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Paclitaxel
Product:
Paclitaxel is a natural
product with potent anticancer activity.
Chemistry:
The chemical name for paclitaxel is 5ß, 20-epoxy-1,2a,4,7ß,
10ß, 13a-hexahydroxytax-11-en-9-one, 4,10-diacetate
2-benzoate 13-ester with (2R, 3S)-N-benzoyl-3-phenylisoserine.
Paclitaxel has the following structural formula:
Chemical
Formula: C47H51NO14
Molecular
Weight: 853.9
Solubility:
Soluble in Cremophor EL and organic solvents. Highly insoluble
in water and aqueous buffers.
Stability:
Samples stored at room temperature for 30 days showed no decomposition
as indicated by UV absorption, TLC or HPLC
Source:
Aphios produces a natural paclitaxel from the needles or leaves
of the American yew, Taxus media “hicksii,” an
ornamental species grown by cloning in nurseries in the United
Sates utilizing its patented SuperFluids™CXP
technology. Aphios also produces paclitaxel from the needles
or leaves of the wild Canadian yew, Taxus Canadensis.
Purity:
> 99% determined by HPLC chromatographic scans
Mechanism
of Action: Paclitaxel has demonstrated a significant
effectiveness against ovarian and breast cancers, and a number
of other cancers in clinical trials. Paclitaxel works by stabilizing
microtubules and preventing unregulated cell mitosis or division.
Paclitaxel is also being used as an adjunct therapy with the
new breed of genetically-engineered drugs as exemplified with
Genentech’s Herceptin.® The adjunct use
of paclitaxel significantly increased the therapeutic effectiveness
of Herceptin.® Paclitaxel has repeatedly demonstrated
an additive or synergistic effect with other drugs. Paclitaxel
and its relatives thus hold the promise to have widespread
applicability to cancer and other non-tumorgenic diseases.
Cremophor®
EL – Registered Trademark of BASF Aktiengesellschaft
Taxol® – Registered Trademark of the
Bristol-Myers Squibb Company
LoTax™ – Trademark of Aphios Corporation
Herceptin® – Registered Trademark of
Genentech
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