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Merck
CN

B8154

巴卡亭III

≥95% (HPLC)

别名:

O-De[(2R,3S)-3-(Benzoylamino)-2-hydroxy-3-phenylpropanoyl]paclitaxel

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关于此项目

经验公式（希尔记法）:
C31H38O11
化学文摘社编号:
27548-93-2
分子量:
586.63
MDL编号:
MFCD00153921
UNSPSC代码:
12352005
PubChem化学物质编号:
57653960
NACRES:
NA.22

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质量水平

100

方案

≥95% (HPLC)

表单

powder

储存温度

2-8°C

SMILES字符串

CC(=O)O[C@H]1C(=O)[C@]2(C)[C@@H](O)C[C@H]3OC[C@@]3(OC(C)=O)[C@H]2[C@H](OC(=O)c4ccccc4)[C@]5(O)C[C@H](O)C(C)=C1C5(C)C

InChI

1S/C31H38O11/c1-15-19(34)13-31(38)26(41-27(37)18-10-8-7-9-11-18)24-29(6,20(35)12-21-30(24,14-39-21)42-17(3)33)25(36)23(40-16(2)32)22(15)28(31,4)5/h7-11,19-21,23-24,26,34-35,38H,12-14H2,1-6H3/t19-,20-,21+,23+,24-,26-,29+,30-,31+/m0/s1

InChI key

OVMSOCFBDVBLFW-VHLOTGQHSA-N

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相关类别

应用

紫杉酚的前体

象形图

Health hazardExclamation mark
GHS08,GHS07

警示用语：

Danger

危险分类

Carc. 1B - Eye Irrit. 2 - Muta. 1B - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCP2901
MKBT4428V
098H1127
098H0559
078H0511

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Young-Hee Lee et al.
International immunopharmacology, 21(2), 487-493 (2014-06-25)
Myeloid-derived suppressor cells (MDSCs) mediate tumor-associated immune suppression in both cancer patients and tumor-bearing animals. Reduction or elimination of MDSCs reduces the rate of tumor progression and improves cancer therapies that employ mechanisms of immunity. Here we show that baccatin
Catherine Loncaric et al.
Chemistry & biology, 13(3), 309-317 (2006-04-28)
The 10beta-acetyltransferase on the biosynthetic pathway of the antineoplastic drug Taxol catalyzes the regiospecific transfer of the acetyl group of acetyl-coenzyme A (CoA) to 10-deacetylbaccatin III. We demonstrate that in addition to acetyl group transfer, the overexpressed enzyme also catalyzes
Mohammad K Parvez et al.
Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 27(3), 389-400 (2019-04-13)
Despite high anti-HBV efficacies, while the nucleoside analogs (e.g., lamivudine) lead to the emergence of drug-resistance, interferons (e.g., IFN-α causes adverse side-effects. Comparatively, various natural or plant products have shown similar or even better efficacy. Hence, new antiviral strategies must
Xin Che et al.
Journal of pharmaceutical and biomedical analysis, 55(5), 1190-1196 (2011-05-03)
The isolation and characterization of the process related impurities and degradation products of larotaxel drug substance were described. Forced degradation of larotaxel was carried out under acidic, basic, oxidation, light and thermal conditions to assess the nature of the impurities.
Hiroshi Izumi et al.
The Journal of organic chemistry, 73(6), 2367-2372 (2008-02-16)
The comparison between measured and conformer-weighted calculated VCD spectra of the baccatin III ring of paclitaxel and visualization of the conformations using the new code for structure-activity relationships are reported for the first time. The VCD spectrum of paclitaxel closely
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