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(4E,5R)-4-亚乙基-1,3,4,5,6,7-六氢-6-亚甲基-2,5-乙桥-2H-氮杂环辛烷并[4,3-b]吲哚 | 3463-93-2

中文名称
(4E,5R)-4-亚乙基-1,3,4,5,6,7-六氢-6-亚甲基-2,5-乙桥-2H-氮杂环辛烷并[4,3-b]吲哚
中文别名
——
英文名称
apparicine
英文别名
(13R,14E)-14-ethylidene-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene
(4E,5R)-4-亚乙基-1,3,4,5,6,7-六氢-6-亚甲基-2,5-乙桥-2H-氮杂环辛烷并[4,3-b]吲哚化学式
CAS
3463-93-2
化学式
C18H20N2
mdl
——
分子量
264.37
InChiKey
LCVACABZTLIWCE-SUSILRQXSA-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

物化性质

  • 熔点:
    198-9°C

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    19
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    参考文献:
    名称:
    [EN] CONOLIDINE ANALOGUES AS SELECTIVE ACKR3 MODULATORS FOR THE TREATMENT OF CANCER AND CARDIOVASCULAR DISEASES
    [FR] ANALOGUES DE LA CONOLIDINE SERVANT DE MODULATEURS SÉLECTIFS D'ACKR3 POUR TRAITER LE CANCER
    摘要:
    本申请公开了化合物的结构公式,如公式(2),(1A),(1B)或(1C),作为选择性非典型趋化因子受体3(ACKR3)调节剂,用于治疗癌症,动脉粥样硬化性血管疾病,心血管疾病,纤维化(例如心脏纤维化),炎症或自身免疫性疾病和病症,过度或异常血管化病症(例如伤口愈合),干细胞分化和移动障碍,脑和神经功能障碍(例如阿尔茨海默病,多发性硬化症和脱髓鞘性疾病),肾功能障碍,肾功能障碍,先兆子痫,人类免疫缺陷病毒(HIV)感染和肥胖症。此外,还提供了这些化合物用于体外或体外诊断、预测、预后和/或监测由ACKR3多肽水平异常特征的疾病或病症的方法,以及用于体外方法,以鉴定作为治疗药物有用的试剂。其中一个示例化合物是WW-1。
    公开号:
    WO2022136486A1
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文献信息

