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MedKoo product information:
Levamisole
Hydrochloride
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MedKoo Code#: 100540
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Name:
Levamisole
hydrochloride
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CAS#: 16595-80-5
Synonym: l-tetramisole
hydrochloride; US brand name: Ergamisol. Foreign brand names:
Ascaridil; Decaris; Ergamisole; Ketrax; Solaskil. Abbreviation:
LEV. Code names: ICI-59623; R 12564; RP-20605. Chemical
structure name: (-)-( S)-2,3,5, 6-tetrahydro-6-phenylimidazo
[2,1-b] thiazole monohydrochloride
IUPAC/Chemical name:
(S)-6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole
hydrochloride
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Chemical structure:
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Theoretical analysis
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Levamisole
Chemical Formula: C11H12N2S
Exact Mass: 204.07212
Molecular Weight: 204.29
m/z: 204.07212 (100.0%), 205.07547 (11.9%),
206.06792 (4.5%)
Elemental Analysis: C, 64.67; H, 5.92; N,
13.71; S, 15.70
Levamisole hydrochloride
Chemical Formula: C11H13ClN2S
Molecular Weight: 240.75
Elemental Analysis: C, 54.88; H, 5.44; Cl,
14.73; N, 11.64; S, 13.32
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Availability and price:
This agent is
available. For quotation, question, and order, please send email to
sales@medkoo.com to describe your needs. A representative
will respond your email shortly. We offer significant discount
for larger quantity order.
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Quality control
data:
Product will be shipped with
supporting analytical data.
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Information about this agent
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levamisole hydrochloride is
the orally bioavailable hydrochloride salt of the synthetic
imidazothiazole derivative levamisole with anthelminthic and
immunostimulating activities. In immunosuppressed states, levamisole
may restore immune function by: 1) stimulating antibody formation,
2) stimulating T-cell activation and proliferation, 3)
potentiatiating monocyte and macrophage phagocytosis and chemotaxis
and 4) increasing neutrophil mobility, adherence, and chemotaxis.
Check for
active clinical trials or
closed clinical trials using this agent. (NCI
Thesaurus)
According to
http://en.wikipedia.org/wiki/Levamisole, Levamisole (marketed as the
hydrochloride salt under the trade name Ergamisol) is an anthelminthic
and immunomodulator belonging to a class of synthetic imidazothiazole
derivatives. It was discovered at Janssen Pharmaceutica in 1966.
Levamisole has been used in humans to treat parasitic worm infections,
and has been studied in combination with other forms of chemotherapy for
colon cancer, melanoma, and head and neck cancer. The drug was withdrawn
from the U.S. and Canadian markets in 2000 and 2003 respectively, due to
the risk of serious side effects and the availability of more effective
replacement medications. Currently, levamisole remains in veterinary use
as a dewormer for livestock. The medication has also been increasingly
used as an adulterant in cocaine sold in the US and Canada, resulting in
serious side effects.
Clinical use
Levamisole was originally used as an
antihelminthic to treat worm infestations in both humans and animals.
Most current commercial preparations are intended for veterinary use as
a dewormer in cattle, pigs, and sheep. However, levamisole has also
gained prominence among aquarists as an effective treatment for
Camallanus roundworm infestations in freshwater tropical fish.
Levamisole has been tested in combination with fluorouracil to treat
colon cancer. There is no good evidence from clinical trials that its
addition to fluorouracil therapy benefits patients with colon cancer,
and it is no longer used for this. It is also used infrequently to treat
melanoma and head and neck cancer. It is unclear from its mechanism of
action why it would have an effect in treating colon cancer, although it
has been shown to have "immune-stimulating" properties in some
situations. A 1984 study on complicated influenza had found levamisole
to be an effective inducer of interferon and had recommended its use in
combination therapy for influenza. It is also used routinely in India to
treat steroid dependent childhood nephrotic syndrome cases, which is
probably based on literature published in a few UK based studies. see
http://en.wikipedia.org/wiki/Levamisole.
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