62284-79-1
62284-79-1
Chemical Structure
(-)-p-Bromotetramisole oxalate
Synonym(s): L-p-Bromotetramisole oxalate; 6-Bromolevamisole oxalate
- CAS No.: 62284-79-1
- Formula:C13H13BrN2O4S
- Molecular Weight:373.22
IUPAC Name: (S)-6-(4-bromophenyl)-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole oxalate
InChIKey: ZULBIBHDIQCNIS-HNCPQSOCSA-N
SMILES: BrC1=CC=C([C@@H]2N=C3SCCN3C2)C=C1.O=C(O)C(O)=O
Biological Activity: (-)-p-Bromotetramisole oxalate (L-p-Bromotetramisole oxalate) is an alkaline phosphatase inhibitor. (-)-p-Bromotetramisole (oxalate) is applicable to research related to erythroleukemia[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(-)-p-Bromotetramisole oxalate | 99.78% | (-)-p-Bromotetramisole oxalate (L-p-Bromotetramisole oxalate) is an alkaline phosphatase inhibitor. (-)-p-Bromotetramisole (oxalate) is applicable to research related to erythroleukemia. | ||||||||||||||||||||
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References
- [1]. Scher BM, et al. The phosphatase inhibitors, orthovanadate and levamisole, inhibit induction of erythroid differentiation and abrogate the associated inhibition of glycolysis. Int J Oncol. 1998;12(5):987-996. [Content Brief]
- [2]. Van Belle H, et al. L-p-Bromotetramisole, a new reagent for use in measuring placental or intestinal isoenzymes of alkaline phosphatase in human serum. Clin Chem. 1977 Mar;23(3):454-9. [Content Brief]
