Inhibitor SourceBook™ Second Edition
Inhibitor SourceBook™ Second Edition
Inhibitor SourceBook™ Second Edition
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Phosphorylation/Dephosphorylation<br />
Protein Phosphatase <strong>Inhibitor</strong>s, continued<br />
Product Cat. No. Comments Size Price<br />
,4-Dimethylendothall 311250 (1,4-Dimethyl-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Acid)<br />
A useful negative control for Canthardic Acid (Cat. No. 2 0 50), Canthardin<br />
(Cat. No. 2 0 55), and Endothall (Cat. No. 324760).<br />
N eIF-2a <strong>Inhibitor</strong>,<br />
Salubrinal<br />
324895 (Sal)<br />
A cell-permeable thiourea compound that acts as a selective inhibitor of eukaryotic<br />
translation initiation factor 2 subunit a (eIF-2a) dephosphorylation by phosphatase<br />
complexes.<br />
Endothall 324760 (7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Acid)<br />
A specific inhibitor of PP2A (IC 50 = 90 nM).<br />
Fenvalerate 341380 [a-Cyano-3-phenoxybenzyl-a-(4-chlorophenyl)isovalerate]<br />
A potent inhibitor of PP2B (IC 50 = 2–4 nM).<br />
Fostriecin, Sodium<br />
Salt, Streptomyces<br />
pulveraceous<br />
b-Glycerophosphate,<br />
Disodium Salt,<br />
Pentahydrate<br />
Microcystin-LF,<br />
Microcystis aeruginosa<br />
Microcystin-LR,<br />
Microcystis aeruginosa<br />
InSolution<br />
Microcystin-LR,<br />
Microcystis aeruginosa<br />
Microcystin-LW,<br />
Microcystis aeruginosa<br />
Microcystin-RR,<br />
Microcystis aeruginosa<br />
344280 (FST; Phosphotrienin)<br />
A potent PP2A inhibitor (IC 50 = 3.2 nM). Inhibits PP only at higher concentrations<br />
(IC 50 = 3 mM).<br />
35675 A phosphate group donor in matrix mineralization studies that acts as a protein<br />
phosphatase inhibitor.<br />
475814 A more cell-permeable analog of Microcystin-LR (Cat. No. 4758 5). Useful for studies<br />
in intact cells. Not available for sale outside the United States.<br />
475815 A cyclic peptide that inhibits PP2A~PP >> PP2B (IC 50 for PP2A = 40 pM and for<br />
PP = .7 nM). Does not enter some mammalian cells. Not available for sale outside<br />
the United States.<br />
475821 A 2.5 mM (250 mg/ 00 ml) of Microcystin-LR, Microcystis aeurginosa<br />
(Cat. No. 4758 5) in DMSO. Not available for sale outside the United States.<br />
475818 A more cell-permeable analog of Microcystin-LR (Cat. No. 4758 5). Useful for studies<br />
in intact cells. Not available for sale outside the United States.<br />
475816 A cyclic peptide that inhibits PP2A~PP >> PP2B (IC 50 = .4 mM). Does not enter some<br />
mammalian cells. Not available for sale outside the United States.<br />
mpV(pic) 475950 [Monoperoxo(picolinato)oxovanadate(V)]<br />
A potent PTP inhibitor. More potent for insulin receptor (IR) dephosphorylation than<br />
EGFR dephosphorylation.<br />
a-Naphthyl<br />
Acid Phosphate,<br />
Monosodium Salt<br />
NFAT Activation<br />
<strong>Inhibitor</strong> III<br />
NIPP- , His•Tag®,<br />
Bovine Thymus,<br />
Recombinant, E. coli<br />
Okadaic Acid,<br />
Prorocentrum<br />
concavum<br />
N InSolution Okadaic<br />
Acid, Prorocentrum<br />
concavum<br />
Okadaic Acid,<br />
Ammonium Salt<br />
0 mg $76<br />
5 mg $ 29<br />
20 mg $55<br />
25 mg $55<br />
0 mg $ 7<br />
60 Orders Phone 800 854 34 7<br />
Calbiochem • <strong>Inhibitor</strong> SourceBook<br />
Fax 800 776 0999<br />
Web www.emdbiosciences.com/calbiochem<br />
50 g<br />
00 g<br />
250 g<br />
$32<br />
$48<br />
$98<br />
25 mg $ 4<br />
500 mg $ 78<br />
250 mg $ 0<br />
25 mg $ 5<br />
250 mg $202<br />
0 mg $ 7<br />
479775 A broad-spectrum protein phosphatase inhibitor. 5 g $44<br />
480403 INCA-6; <strong>Inhibitor</strong> of NFAT-Calcineurin Association-6<br />
A cell-permeable quinone compound that acts as a potent and selective inhibitor of<br />
Calcineurin-NFAT (Nuclear Factor of Activated T cells) signaling. Binds to calcineurin with<br />
high affinity (K d = 800 nM), disrupts its interaction with NFAT and completely blocks its<br />
dephosphorylation, nuclear import of NFAT (~40 mM in C .7W2 T cells), and induction of<br />
cytokine mRNAs. Unlike CsA (Cat. No. 239835) and FK506, INCA-6 does not affect calcineurin<br />
activity or its downstream signaling.<br />
482251 (Nuclear <strong>Inhibitor</strong> of Protein Phosphatase-1)<br />
A potent and specific inhibitor or protein phosphatase (PP ; K i = – 0 pM) that can be used<br />
to distinguish PP from other major serine/threonine protein phosphatases, including PP2A,<br />
PP2B, and PP2C.<br />
495604 (OA)<br />
A cell-permeable inhibitor of PP2A > PP >> PP2B. (IC 50 for PP2A = 00 pM;<br />
for PP = 0– 5 nM; and for PP2B = 5 mM).<br />
495609 A 250 mM (25 mg/ 24 ml) solution of Okadaic Acid, Prorocentrum concavum<br />
(Cat. No. 495604) in DMSO.<br />
459616 A water-soluble form of Okadaic Acid (Cat. No. 495604). Inhibits protein phosphatases<br />
and 2A.<br />
5 mg $90<br />
0 mg<br />
25 mg<br />
00 mg<br />
mg $95<br />
$40<br />
$65<br />
$2 2<br />
25 mg $65<br />
25 mg $60