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Merck
모든 사진(1)

Key Documents

추가 자료

B8154

Sigma-Aldrich

Baccatin III

≥95% (HPLC)

동의어(들):

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

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C31H38O11
CAS Number:
27548-93-2
Molecular Weight:
586.63
MDL number:
MFCD00153921
UNSPSC 코드:
12352005
PubChem Substance ID:
57653960

Quality Level

100

분석

≥95% (HPLC)

형태

powder

저장 온도

2-8°C

SMILES string

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

관련 카테고리

애플리케이션

Precursor to paclitaxel

픽토그램

Exclamation markHealth hazard
GHS07,GHS08

신호어

Danger

유해 및 위험 성명서

H315 - H319 - H335 - H340 - H350

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

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

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 5

1 of 5

Paclitaxel, Taxus sp. Antitumor and antileukemic agent isolated from the bark of the yew tree.

Sigma-Aldrich

580555

Paclitaxel, Taxus sp.

Paclitaxel United States Pharmacopeia (USP) Reference Standard

USP

1491332

Paclitaxel

D-(−)-Quinic acid 98%

Sigma-Aldrich

138622

D-(−)-Quinic acid

Docetaxel purum, ≥97.0% (HPLC)

Sigma-Aldrich

01885

Docetaxel

Paclitaxel from semisynthetic, ≥98%

Sigma-Aldrich

T7191

Paclitaxel

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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