3-苄氧羰基氨基哌啶盐酸盐 | 31648-54-1

• 物质功能分类: 有机原料 - 杂环化合物
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-苄氧羰基氨基哌啶盐酸盐
• 中文别名: 3-苄氧羰基氨基哌啶；3-Cbz-氨基哌啶；3-CBZ-氨基哌啶
• 英文名称: (RS)-benzyl piperidin-3-ylcarbamate
• 英文别名: Benzyl piperidin-3-ylcarbamate；benzyl N-piperidin-3-ylcarbamate
• CAS: 31648-54-1
• 化学式: C₁₃H₁₈N₂O₂
• mdl: MFCD04115317
• 分子量: 234.298
• InChiKey: GEHZGURGZRSODK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.461
• 拓扑面积：
  50.4
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 海关编码：
  2933399090
• 危险性防范说明：
  P261,P280,P301+P312,P302+P352,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335

反应信息

• 作为反应物：
  描述：

  3-苄氧羰基氨基哌啶盐酸盐 在 palladium 10% on activated carbon 、 氢气 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 为溶剂， 20.0 ℃ 、101.33 kPa 条件下， 反应 21.5h， 生成 1-cyclohexylpiperidin-3-amine
  参考文献：
  名称：

  Discovery of 2-substituted 1 H -benzo[ d ]immidazole-4-carboxamide derivatives as novel poly(ADP-ribose)polymerase-1 inhibitors with in vivo anti-tumor activity

  摘要：

  Novel 1H-benzo[d]immidazole-4-carboxamide derivatives bearing five-membered or six-membered N-heterocyclic moieties at the 2-position were designed and synthesized as PARP-1 inhibitors. Structure activity relationships were conducted and led to a number of potent PARP-1 inhibitors having IC50 values in the single or double digit nanomolar level. Some potent PARP-1 inhibitors also had similar inhibitory activities against PARP-2. Among all the synthesized compounds, compound 10a and 11e displayed strong potentiation effects on temozolomide (TMZ) in MX-1 cells (PF50 = 7.10, PF50 = 4.17). In vivo tumor growth inhibition was investigated using compound 10a in combination with TMZ, and it was demonstrated that compound 10a could strongly potentiate the cytotoxicity of TMZ in MX-1 xenograft tumor model. Two co-crystal structures of compounds 11b and 15e complexed with PARP-1 were achieved and demonstrated a unique binding mode of these benzo-imidazole derivatives. (C) 2017 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2017.03.013
• 作为产物：
  描述：

  1-叔丁氧羰基-3-氨基哌啶 在 N,N-二异丙基乙胺 、 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 生成 3-苄氧羰基氨基哌啶盐酸盐
  参考文献：
  名称：

  Discovery of 2-substituted 1 H -benzo[ d ]immidazole-4-carboxamide derivatives as novel poly(ADP-ribose)polymerase-1 inhibitors with in vivo anti-tumor activity

  摘要：

  Novel 1H-benzo[d]immidazole-4-carboxamide derivatives bearing five-membered or six-membered N-heterocyclic moieties at the 2-position were designed and synthesized as PARP-1 inhibitors. Structure activity relationships were conducted and led to a number of potent PARP-1 inhibitors having IC50 values in the single or double digit nanomolar level. Some potent PARP-1 inhibitors also had similar inhibitory activities against PARP-2. Among all the synthesized compounds, compound 10a and 11e displayed strong potentiation effects on temozolomide (TMZ) in MX-1 cells (PF50 = 7.10, PF50 = 4.17). In vivo tumor growth inhibition was investigated using compound 10a in combination with TMZ, and it was demonstrated that compound 10a could strongly potentiate the cytotoxicity of TMZ in MX-1 xenograft tumor model. Two co-crystal structures of compounds 11b and 15e complexed with PARP-1 were achieved and demonstrated a unique binding mode of these benzo-imidazole derivatives. (C) 2017 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2017.03.013

