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3-ethoxy-1-adamantylamine | 1098072-03-7

中文名称
——
中文别名
——
英文名称
3-ethoxy-1-adamantylamine
英文别名
3-Ethoxyadamantan-1-amine
3-ethoxy-1-adamantylamine化学式
CAS
1098072-03-7
化学式
C12H21NO
mdl
——
分子量
195.305
InChiKey
AKPWQXXITUXNMB-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):
    1.4
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    35.2
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    3-ethoxy-1-adamantylamine4-甲酰基肉桂酸甲酯 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 4.0h, 生成 methyl 3-[4-[[(3-ethoxy-1-adamantyl)amino]methyl]phenyl]prop-2-enoate
    参考文献:
    名称:
    Discovery of adamantane based highly potent HDAC inhibitors
    摘要:
    Herein, we report the development of highly potent HDAC inhibitors for the treatment of cancer. A series of adamantane and nor-adamantane based HDAC inhibitors were designed, synthesized and screened for the inhibitory activity of HDAC. A number of compounds exhibited GI(50) of 10-100 nM in human HCT116, NCI-H460 and U251 cancer cells, in vitro. Compound 32 displays efficacy in human tumour animal xenograft model. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.03.002
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文献信息

  • ORGANIC COMPOUNDS
    申请人:Hassiepen Ulrich
    公开号:US20100256080A1
    公开(公告)日:2010-10-07
    The present invention relates to a compound The instant invention relates to a compound of formulae (I A), (I B), (X A), (X B), (Y A) or (Y B), wherein R′ represents and R″ represents hydrogen, hydroxy, C 1 -C 7 alkoxy, C 1 -C 8 -alkanoyloxy, or R 5 R 4 N—CO—O—, where R 4 and R 5 independently are C 1 -C 7 alkyl or phenyl which is unsubstituted or substituted by a substitutent selected from C 1 -C 7 alkyl, C 1 -C 7 alkoxy, halogen and trifluoromethyl and where R 4 additionally is hydrogen; or R 4 and R 5 together represent C 3 -C 6 alkylene; in free form or in form of a pharmaceutically acceptable acid addition salt. Compounds of formulae (I A), (I B), (X A), (X B), (Y A) or (Y B) inhibit DPP-IV (dipeptidyl-peptidase-IV) activity. They are therefore indicated for use as pharmaceuticals in inhibiting DPP-IV and in the treatment of conditions mediated by DPP-IV, such as non-insulin-dependent diabetes mellitus, arthritis, obesity, osteoporosis and further conditions of impaired glucose tolerance.
    本发明涉及一种化合物。本发明涉及一种具有式(I A)、(I B)、(X A)、(X B)、(Y A)或(Y B)的化合物,其中R′代表,R″代表氢、羟基、C1-C7烷氧基、C1-C8-烷酰氧基,或R5R4N—CO—O—,其中R4和R5独立地为C1-C7烷基或苯基,未取代或被C1-C7烷基、C1-C7烷氧基、卤素和三甲基等取代基取代,且R4另外为氢;或者R4和R5共同表示C3-C6烷基链;以自由形式或药学上可接受的酸盐形式存在。式(I A)、(I B)、(X A)、(X B)、(Y A)或(Y B)的化合物抑制DPP-IV(二肽基肽酶-IV)活性。因此,它们适用于作为药物用于抑制DPP-IV和治疗由DPP-IV介导的疾病,如非胰岛素依赖型糖尿病、关节炎、肥胖症、骨质疏松症以及其他葡萄糖耐量受损疾病。
  • [EN] N-SUBSTITUTED 2-CYANOPYRROLIDINES<br/>[FR] 2-CYANOPYRROLIDINES N-SUBSTITUES
    申请人:NOVARTIS AG
    公开号:WO2000034241A1
    公开(公告)日:2000-06-15
    The present invention relates to a compound of formula (I), wherein R is substituted adamantyl; and n is 0 to 3; in free form or in acid addition salt form. Compounds of formula (I) inhibit DPP-IV (dipeptidyl-peptidase-IV) activity. They are therefore indicated for use as pharmaceuticals in inhibiting DPP-IV and in the treatment of conditions mediated by DPP-IV, such as non-insulin-dependent diabetes mellitus, arthritis, obesity, osteoporosis and further conditions of impaired glucose tolerance.
    本发明涉及一种式为(I)的化合物,其中R是取代的金刚烷基;n为0至3;以自由形式或酸加成盐形式存在。式(I)的化合物能够抑制DPP-IV(二肽基肽酶-IV)的活性。因此,它们适用于作为药物用于抑制DPP-IV和治疗由DPP-IV介导的疾病,如非胰岛素依赖性糖尿病、关节炎、肥胖症、骨质疏松症和其他葡萄糖耐量受损的疾病。
  • Compound for resist and radiation-sensitive composition
    申请人:MITSUBISHI GAS CHEMICAL COMPANY, INC.
    公开号:EP2662727A2
    公开(公告)日:2013-11-13
    A radiation-sensitive composition containing 1 to 80% by weight of a solid component and 20 to 99% by weight of a solvent. The solid component contains a compound B which has (a) a structure derived from a polyphenol compound A by introducing an acid-dissociating group to at least one phenolic hydroxyl group of the polyphenol compound A which is synthesized by a condensation between a compound selected from the group consisting of compounds such as for instance diformylbenzene, diacetylbenzene and diformyltoluene; or a di- to tetrafunctional aromatic ketone or aromatic aldehyde each having 12 to 36 carbon atoms with a compound having 1 to 3 phenolic hydroxyl groups and 6 to 15 carbon atoms, and (b) a molecular weight of 400 to 2000. The composition containing the compound B is useful as an acid-amplified, non-polymeric resist material, because it is highly sensitive to radiation such as KrF excimer lasers, extreme ultraviolet rays, electron beams, and X-rays, and provides resist patterns with a high resolution, high heat resistance, and high etching resistance.
    一种辐射敏感组合物,含有 1%至 80%(按重量计)的固体成分和 20%至 99%(按重量计)的溶剂。固体成分含有一种化合物 B,该化合物 B 具有 (a) 由多酚类化合物 A 衍生出的结构,该结构是通过在多酚类化合物 A 的至少一个羟基上引入酸解离基团而形成的,该多酚类化合物 A 是由选自以下组成的化合物组的化合物缩合合成的:例如二甲酰基苯、二乙酰基苯和二甲酰基甲苯;(b) 分子量为 400 至 2000。含有化合物 B 的组合物可用作酸放大的非聚合抗蚀剂材料,因为它对诸如 KrF 准分子激光、极紫外线、电子束和 X 射线等辐射高度敏感,并能提供具有高分辨率、高耐热性和高抗蚀性的抗蚀图案。
  • N-SUBSTITUTED 2-CYANOPYRROLIDINES
    申请人:Novartis AG
    公开号:EP1137635B1
    公开(公告)日:2005-10-19
  • ADAMANTYL O-GLUCURONIDE DERIVATIVES AS INHIBITORS OF DIPEPTIDYL PEPTIDASE IV FOR THE TREATMENT OF DIABETES
    申请人:Novartis AG
    公开号:EP2247602A2
    公开(公告)日:2010-11-10
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