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Docetaxel, 99%, Thermo Scientific™

Docetaxel, CAS # 114977-28-5, is a cytotoxic, semisynthetic, second-generation taxane derived from the needles of the European yew tree and displays antineoplastic, antibiotic, and antimicrotubule activities.

£113.00 - £570.98

Chemical Identifiers

CAS 114977-28-5
Molecular Formula C43H53NO14
Molecular Weight (g/mol) 807.89
MDL Number MFCD00800737
InChI Key ZDZOTLJHXYCWBA-VCVYQWHSSA-N
Synonym docetaxel, taxotere, docetaxel anhydrous, docetaxol, emdoc, docetaxel, trihydrate, docetaxel inn, taxotere tn, unii-699121phca, txl
PubChem CID 148124
ChEBI CHEBI:4672
SMILES CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)OC(C)(C)C)O)O)OC(=O)C6=CC=CC=C6)(CO4)OC(=O)C)O)C)O
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Product Code Brand Quantity Price Quantity & Availability  
15462989
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Thermo Scientific Alfa Aesar
J60174.MC
100mg
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Thermo Scientific Alfa Aesar
J60174.ME
500mg
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£322.00
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Thermo Scientific Alfa Aesar
J60174.03
1g
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£584.00
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Description

Description

This Thermo Scientific brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific.

General Description

• Docetaxel is an analog of taxol, and is considered to be a cytotoxic, semisynthetic, second-generation taxane that exhibits antineoplastic, antibiotic, and antimicrotubule activities
• Docetaxel is capable of inhibiting cellular mitosis. This compound promotes the assembly of microtubules from tubulin dimers and stabilizes microtubules by preventing depolymerization. This stability inhibits the normal dynamic reorganization of the microtubule network that is essential for vital interphase and mitotic cellular functions. This results in the persistence of abnormal microtubule structures leading to cell-cycle arrest and cell death

Application

• Docetaxel can inhibit angiogenesis both in vitro and in vivo by acting on vascular endothelial growth factor (VEGF) associated with cancer cells
• This compound has been used to investigate the effect of lysosomal autophagic flux in gastric cancer cells
• Some in vitro and in vivo studies have been performed in order to understand if the combination of docetaxel with stearidonic acid enhances cell death in human prostate cancer cells
• It has been used in vitro in prostate cancer stem-like cells (PCSCs) to test its effect on the notch signaling pathway

Specifications

Chemical Identifiers

114977-28-5
807.89
ZDZOTLJHXYCWBA-VCVYQWHSSA-N
148124
CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)OC(C)(C)C)O)O)OC(=O)C6=CC=CC=C6)(CO4)OC(=O)C)O)C)O
C43H53NO14
MFCD00800737
docetaxel, taxotere, docetaxel anhydrous, docetaxol, emdoc, docetaxel, trihydrate, docetaxel inn, taxotere tn, unii-699121phca, txl
CHEBI:4672

Specifications

114977-28-5
MFCD00800737
docetaxel, taxotere, docetaxel anhydrous, docetaxol, emdoc, docetaxel, trihydrate, docetaxel inn, taxotere tn, unii-699121phca, txl
ZDZOTLJHXYCWBA-VCVYQWHSSA-N
807.89
CHEBI:4672
99%
C43H53NO14
14,3397
Soluble in dimethyl sulfoxide and ethanol; Insoluble in water.
CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)OC(C)(C)C)O)O)OC(=O)C6=CC=CC=C6)(CO4)OC(=O)C)O)C)O
148124
807.88
Docetaxel
Videos
Safety and Handling

Safety and Handling

P201-P202-P261-P264b-P271-P280i-P281-P302+P352-P304+P340-P305+P351+P338-P308+P313-P332+P313-P362-P501c

H315-H319-H335-H361fd

missing translation for 'rtecsNumber' : DA4172750

missing translation for 'tsca' : No

Recommended Storage : Store at -20°C

SDS
Documents

Documents

Product Certifications

RUO – Research Use Only

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