前往化源商城

品牌现货直购
供应商:我要出现这里






查看所有供应商和价格请点击:

105454-04-4生产厂家

105454-04-4价格

105454-04-4

105454-04-4结构式
105454-04-4结构式
  • 常用中文名:7-表紫杉醇
  • 常用英文名:7-Epitaxol
  • CAS号:105454-04-4
  • 分子式:C47H51NO14
  • 分子量:853.906
  • 相关类别: 生物化工 植物提取物
  • 发布时间:2018-02-06 08:00:00
  • 更新时间:2026-07-01 15:27:04
  • 7-epi-Taxol 是 taxol 的活性代谢物,在抑制细胞增殖及微管 (microtubule) 解离,诱导微管聚合等方面与 taxol 作用相当。

化源商城直购

中文名 7-表紫杉醇
英文名 7-Epitaxol
中文别名 紫杉醇杂质E(7-表紫杉醇)
7-表紫杉醇,10 MM DMSO 溶液
表紫杉醇
7-表紫杉醇/HPLC
紫杉醇杂质Ⅲ(7-表-紫杉醇)(2 ,4R ,4aS ,6R ,9S , llS ,12,12bS )- l ,2a ,3 ,4 ,4a ,6 ,9,10,11,12,12a,12b)-十二氢-4,6,9,11,12,12b-六羟基-4a,8,13,13-四甲基-7,11-亚甲基-5H-环芳癸[ 3,4 ]苯并[ 1,2-b]氧杂环丁烷-5酮-6,12b-二醋酸酯,12-苯甲酸酯,9-(2R,3S) -N-苯甲酰-3-苯基异丝氨酸酯
紫杉醇杂质Ⅲ(7-表-紫杉醇)(2 ,4R ,4AS ,6R ,9S , LLS ,12,12BS )- L ,2A ,3 ,4 ,4A ,6 ,9,10,11,12,12A,12B)-十二氢-4,6,9,11,12,12B-六羟基-4A,8,13,13-四甲基-7,11-亚甲基-5H-环芳癸[ 3,4 ]苯并[ 1,2-B]氧杂环丁烷-5酮-6,12B-二醋酸酯,12-苯甲酸酯,9-(2R,3S) -N-苯甲酰-3-苯基异丝氨酸酯
紫杉醇杂质E(7- I紫杉醇)
紫杉醇
紫杉醇杂质E
7-表紫杉醇(标准品)
7-I紫杉醇
紫杉醇杂质5(紫杉醇杂质E)
7-表皮素
7-差向紫杉醇
(2,4R,4aS,6R,9S,11S,12S,12,12bS)-9-(((2R,3S)-3-苯甲酰胺-2-羟基-3-苯基丙酰基)氧基)-12-(苯甲酰氧基)-4,11-二羟基-4a,8,13,13-四甲基-5-氧代-3,4,4a,5,6,9,10,11,12,12a-十氢-1H-7,11-甲桥环癸并[3,4]苯并[1,2-b]oxete-6,12b(2aH)-二基 二乙酸酯
7-表-紫杉醇(紫杉醇杂质III)
紫杉醇杂质
紫杉醇杂质III
7-表紫杉醇(对照品)
7-表紫杉醇,7-差向紫杉醇
紫杉醇杂质E(7-差向紫杉醇)
7-表紫杉醇, 来源于红豆杉
7-差向紫杉酚
7-表位紫杉醇(紫杉醇杂质E)
英文别名 ITAXOL,7- SOLUTION(2.4mg/mL)(P)
Paclitaxel Impurity 5(Paclitaxel Impurity E)
inhibit,Microtubule/Tubulin,7 i Taxol,7iTaxol,Inhibitor
(2α,5β,7α,10β,13α)-4,10-Diacetoxy-13-{[(2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoyl]oxy}-1,7-dihydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate
5b,20-Epoxy-1,2a,4,7b,10b,13a-hexahydroxytax-11-en-9-one 4,10-Diacetate 2-Benzoate 13-Ester with (2R,3S)-N-Benzoyl-3-phenylisoserine
Yewtaxan
Paclitaxel Impurity E
benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, 6,12B-bis(acetyloxy)-12-(benzoyloxy)-2A,3,4,4A,5,6,9,10,11,12,12A,12B-dodecahydro-4,11-dihydroxy-4A,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca(3,4)benz(1,2-B)oxet-9-yl ester, (2- (2aalpha,4alpha,4abeta,6beta,9alpha(alph*,betas*),11alpha,12alpha,12aalpha,12balpha))
TaxAlbin
Paclitaxel Impurity Ⅲ:(7-i-Paclitaxel)
Paclitaxel 7-i-Impurity
Epitaxol
(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Bis(acetyloxy)-1,9-dihydroxy-15-({(2R,3S)-2-hydroxy-3-phenyl-3-[(phenylcarbonyl)amino]propanoyl}oxy)-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.0.0]heptadec-13-en-2-ylbenzolcarboxylat
7-i-Taxol, 10 mM in DMSO
Taxol A
7,11-Methano-1H-cyclodeca[3,4]benz[1,2-b]oxete benzenepropanoic acid derivative
Paclitaxel Impurity E (7-Diverse Taxol)
7-i-Paclitaxel(7-itaxol)
(2,4R,4aS,6R,9S,11S,12S,12,12bS)-9-(((2R,3S)-3-Benzamido-2-hydroxy-3-phenylpropanoyl)oxy)-12-(benzoyloxy)-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-3,4,4a,5,6,9,10,11,12,12a-decahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxete-6,12b(2aH)-diyl diacetate
benzenepropanoic acid, β-(benzoylamino)-α-hydroxy-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, [2-[2aα,4α,4aβ,6β
7-epi-Taxol
7-itaxol 7-ipaclitaxel
(2α,5β,7β,10β,13α)-4,10-bis(acetyloxy)-1,7-dihydroxy-13-({(2R,3S)-2-hydroxy-3-phenyl-3-[(phenylcarbonyl)amino]propanoyl}oxy)-9-oxo-5,20-epoxytax-11-en-2-yl benzoate
UNII-P88XT4IS4D
Paclitaxel Impurity E (7-i Paclitaxel)
(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-bis(acetyloxy)-1,9-dihydroxy-15-({(2R,3S)-2-hydroxy-3-phenyl-3-[(phenylcarbonyl)amino]propanoyl}oxy)-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.0.0]heptadec-13-en-2-yl benzoate
7-ipaclitaxel, froM Taxus chinensis
BMS 181339-01
7-i Paclitaxel (Paclitaxel Impurity E)
itaxol
Plaxicel
Paxceed
benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, (2,4R,4as,6R,9S,11S,12S,12,12bs)-6,12B-bis(acetyloxy)-12-(benzoyloxy)- 2A,3,4,4A,5,6,9,10,11,12,12A,12B-dodecahydro-4,11-dihydroxy-4A,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca(3,4)benz(1,2-B)oxet-9-yl ester, (alph,betas)
(2a,5b,7b,10b,13a)-4,10-bis(acetyloxy)-13-{[(2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoyl]oxy}-1,7-dihydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate
(2α,5β,7β,10β,13α)-4,10-Diacetoxy-13-{[(2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoyl]oxy}-1,7-dihydroxy-9-oxo-5,20-epoxytax-11-en-2-yl benzoate
7-ipaclitaxel(crude)
Paclitaxel
(2,4R,4aS,6R,9S,11S,12S,12,12bS)-9-(((2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl)oxy)-12-(benzoyloxy)-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-1
7-ipaclitaxelQ: What is 7-ipaclitaxel Q: What is the CAS Number of 7-ipaclitaxel Q: What is the storage condition of 7-ipaclitaxel Q: What e the applications of 7-ipaclitaxel
7-itaxol ,S9265
7-ipaclitaxel from Taxus chinensis (Pilg.) Rehder
Propanedioicacid,2-(2-propyn-6-yl)-,diethylester
Peclitaxel
Taxol
ITAXOL, 7
Paxene
Paclitaxel Imp. I : 10-O-[(2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoyl]-10-O-deacetylpaclitaxel
benzenepropanoic acid, β-(benzoylamino)-α-hydroxy-, (2,4R,4aS,6R,9S,11S,12S,12,12bS)-6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, (αR,βS)
benzenepropanoicacid,beta-(benzoylaMino)-alpha-hydroxy-,6,12B-bis(acetyloxy)-12-(benzoyloxy)-2A,3,4,4A,5,6,9,10,11,12,12A,12B-dodecahydro-4,11-dihydroxy-4A,8,13,13-tetraMethyl-5-oxo-7,11-Methano-1H-cyclodeca(3,4)benz(1,2-B)oxet-9-ylester,(2-(
7-i-Taxol, Metabolite of Paclitaxel
7-IPACLITAXEL; 7-ITAXOL; 7-I-PACLITAXEL; ITAXOL
LipoPac
7-Epi Paclitaxel
Ebetaxel
Anzatax
baccatin III N-benzyl-b-phenylisoserine ester
Onxol
(2,4R,4aS,6R,9S,11S,12S,12,12bS)-9-(((2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl)oxy)-12-(benzoyloxy)-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxete-6,12b-diyl diacetate
描述 7-epi-Taxol 是 taxol 的活性代谢物,在抑制细胞增殖及微管 (microtubule) 解离,诱导微管聚合等方面与 taxol 作用相当。
相关类别
靶点

