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phenyl hydrogen (1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methylphosphonate | 1609111-41-2

中文名称
——
中文别名
——
英文名称
phenyl hydrogen (1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methylphosphonate
英文别名
Tenofovir alafenamide Intermediate 1;1-(6-aminopurin-9-yl)propan-2-yloxymethyl-phenoxyphosphinic acid
phenyl hydrogen (1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methylphosphonate化学式
CAS
1609111-41-2
化学式
C15H18N5O4P
mdl
——
分子量
363.313
InChiKey
ITAMCOCNZJPJDF-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):
    2.04
  • 重原子数:
    25.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    125.38
  • 氢给体数:
    2.0
  • 氢受体数:
    8.0

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

点击查看最新优质反应信息

文献信息

  • [EN] SALTS OF ANTIVIRAL PHOSPHONATE ANALOGUES AND PROCESS FOR PREPARATION THEREOF<br/>[FR] SELS D'ANALOGUES DE PHOSPHONATE ANTIVIRAUX ET LEUR PROCÉDÉ DE PRÉPARATION
    申请人:CIPLA LTD
    公开号:WO2018167515A1
    公开(公告)日:2018-09-20
    The present invention relates to certain acid salts of (((1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)(phenoxy) phosphoryloxy)methyl pivalateof Formula (I), to processes for their preparation; to pharmaceutical compositions comprising such compounds,and methods of treating a disease which responds to inhibition of nucleotide reverse transcriptase activity.
    本发明涉及一种特定的酸盐,化学式为(((1-(6-氨基-9H-嘌呤-9-基)丙基氧基)甲基(苯氧基)磷酰氧基)甲基)季戊酸盐(I),以及其制备方法;包含这类化合物的药物组合物;以及治疗对核苷酸逆转录酶活性抑制有响应的疾病的方法。
  • PHOSPHONAMIDE ESTER COMPOUND, SALT THEREOF, RELATED CRYSTAL FORM THEREOF, PREPARATION METHOD THEREFOR AND USE THEREOF
    申请人:SICHUAN KELUN-BIOTECH BIOPHARMACEUTICAL CO., LTD.
    公开号:US20210179647A1
    公开(公告)日:2021-06-17
    The present invention relates to compounds represented by formula (I) and formula (II) and a chiral synthesis and chiral isolation method therefor, further relating to a salt and crystal form of the compound represented by formula (I), a preparation method therefor, a pharmaceutical composition comprising the same, and use thereof in the preparation of a medicament used for the treatment of a viral infectious disease such as hepatitis B.
    本发明涉及由式(I)和式(II)表示的化合物及其手性合成和手性分离方法,进一步涉及由式(I)表示的化合物的盐和晶体形式、其制备方法、包含其的药物组合物以及在制备用于治疗病毒性传染病如乙型肝炎的药物中的用途。
  • ACYCLIC NUCLEOSIDE PHOSPHONATE DIESTERS
    申请人:The Regents of the University of California, a California Corporation
    公开号:US20140364397A1
    公开(公告)日:2014-12-11
    The present disclosure relates, inter alia, to compositions and methods for treating viral diseases and cancer. There are disclosed lipophilic antiviral and anticancer acyclic nucleoside phosphonate diesters, preparation thereof, and methods of using the compounds to treat viral diseases and cancer.
    本公开涉及治疗病毒性疾病和癌症的组合物和方法,其中包括脂溶性抗病毒和抗癌无环核苷酸膦酸二酯,其制备方法以及使用该化合物治疗病毒性疾病和癌症的方法。
  • Antiviral Phosphonate Analogues and Process for Preparation Thereof
    申请人:Cipla Limited
    公开号:US20150291639A1
    公开(公告)日:2015-10-15
    The present invention provides a compound of the Formula (I) wherein R is 9-isopropyl-9H-purin-6-amine; 2-amino-9-isopropyl-1H-purin-6(9H)-one; 4-amino-1-isopropyl pyrimidin-2(1H)-one; or 1-isopropyl-5-methylpyrimidine-2,4(1H,3H)-dione, R′ is —CH 2 OC(O)R″, and R″ is —C(CH 3 ) 3 or —CH(CH 3 ) 2 including pharmaceutically acceptable salts thereof. The present invention also provides a process for preparing a compound of formula (Ia) and a compound of formula (I) for use in treating a viral infection.
    本发明提供了一种式(I)的化合物,其中R为9-异丙基-9H-嘌呤-6-胺;2-氨基-9-异丙基-1H-嘌呤-6(9H)-酮;4-氨基-1-异丙基嘧啶-2(1H)-酮;或1-异丙基-5-甲基嘧啶-2,4(1H,3H)-二酮,R′为—CH2OC(O)R″,R″为—C(CH3)3或—CH(CH3)2,包括其药学上可接受的盐。本发明还提供了制备式(Ia)和式(I)化合物的方法,用于治疗病毒感染。
  • Phosphonamide ester compound, salt thereof, related crystal form thereof, preparation method therefor and use thereof
    申请人:SICHUAN KELUN-BIOTECH BIOPHARMACEUTICAL CO., LTD.
    公开号:US11186599B2
    公开(公告)日:2021-11-30
    The present invention relates to compounds represented by formula (I) and formula (II) and a chiral synthesis and chiral isolation method therefor, further relating to a salt and crystal form of the compound represented by formula (I), a preparation method therefor, a pharmaceutical composition comprising the same, and use thereof in the preparation of a medicament used for the treatment of a viral infectious disease such as hepatitis B.
    本发明涉及式(I)和式(II)代表的化合物及其手性合成和手性分离方法,还涉及式(I)代表的化合物的盐和晶体形式、其制备方法、包含其的药物组合物,以及其在制备用于治疗乙型肝炎等病毒性传染病的药物中的用途。
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