trans-3-Isopropyl-cyclobutylamin | 16453-24-0

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: trans-3-Isopropyl-cyclobutylamin
• CAS: 16453-24-0
• 化学式: C₇H₁₅N
• 分子量: 113.203
• InChiKey: DWFAIIJUKMDTLJ-LJGSYFOKSA-N

反应信息

• 作为产物：
  描述：

  3-异丙基环丁基甲酸 在 sodium azide 、 硫酸 作用下， 生成 trans-3-Isopropyl-cyclobutylamin
  参考文献：
  名称：

  Nonplanar cyclobutane. Evidence for a conformationally controlled, classic mechanism in the deamination of cis- and trans-3-isopropylcyclobutylamine

  摘要：

  DOI：

  10.1021/jo01274a033

文献信息

• Substituted Cyclohexylamine Compounds
  申请人：EPIZYME, INC.

  公开号：US20200123142A1

  公开（公告）日：2020-04-23

  The present disclosure provides substituted cyclohexylamine compounds having Formula (I): and the pharmaceutically acceptable salts and solvates thereof, wherein R 1 , R 2a , R 2b , R 3a , R 3b , R 4 , R 5 , and R 7 are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula I to treat a disorder responsive to the blockade of SMYD proteins such as SMYD3 or SMYD2. Compounds of the present disclosure are especially useful for treating cancer.

  本公开提供具有化学式（I）的替代环己胺化合物及其药用可接受的盐和溶剂化合物，其中R1、R2a、R2b、R3a、R3b、R4、R5和R7如规范中所定义。本公开还涉及使用化合物I的方法来治疗对SMYD蛋白如SMYD3或SMYD2阻断产生反应的疾病。本公开的化合物特别适用于治疗癌症。
• [EN] 2,3,5-TRISUBSTITUTED PYRAZOLO[1,5-A]PYRIMIDINE COMPOUNDS<br/>[FR] COMPOSÉS DE PYRAZOLO[1,5-A]PYRIMIDINE 2,3,5-TRISUBSTITUÉS
  申请人：ARCUS BIOSCIENCES INC

  公开号：WO2020247496A1

  公开（公告）日：2020-12-10

  Compounds that inhibit PI3Kγ, and compositions containing the compound(s) and methods for synthesizing the compounds, are described herein. Also described are the use of such compounds and compositions for the treatment of a diverse array of diseases, disorders, and conditions, including cancer- and immune-related disorders that are mediated, at least in part, by PI3Kγ.

  本文描述了抑制PI3Kγ的化合物，以及含有该化合物的组合物和合成该化合物的方法。还描述了利用这些化合物和组合物治疗各种疾病、疾病和疾病的用途，包括至少部分由PI3Kγ介导的癌症和免疫相关疾病。
• DIHYDROPYRROLOPYRIMIDINE DERIVATIVES
  申请人：PFIZER INC.

  公开号：US20150291604A1

  公开（公告）日：2015-10-15

  The present invention relates to compounds of formula (X) or pharmaceutically acceptable salts thereof, wherein R 1 -R 50 , a, b, d, e, f, g, h, i, j, k, l, o, p, q, r, s, t, u, y, and z are defined herein. The novel dihydropyrrolopyrimidine derivatives are useful in the treatment of abnormal cell growth, such as cancer, in mammals. Additional embodiments relate to pharmaceutical compositions containing the compounds and to methods of using the compounds and compositions in the treatment of abnormal cell growth in mammals.

  本发明涉及式（X）化合物或其药学上可接受的盐，其中R1-R50，a，b，d，e，f，g，h，i，j，k，l，o，p，q，r，s，t，u，y和z在此定义。这种新型二氢吡咯吡咪啉衍生物在哺乳动物的异常细胞生长，如癌症治疗中有用。其他实施例涉及含有该化合物的制药组合物以及在哺乳动物中治疗异常细胞生长的方法。
• PRODRUG BIPYRIDYLAMINOPYRIDINES AS SYK INHIBITORS
  申请人：HAIDLE Andrew M.

  公开号：US20150299125A1

  公开（公告）日：2015-10-22

  The present invention provides compounds of Formula (I), which are prodrugs of trans-4-[(1R)-(6-[4-(difluoromethyl)pyridin-2-yl]amino}-4-methyl-2,3′-bipyridin-6′-yl)-1-hydroxyethyl]cyclohexanecarboxylic acid, a potent inhibitor of Syk. The compounds are useful in the treatment and prevention of diseases mediated by the enzyme, such as asthma, COPD, rheumatoid arthritis and cancer.

  本发明提供了式（I）的化合物，它们是trans-4-[(1R)-(6-[4-(二氟甲基)吡啶-2-基]氨基}-4-甲基-2,3′-联苯并[6′]-基)-1-羟基乙基]环己烷羧酸的前药，是Syk的有效抑制剂。这些化合物在治疗和预防由该酶介导的疾病，如哮喘、COPD、类风湿性关节炎和癌症方面是有用的。
• INHIBITION AND ENHANCEMENT OF REPROGRAMMING BY CHROMATIN MODIFYING ENZYMES
  申请人：Children's Medical Center Corporation

  公开号：US20140242046A1

  公开（公告）日：2014-08-28

  Methods and compositions are provided for the production of stem cells and induced pluripotent stem cells, and for uses thereof.