ALK inhibitor 2 |
A3155-10 |
ApexBio |
10 mg |
EUR 837.6 |
Description: ALK inhibitors are potential anti-cancer drugs that act on tumours with variations of anaplastic lymphoma kinase (ALK) such as an EML4-ALK [1]. As the same as ALK inhibitor 1, ALK inhibitor 2 is a novel and selective inhibitor for the ALK kinase as well. |
Ace2 Inhibitor Laboratories manufactures the ace-2 inhibitor reagents distributed by Genprice. The Ace-2 Inhibitor reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact ACE2 Inhibitor. Other Ace-2 products are available in stock. Specificity: Ace-2 Category: Inhibitor
BCATc Inhibitor 2 |
ApexBio |
5 mg |
EUR 324 |
Description: BCATc Inhibitor 2 is an active and selective inhibitor of cytosolic BCAT (BCATc)[1]. |
BCATc Inhibitor 2 |
ApexBio |
50 mg |
EUR 1666.8 |
Description: BCATc Inhibitor 2 is an active and selective inhibitor of cytosolic BCAT (BCATc)[1]. |
Serum / Plasma information
MMP-2 Inhibitor I |
C5615-10 |
ApexBio |
10 mg |
EUR 189.6 |
Description: MMP-2 Inhibitor I, a hydroxamate-based, long-chain fatty acid, is a reversible inhibitor of matrix metalloproteinase (MMP)-2.Matrix metalloproteinases (MMPs) have been involved in the degradation of extracellular matrix. |
MMP-2 Inhibitor I |
C5615-5 |
ApexBio |
5 mg |
EUR 146.4 |
Description: MMP-2 Inhibitor I, a hydroxamate-based, long-chain fatty acid, is a reversible inhibitor of matrix metalloproteinase (MMP)-2.Matrix metalloproteinases (MMPs) have been involved in the degradation of extracellular matrix. |
PIM-1 Inhibitor 2 |
A4519-10 |
ApexBio |
10 mg |
EUR 268.8 |
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM). |
PIM-1 Inhibitor 2 |
A4519-5 |
ApexBio |
5 mg |
EUR 205.2 |
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM). |
MMP-2 Inhibitor II |
C5818-1 |
ApexBio |
1 mg |
EUR 132 |
Description: MMP-2 Inhibitor II is an irreversible, potent and selective MMP-2 inhibitor with Ki value of 2.4 ?M [1]. Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that play important roles in physiological and pathological conditions. |
MMP-2 Inhibitor II |
C5818-10 |
ApexBio |
10 mg |
EUR 648 |
Description: MMP-2 Inhibitor II is an irreversible, potent and selective MMP-2 inhibitor with Ki value of 2.4 ?M [1]. Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that play important roles in physiological and pathological conditions. |
MMP-2 Inhibitor II |
C5818-5 |
ApexBio |
5 mg |
EUR 390 |
Description: MMP-2 Inhibitor II is an irreversible, potent and selective MMP-2 inhibitor with Ki value of 2.4 ?M [1]. Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that play important roles in physiological and pathological conditions. |
SIRT1/2 Inhibitor IV |
27323 |
BPS Bioscience |
25 mg |
EUR 420 |
Description: SIRT1/2 Inhibitor IVCatalog #: 27323Size: 25 mgSIRT1 and 2 Inhibitor |
SIRT1/2 Inhibitor IV |
C5522-10 |
ApexBio |
10 mg |
EUR 351.6 |
Description: SIRT1/2 Inhibitor IV is a cell-permeable inhibitor of SIRT1 and SIRT2 with IC50 values of 56 ?M and 59 ?M, respectively [1]. Sirtuin proteins are nicotinamide adenine dinucleotide (NAD+)-dependent deacetylases. |
SIRT1/2 Inhibitor IV |
C5522-25 |
ApexBio |
25 mg |
EUR 686.4 |
Description: SIRT1/2 Inhibitor IV is a cell-permeable inhibitor of SIRT1 and SIRT2 with IC50 values of 56 ?M and 59 ?M, respectively [1]. Sirtuin proteins are nicotinamide adenine dinucleotide (NAD+)-dependent deacetylases. |
SIRT1/2 Inhibitor IV |
C5522-5 |
ApexBio |
5 mg |
EUR 216 |
Description: SIRT1/2 Inhibitor IV is a cell-permeable inhibitor of SIRT1 and SIRT2 with IC50 values of 56 ?M and 59 ?M, respectively [1]. Sirtuin proteins are nicotinamide adenine dinucleotide (NAD+)-dependent deacetylases. |
Cdk1/2 Inhibitor III |
C3679-1 |
ApexBio |
1 mg |
EUR 192 |
Description: IC50: 0.6 and 0.5 nM forCdk1/cyclin B and Cdk2/cyclin A, respectivelyCdk1/2 Inhibitor III is a Cdk inhibitor.Cyclin-dependent kinases (CDKs) are a family members of serine-threonine protein kinases responsible for regulation of the eukaryotic cell cycle. |