨基-3,3-二甲基-2,3-二氢吲哚盐酸 、 sodium nitrite 、 potassium iodide 作用下, 以 氯仿 为溶剂, 反应 0.67h, 以65%的产率得到1-(6-iodo-3,3-dimethylindolin-1-yl)ethanone
    参考文献:
    名称:
    [EN] ALKYNYL ALCOHOLS AS KINASE INHIBITORS
    [FR] ALCOOLS D'ALCYNYLE UTILISÉS COMME INHIBITEURS DE KINASES
    摘要:
    选定的化合物对预防和治疗炎症和炎症性疾病,如NIK介导的疾病,具有有效性。该发明涵盖了新颖的化合物、类似物、前药及其药用可接受的盐,以及用于预防和治疗涉及炎症等疾病和其他疾病或病症的药物组合物和方法。
    公开号:
    WO2009158011A1
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文献信息

  • [EN] VANILLOID RECEPTOR LIGANDS AND THEIR USE IN TREATMENTS<br/>[FR] LIGANDS DE RECEPTEUR VANILLOIDE ET LEUR UTILISATION DANS DES TRAITEMENTS
    申请人:AMGEN INC
    公开号:WO2004014871A1
    公开(公告)日:2004-02-19
    Compounds having the general structure and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.
    含有通用结构和组成的化合物及其组合物,用于治疗急性、炎症性和神经痛、牙痛、普通头痛、偏头痛、集群性头痛、混合性血管和非血管综合症、紧张性头痛、普通炎症、关节炎、风湿性疾病、骨关节炎、炎症性肠病、炎症性眼病、炎症性或不稳定的膀胱疾病、牛皮癣、带有炎症成分的皮肤病、慢性炎症状况、炎症性疼痛及相关的高敏性和触痛,神经痛及相关的高敏性和触痛、糖尿病神经病疼痛、烧伤后神经痛、交感神经维持的疼痛、去神经症候群、哮喘、上皮组织损伤或功能障碍、单纯疱疹、呼吸道、泌尿生殖系统、胃肠道或血管区域的内脏运动障碍、伤口、烧伤、过敏性皮肤反应、瘙痒、白癜风、普通胃肠疾病、胃溃疡、十二指肠溃疡、腹泻、坏死性剂引起的胃病变、毛发生长、血管运动或过敏性鼻炎、支气管疾病或膀胱疾病。
  • Vanilloid receptor ligands and their use in treatments
    申请人:——
    公开号:US20040082780A1
    公开(公告)日:2004-04-29
    Compounds having the general structure 1 and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.
    具有一般结构1的化合物及其组成物,用于治疗急性、炎症和神经痛、牙痛、普通头痛、偏头痛、集群头痛、混合血管和非血管综合症、紧张性头痛、普通炎症、关节炎、风湿性疾病、骨关节炎、炎症性肠病、炎症性眼疾、炎症性或不稳定的膀胱疾病、牛皮癣、具有炎症成分的皮肤病、慢性炎症状况、炎症性疼痛及相关的高敏感性和触痛、神经痛及相关的高敏感性和触痛、糖尿病神经病痛、烧灼性疼痛、交感神经维持性疼痛、去神经症候群、哮喘、上皮组织损伤或功能障碍、单纯疱疹、呼吸、泌尿、胃肠或血管区域的内脏运动障碍、伤口、烧伤、过敏性皮肤反应、瘙痒、白癜风、普通胃肠障碍、胃溃疡、十二指肠溃疡、腹泻、坏死剂诱导的胃病变、毛发生长、血管运动或过敏性鼻炎、支气管疾病或膀胱疾病。
  • Alkyne-substituted pyridone compounds and methods of use
    申请人:White Ryan
    公开号:US20080032977A1
    公开(公告)日:2008-02-07
    The present invention comprises a new class of compounds capable of modulating the c-kit receptor and, accordingly, useful for treatment of c-kit mediated diseases, including various inflammatory, fibrotic and/or mast cell mediated diseases such as mastocytosis. The compounds have a general Formula I wherein A 1-3 , R 1 and R 3-6 are defined herein. The invention further comprises pharmaceutical compositions, methods for treatment of c-kit mediated diseases, and intermediates and processes useful for the preparation of compounds of the invention.
    本发明涉及一类新的化合物,能够调节c-kit受体,因此对于治疗c-kit介导的疾病,包括各种炎症、纤维化和/或肥大细胞介导的疾病如肥大细胞增多症等非常有用。该化合物具有一般的公式I,其中A1-3,R1和R3-6在此定义。本发明还包括制备该化合物的药物组合物、治疗c-kit介导疾病的方法,以及中间体和用于制备本发明化合物的方法。
  • Substituted pyridone compounds and methods of use
    申请人:Hu Essa
    公开号:US20080249090A1
    公开(公告)日:2008-10-09
    The present invention comprises a new class of compounds capable of modulating the c-kit receptor and, accordingly, useful for treatment of c-kit mediated diseases, including various inflammatory, fibrotic and/or mast cell mediated diseases such as mastocytosis. The compounds have a general Formula I wherein A 0-3 and R 1-6 are defined herein. The invention further comprises pharmaceutical compositions, methods for treatment of c-kit mediated diseases, and intermediates and processes useful for the preparation of compounds of the invention.
    本发明涉及一类新的化合物,能够调节c-kit受体,因此可用于治疗c-kit介导的疾病,包括各种炎症性、纤维化和/或肥大细胞介导的疾病,如肥大细胞增多症。该化合物具有一般的I式,其中A0-3和R1-6在此定义。本发明还涉及制药组合物、治疗c-kit介导的疾病的方法,以及制备本发明化合物的中间体和方法。
  • ALKYNYL ALCOHOLS AS KINASE INHIBITORS
    申请人:Chen Guoqing
    公开号:US20110086834A1
    公开(公告)日:2011-04-14
    Selected compounds are effective for prophylaxis and treatment of inflammation and inflammatory disorders, such as NIK-mediated disorders. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, inflammation and the like.
    所选化合物对于预防和治疗炎症和炎症性疾病(如NIK介导的疾病)有效。本发明涵盖新的化合物、类似物、前药和其药学上可接受的盐、制药组合物和预防和治疗涉及炎症等疾病和其他疾病或病症的方法。
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