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象牙酮宁 | 474-00-0

中文名称
象牙酮宁
中文别名
——
英文名称
(-)-eburnamonine
英文别名
Eburnamenin-14(15H)-one;(15R,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-one
象牙酮宁化学式
CAS
474-00-0
化学式
C19H22N2O
mdl
——
分子量
294.396
InChiKey
WYJAPUKIYAZSEM-RBUKOAKNSA-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:
    174°
  • 比旋光度:
    D25 +89° (chloroform)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    25.2
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:7f26379201cd025b686fe45355c84582
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
    —— ent-19-oxo-eburnamonine 110421-51-7 C19H20N2O2 308.38
    —— (+/-)-eburnamine —— C19H24N2O 296.412
    长春酸胺 Vincaminsaeure 28152-73-0 C20H24N2O3 340.422
    —— (+)-eburnamenine 517-30-6 C19H22N2 278.397
    —— ent-1β-ethyl-4-oxo-1,2,3,4,6,7,12,12β-octahydro-1,3-cycloindolo<2,3-a>quinolizin-3β-carboxylic acidmethylester 113974-84-8 C19H20N2O3 324.379
    —— 3-((1R,12bR)-1-Ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-yl)-2-[(E)-hydroxyimino]-propionic acid methyl ester 86708-31-8 C21H27N3O3 369.464
    —— 2-((1R,12bR)-1-ethyl-1,2,3,4,6,7,12,12b octahydroindolo[2,3-a]quinolizin-1-yl)ethanol 1395097-95-6 C19H26N2O 298.428
    —— (1RS,12bRS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-ethanol 119459-52-8 C19H26N2O 298.428
    —— (-)-1β-cyanomethyl-1α-ethyl-1,2,3,4,6,7,12,12bα-octahydro-indolo<2,3-a>quinolizine 53430-06-1 C19H23N3 293.412
    —— (3,4,6,7,12,12b-hexahydro-2H-indolo[2,3-a]quinolizin-1-ylidene)-acetic acid ethyl ester 38199-33-6 C19H22N2O2 310.396
    • 1
    • 2
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    —— (+)-17β-hydroxyeburnamonine 1202363-21-0 C19H22N2O2 310.396
    —— (+/-)-eburnamine —— C19H24N2O 296.412
    —— (+)-isoeburnamine 4201-84-7 C19H24N2O 296.412
    埃那胺 eburnamine 473-99-4 C19H24N2O 296.412
    —— vincaminol 54422-34-3 C20H24N2O 308.423
    —— (+/-)-apovincamine —— C21H24N2O2 336.434
    —— (+)-eburnamenine 517-30-6 C19H22N2 278.397
    —— (-)-Norpleiomutine —— C40H48N4O2 616.847
    —— 1β-carboxymethyl-1α-ethyl-1,2,3,4,6,7,12,12bα-octahydroindolo<2,3-a>quinolizine 63038-12-0 C19H24N2O2 312.412
    —— (1RS,12bRS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-ethanol 119459-52-8 C19H26N2O 298.428
    • 1
    • 2

