摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-[[2-(Diethylamino)ethyl]amino]-4-(hydroxymethyl)-7-methoxy-9H-thioxanthen-9-one | 86456-06-6

中文名称
——
中文别名
——
英文名称
1-[[2-(Diethylamino)ethyl]amino]-4-(hydroxymethyl)-7-methoxy-9H-thioxanthen-9-one
英文别名
1-<<2-(diethylamino)ethyl>amino>-4-(hydroxymethyl)-7-methoxy-9H-thioxanthen-9-one;7-methoxy-hycanthone;1-[[2-(diethylamino)-ethyl]amino]-4-(hydroxymethyl)-7-methoxythioxanthen-9-one;1-[[2-(diethylamino)ethyl]amino]-4-(hydroxymethyl)-7-methoxythioxanthen-9-one;1-{[2-(diethylamino)ethyl]amino}-4-(hydroxymethyl)-7-methoxy-9H-thioxanthen-9-one;1-[2-(diethylamino)ethylamino]-4-(hydroxymethyl)-7-methoxythioxanthen-9-one
1-[[2-(Diethylamino)ethyl]amino]-4-(hydroxymethyl)-7-methoxy-9H-thioxanthen-9-one化学式
CAS
86456-06-6
化学式
C21H26N2O3S
mdl
——
分子量
386.515
InChiKey
UPQPNCOOROMTAO-UHFFFAOYSA-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:
    1.250±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    27
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    87.1
  • 氢给体数:
    2
  • 氢受体数:
    6

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Analogs of hycanthone and lucanthone as antitumor agents
    摘要:
    Hycanthone analogues (5 and 6) containing 7-substituted hydroxyl groups were prepared and evaluated as antitumor agents. These compounds were significantly more active than the corresponding unsubstituted derivatives. The 7-hydroxylated 4-(hydroxymethyl)-9H-xanthen-9-ones, 11 and 12, were also active antitumor agents. However, the 7-hydroxy-9H-xanthen-9-one counterparts of the 7-hydroxylucanthones were totally devoid of antitumor activity. Results obtained thus far are consistent with the hypothesis that 4-hydroxymethyl substituents in the 9H-xanthen-9-one and 9H-thioxanthen-9-one series are required for antitumor activity.
    DOI:
    10.1021/jm00363a007
  • 作为产物:
    参考文献:
    名称:
    Analogs of hycanthone and lucanthone as antitumor agents
    摘要:
    Hycanthone analogues (5 and 6) containing 7-substituted hydroxyl groups were prepared and evaluated as antitumor agents. These compounds were significantly more active than the corresponding unsubstituted derivatives. The 7-hydroxylated 4-(hydroxymethyl)-9H-xanthen-9-ones, 11 and 12, were also active antitumor agents. However, the 7-hydroxy-9H-xanthen-9-one counterparts of the 7-hydroxylucanthones were totally devoid of antitumor activity. Results obtained thus far are consistent with the hypothesis that 4-hydroxymethyl substituents in the 9H-xanthen-9-one and 9H-thioxanthen-9-one series are required for antitumor activity.
    DOI:
    10.1021/jm00363a007
点击查看最新优质反应信息

文献信息

  • Thioxanthenone antitumor agents
    申请人:Sterling Winthrop Inc.
    公开号:US05346917A1
    公开(公告)日:1994-09-13
    1-[[(Dialkylamino)alkyl]amino]-4-substituted-thioxanthen-9-ones are disclosed as antitumor agents. Compositions containing the thioxanthenones and methods of treating tumors and cancer in mammals with the thioxanthenones are also disclosed.
    1-[[(二烷基氨基)烷基]氨基]-4-取代-噻吨-9-酮被披露为抗肿瘤剂。还披露了含有噻吨酮的制剂以及使用噻吨酮治疗哺乳动物肿瘤和癌症的方法。
  • Lyophilized thioxanthenone antitumor agents
    申请人:Sanofi Winthrop, Inc.
    公开号:US05665760A1
    公开(公告)日:1997-09-09
    Disclosed are reconstituted lyophilized formulations for the treatment of mammalian tumors comprising a thioxanthenone antitumor agent in combination with mannitol or sucrose as a stabilizer in a lactate buffer.
    公开了用于治疗哺乳动物肿瘤的重组冻干制剂,该制剂包括一种噻吨酮类抗肿瘤剂,并与乳糖酸缓冲液中的甘露醇或蔗糖作为稳定剂结合使用。
  • 7-Hydroxylucanthone, 7-hydroxhycanthone and their analogs
    申请人:Rensselaer Polytechnic Institute
    公开号:US04539412A1
    公开(公告)日:1985-09-03
    7-Hydroxylucanthone and 7-hydroxyhycanthone derivatives have been found to have significant antitumor effect. The derivatives are of the general formula: ##STR1## wherein the radicals R.sup.1 and R.sup.2 are lower alkyl groups or other simple groups and R.sup.3 is OH where X.dbd.O, and H or OH where X.dbd.S.
    7-羟基卢坎通和7-羟基海坎通衍生物已被发现具有显著的抗肿瘤效果。这些衍生物的一般化学式为:其中基团R.sup.1和R.sup.2为较低的烷基基团或其他简单基团,R.sup.3为OH,其中X=dbd.O,以及X=dbd.S时为H或OH。
  • One Step Synthesis of <i>N</i>-[1-(2-Diethylamino-ethylamino)-7-(<i>H</i> or methoxy)-9-oxo-9<i>H</i>-thioxanthen-4-ylmethyl]-formamides and, Acetamide from Their Corresponding Alcohols, Hycanthone, and 7-Methoxy-hycanthone
    作者:Hua-Zhong He、Chul-Hoon Kwon
    DOI:10.1081/scc-120021833
    日期:2003.1.8
    Abstract N-[1-(2-Diethylamino-ethylamino)-7-(H or methoxy)-9-oxo-9H-thioxanthen-4-ylmethyl]-formamides and acetamide were synthesized from their corresponding alcohols, hycanthone and 7-methoxy-hycanthone, in one step procedure and 45% yield.
    摘要 N-[1-(2-二乙氨基-乙氨基)-7-(H 或甲氧基)-9-氧代-9H-噻吨-4-基甲基]-甲酰胺和乙酰胺由其相应的醇、乙氧基和7-甲氧基合成。 -hycanthone,一步法,产率45%。
  • [EN] LYOPHILIZED THIOXANTHENONE ANTIMUMOR AGENTS<br/>[FR] THIOXANTHENONE LYOPHILISEE COMME AGENTS ANTITUMORAUX
    申请人:SANOFI
    公开号:WO1997010809A1
    公开(公告)日:1997-03-27
    (EN) Disclosed are reconstituted lyophilized formulations for the treatment of mammalian tumors comprising a thioxanthenone antitumor agent in combination with mannitol or sucrose as a stabilizer in a lactate buffer.(FR) La présente invention concerne des formulations lyophilisées reconstituées destinées au traitement de tumeurs de mammifères. Ces formulations comprennent un agent antitumoral, à savoir la thioxanthénone, combinée à un stabilisant, en l'occurrence le mannitol ou le saccharose, dans un tampon de lactate.
    揭示了一种重组冻干配方,用于治疗哺乳动物肿瘤,包括一种硫代三环酮抗肿瘤剂与甘露醇或蔗糖作为稳定剂,在乳酸缓冲液中组合使用。
查看更多