文献信息

• Discovery of Branebrutinib (BMS-986195): A Strategy for Identifying a Highly Potent and Selective Covalent Inhibitor Providing Rapid in Vivo Inactivation of Bruton’s Tyrosine Kinase (BTK)
  作者：Scott H. Watterson、Qingjie Liu、Myra Beaudoin Bertrand、Douglas G. Batt、Ling Li、Mark A. Pattoli、Stacey Skala、Lihong Cheng、Mary T. Obermeier、Robin Moore、Zheng Yang、Rodney Vickery、Paul A. Elzinga、Lorell Discenza、Celia D’Arienzo、Kathleen M. Gillooly、Tracy L. Taylor、Claudine Pulicicchio、Yifan Zhang、Elizabeth Heimrich、Kim W. McIntyre、Qian Ruan、Richard A. Westhouse、Ian M. Catlett、Naiyu Zheng、Charu Chaudhry、Jun Dai、Michael A. Galella、Andrew J. Tebben、Matt Pokross、Jianqing Li、Rulin Zhao、Daniel Smith、Richard Rampulla、Alban Allentoff、Michael A. Wallace、Arvind Mathur、Luisa Salter-Cid、John E. Macor、Percy H. Carter、Aberra Fura、James R. Burke、Joseph A. Tino

  DOI：10.1021/acs.jmedchem.9b00167

  日期：2019.4.11

  Bruton's tyrosine kinase (BTK), a non-receptor tyrosine kinase, is a member of the Tec family of kinases and is essential for B cell receptor (BCR) mediated signaling. BTK also plays a critical role in the downstream signaling pathways for the Fcγ receptor in monocytes, the Fcε receptor in granulocytes, and the RANK receptor in osteoclasts. As a result, pharmacological inhibition of BTK is anticipated

  布鲁顿酪氨酸激酶（BTK）是一种非受体酪氨酸激酶，是Tec家族激酶的成员，对于B细胞受体（BCR）介导的信号传导至关重要。BTK在单核细胞中Fcγ受体，粒细胞中的Fcε受体和破骨细胞中的RANK受体的下游信号通路中也起着关键作用。结果，预期对BTK的药理学抑制将为临床治疗自身免疫性疾病例如类风湿性关节炎和狼疮提供有效的策略。本文将概述我们用于鉴定共价，不可逆的BTK抑制剂的策略的发展，该抑制剂具有在非常低的剂量下全身快速灭活所需的内在效力，选择性和药代动力学特性。
• [EN] MACROCYCLIC INHIBITORS OF PEPTIDYLARGININE DEIMINASES<br/>[FR] INHIBITEURS MACROCYCLIQUES DE PEPTIDYLARGININE DÉIMINASES
  申请人：GILEAD SCIENCES INC

  公开号：WO2021222353A1

  公开（公告）日：2021-11-04

  The present disclosure relates to novel compounds for use in therapeutic treatement of a disease associated with peptidylarginine deiminases (PADs), such as peptidylarginine deiminase type 4 (PAD4). The present disclosure also relates to processes and intermediates for the preparation of such compounds, methods of using such compounds and pharmaceutical compositions comprising the compounds described herein.

  本公开涉及用于治疗与肽精氨酸脱亚氨酶（PADs）相关的疾病的新化合物，例如肽精氨酸脱亚氨酶类型4（PAD4）。本公开还涉及用于制备这些化合物的过程和中间体，使用这些化合物的方法以及包含所述化合物的药物组合物。
• [EN] PIPERIDINES, PYRROLIDINES AND HEXAHYDRO-1H-AZEPINES PROMOTE RELEASE OF GROWTH HORMONE<br/>[FR] PIPERIDINES, PYRROLIDINES ET HEXAHYDRO-1H-AZEPINES FAVORISANT LA LIBERATION DE L'HORMONE DE CROISSANCE
  申请人：MERCK & CO., INC.

