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Protease Inhibitors and Phosphatase Inhibitors

Cocktails, tablets, capsules, and individual purified formulations of protease inhibitors and phosphatase inhibitors designed to protect proteins from degradation during cell lysis and extraction.
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1 – 15 of 30 results
1

MilliporeSigma™ Calbiochem™ Adenosine Receptor Agonist, NECA

A cell-permeable adenosine analog that acts a potent non-selective agonist of adenosine receptors (Ki = 14 nM, 20 nM

2

MilliporeSigma™ Calbiochem™ Adenosine Deaminase Inhibitor, DCF

The Adenosine Deaminase Inhibitor, DCF, also referenced under CAS 53910-25-1, controls the biological activity of Adenosine Deaminase.

3

MilliporeSigma™ Calbiochem™ Adenosine 3',5'-cyclic Monophosphate, Sodium Salt

A key regulator of many cellular reactions.

Content And Storage Hygroscopic
CAS 37839-81-9
Form Solid
Target Proteins Protein kinase A
Solubility H2O
Color White
Purity 98% by HPLC
Molecular Formula C10H11N5O6P·Na
Formula Weight 351.2g/mol
4

MilliporeSigma™ Calbiochem™ Adenosine A1 Receptor Antagonist I, DPCPX

A blood-brain barrier permeable xanthine derivative that acts as a highly selective antagonist of Adenosine A1 receptor (A1R; Ki

5

MilliporeSigma™ Calbiochem™ Adenosine A1 Receptor Agonist II, CCPA

An adenosine analog that acts as a selective, high affinity agonist for Adenosine A1 receptor (A1R) (Ki = 800 pM

6

MilliporeSigma™ Calbiochem™ Adenosine A1 Receptor Agonist I, CPA

A potent and selective agonist of adenosine A1 receptor (A1R) (Ki

7

MilliporeSigma™ Calbiochem™ Adenosine A2A Receptor Antagonist I, ZM 241385

A highly potent, selective, non-xanthine adenosine A2A receptor antagonist (Ki = 800 pM for human adenosine A2AR stably expressed in HEK-293 cells).

8

MilliporeSigma™ Calbiochem™ Adenosine A2A Receptor Antagonist II, SCH-58261

A highly potent and selective antagonist of adenosine A2A receptor (Ki = 6

9

MilliporeSigma™ Calbiochem™ Adenosine A2A Receptor Agonist I, CGS 21680, Hydrochloride

A xanthin derivative that acts as a potent agonist of adenosine A2A receptors (Ki =

11

MilliporeSigma™ Calbiochem™ Adenosine 3',5'-cyclic Monophosphate, 8-Bromo-, Sodium Salt

Cell-permeable cAMP analog that has greater resistance to phosphodiesterases than cAMP.

12

MilliporeSigma™ Calbiochem™ Adenosine 3',5'-cyclic Monophosphate, N6,O2'-Dibutyryl-, Sodium Salt

This Dibutyryl-cAMP, CAS 16980-89-5, is a cell-permeable cAMP analog that preferentially activates PKA.

Content And Storage Hygroscopic
CAS 16980-89-5
Form Lyophilized
Target Proteins PKA
Solubility H2O
Color White
Purity 95% by HPLC
Molecular Formula C18H23N5O8P·Na
Formula Weight 491.4g/mol
13

MilliporeSigma™ Calbiochem™ Adenosine A3 Receptor Agonist, 2-Cl-IB-MECA

A highly selective agonist of adenosine A3 receptor (Ki = 330 pM).

14

MilliporeSigma™ Calbiochem™ Adenosine 3',5'-cyclic Monophosphate, 8-(4-Chlorophenylthio)-, Sodium Salt

Cell-permeable cAMP analog that activates both protein kinase A and protein kinase G.

15

MilliporeSigma™ Calbiochem™ Adenosine 3',5'-cyclic Monophosphorothioate, 8-Bromo-, Rp-Isomer, Sodium Salt

A potent, cell-permeable, and reversible metabolically-stable cAMP antagonist that inhibits cAMP-dependent protein kinase and shows preference for PKA type I.