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Merck
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B8154

Sigma-Aldrich

巴卡亭III

≥95% (HPLC)

别名:

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

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About This Item

经验公式（希尔记法）:
C31H38O11
CAS号:
27548-93-2
分子量:
586.63
MDL號碼:
MFCD00153921
分類程式碼代碼:
12352005
PubChem物質ID:
57653960
NACRES:
NA.22

化驗

≥95% (HPLC)

形狀

powder

儲存溫度

2-8°C

SMILES 字串

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 密鑰

OVMSOCFBDVBLFW-VHLOTGQHSA-N

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相关类别

應用

紫杉酚的前体

象形圖

Health hazardExclamation mark
GHS08,GHS07

訊號詞

Danger

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

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

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

从最新的版本中选择一种：

分析证书(COA)

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

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Chia-Hsiang Hwang et al.
Phytotherapy research : PTR, 26(4), 528-534 (2011-09-15)
7,7''-Dimethoxyagastisflavone (DMGF), a biflavonoid isolated from the needles of Taxus × media cv. Hicksii, was evaluated for its antiproliferative and antineoplastic effects in three human cancer cell lines. Interestingly, DMGF caused cell death via different pathways in different cancer cells.
Takayuki Doi et al.
Chemistry, an Asian journal, 1(3), 370-383 (2007-04-19)
A 36-step synthesis was carried out in automated synthesizers to provide a synthetic key intermediate of taxol. A key step involved a microwave-assisted alkylation reaction to construct the ABC ring system from an AC precursor. Subsequent formation of the D
Jared T Spletstoser et al.
Bioorganic & medicinal chemistry letters, 16(3), 495-498 (2005-11-18)
A single-site modification of paclitaxel analogs at the C10 position on the baccatin III core that reduces interaction with P-glycoprotein in bovine brain microvessel endothelial cells is described. Modification and derivatization of the C10 position were carried out using a
Bing-Juan Li et al.
Nature communications, 8, 15544-15544 (2017-05-19)
The natural concentration of the anticancer drug Taxol is about 0.02% in yew trees, whereas that of its analogue 7-β-xylosyl-10-deacetyltaxol is up to 0.5%. While this compound is not an intermediate in Taxol biosynthetic route, it can be converted into
Elizabeth M Heider et al.
Physical chemistry chemical physics : PCCP, 9(46), 6083-6097 (2008-01-03)
The three-dimensional structure of a unique polymorph of the anticancer drug paclitaxel (Taxol) is established using solid state NMR (SSNMR) tensor ((13)C & (15)N) and heteronuclear correlation ((1)H-(13)C) data. The polymorph has two molecules per asymmetric unit (Z' = 2)
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实验方案

HPLC Analysis of Paclitaxel and Related Compounds on Ascentis® Express F5

HPLC Analysis of Paclitaxel and Related Compounds on Ascentis® Express F5

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