  公开号：WO1995013069A1

  公开（公告）日：1995-05-18

  (EN) The present invention is directed to certain piperidine, pyrrolidine, and hexahydro-1H-azepine compounds of general structural formula (I) wherein R1, R3, R4, R5, A, W, X, Y, and n are as defined herein. These compounds promote the release of growth hormone in humans and animals. This property can be utilized to promote the growth of food animals to render the production of edible meat products more efficient, and in humans, to treat physiological or medical conditions characterized by a deficiency in growth hormone secretion, such as short stature in growth hormone deficient children, and to treat medical conditions which are improved by the anabolic effects of growth hormone. Growth hormone releasing compositions containing such compounds as the active ingredient thereof are also disclosed.(FR) L'invention concerne certains composés de pipéridine, de pyrrolidine, et d'hexahydro-1H-azépine de formule structurale (I) dans laquelle R1, R3, R4, R5, A, W, X, Y et n sont définis dans la description. Ces composés favorisent la libération de l'hormone de croissance chez les humains et les animaux. Cette propriété peut être utilisée pour favoriser la croissance d'animaux destinés à l'alimentation et augmenter la production de produits de viande comestibles, et, chez les humains, pour traiter des états physiologiques ou médicaux caractérisés par une insuffisance de sécrétion de l'hormone de croissance telle que l'insuffisance staturale chez l'enfant, et traiter des états médicaux pouvant être améliorés par les effets anabolisants de l'hormone de croissance. L'invention porte également sur des compositions libérant l'hormone de croissance dans lesquelles lesdits composés sont utilisés comme principes actifs.

  本发明涉及通式（I）中R1、R3、R4、R5、A、W、X、Y和n所定义的某些哌啶、吡咯烷和六氢-1H-氮杂环化合物。这些化合物促进人类和动物的生长激素释放。这种特性可用于促进食用动物的生长，使可食肉类产品的生产更加高效，以及在人类中，用于治疗生长激素分泌不足所表现出的生理或医学状况，例如生长激素缺乏症儿童的矮小症，以及治疗通过生长激素的合成代谢作用得到改善的医学状况。还公开了含有该化合物作为活性成分的生长激素释放组合物。
• HETEROAROMATIC COMPOUNDS USEFUL FOR THE TREATMENT OF PROLFERATIVE DISEASES
  申请人：SYROS PHARMACEUTICALS, INC.

  公开号：US20160264551A1

  公开（公告）日：2016-09-15

  The present invention provides novel compounds of Formula (I), and pharmaceutically acceptable salts, solvates, hydrates, tautomers, stereoisomers, isotopically labeled derivatives, and compositions thereof. Also provided are methods and kits involving the compounds or compositions for treating or preventing proliferative diseases (e.g., cancers (e.g., leukemia, melanoma, multiple myeloma), benign neoplasms, angiogenesis, inflammatory diseases, autoinflammatory diseases, and autoimmune diseases) in a subject. Treatment of a subject with a proliferative disease using a compound or composition of the invention may inhibit the aberrant activity of a kinase, such as a cyclin-dependent kinase (CDK) (e.g., cyclin-dependent kinase 7 (CDK7)), and therefore, in duce cellular apoptosis and/or inhibit transcription in the subject.

  本发明提供了式（I）的新化合物，以及其药学上可接受的盐、溶剂合物、水合物、互变异构体、立体异构体、同位素标记衍生物和组合物。还提供了涉及这些化合物或组合物的方法和试剂盒，用于治疗或预防主体中的增殖性疾病（例如，癌症（例如白血病、黑色素瘤、多发性骨髓瘤）、良性肿瘤、血管生成、炎症性疾病、自身炎症性疾病和自身免疫性疾病）。使用本发明的化合物或组合物治疗主体的增殖性疾病可能抑制激酶的异常活性，例如细胞周期依赖性激酶（CDK）（例如细胞周期依赖性激酶7（CDK7）），从而在主体中诱导细胞凋亡和/或抑制转录。
• MANUFACTURING METHOD FOR A PIPERIDINE-3-YLCARBAMATE COMPOUND AND OPTICAL RESOLUTION METHOD THEREFOR
  申请人：Watanabe Yosuke

  公开号：US20110021780A1

  公开（公告）日：2011-01-27

  Provided is a manufacturing method for a piperidine-3-ylcarbamate compound in which a pyridine-3-ylcarbamate compound and hydrogen are brought into contact in the presence of a palladium catalyst.

  提供了一种制造哌啶-3-基氨基甲酸酯化合物的方法，其中在钯催化剂的存在下，将吡啶-3-基氨基甲酸酯化合物和氢气接触。