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isoemetine | 522-99-6

中文名称
——
中文别名
——
英文名称
isoemetine
英文别名
emetine;10,11,6',7'-tetramethoxy-emetane;(-)-Isoemetin;methyl cephaeline;Isoemetin;(2S,3R,11bS)-2-[[(1S)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl]-3-ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizine
isoemetine化学式
CAS
522-99-6
化学式
C29H40N2O4
mdl
——
分子量
480.648
InChiKey
AUVVAXYIELKVAI-YMLRZMTOSA-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

  • 沸点:
    600.3±55.0 °C(Predicted)
  • 密度:
    1.17±0.1 g/cm3(Predicted)
  • 熔点:
    50-55 °C

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    35
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    52.2
  • 氢给体数:
    1
  • 氢受体数:
    6

SDS

SDS:9c26ee5c1eb4012cf6fd9bfc6868197e
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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

反应信息

点击查看最新优质反应信息

文献信息

  • Studies on the syntheses of heterocyclic compounds. Part 875. The total stereoselective retro mass spectral synthesis of (±)-emetine
    作者:Tetsuji Kametani、Samuel A. Surgenor、Keiichiro Fukumoto
    DOI:10.1039/p19810000920
    日期:——
    Addition of 3,4-dihydro-6,7-dimethoxy-1-methylisoquinoline (5) to 3-methoxycarbonyl-1,6,7,11b-tetrahydro-9,10-dimethoxybenzo[a]quinolizin-4-one (4) produced 2-[3,4-dihydro-6,7-dimethoxy-1-isoquinolyl)methyl]-3-methoxycarbonyl-1,2,3,6,7,11b-hexahydro-9,10-dimethoxybenzo[a]quinolizin-4-one (6A). The same reaction of 3,4-dihydro-1-methyl-9H-pyrido[3,4-b]indole (15) with (4) afforded 2-(3,4-dihydro-9H-pyrido[3
    将3,4-二氢-6,7-二甲氧基-1-甲基异喹啉(5)加至3-甲氧基羰基-1,6,7,11b-四氢-9,10-二甲氧基苯并[ a ]喹诺嗪-4-酮(4 )制得的2- [3,4-二氢-6,7-二甲氧基-1-异喹啉基)甲基] -3-甲氧基羰基-1,2,3,6,7,11b-六氢-9,10-二甲氧基苯并[ a ]喹诺酮-4-酮(6A)。3,4-二氢-1-甲基-9 H-吡啶[3,4- b ]吲哚(15)与(4)的相同反应得到2-(3,4-二氢-9 H-吡啶基[3, 4 - b ] -1-吲哚基)甲基] -1,2,3,6,7,11b-六氢-9,10-二甲氧基-3-甲氧基羰基苯并[ a ]喹啉嗪-4-酮(16)。前迈克尔加合物(6A)经六步转化为(±)-依替丁(1)。
  • Concise Total Synthesis of Dihydrocorynanthenol, Protoemetinol, Protoemetine, 3-epi-Protoemetinol and Emetine
    作者:Shuangzheng Lin、Luca Deiana、Abrehet Tseggai、Armando Córdova
    DOI:10.1002/ejoc.201101296
    日期:2012.1
    A concise asymmetric assembly of secologanine tryptamine and dopamine alkaloids by means of a one-pot three-component cascade reaction methodology is disclosed. This is demonstrated by the expediti ...
    公开了一种通过一锅三组分级联反应方法对 secologanine 色胺和多巴胺生物碱进行简明不对称组装的方法。这体现在快速...
