CAS 14769-73-4: Levamisole
Formula:C11H12N2S
InChI:InChI=1S/C11H12N2S/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10/h1-5,10H,6-8H2/t10-/m1/s1
InChI key:InChIKey=HLFSDGLLUJUHTE-SNVBAGLBSA-N
SMILES:[C@@H]1(CN2C(=N1)SCC2)C3=CC=CC=C3
Synonyms:- (-)-2,3,5,6-Tetrahydro-6-phenylimidazo[2.1-b]thiazole
- (-)-Tetramisole
- (6S)-2,3,5,6-Tetrahydro-6-phenylimidazo[2,1-b]thiazole
- (6S)-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole
- (6S)-6-Phenyl-2H,3H,5H,6H-imidazo[2,1-b][1,3]thiazole
- (S)-(-)-Levamisole
- (S)-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole
- <span class="text-smallcaps">L</span>-Tetramisole
- Anthelsol
- Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, (S)-
- Ketrax
- See more synonyms
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Found 10 products.
Levamisol 100 µg/mL in Acetonitrile
CAS:Formula:C11H12N2SColor and Shape:Single SolutionMolecular weight:204.29Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, (6S)-
CAS:Formula:C11H12N2SPurity:97%Color and Shape:SolidMolecular weight:204.2914"(S)-6-Phenyl-2,3,5,6-Tetrahydroimidazo[2,1-B]Thiazole"
CAS:"(S)-6-Phenyl-2,3,5,6-Tetrahydroimidazo[2,1-B]Thiazole"Purity:99%Molecular weight:204.29g/molLevamisole
CAS:Formula:C11H12N2SPurity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:204.29(S)-2,3,5,6-Tetrahydro-6-phenylimidazo[2,1-b]thiazole
CAS:The drug, 2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazole (TEM), is a small molecule with potent immunomodulatory properties. TEM is a competitive inhibitor of the enzyme histamine N-methyltransferase and inhibits the synthesis of histamine and other proinflammatory mediators. It also has anthelmintic activity against nematodes and exhibits anti-inflammatory activities in animal models of autoimmune diseases such as lupus erythematosus and inflammatory skin diseases such as psoriasis. TEM is also a potent inhibitor of lymphocyte transformation. This drug can be used for the treatment of chronic viral hepatitis, which is caused by hepatitis B or C virus infections. TEM binds to the active site on the enzyme RNA polymerase II that catalyzes DNA transcription to produce messenger RNA. TEM blocks RNA synthesis by binding to the template strand of DNA, preventingFormula:C11H12N2SPurity:Min. 97 Area-%Color and Shape:PowderMolecular weight:204.29 g/mol(S)-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:204.28999328613284-Carboxy Levamisole
CAS:Controlled ProductFormula:C12H12N2O2SColor and Shape:NeatMolecular weight:248.3
![Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-, (6S)-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA001F3K.jpg&w=3840&q=75)
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![(S)-2,3,5,6-Tetrahydro-6-phenylimidazo[2,1-b]thiazole](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb%2FFL138922.jpg&w=3840&q=75)
![(S)-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb%2FF241597.jpg&w=3840&q=75)
