American Journal of Engineering & Natural Sciences (AJENS) ISSN 2074-112X

Original Research Contributions in Genetic Biongineering And Natural Genome Editing

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Ace-2 Inhibitor

ALK inhibitor 2

A3155-10 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

5 mg
EUR 324
Description: BCATc Inhibitor 2 is an active and selective inhibitor of cytosolic BCAT (BCATc)[1].

BCATc Inhibitor 2

50 mg
EUR 1666.8
Description: BCATc Inhibitor 2 is an active and selective inhibitor of cytosolic BCAT (BCATc)[1].

Cathepsin Inhibitor 2

10mg
EUR 11300.4

Btk inhibitor 2

100mg
EUR 1230

Lck inhibitor 2

10mM/1mL
EUR 570

MAT2A inhibitor 2

100mg
EUR 2332.8

ROCK inhibitor-2

5mg
EUR 542.4

Serum / Plasma information

HPGDS inhibitor 2

HY-126134 10mM/1mL
EUR 590.4

Cathepsin Inhibitor 2

HY-U00377 10mg
EUR 11300.4

PI3K/mTOR Inhibitor-2

HY-111508 100mg
EUR 3159.6

MMP-2 Inhibitor I

C5615-10 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 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 10 mg
EUR 268.8
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM).

PIM-1 Inhibitor 2

A4519-5 5 mg
EUR 205.2
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM).

MMP-2 Inhibitor II

C5818-1 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 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 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.

MK-2 Inhibitor III

HY-112457 5mg
EUR 542.4

SEC inhibitor KL-2

HY-123972 10mg
EUR 817.2

SIRT1/2 Inhibitor IV

27323 25 mg
EUR 420
Description: SIRT1/2 Inhibitor IVCatalog #: 27323Size: 25 mgSIRT1 and 2 Inhibitor

SIRT1/2 Inhibitor IV

C5522-10 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 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 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 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.

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