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Merck

D3676

Sigma-Aldrich

10-脱乙酰基巴卡汀III 来源于浆果紫杉

≥95% (HPLC)

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5 MG
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5 MG
$334.00

About This Item

经验公式(希尔记法):
C29H36O10
CAS号:
分子量:
544.59
MDL编号:
UNSPSC代码:
51102829
PubChem化学物质编号:
NACRES:
NA.85

$334.00


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生物来源

Taxus baccata

方案

≥95% (HPLC)

表单

solid

分子量

544.59 g/mol

颜色

white

溶解性

methanol: soluble, clear, colorless (5 mg + 0.1 mL MeOH)

抗生素抗菌谱

neoplastics

作用机制

DNA synthesis | interferes

储存温度

2-8°C

SMILES字符串

[H][C@@]12C[C@H](O)[C@@]3(C)C(=O)[C@H](O)C4=C(C)[C@@H](O)C[C@@](O)([C@@H](OC(=O)c5ccccc5)[C@]3([H])[C@@]1(CO2)OC(C)=O)C4(C)C

InChI

1S/C29H36O10/c1-14-17(31)12-29(36)24(38-25(35)16-9-7-6-8-10-16)22-27(5,23(34)21(33)20(14)26(29,3)4)18(32)11-19-28(22,13-37-19)39-15(2)30/h6-10,17-19,21-22,24,31-33,36H,11-13H2,1-5H3/t17-,18-,19+,21+,22-,24-,27+,28-,29+/m0/s1

InChI key

YWLXLRUDGLRYDR-ZHPRIASZSA-N

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应用

10-脱乙酰基浆果赤霉素III被用作制备抗癌药物紫杉醇(紫杉醇)的一种化学中间体。它被用于研究紫杉醇生物合成途径[1][2][3]

生化/生理作用

10-脱乙酰基浆果赤霉素III是紫杉醇生物合成的第五中间体。该生物合成通路由大约20个尚未被完全阐明的酶促步骤组成[1]

象形图

Health hazardExclamation mark

警示用语:

Danger

危险分类

Carc. 1B - Eye Irrit. 2 - Muta. 1B - Skin Irrit. 2 - STOT RE 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

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

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H Gelderblom et al.
Drug metabolism and disposition: the biological fate of chemicals, 27(11), 1300-1305 (1999-10-26)
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Simona Mozzetti et al.
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Denis, J-N., et al.
Journal of the American Chemical Society, 110, 5917-5917 (1988)
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Journal of biotechnology, 288, 41-47 (2018-11-06)
Formation of disulfide bonds between heavy and light chains is challenge for production of recombinant immunoglobulin G (IgG) and fragment antigen-binding (Fab). Insufficient formation of the bond influences productive yield and quality of recombinant IgG and Fab. To investigate how

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