  • Syntheseversuche in der Emetin-Reihe. 6. Mitteilung. Eine weitere Totalsynthese von<i>rac</i>. Emetin
    作者:A. Grüssner、E. Jaeger、J. Hellerbach、O. Schnider
    DOI:10.1002/hlca.19590420714
    日期:——
    Confirming results from a recent publication by BURGSTAHLER and BITHOS, emetine and isoemetine have been prepared from a new tricyclic intermediate.
    BURGSTAHLER和BITHOS最近发表的出版物中证实的结果是,从一种新的三环中间体制得了依米汀和异麦汀。
  • Three New O-Methyltransferases Are Sufficient for All O-Methylation Reactions of Ipecac Alkaloid Biosynthesis in Root Culture of Psychotria ipecacuanha
    作者:Taiji Nomura、Toni M. Kutchan
    DOI:10.1074/jbc.m109.086157
    日期:2010.3
    ipecacuanha produces ipecac alkaloids, a series of monoterpenoid-isoquinoline alkaloids such as emetine and cephaeline, whose biosynthesis derives from condensation of dopamine and secologanin. Here, we identified three cDNAs, IpeOMT1-IpeOMT3, encoding ipecac alkaloid O-methyltransferases (OMTs) from P. ipecacuanha. They were coordinately transcribed with the recently identified ipecac alkaloid beta-glucosidase
    药用植物Psychotria ipecacuanha 产生吐根生物碱,这是一系列单萜-异喹啉生物碱,如依米丁和头孢碱,其生物合成来源于多巴胺和secologanin 的缩合。在这里,我们鉴定了三个 cDNA,即 IpeOMT1-IpeOMT3,它们编码来自吐根假单胞菌的吐根生物碱 O-甲基转移酶 (OMT)。它们与最近发现的吐根生物碱 β-葡萄糖苷酶 Ipeglu1 协同转录。它们的氨基酸序列彼此密切相关,而不是与参与苄基异喹啉生物碱生物合成的 OMT 相关,而不是与类黄酮 OMT 相关。重组 IpeOMT 酶的表征与 IpeGlu1 的酶学特性的整合表明,通过 IpeOMT1 的 6-O-甲基化,emetine 生物合成从 N-脱乙酰异胡椒苷分枝出来,IpeOMT2 的贡献较小,然后是 IpeGlu1 的去糖基化。苷元异喹啉骨架的 7-羟基在形成与第二个多巴胺分子缩合的原甲基化之前被 IpeOMT3
  • Ipecac alkaloids from Cephaelis acuminata
    作者:Atsuko Itoh、Yuki Ikuta、Yoshikazu Baba、Takao Tanahashi、Naotaka Nagakura
    DOI:10.1016/s0031-9422(99)00361-1
    日期:1999.11
    From the dried roots of Cephaelis acuminata, five ipecac alkaloids, neocephaeline, 7'-O-demethylcephaeline, 10-O-demethylcephaeline, 2'-N-(1"-deoxy-1"-beta-D-fructopyranosyl)cephaeline and 2'-N-(1"-deoxy-1"-beta-D-fructopyranosyl)neocephaeline, were isolated, along with emetine, cephaeline, psychotrine, protoemetine, 9-demethylprotoemetinol and isocephaeline. Structures were determined by spectroscopic
    来自尖尖头麻的干燥根、五种吐根生物碱、新头麻碱、7'-O-去甲基头麻碱、10-O-去甲基头麻碱、2'-N-(1"-deoxy-1"-β-D-吡喃果糖基)头麻碱和 2 '-N-(1"-deoxy-1"-beta-D-fructopyranosyl)neocephaeline,与 emetine、cephaeline、psychotrine、protoemetine、9-demethylprotoemetinol 和 isocephaeline 一起被分离出来。通过光谱和化学方法确定结构。
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同类化合物