  • [EN] CONOLIDINE ANALOGUES AS SELECTIVE ACKR3 MODULATORS FOR THE TREATMENT OF CANCER AND CARDIOVASCULAR DISEASES<br/>[FR] ANALOGUES DE LA CONOLIDINE SERVANT DE MODULATEURS SÉLECTIFS D'ACKR3 POUR TRAITER LE CANCER
    申请人:LUXEMBOURG INST OF HEALTH LIH
    公开号:WO2022136486A1
    公开(公告)日:2022-06-30
    The present application discloses compounds of e.g. formulae (2), (1A), (1B) or (1C) as selective atypical chemokine receptor 3 (ACKR3) modulators for the treatment of e.g. cancer, atherosclerotic vascular disease, cardiovascular diseases, fibrosis (e.g. cardiac fibrosis), inflammatory or autoimmune diseases and conditions, conditions of excessive or abnormal vascularization (e.g. wound healing), stem cell differentiation and mobilization disorders, brain and neuronal dysfunctions (e.g. Alzheimer's disease, multiple sclerosis and demyelinating diseases), kidney dysfunction, renal dysfunction, preeclampsia, human immunodeficiency virus (HIV) infection and obesity. Further provided are said compounds for use in methods for in vitro or ex vivo diagnosis, prediction, prognosis and/or monitoring of a disease or condition characterized by an aberrant level of ACKR3 polypeptide, as well as for use in in vitro methods for identifying an agent useful as a therapeutic. An exemplary compound is e.g. WW-1.
    本申请公开了化合物的结构公式,如公式(2),(1A),(1B)或(1C),作为选择性非典型趋化因子受体3(ACKR3)调节剂,用于治疗癌症,动脉粥样硬化性血管疾病,心血管疾病,纤维化(例如心脏纤维化),炎症或自身免疫性疾病和病症,过度或异常血管化病症(例如伤口愈合),干细胞分化和移动障碍,脑和神经功能障碍(例如阿尔茨海默病,多发性硬化症和脱髓鞘性疾病),肾功能障碍,肾功能障碍,先兆子痫,人类免疫缺陷病毒(HIV)感染和肥胖症。此外,还提供了这些化合物用于体外或体外诊断、预测、预后和/或监测由ACKR3多肽水平异常特征的疾病或病症的方法,以及用于体外方法,以鉴定作为治疗药物有用的试剂。其中一个示例化合物是WW-1。
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白坚木辛碱 瓦来萨明碱N-氧化物 19,20-(E)-瓦来萨明碱 (4E,5R)-4-亚乙基-1,3,4,5,6,7-六氢-6-亚甲基-2,5-乙桥-2H-氮杂环辛烷并[4,3-b]吲哚 Brafouedine Gomezine Isobrafouedine 16S-Hydroxy-16,22-dihydro-(-)-apparicine Gomezine hydrochloride (12R,13S,14Z)-14-ethylidene-12-methyl-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraen-12-ol (±)-(15S*,16R*)-16-hydroxy-16,22-dihydroapparicine Tabernoschizine (13S,14Z)-14-ethylidene-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene 16(S)-Hydroxy-16,22-dihydroapparicine 2,5-Ethano-2H-azocino[4,3-b]indole-6-carboxylic acid, 4-ethylidene-1,3,4,5,6,7-hexahydro-6-(hydroxymethyl)-, methyl ester 2,5-Ethano-2H-azocino[4,3-b]indole-6-carboxylic acid, 6-[(acetyloxy)methyl]-4-ethylidene-1,3,4,5,6,7-hexahydro-, methyl ester (14E)-14-ethylidene-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene;hydron;chloride methyl (12R,13S,14E)-14-ethylidene-12-methoxy-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate methyl (13S,14E)-14-ethylidene-12-(hydroxymethyl)-1-oxido-10-aza-1-azoniatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate methyl (12S,13S)-14-ethylidene-12-(hydroxymethyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate (13S)-14-ethylidene-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene (+/-)-apparicine 14-Ethylidene-6-methoxy-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4(9),5,7-tetraene 14-Oxa-1,10-diazapentacyclo[15.3.1.03,11.04,9.012,18]henicosa-3(11),4,6,8,16-pentaene-12-carboxylic acid Methyl 15-ethenyl-14-oxa-1,10-diazapentacyclo[13.3.1.03,11.04,9.012,16]nonadeca-3(11),4,6,8-tetraene-12-carboxylate 14-Ethylidene-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4(9),5,7-tetraen-6-ol Methyl 15-ethenyl-16-hydroxy-14-oxa-1,10-diazapentacyclo[13.3.1.03,11.04,9.012,16]nonadeca-3(11),4,6,8-tetraene-12-carboxylate 14-Ethylidene-12-methyl-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraen-12-ol Apparicin Methyl 14-ethylidene-12-(hydroxymethyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate [14-Ethylidene-12-(2-hydroxyacetyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraen-12-yl]methyl acetate angustilobine B, (rac)- 12,14-Dimethyl-13-oxa-1,10-diazapentacyclo[13.3.1.03,11.04,9.012,16]nonadeca-3(11),4,6,8-tetraen-15-ol 14-Ethylidene-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraen-13-ol 1-[14-Ethylidene-12-(hydroxymethyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraen-12-yl]-2-hydroxyethanone 14-Ethylidene-6-methoxy-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4(9),5,7-tetraen-13-ol 3'-Methyl-12-methylidenespiro[1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-14,2'-oxirane] Methyl 12-(acetyloxymethyl)-14-ethylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate