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AMD 7276 | 297770-95-7

中文名称
——
中文别名
——
英文名称
AMD 7276
英文别名
N-(1-methylbenzimidazol-2-ylmethyl)-N'-(2-pyridinylmethyl)-N-(6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-yl)-1,4-benzenedimethanamine;N-[(1-methylbenzimidazol-2-yl)methyl]-N-[[4-[(pyridin-2-ylmethylamino)methyl]phenyl]methyl]-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-amine
AMD 7276化学式
CAS
297770-95-7
化学式
C33H36N6
mdl
——
分子量
516.689
InChiKey
PGPVOBTXVGCPBN-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):
    4.4
  • 重原子数:
    39
  • 可旋转键数:
    9
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    58.9
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • Methods to mobilize progenitor/stem cells
    申请人:Genzyme Global S.à.r.l.
    公开号:EP2371361A1
    公开(公告)日:2011-10-05
    Methods to elevate progenitor and stem cell counts in animal subjects using compounds which bind to the chemokine receptor CXCR4 are disclosed. Preferred embodiments of such compounds are of the formula Z-linker-Z' (1) or pharmaceutically acceptable salt thereofwherein Z is a cyclic polyamine containing 9-32 ring members of which 3-8 are nitrogen atoms, said nitrogen atoms separated from each other by at least 2 carbon atoms, and wherein said heterocycle may optionally contain additional heteroatoms besides nitrogen and/or may be fused to an additional ring system; or Z is of formula (a), wherein A comprises a monocyclic or bicyclic fused ring system containing at least one N and B is H or an organic moiety of 1-20 atoms, Z' may be embodied in a form as defined by Z above, or alternatively may be of the formula -N(R)-(CR2)n-X wherein each R is independently H or straight, branched or cyclic alkyl (1-6C), n is 1 or 2, and X is an aromatic ring, including heteroaromatic rings, or is a mercaptan; "linker" represents a bond, alkylene (1-6C) or may comprise aryl, fused aryl, oxygen atoms contained in an alkylene chain, or may contain keto groups or nitrogen or sulphur atoms.
    本研究公开了使用与趋化因子受体 CXCR4 结合的化合物提高动物体内祖细胞和干细胞数量的方法。此类化合物的优选实施方案为式 Z-linker-Z' (1) 或其药学上可接受的盐,其中 Z 是环状多胺,包含 9-32 个环成员,其中 3-8 个为氮原子,所述氮原子之间至少相隔 2 个碳原子,所述杂环除氮原子外还可选择包含其他杂原子和/或可与其他环系统融合;或 Z 为式(a),其中 A 包含单环或双环融合环系统,至少含有一个 N,B 为 H 或 1-20 个原子的有机分子,Z'可以如上文 Z 所定义的形式体现,或者可以为式-N(R)-(CR2)n-X,其中每个 R 独立地为 H 或直链、支链或环状烷基(1-6C),n 为 1 或 2,X 为芳香环,包括杂芳香环,或者为醇;"连接剂 "代表键、亚烷基(1-6C),或可包括芳基、融合芳基、亚烷基链中包含的氧原子,或可包含酮基或氮或原子。
  • CHEMOKINE RECPETOR BINDING HETEROCYCLIC COMPOUNDS
    申请人:ANORMED INC.
    公开号:EP1163238B1
    公开(公告)日:2006-05-31
  • DOSING REGIMENS FOR THE MOBILIZATION OF HEMATOPOIETIC STEM AND PROGENITOR CELLS
    申请人:Magenta Therapeutics, Inc.
    公开号:EP3720494A2
    公开(公告)日:2020-10-14
  • COMPOSITIONS AND METHODS FOR THE EXPANSION OF HEMATOPOIETIC STEM AND PROGENITOR CELLS AND TREATMENT OF INHERITED METABOLIC DISORDERS
    申请人:Magenta Therapeutics, Inc.
    公开号:EP3735412A1
    公开(公告)日:2020-11-11
  • CXCR4 ANTAGONISTS FOR KIDNEY INJURY
    申请人:Zuk Anna
    公开号:US20110245265A1
    公开(公告)日:2011-10-06
    Methods to treat or prevent acute kidney injury and chronic kidney injury in subjects using CXCR4 antagonists are disclosed.
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