盐酸吐根酚碱 盐酸吐根碱 吐根碱氢溴酸盐 吐根碱氢溴酸盐 吐根碱 依米丁二盐酸盐水合物 依米丁 二盐酸吐根碱 九节碱 7',10,11-三甲氧基-1',2'-二去氢依米丁-6'-醇草酸盐(1:1) 2-[(6,7-二甲氧基-1,2,3,4-四氢异喹啉-1-基)甲基]-3-乙基-9,10-二甲氧基-2,3,4,6,7,11b-六氢-1H-吡啶并[2,1-a]异喹啉四水合物二盐酸盐 1',2'-二去氢-7',10,11-三甲氧基依米丁-6',9-二醇 (+)-吐根素二盐酸盐水合物 (1RS,2S,3R,11bR)-2-benzoyl-1-(3-ethyl-9,10-dimethoxy-4-oxo-1,3,4,6,7,11b-hexahydro-2H-benzo[a]quinolizin-2-ylmethyl)-6-7-dimethoxy-1,2-dihydroisoquinoline-1-carbonitrile (2SR,3RS,11bSR)-2-benzoyl-1-(3-ethyl-9,10-dimethoxy-4-oxo-1,3,4,6,7,11b-hexahydro-2H-benzo[a]quinolizin-2-ylmethyl)-6,7-dimethoxy-1,2-dihydroisoquinoline-1-carbonitrile 2'-N-(1''-deoxy-1''-β-D-fructopyranosyl)cephaeline 7'-O-demethylcephaeline 7′,10-dide-O-methylcephaeline 2′-(N-carboxy-β-alanyl)-tert-butyl emetine ester 7'-O-demethylisocephaeline N-Methyl-emetin Emetine (or isoemetine), dihydrochloride Emetine hydrobromide 2H-Benzo(a)quinolizine, 1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2-((1,2,3,4-tetrahydro-6,7-dimethoxy-2-(3-(o-anisyloxy)-2-hydroxypropyl)-1-isoquinolyl)methyl)-, dihydrochloride 2H-Benzo(a)quinolizine, 3-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2-((1,2,3,4-tetrahydro-6-isopentoxy-7-methoxy-1-isoquinolyl)methyl)-, phosphate (2S,3R,11bS)-2-[[(1R)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl]-3-ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizine;triiodobismuthane 2-[(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]-3-ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizine;hydron;dichloride 11b-epi-emetine 11b-epi-isoemetine (2S,3R,11bS)-2-[(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]-3-ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizine;hydron;dibromide 1-[(1R)-1-[[(2R,3R,11bS)-3-ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-2-yl]methyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-3-tert-butylsulfanylpropan-2-ol;hydron;dichloride Emetine, 2'-(3-(6-chloro-o-toluidino)-2-hydroxypropyl)-, trihydrochloride Emetine, 2'-(2-hydroxy-3-(4-methyl-1-piperazinyl)propyl)-, tetrahydrochloride 1-[(1R)-1-[[(2R,3R,11bS)-3-ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-2-yl]methyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-3-(furan-2-ylmethylsulfanyl)propan-2-ol;hydron;dichloride 2H-Benzo(a)quinolizine, 1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2-((1,2,3,4-tetrahydro-6,7-dimethoxy-2-(3-(2-ethylhexyloxy)-2-hydroxypropyl)-1-isoquinolyl)methyl)-, dihydrochloride 2H-Benzo(a)quinolizine, 1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2-((1,2,3,4-tetrahydro-6,7-dimethoxy-2-(2-hydroxy-3-(1-methylpropylthio)propyl)-1-isoquinolyl)methyl)-, dihydrochloride, trihydrate 2H-Benzo(a)quinolizine, 1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2-((1,2,3,4-tetrahydro-6,7-dimethoxy-2-(3-(3,4-dimethoxycarbaniloylmethylthio)-2-hydroxypropyl)-1-isoquinolyl)methyl)-, dihydrochloride <2S-<2α(S*),3β,11β>>-9-benzyloxy-2-(6-benzyloxy-7-methoxy-1,2,3,4-tetrahydro-1-isoquinolyl)methyl-3-ethyl-1,3,4,6,7,11b-hexahydro-10-methoxy-2H-benzoquinolizine <2S-<2α(S*),3β,11β>>-3-ethyl-1,3,4,6,7,11b-hexahydro-9-hydroxy-2-(6-benzyloxy-7-methoxy-1,2,3,4-tetrahydro-1-isoquinolyl)methyl-10-methoxy-2H-benzoquinolizine <2S-<2α(R*),3β,11β>>-9-benzyloxy-2-(6-benzyloxy-7-methoxy-1,2,3,4-tetrahydro-1-isoquinolyl)methyl-3-ethyl-1,3,4,6,7,11b-hexahydro-10-methoxy-2H-benzoquinolizine Emetine, N-(1-carboxyprolyl)-, benzyl ester Emetine, 2'-(N-carboxyglycyl)-, tert-butyl ester Emetine dihydrobromide tetrahydrate 16,17-Dinoremetan, 1-ethyl-6',7',10,11-tetramethoxy-, dihydrochloride, (1-beta)-(+-)- 16,17-Dinoremetan, 1-methyl-6',7',10,11-tetramethoxy-, dihydrochloride, (1-alpha,2-alpha)-(+-)- 16,17-Dinoremetan, 1-methyl-6',7',10,11-tetramethoxy-, dihydrochloride, (1-beta)-(+-)- 16,17-Dinoremetan, 1',2'-didehydro-1-methyl-6',7',10,11-tetramethoxy-, dihydrochloride, (1-alpha)-(+-)- 16,17-Dinoremetan, 1',2'-didehydro-1-methyl-6',7',10,11-tetramethoxy-, dihydrochloride, (1-beta)-(+-)- 16,17-Dinoremetan, 1-methyl-6',7',10,11-tetramethoxy-, dihydrochloride, (1-alpha)-(+-)- 16,17-Dinoremetan, 1',2'-didehydro-1-methyl-6',7',10,11-tetramethoxy-, dihydrochloride, (1-alpha,2-alpha)-(+-)-