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2-甲酰基呋喃-3-硼酸频那醇酯 | 1055881-23-6

中文名称
2-甲酰基呋喃-3-硼酸频那醇酯
中文别名
2-甲酰基呋喃-3-硼酸频哪醇酯
英文名称
3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-carbaldehyde
英文别名
2-formylfuran-3-boronic acid pinacol ester
2-甲酰基呋喃-3-硼酸频那醇酯化学式
CAS
1055881-23-6
化学式
C11H15BO4
mdl
MFCD07368242
分子量
222.049
InChiKey
PYPDEWSBYDJVFU-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):
    2.52
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.545
  • 拓扑面积:
    48.7
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:3c8e402360b7005bb056016ce3a710c3
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反应信息

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文献信息

  • [EN] HETEROCYCLIC COMPOUNDS AS JANUS KINASE INHIBITORS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES UTILISABLES EN TANT QU'INHIBITEURS DES JANUS KINASES
    申请人:BIOCRYST PHARM INC
    公开号:WO2013033093A1
    公开(公告)日:2013-03-07
    The invention provides compounds of formula I: (I) or a salt thereof as described herein. The invention also provides pharmaceutical compositions comprising a compound of formula I, processes for preparing compounds of formula I, intermediates useful for preparing compounds of formula I and therapeutic methods for suppressing an immune response or treating cancer, including a hematologic malignancy, using compounds of formula I.
    该发明提供了如下式I的化合物:(I)或其盐,如本文所述。该发明还提供了包括如下式I的化合物的药物组合物,制备如下式I的化合物的方法,用于制备如下式I的化合物的有用中间体,以及使用如下式I的化合物抑制免疫反应或治疗癌症,包括血液恶性肿瘤的治疗方法。
  • [EN] TRICYCLIC COMPOUNDS AND METHDS OF MAKING AND USING SAME<br/>[FR] COMPOSÉS TRICYCLIQUES ET PROCÉDÉS POUR LES PRÉPARER ET LES UTILISER
    申请人:ZAFGEN CORP
    公开号:WO2012012642A1
    公开(公告)日:2012-01-26
    The invention provides tricyclic compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tricyclic compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
    该发明提供了三环化合物及其在治疗医学疾病(如肥胖症)中的用途。提供了制备各种三环化合物的药物组合物和方法。这些化合物被认为具有对蛋氨酸氨肽酶2的活性。
  • Benzoxazepine derivatives and use thereof
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US08247403B2
    公开(公告)日:2012-08-21
    Compounds represented by the general formula (I): wherein each symbol is as defined in the description [with the proviso that 9-chloro-7-(1,1-dimethylethyl)-2,3,4,5-tetrahydro-1,4-benz-oxazepine and N-[[(5S)-2-oxo-3-(2,3,4,5-tetrahydro-1,4-benz-oxazepin-7-yl)-5-oxazolidinyl]methyl]acetamide are excluded], salts of the same, and prodrugs thereof have selective activation effect on serotonin 5-HT2C receptor and are useful as preventive and therapeutic agents for lower urinary tract diseases, obesity, and/or pelvic organ prolapse.
    一般式(I)所代表的化合物:其中每个符号如描述中所定义[但9-氯-7-(1,1-二甲基乙基)-2,3,4,5-四氢-1,4-苯并噁唑环和N-[[(5S)-2-氧代-3-(2,3,4,5-四氢-1,4-苯并噁唑-7-基)-5-噁唑烷基]甲基]乙酰胺被排除],其盐和前药在选择性激活5-羟色胺5-HT2C受体方面具有作用,并可用作预防和治疗下尿路疾病、肥胖症和/或盆腔器官脱垂的药物。
  • Partially Saturated Tricyclic Compounds and Methods of Making and Using Same
    申请人:Cramp Susan Mary
    公开号:US20140088078A1
    公开(公告)日:2014-03-27
    The invention provides tricyclic compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tricyclic compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
    本发明提供了三环化合物及其在治疗医学疾病,如肥胖症中的应用。同时提供了制备各种三环化合物的药物组合物和方法。这些化合物被认为对甲硫氨酰基氨肽酶2具有活性。
  • Tricyclic Compounds and Methods of Making and Using Same
    申请人:Clark David
    公开号:US20130123235A1
    公开(公告)日:2013-05-16
    The invention provides tricyclic compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tricyclic compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
    本发明提供三环化合物及其在治疗医学障碍(如肥胖症)中的应用。还提供了制备各种三环化合物的制药组合物和方法。这些化合物被认为具有对甲硫氨酰基氨肽酶2的活性。
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