Microtubule/Tubulin[2]

体外研究 7-epi-Taxol(7-Epitaxol)是紫杉醇的代谢产物[1]。 7-epi-Taxol具有与紫杉醇相当的活性,可用于细胞复制,微管束形成和体外微管聚合[2]。
参考文献

[1]. Royer I, et al. Paclitaxel metabolites in human plasma and urine: identification of 6 alpha-hydroxytaxol, 7-epitaxol and taxol hydrolysis products using liquid chromatography/atmospheric-pressure chemical ionization mass spectrometry. Rapid Commun Mass Spectrom. 1995;9(6):495-502.

[2]. Ringel I, et al. Taxol is converted to 7-epitaxol, a biologically active isomer, in cell culture medium. J Pharmacol Exp Ther. 1987 Aug;242(2):692-8.

密度 1.4±0.1 g/cm3
沸点 957.1±65.0 °C at 760 mmHg
熔点 168-170?C
分子式 C47H51NO14
分子量 853.906
闪点 532.6±34.3 °C
精确质量 853.330933
PSA 221.29000
LogP 7.38
外观性状 粉末
蒸汽压 0.0±0.3 mmHg at 25°C
折射率 1.637
储存条件 -20°C Freezer, Under Inert Atmosphere
海关编码 2932999026
上游产品  0

下游产品  2

海关编码 2932999026
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。