Paclitaxel

CAS No. 33069-62-4

Paclitaxel( NSC 125973 )

Catalog No. M14100 CAS No. 33069-62-4

Paclitaxel is a novel antineoplastic agent, which was discovered in a screen of extracts of thousands of plants and natural products for antineoplastic activity by a National Y Institute program.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 48 In Stock
25MG 32 In Stock
50MG 45 In Stock
100MG 73 In Stock
200MG Get Quote In Stock
500MG 110 In Stock
1G 161 In Stock

Biological Information

  • Product Name
    Paclitaxel
  • Note
    Research use only, not for human use.
  • Brief Description
    Paclitaxel is a novel antineoplastic agent, which was discovered in a screen of extracts of thousands of plants and natural products for antineoplastic activity by a National Y Institute program.
  • Description
    Paclitaxel is a novel antineoplastic agent, which was discovered in a screen of extracts of thousands of plants and natural products for antineoplastic activity by a National Y Institute program. Alought it functions as a mitotic inhibitor like vinca alkaloids, paclitaxel promotes the polymerization of tubulin instead of inducing the disassembly of microtubules, which inhibits the microtubules disassembly and promotes the formation of excessively stable, dysfunctional microtubules. Paclitaxel has exhibited antitumor activity against a broad spectrum of human Ys, including ovarian, breast, head and neck, and lung Y, in a large number of studies.(In Vitro):Paclitaxel (20 nM; 48 hours) induces programmed cell death and exists a block at the G2/M phase of the cell cycle.Paclitaxel (20 nM; 48 hours) induces a consistent increase in the level of p53.(In Vivo):Paclitaxel (1-20 mg/kg; i.p.; 1 time/2 days for five cycles) obviously induces liver metastases at the low-Paclitaxel group with little influence on primary tumor growth.
  • In Vitro
    Apoptosis Analysis Cell Line:MCF-7, MDA-MB-231 cells Concentration:20 nM Incubation Time:48 hours Result:Induced programmed cell death.Cell Cycle Analysis Cell Line:MCF-7, MDA-MB-231 cells Concentration:20 nM Incubation Time:48 hours Result:>60% of MCF-7 cells and 50% of MDA-MB-231 cells were in the G2/M phase following 24 h treament.Western Blot Analysis Cell Line:MCF-7 cells (harboring wild-type p53 ) Concentration:20 nM Incubation Time:48 hours Result:Induced a consistent increase in the level of p53.
  • In Vivo
    Animal Model:MDA-231 xenograft-bearing miceDosage:1, 20 mg/kg Administration:Intraperitoneal injection; five cycles (1 time/2 days)Result:Liver metastases were obviously induced in the low-PTX (1 mg/kg) group with little influence on primary tumor growth compared with high-PTX group.
  • Synonyms
    NSC 125973
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Microtubule/Tubulin
  • Recptor
    microtubule
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    33069-62-4
  • Formula Weight
    853.92
  • Molecular Formula
    C47H51NO14
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 18 mg/mL (21.07 mM); DMSO: 171 mg/mL (200.25 mM)
  • SMILES
    O=C1[C@H](OC(C)=O)C(C2(C)C)=C(C)[C@@H](OC([C@H](O)[C@@H](NC(C3=CC=CC=C3)=O)C4=CC=CC=C4)=O)C[C@@]2(O)[C@@H](OC(C5=CC=CC=C5)=O)[C@@]6([H])[C@@]1(C)[C@@H](O)C[C@@]7([H])OC[C@]76OC(C)=O
  • Chemical Name
    (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-9-(((2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl)oxy)-12-(benzoyloxy)-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxete-6,12b-diyl diacetate

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Wang J, et al. anticancer Drugs. 2003, 14(1), 13-19.
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