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1-(triphenyl-λ5-phosphanyl)butan-2-one

中文名称
——
中文别名
——
英文名称
1-(triphenyl-λ5-phosphanyl)butan-2-one
英文别名
——
1-(triphenyl-λ5-phosphanyl)butan-2-one化学式
CAS
——
化学式
C22H23OP
mdl
——
分子量
334.4
InChiKey
REIOBUGTSZRADY-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):
    4.8
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • [EN] TREATMENT AND PREVENTION OF HBV DISEASES BY CYCLOSPORINE ANALOGUE MOLECULES MODIFIED AT AMINO ACIDES 1 AND 3<br/>[FR] TRAITEMENT ET PRÉVENTION DE MALADIES DU VHB PAR DES MOLÉCULES ANALOGUES DE CYCLOSPORINE MODIFIÉES AU NIVEAU DES ACIDES AMINÉS 1 ET 3
    申请人:CONTRAVIR PHARMACEUTICALS INC
    公开号:WO2018106928A1
    公开(公告)日:2018-06-14
    The present application relates to a method of treating and/or preventing a hepatitis B virus (HBV) disease through inhibiting the interaction of CypA with HBV X protein (HBx) and/or Hepatitis B surface antigen (HBsAg), comprising administering to a subject in need thereof a compound of Formula L.
    本申请涉及一种通过抑制CypA与乙型肝炎病毒(HBV)X蛋白(HBx)和/或乙型肝炎表面抗原(HBsAg)的相互作用来治疗和/或预防乙型肝炎病毒(HBV)疾病的方法,包括向需要的受试者施用一种L式化合物。
  • CYCLOSPORINE ANALOGUE MOLECULES MODIFIED AT AMINO ACID 1 AND 3
    申请人:ContraVir Pharmaceuticals, Inc.
    公开号:EP3461835A1
    公开(公告)日:2019-04-03
    Analogues of cyclosporin-A are disclosed comprising modifications of the substituents as the positions of amino acids 1 and 3, according to the following Formula (I). The disclosed compounds include compounds having affinity for cyclophilin, including cyclophilin-A, and reduced immunosuppressivity in comparison with cyclosporin-A and analogs thereof modified solely at position 1.
    根据下式(I),环孢素-A 的类似物包括氨基酸 1 和 3 位置的取代基修饰。所公开的化合物包括与环孢素-A 及其仅在 1 位修饰的类似物相比,对包括环纤蛋白酶-A 在内的环纤蛋白酶具有亲和性并降低免疫抑制性的化合物。
  • NONIMMUNOSUPPRESSIVE CYCLOSPORINE ANALOGUE MOLECULES
    申请人:Hegmans Alexander
    公开号:US20130190223A1
    公开(公告)日:2013-07-25
    The compounds of the present invention are non-immunosupressive cyclosporine analogue molecules that are able to bind cyclophilin. Said compounds include a modified side chain of amino acid I of cyclosporin A, consisting of an oxyalkyl having substituents R′, R1 and R2, where R′ is H or Acetyl; R1 is a saturated or unsaturated straight chain or branched aliphatic carbon chain; and R2 may be a hydrogen; a unsubstituted, N substituted or NN disubstituted amide; a N substituted or unsubstituted acyl protected amine; a carboxylic acid; a N substituted or unsubstituted amine; a nitrile; a ester; a ketone; a hydroxy, dihydroxy, trihydroxy or polyhydroxy alkyl; or a substituted or unsubstituted aryl.
  • Cyclosporine Analogue Molecules Modified At Amino Acid 1 and 3
    申请人:Ciclofilin Pharmaceuticals Corp.
    公开号:US20160207961A1
    公开(公告)日:2016-07-21
    Analogues of cyclosporin-A are disclosed comprising modifications of the substituents as the positions of amino acids 1 and 3, according to the following Formula. The disclosed compounds include compounds having affinity for cyclophilin, including cyclophilin-A, and reduced immunosuppressivity in comparison with cyclosporin-A and analogs thereof modified solely at position 1.
  • US9200038B2
    申请人:——
    公开号:US9200038B2
    公开(公告)日:2015-12-01
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同类化合物

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