| Product |
Cat. No. |
Size |
Purity |
Biological Activity |
| Bioallethrin |
B-300 |
1 mg |
>98% |
Although bioallethrin is a type I pryrethroid, its effects on calcineurin resemble those of Type II Pyrethrins which are very weak, bioallethrin is a potent calcinerin inhibitor, with an IC50 of about 1-2 nM.
|
| Calyculin A |
C-100 |
10 ¥ìg |
>99% |
Highly specific inhibitor for PP-1 and PP-2A phosphatases in comparison to its effect in various acid,alkaline,and protein tyrosine phosphatases.CA is 20-300-fold more potent than OA in inhibiting various PP-1 phosphatases.Its concentrationdependent effects in intact cells are easier to interpret than those of OA.
|
| Cantharidic Acid |
C-250 |
1 mg |
>99% |
Like Cantharidin, Cantharidinic Acid has been a useful tool in studying the role of protein phosphatase in regulation of various physiological functions.
|
| Cantharidin |
C-170 |
1 mg |
>98% |
Potent inhibitor of protein phosphatase 2A(IC50=40nM).
|
| Cyclosporin A |
C-900 |
25 mg |
>97% |
Cyclosporin A is a cyclic peptide that serves as an immunosuppresant, hypertension inducer and antifungal agent by its ability to inhibit Calcineurin (PP-2B).
|
| Cypermethrin |
C-470 |
1 mg |
>98% |
A type II pyrethrin; potent inhibitor of calcineurin, with an IC50 of about 40 pM (the dose-response curve is complex, however).
|
| Deltamethrin |
D-500 |
0.5 mg |
>99% |
Potent pyrethroid insecticide, specific inhibitor of Calcineurin (PP-2B) with an IC50 of about 100 pM.
|
| Endothall |
E-180 |
5 mg |
>98% |
Like other Cantharidin analogs, Endothall has been employed as a useful PP-2A inhibitor. In addition, protein phosphatase inhibition by Endothall has been used in the study of cardiac contractile, electrophysiological nd biochemical aspects, and characterization of hepatocellular carcinoma cell lines from diethylnitrosamine phenobarbital-trided rats.
|
| Fenvalerate |
F-420 |
1 mg |
>99% |
A type II pyrethroid; potent inhibitor of calcineurin, with an IC50 of about 2-4nM.
|
| FK-506 |
F-900 |
1 mg |
>98% |
FK 506 is potent immunosuppressive compounds that inhibit T-cell activation (10 to 100 times more potent than Cyclosporin A). FK-506 inhibits the heterodimeric Ca2+ /calmodulin-dependent phosphatase Calcineurin.
|
| Okadaic Acid (Ammonium Salt) |
O-800 |
25 ¥ìg |
>98% |
Okadaic Acid is a marine toxin, polyether derivative, produced by dinoflagellates. It is a potent, ell-permeable, specific inhibitor of PP-1 and PP2A, in numerous cell types.
|
| Okadaol |
O-700 |
10 ¥ìg |
>98% |
Okadaic acid derivate with novel pharmacological profile.
|
| Okadiac Acid (Sodium Salt) |
O-900 |
25 ¥ìg |
>98% |
Okadaic Acid is a marine toxin, polyether derivative, produced by dinoflagellates. It is a potent, ell-permeable, specific inhibitor of PP-1 and PP2A, in numerous cell types.
|
| Permethrin |
P-400 |
0.4 mg |
>99% |
A type I pyrethroid; weakly active negative control for studies of calcineurin inhibition by the more active type II pyrethroids such as Deltamethrin and Fenvalerate.
|
| Phenylarsine Oxide |
- |
100 mg |
>99% |
Putative inhibitor of tyrosine phosphatases activity. Does not affect tyrosine kinase.
|
| Pyrophosphate (Sodium Salt) |
- |
500 mg |
>98% |
Strong inhibitor of protein phosphatases. Effect similar to sodium fluoride and Vanadate.
|
| Sodium Fluoride |
- |
500 mg |
>99% |
Strong inhibitor of protein phosphatases (acid, alkaline, P2, 2A). Effect similar to Pyro-phosphate and Vanadate.
|
| Vanadate (Orthovanadate) |
- |
100 mg |
>95% |
A general potent protein phosphatases inhibitor. |