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

2-debenzoyl-2-(3-methoxybenzoyl)-7-triethylsilyl-10-deacetyl-10-(2-methoxybenzoyl)-13-oxo-baccatin III | 1031783-62-6

中文名称
——
中文别名
——
英文名称
2-debenzoyl-2-(3-methoxybenzoyl)-7-triethylsilyl-10-deacetyl-10-(2-methoxybenzoyl)-13-oxo-baccatin III
英文别名
——
2-debenzoyl-2-(3-methoxybenzoyl)-7-triethylsilyl-10-deacetyl-10-(2-methoxybenzoyl)-13-oxo-baccatin III化学式
CAS
1031783-62-6
化学式
C44H56O13Si
mdl
——
分子量
821.006
InChiKey
LIBYBFGZVAVGEP-KXEYATMGSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.2
  • 重原子数:
    58.0
  • 可旋转键数:
    12.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    170.19
  • 氢给体数:
    1.0
  • 氢受体数:
    13.0

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

  • 作为反应物:
    描述:
    2-debenzoyl-2-(3-methoxybenzoyl)-7-triethylsilyl-10-deacetyl-10-(2-methoxybenzoyl)-13-oxo-baccatin III 在 sodium tetrahydroborate 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 5.0h, 以40%的产率得到2-debenzoyl-2-(3-methoxybenzoyl)-7-triethylsilyl-10-deacetyl-10-(2-methoxybenzoyl)baccatin III
    参考文献:
    名称:
    Design, Synthesis, and Biological Evaluation of New-Generation Taxoids
    摘要:
    Novel second-generation taxoids with systematic modifications at the C2, C10, and C3'N positions were synthesized and their structure-activity relationships studied. A number of these taxoids exhibited exceptionally high potency against multidrug-resistant cell lines, and several taxoids exhibited virtually no difference in potency against the drug-sensitive and drug-resistant cell lines. These exceptionally potent taxoids were termed "third-generation taxoids". 19 (SB-T-1214), 14g(SB-T-121303), and 14i (SB-T-1213031) exhibited excellent activity against paclitaxel-resistant ovarian cancer cell lines with mutations in beta-tubulin as well, wherein the drug resistance is mediated by the beta-tubulin mutation. These taxoids were found to possess exceptional activity in promoting tubulin assembly, forming numerous very short microtubules similar to those formed by discodermolide. Taxoids 19 and 14g also showed excellent cytotoxicity against four pancreatic cancer cell lines, expressing three to four multidrug-resistant genes. Moreover, taxoid 19 exhibited excellent in vivo efficacy against highly drug-resistant CFPAC-1 pancreatic as well as DLD-1 human colon tumor xenografts in mice.
    DOI:
    10.1021/jm800086e
  • 作为产物:
    描述:
    2-debenzoyl-2-(3-methoxybenzoyl)-7-triethylsilyl-10-deacetyl-13-oxo-baccatin III甲氧基苯甲酰氯4-二甲氨基吡啶三乙胺 作用下, 以 二氯甲烷 为溶剂, 以100%的产率得到2-debenzoyl-2-(3-methoxybenzoyl)-7-triethylsilyl-10-deacetyl-10-(2-methoxybenzoyl)-13-oxo-baccatin III
    参考文献:
    名称:
    Design, Synthesis, and Biological Evaluation of New-Generation Taxoids
    摘要:
    Novel second-generation taxoids with systematic modifications at the C2, C10, and C3'N positions were synthesized and their structure-activity relationships studied. A number of these taxoids exhibited exceptionally high potency against multidrug-resistant cell lines, and several taxoids exhibited virtually no difference in potency against the drug-sensitive and drug-resistant cell lines. These exceptionally potent taxoids were termed "third-generation taxoids". 19 (SB-T-1214), 14g(SB-T-121303), and 14i (SB-T-1213031) exhibited excellent activity against paclitaxel-resistant ovarian cancer cell lines with mutations in beta-tubulin as well, wherein the drug resistance is mediated by the beta-tubulin mutation. These taxoids were found to possess exceptional activity in promoting tubulin assembly, forming numerous very short microtubules similar to those formed by discodermolide. Taxoids 19 and 14g also showed excellent cytotoxicity against four pancreatic cancer cell lines, expressing three to four multidrug-resistant genes. Moreover, taxoid 19 exhibited excellent in vivo efficacy against highly drug-resistant CFPAC-1 pancreatic as well as DLD-1 human colon tumor xenografts in mice.
    DOI:
    10.1021/jm800086e
点击查看最新优质反应信息

同类化合物

([2-(萘-2-基)-4-氧代-4H-色烯-8-基]乙酸) (R)-斯替戊喷酯-d9 (E,Z)-他莫昔芬N-β-D-葡糖醛酸 (E)-3-(4-(叔丁基)苯基)丙烯酸乙酯 (E)-3-(2-(三氟甲基)苯基)丙烯酸乙酯 (E)-3-(2,4-二甲氧基苯基)丙烯酸乙酯 (E/Z)-他莫昔芬-d5 (5Z)-7-氧杂烯醇 (4S,5R)-4,5-二苯基-1,2,3-恶噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S,5R,5''R)-2,2''-(1-甲基亚乙基)双[4,5-二氢-4,5-二苯基恶唑] (4R,5S)-4,5-二苯基-1,2,3-恶噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4R,4''R,5S,5''S)-2,2''-(1-甲基亚乙基)双[4,5-二氢-4,5-二苯基恶唑] (4-甲氧基-6-[(E)-2-(3-甲氧基苯基)乙烯基]-5,6-二氢-2H-吡 (2Z)-1,3-二苯基-2-丙烯-1-酮,2-丙烯-1-酮,1,3-二苯基-,(2Z)- (2E)-N-[2-(3-羟基-2-氧代-2,3-二氢-1H-吲哚-3-基)乙基]-3-苯基丙-2-烯酰胺 (1R,2R)-2-(二苯基膦基)-1,2-二苯基乙胺 (11aR)-3,7-双(3,5-二甲基苯基)-10,11,12,13-四氢-5-羟基-5-氧化物-二茚基[7,1-de:1'',7''-fg][1,3,2]二氧杂膦酸 龙血素D 龙血素C 龙血素A 龙血素 B 龙血树脂红血树脂 鼠李素 鼠李柠檬素3-O-beta-D-鼠李三糖苷 鼠李柠檬素 鼠李亭3-O-beta-吡喃葡萄糖苷 鼓槌石斛素 黄麦格霉素 黄金树苷 黄酮醇-2-磺酸钠盐 黄酮胺 黄酮榕碱 黄酮地洛 黄酮哌酯 黄酮 黄豆黄苷 黄豆黄素 黄豆苷元-D6 黄豆苷元-4,7-二葡糖苷 黄诺马甙 黄苏木素 黄花夹竹桃黄酮 黄芪总皂甙 黄芪异黄烷苷,7,2'-二羟基-3',4'-二甲氧基异黄烷 黄芩黄酮II 黄芩黄酮I 黄芩黄酮 黄芩苷甲酯 黄芩苷 黄芩素磷酸酯