09.03.2013 Views

Inhibitor SourceBook™ Second Edition

Inhibitor SourceBook™ Second Edition

Inhibitor SourceBook™ Second Edition

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

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

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!