Chemodex

Paclitaxel

CHF 68.00
In stock
CDX-P0188-M01010 mgCHF 68.00
CDX-P0188-M05050 mgCHF 177.00
More Information
Product Details
Synonyms Taxol; BMS 181339-01; NSC 125973
Product Type Chemical
Properties
Formula

C47H51NO14

MW 853.91
CAS 33069-62-4
Source/Host Chemicals Synthetic.
Purity Chemicals ≥98% (NMR)
Appearance White to off-white powder.
Solubility Soluble in DMSO (50 mg/ml), methanol (50 mg/ml) or ethanol.
Identity Determined by NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key RCINICONZNJXQF-MZXODVADSA-N
Smiles O[C@](C(C)(C)C1=C(C)[C@H]2OC([C@@H]([C@H](C3=CC=CC=C3)NC(C4=CC=CC=C4)=O)O)=O)(C2)[C@H]([C@]([C@]([C@@H](O)C5)(C)C([C@@H]1OC(C)=O)=O)([H])[C@]6([C@]5([H])OC6)OC(C)=O)OC(C7=CC=CC=C7)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Anticancer compound. Chemotherapeutic used in patients with cancer and advanced forms of Kaposi's sarcoma. Microtubule assembly stabilizer. Reversibly binds to polymerized tubulin. Mitotic spindle assembly, chromosome segregation and cell division inhibitor. Induces cell cycle arrest at the G2/M phase. Apoptosis inducer through aberrant activation of cyclin-dependent kinases (CKDs) and the c-Jun N-terminal kinase/stress activated protein kinase (JNK/SAPK). Immunosuppressor, immunostimulant and TRAIL sensitizer.

Product References

(1) J.E. Liebmann, et al.; Br. J. Cancer 68, 1104 (1993) | (2) R. Foa, et al.; Int. J. Clin. Lab. Res. 24, 6 (1994) (Review) | (3) M. Woods, et al.; Mol. Med. 1, 506 (1995) | (4) A. Jordan, et al.; Med. Res. Rev. 18, 259 (1998) | (5) L.A. Amos & J. Löwe; Chem. Biol. 6, R65 (1999) (Review) | (6) M.V. Blagosklonny & T. Fojo; Int. J. Cancer 83, 151 (1999) | (7) T.H. Wang, et al.; J. Biol. Chem. 274, 8208 (1999) | (8) T.H. Wang, et al.; Cancer 88, 2619 (2000) | (9) T.M. Mekhail & M. Markman; Expert Opin. Pharmacother. 3, 755 (2002) | (10) A. Javeed, et al.; Eur. J. Pharm. Sci. 38, 283 (2009) (Review) | (11) D. Finlay, et al.;PLoS One 5, e13375 (2010) | (12) B. Ai, et al.; Am. J. Cancer Res. 6, 1624 (2016) (Review)

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