反应信息

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文献信息

  • Dibenzyl Amine Compounds and Derivatives
    申请人:Chang George
    公开号:US20070213371A1
    公开(公告)日:2007-09-13
    Dibenzyl amine compounds and derivatives, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases in some mammals, including humans.
    二苯基胺化合物及其衍生物,含有这种化合物的药物组合物以及使用这种化合物提高某些血浆脂质水平,包括高密度脂蛋白胆固醇,并降低其他一些血浆脂质水平,如低密度脂蛋白胆固醇和甘油三酯,并据此治疗由高密度脂蛋白胆固醇水平低和/或低密度脂蛋白胆固醇和甘油三酯水平高加重的疾病,如动脉粥样硬化和心血管疾病在某些哺乳动物,包括人类。
  • SUBSTITUTED AMIDE COMPOUNDS
    申请人:Pfizer Inc.
    公开号:US20140315928A1
    公开(公告)日:2014-10-23
    The present invention is directed at substituted amide compounds, pharmaceutical compositions containing such compounds and the use of such compounds to reduce plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases, in mammals, including humans.
    本发明涉及替代酰胺化合物,含有这种化合物的药物组合物以及利用这种化合物降低血浆脂质水平,如LDL-胆固醇和甘油三酯,并据此治疗由高水平的LDL-胆固醇和甘油三酯加重的疾病,如动脉粥样硬化和心血管疾病,在哺乳动物,包括人类中的应用。
  • Tyrosine kinase inhibitors
    申请人:——
    公开号:US20020137755A1
    公开(公告)日:2002-09-26
    The present invention relates to compounds which inhibit, regulate and/or modulate tyrosine kinase signal transduction, compositions which contain these compounds, and methods of using them to treat tyrosine kinase-dependent diseases and conditions, such as angiogenesis, cancer, tumor growth, atherosclerosis, age related macular degeneration, diabetic retinopathy, inflammatory diseases, and the like in mammals.
    本发明涉及抑制、调节和/或调控酪氨酸激酶信号传导的化合物,含有这些化合物的组合物,以及使用它们治疗依赖于酪氨酸激酶的疾病和病况的方法,如在哺乳动物中的血管生成、癌症、肿瘤生长、动脉粥样硬化、老年性黄斑变性、糖尿病视网膜病变、炎症性疾病等。
  • Tetrahydroisoquinoline LXR modulators
    申请人:Yang Wu
    公开号:US20070093523A1
    公开(公告)日:2007-04-26
    A compound of formula I wherein X, R 1 , R 2a , R 3a , R 3b , R 4a , R 4b , R 4c and R 5 are defined herein.
    其中X,R1,R2a,R3a,R3b,R4a,R4b,R4c和R5在此处定义。
  • [EN] INDOLINE COMPOUNDS AND THEIR USE IN THE TREATMENT OF ARTERIOSCLEROSIS<br/>[FR] COMPOSES A BASE D'INDOLINE ET LEUR UTILISATION DANS LE TRAITEMENT DE L'ARTERIOSCLEROSE
    申请人:PFIZER PROD INC
    公开号:WO2006032987A1
    公开(公告)日:2006-03-30
    Indoline compounds, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases in some mammals, including humans.
    吲哚啉化合物,含有这种化合物的药物组合物,以及使用这种化合物来提高某些血浆脂质水平,包括高密度脂蛋白胆固醇,并降低其他一些血浆脂质水平,如低密度脂蛋白胆固醇和甘油三酯,并据此治疗由高密度脂蛋白胆固醇水平低和/或低密度脂蛋白胆固醇和甘油三酯水平高加重的疾病,如动脉粥样硬化和心血管疾病在某些哺乳动物中,包括人类。
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同类化合物

阿扑长春胺 长春醇 长春酸胺 长春西汀杂质N 长春西汀杂质L 长春西汀杂质K 长春西汀杂质J 长春西汀杂质I 长春西汀杂质27 长春西汀杂质1 长春西汀杂质 A 长春西汀 长春胺杂质 长春胺杂质 长春胺乙酯 长春胺 长春泊林 长春布宁 长春倍酯 长春乙酯羧酸 象牙酮宁 溴长春胺 富马酸溴长春胺 埃那胺 7-氨基-4-羟基-3-(苯偶氮基)萘-2-磺基酸 14,15-二氢阿扑长春胺乙酯 13alpha-乙基-2,3,5,6,13a,13b-六氢-1H-吲哚并(3,2,1-去)吡啶并(3,2,1-ij)(1,5)-萘啶-12-羧酸甲氧基甲基酯 (3alpha,16alpha)-6-羟基-象牙洪达木烯宁-14(15H)-酮 (3alpha,14beta,16alpha)-14,15-二氢-14-羟基埃那美宁-14-甲醇 (+)-(14beta)-二氢长春西丁 (+/-)-vincaminine (3α)-Eburnamenine-14-carbonyl chloride hydrochloride (-)-3S,16R-14-benzoyloxymethyl-eburnamenine apovincamine acetylsalicylate (+)-vinpocetine-9,11-disulfonic acid (3-methoxypropyl)diamide 14-(aminomethyl)-vincane O-((eburnamenine-14-yl)methyl)(4-methoxyphenyl)carbamothioate O-((eburnamenine-14-yl)methyl)(4-chlorophenyl)carbamothioate O-((eburnamenine-14-yl)methyl)(morpholine-4-carbonyl)(phenyl)carbamothioate (+)-14-carboxy-eburnamenine(3,16)-10-sulfonamide vinpocetine hydrochloride (+)-14-(2-chloro)carboethoxy-eburnamenine(3,16)-10-sulfonic acid (3-methoxypropyl)amide (+)-14-carbopropyloxy-eburnamenine(3,16)-10-sulfonic acid (3-methoxypropyl)amide (+)-apovincamine-10-sulfonic acid (3-methoxypropyl)amide 4-oxide 6-hydroxy-py-tetrahydroapovincamine chloride 10-nitro-6-oxovincamine (41S,13aS)-13a-ethyl-N,N-dimethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5] naphthyridine-12-carboxamide N-(((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)methyl)isobutyramide vincamine acetylsalicylate 6-hydroxy-py-tetrahydro-16-deoxyepivincamine chloride