同类化合物

贝恩酮盐酸盐 苯并噻喃并[4,3-b]吲哚 苯并[e][1]苯并噻喃并[4,3-b]吲哚 苯并[c]噻吨-7-酮 苯并[a]噻吨-12-酮 硫坎酮 硫代色烯-2-酮 海蒽酮甲磺酸盐 海蒽酮N-甲基氨基甲酸酯 海恩酮 异丙基硫代呫吨酮 噻吨酮-3-甲酰胺 [[(9-氧代-9H-噻吨-2-基)甲基]硫代]乙酸 N-[2-(二甲氨基)乙基]-9-羰基-9H-硫代占吨-4-甲酰胺 N,N-二甲基-N'-4H-硫代色烯-4-基酰亚胺基甲酰胺 N'-[4-(羟基甲基)-9-氧代-9H-噻吨-1-基]-N,N-二乙基乙烷-1,2-二胺N-氧化物 9-氧代噻吩-4-羧酸乙酯 9-氧代噻吨-1-羧酸甲酯 9-氧代-9h-硫代氧杂蒽-2-羧酸 9-氧代-9h-硫代氧杂蒽-2-羧酸 9-氧代-9H-硫代氧杂蒽-1-羧酸 9-氧代-9H-噻吨-3-甲腈 9-氧代-9H-噻吨-2-羧酸乙酯 9-氧代-3-(苯基磺酰基)-9H-噻吨-1-羧酸乙酯 9-噻吨酮 8H-苯并噻喃并[7,8-D][1,3]噻唑 8H-苯并噻喃并[6,7-D][1,3]噻唑 8-甲基-4H-硫色烯-4-酮 8-氯-N,N-二乙基-5-甲基-2H-[1]苯并噻喃并[4,3,2-cd]吲唑-2-乙胺N-氧化物 8-氯-5-甲基-N,N-二乙基-2H-[1]苯并噻喃并[4,3,2-cd]吲唑-2-乙烷-1-胺 8-氯-5-(羟基甲基)-N,N-二乙基-2H-[1]苯并噻喃并[4,3,2-cd]吲唑-2-乙烷-1-胺N-氧化物 7H-苯并噻喃并[6,5-d][1,3]噻唑 7-甲氧基-2-甲基-4H-硫代色烯-4-酮 7-甲基-9-氧代噻吨-3-羧酸乙酯 7-氨基-1-[[2-(二乙胺)乙基]氨基]-4-甲基-L-9H-噻吨-9-酮 6H-苯并噻喃并[7,6-D][1,3]噻唑 6-甲氧基-2-甲基-4H-硫代色烯-4-酮 6-甲基-4H-硫代色烯-4-酮 6-氯-1-({2-[乙基(2-羟基乙基)氨基]乙基}氨基)-4-(羟甲基)-9H-硫代占吨-9-酮 6-氟-4H-硫代色烯-4-酮 6-氟-2-(三氟甲基)-9H-噻吨-9-酮 6-(2-二乙基氨基乙胺)-1,2,3,4-四氢苯并[a]噻吨-12-酮 5-[(2-氨基乙基)氨基]-2-[2-(二乙基氨基)乙基]-2H-苯并噻喃并[4,3,2-Cd]吲唑-8-醇三盐酸盐 5-(2-二乙基氨基乙胺)-1,2,3,4-四氢苯并[c]噻吨-7-酮 4H-1-苯并噻喃-4-酮 1,1-二氧化物 4-羟基硫代香豆素 4-甲基-9H-噻吨-9-酮 4-氯-9H-噻吨-9-酮 4-氯-3-硝基硫代香豆素 4-氯-2H-1-苯并噻喃-3-甲醛