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4-dedimethylamino-7-dimethylamino-6-demethyl-6-deoxytetracycline | 180002-76-0

中文名称
——
中文别名
——
英文名称
4-dedimethylamino-7-dimethylamino-6-demethyl-6-deoxytetracycline
英文别名
4-de(dimethylamino)-minocycline;(12aα)-7-dimethylamino-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide;7-dimethylamino-6-demethyl-6-deoxy-4-de(dimethylamino)tetracycline;4-dedimethylamino-6-demethyl-6-deoxy-7-dimethylaminotetracycline;7-dimethylamino-6-demethyl-6-deoxy-4-dedimethylaminotetracycline;4-de(dimethylamino)minocycline
4-dedimethylamino-7-dimethylamino-6-demethyl-6-deoxytetracycline化学式
CAS
180002-76-0
化学式
C21H22N2O7
mdl
——
分子量
414.415
InChiKey
BADNNDSCJPGEII-HORACTTISA-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

物化性质

  • 熔点:
    212 °C (decomp)
  • 沸点:
    802.9±65.0 °C(Predicted)
  • 密度:
    1.62±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.65
  • 重原子数:
    30.0
  • 可旋转键数:
    2.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    161.39
  • 氢给体数:
    5.0
  • 氢受体数:
    8.0

SDS

SDS:c014810144f6c290c6e071b9b11bbf2d
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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

反应信息

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文献信息

  • [EN] TETRACYCLINES AND THEIR USE AS CALPAIN INHIBITORS<br/>[FR] TETRACYCLINES ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE LA CALPAINE
    申请人:CA NAT RESEARCH COUNCIL
    公开号:WO2005082860A1
    公开(公告)日:2005-09-09
    Tetracyclines are useful as calpain inhibitors, particularly inhibitors of calpain I and II, as demonstrated in enzymatic assays as well as at the cellular and animal levels. Tetracyclines may be used in the treatment of a wide range of conditions implicated by or associated with calpain activity or activation, including cellular protection from apoptosis and necrosis, particularly n eu ro protection, prevention of cell motility (e.g. anti-metastasis of cancer) and treatment of certain infectious diseases (e.g. malaria and AIDS). Some tetracyclines are particularly useful as calpain inhibitors since they are also antioxidants, oxidative stress often being associated with conditions where calpain is activated.
    四环素类药物可作为卡尔佩因子的抑制剂,特别是卡尔佩因子I和II的抑制剂,在酶活性测定以及细胞和动物平上得到证实。四环素类药物可用于治疗与卡尔佩因子活性或激活有关的或相关的一系列疾病,包括细胞保护免受凋亡和坏死的影响,特别是神经保护,防止细胞活动(例如抗癌转移)以及治疗某些传染病(例如疟疾和艾滋病)。一些四环素类药物特别适用作为卡尔佩因子的抑制剂,因为它们也是抗氧化剂,氧化应激常常与卡尔佩因子激活的疾病有关。
  • 10-substituted tetracyclines and methods of use thereof
    申请人:Abato Paul
    公开号:US20070093455A1
    公开(公告)日:2007-04-26
    10-Substituted tetracycline compounds are described.
    描述了10-取代四环素化合物。
  • TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES
    申请人:Paratek Pharmaceuticals, Inc.
    公开号:US20180016225A1
    公开(公告)日:2018-01-18
    Methods and compounds for treating diseases with tetracycline compounds having a target therapeutic activity are described.
    使用具有目标治疗活性的四环素化合物治疗疾病的方法和化合物被描述。
  • Methods of simultaneously treating ocular rosacea and acne rosacea
    申请人:——
    公开号:US20030229055A1
    公开(公告)日:2003-12-11
    A method for simultaneously treating ocular rosacea and acne rosacea in a human in need thereof comprising administering systemically to said human a tetracycline compound in an amount that is effective to treat ocular rosacea and acne rosacea but has substantially no antibiotic activity.
    一种用于同时治疗需要治疗的人体中的眼部酒渣鼻和痤疮性酒渣鼻的方法,包括向该人体系统内给予四环素化合物,其用量足以治疗眼部酒渣鼻和痤疮性酒渣鼻,但几乎没有抗生素活性。
  • Methods of treating acne
    申请人:——
    公开号:US20030130240A1
    公开(公告)日:2003-07-10
    A method of treating acne in a human in need thereof comprising administering systemically to said human a tetracycline compound in an amount that is effective to treat acne but has substantially no antibiotic activity, without administering a bisphosphonate compound.
    治疗需要的人体痤疮的方法包括系统地向该人体施用四环素类化合物,其剂量足以治疗痤疮但基本没有抗生素活性,而不施用双膦酸盐化合物。
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