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MedKoo product information:

 Levamisole Hydrochloride

MedKoo Code#:  100540

Name:  Levamisole hydrochloride

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

 

Chemical structure:

Theoretical analysis :

 

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

 

 

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.

 

Quality control data:

Product will be shipped with supporting analytical data.

 

 

Information about this agent

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 The drug was withdrawn from the U.S. and Canadian markets in 2000 and 2003 respectively, due to the risk of serious side effects and the availability of more effective replacement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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380: Galasso GJ. An assessment of antiviral drugs for the management of infectious diseases in humans. Antiviral Res. 1981 Jun;1(2):73-96. Review. PubMed PMID: 6175275.

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385: Abe T. [Development and clinical use of chemical immunomodulators]. Nippon Rinsho. 1981 Apr;39(4):1893-901. Review. Japanese. PubMed PMID: 6796722.

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388: Zernov NG, Kirillov VI. [Achievements and prospects of immunotherapy in urinary tract infection and pyelonephritis in children]. Pediatriia. 1981 Mar;(3):63-6. Review. Russian. PubMed PMID: 7012779.

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390: Amery WK. Cancer immunotherapy: some critical comments regarding immunological monitoring. Int J Immunopharmacol. 1981;3(4):339-48. Review. PubMed PMID: 7037663.

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