33069-62-4

  • Product Name:Paclitaxel
  • Molecular Formula:C47H51NO14
  • Purity:99%
  • Molecular Weight:853.92
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Product Details;

CasNo: 33069-62-4

Molecular Formula: C47H51NO14

Appearance: white powder

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1.What is the Paclitaxel ?

Paclitaxel (Taxol) is a highly complex, organic compound isolated from the bark of the Pacific yew tree. It binds to tubulin dimers and microtubulin filaments, promoting the assembly of filaments and preventing their depolymerization. This increase in the stability of microfilaments results in disruption of mitosis and cytotoxicity and disrupts other normal microtubular functions, such as axonal transport in nerve fibers. The major mechanism of resistance that has been identified for paclitaxel is transport out of tumor cells, which leads to decreased intracellular drug accumulation. This form of resistance is mediated by the multidrug transporter P-glycoprotein.

Paclitaxel is an antineoplastic that used to treat patients with lung, ovarian, breast cancer, head and neck cancer, and advanc ed forms of Kaposi's sarcoma. Paclitaxel is a mitotic inhibitor used in cancer chemotherapy. It is also used in the study of structure and function of microtubles into tubulin.

acetic anhydride
108-24-7

acetic anhydride

7-O-(β-xylosyl)-10-deacetyltaxol
90332-63-1

7-O-(β-xylosyl)-10-deacetyltaxol

taxol
33069-62-4

taxol

2'-O-acetyl-paclitaxel
92950-40-8

2'-O-acetyl-paclitaxel

Conditions
Conditions Yield
7-O-(β-xylosyl)-10-deacetyltaxol; With sodium periodate; sulfuric acid; In methanol; chloroform; water; at 20 ℃; for 3h;
acetic anhydride; With pyridine; at 100 ℃; for 0.5h;
With acetic acid; phenylhydrazine; In methanol; at 50 - 60 ℃; for 3h;
7-O-(β-xylosyl)-10-deacetyltaxol; With sodium periodate; sulfuric acid; In methanol; chloroform; at 20 ℃; for 3h;
acetic anhydride; With pyridine; at 100 ℃; for 0.05h;
With acetic acid; phenylhydrazine; In methanol; at 50 - 60 ℃; for 3h;
C<sub>54</sub>H<sub>59</sub>N<sub>5</sub>O<sub>16</sub>

C54H59N5O16

taxol
33069-62-4

taxol

(S)-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione
3705-27-9

(S)-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

Conditions
Conditions Yield
With trimethylphosphane; In tetrahydrofuran; water;
92%

2.What is the CAS number for Paclitaxel ?

The CAS number of Paclitaxel is 33069-62-4.

More information of Paclitaxel 33069-62-4 are:

CAS Number

33069-62-4

Density

1.39 g/cm3

Melting Point

213 °C

Boiling Point

957.115 °C at 760 mmHg

Flash Point

532.644 °C

Vapor Pressure

0mmHg at 25°C

Refractive Index

-49 ° (C=1, MeOH)

HS CODE

2939.90

PSA

221.29000

LogP

4.12660

Pka

11.90±0.20(Predicted)

3.What are another words for Paclitaxel ?

Synonyms for Paclitaxel 33069-62-4:BMS 181339-01;Benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca(3,4)benz(1,2-b)oxet-9-yl ester, (2aR-(2a-alpha,4-beta,4a-beta,6-beta,9-alpha(alpha-R*,beta-S*),11-alpha,12-alpha,12a-alpha, 12b-alpha))-;Taxol.RTM. (Registered Trademark);QW 8184;MBT 0206;12-benzoate, 9-ester with (2R,3S)-N-benzoyl-3-phenylisoserine;Palcitaxel;Benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca(3,4)benz(1,2-b)oxet-9-yl ester, (2aR-(2aalpha,4beta,4abeta,6beta,9alpha(alphaR*,betaS*),11alpha,12alpha,12aalpha,12balpha))-;Prestwick_459;Abraxane;Taxol (TN);Paxceed;NSC-125973;Paxene;Plaxicel;Onxol;Indirubin;Paclitaxle;Paclitaxel Semi-Synthetic USP30;

4.What is the molecular formula of Paclitaxel?

The chemical formula of  Paclitaxel is C47H51NO14 which containing 47 Carbon atoms,51 Hydrogen atoms,1 Nitrogen atoms and 14 Oxygen atoms,and the molecular weight of  Paclitaxel is 853.92.

5.What is Paclitaxel (33069-62-4) used for?

Paclitaxel, a natural product isolated from the bark of the Pacific yew, is effective in treating refractory metastatic ovarian cancer. Unlike any other antineoplastic agents, paclitaxel appears to have several possible mechanisms of action, including an antimicrotubule action through the promotion of tubulin polymerization and stabilization of microtubules, thereby, halting mitosis and promoting cell death. The supply of paclitaxel is limited by its low natural abundance and currently it is being manufactured by a semi-synthetic route from deacetylbaccatin Ⅲ that is isolated from the needles of the yew tree. Recent completion of two total syntheses of taxol conquered the structural complexity of the title compound and may be useful in obtaining certain closely related analogs, some of which have been found to have antitumor activity. Paclitaxel has potential uses in the treatment of metastatic breast cancer, lung cancer, head and neck cancer, and malignant melanoma.

InChI:InChI=1/C47H51NO14/c1-25-31(60-43(56)36(52)35(28-16-10-7-11-17-28)48-41(54)29-18-12-8-13-19-29)23-47(57)40(61-42(55)30-20-14-9-15-21-30)38-45(6,32(51)22-33-46(38,24-58-33)62-27(3)50)39(53)37(59-26(2)49)34(25)44(47,4)5/h7-21,31-33,35-38,40,51-52,57H,22-24H2,1-6H3,(H,48,54)/t31?,32-,33+,35?,36?,37+,38?,40?,45+,46-,47+/m0/s1

Relevant articles related to Paclitaxel:

Article

Source

CoA recycling by a benzoate coenzyme A ligase in cascade reactions with aroyltransferases to biocatalyze paclitaxel analogs

Nawarathne, Irosha N.,Sullivan, Sean A.,Walker, Kevin D.

, (2020)

Intermediate compound for preparing paclitaxel, synthetic method of intermediate compound and synthetic method of paclitaxel

-

, (2022/01/12)

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