15544 Results for: "GLUT+inhibitor-1"

Supplier: Thermo Scientific Chemicals

Calpain Inhibitor XII

Supplier: ABCAM INC CA

Potent, selective and dual site Src family tyrosine kinase inhibitor (IC₅₀ values are 44 and 88 nM for Src and Lck, respectively). Cell-permeable, reversible and ATP-competitive. Interacts with both ATP and peptide-binding sites. Additionally inhibits VEGFR2 and C-fms (IC₅₀ values are 0.32 and 30 μM, respectively). Induces apoptosis.

Supplier: Enzo Life Sciences

Potent inhibitor of Akt1, Akt2 and Akt3 activity.

Supplier: Thermo Scientific Chemicals

Pale yellow Solid

Supplier: MilliporeSigma

A potent, cell-permeable, and irreversible inhibitor of caspase-1 (ICE) and caspase-4.

Supplier: Thermo Scientific Chemicals

A cell-permeable oxazolidinone-carboxamidine compound that acts as a potent, selective, and active-site targeting inhibitor of urokinase-type plasminogen activator

Supplier: BeanTown Chemical

Inhibitor removal resin, CAS Number: 9003-70-7, Molecular Formula: [CH2CH(C6H5)]x[CH2CH[C6H4(CHCH2)]]y, Size: 100G

Supplier: Enzo Life Sciences

Potent MMP-13 inhibitor.

Supplier: Enzo Life Sciences

Potent inhibitor of GSK-3 ATP-binding site.

Supplier: Enzo Life Sciences

Potent, selective, and ATP-competitive inhibitor of Cdks

Supplier: ABCAM INC CA

Cell-permeable SIRT2 inhibitor (IC₅₀ = 13 μM). Increases acetylated tubulin levels. Shows neuroprotective effects in vivo.

Supplier: Enzo Life Sciences

Cell-permeable, potent and AMP-competitive inhibitor of glycogen phosphorylase.

Supplier: Thermo Scientific Chemicals

Off-white solid

Supplier: ABCAM INC CA

Cell-permeable, irreversible MALT1 inhibitor (IC₅₀ = 5.8 μM). Suppresses protease function, decreases NF-κB activity and inhibits cell proliferation. Antitumor agent. Active in vitro, in vivoand ex vivo.

Supplier: Thermo Scientific Chemicals

Pale yellow solid

Supplier: Ambeed

YAP/TAZ inhibitor-2 98%

Supplier: ABCAM INC CA

Potent FLT3 receptor tyrosine kinase inhibitor (IC₅₀ =42 nM). Selective over 22 other kinases. Shows antiproliferative effects (IC₅₀ =340 nM for Human acute myelocytic leukemia MV4-11 cells).

Supplier: MilliporeSigma

SIRT2 Inhibitor II, AK-1

Supplier: ABCAM INC CA

Selective caspase 3 and 7 inhibitor (IC₅₀ =1.7 μM, caspase-3). Reduces ischemic-induced apoptosis (IC₅₀ =0.5 μM). Shows cardioprotective effects.

Supplier: Ambeed

PTP1B inhibitor ≥95%

Supplier: Adipogen

Potent cyclooxygenase-2 (COX-2) inhibitor. Inhibits inflammatory prostaglandin E2 (PGE2) production.

Supplier: Ambeed

Flt-3 inhibitor 98+%

Supplier: Ambeed

FABP4 inhibitor 98%

Supplier: Bachem Americas

Sequence: 4-Abz-Gly-Pro-D-Leu-D-Ala-NHOH
Synonym(s): MMP Inhibitor 1

Supplier: ABCAM INC CA

Potent, reversible and selective ATP-binding site-targeting Tie2 kinase inhibitor (IC₅₀ = 250 nM). Anti- angiogenesis agent. Active in vivoand in vivo. Cell-permeable.

Supplier: Cayman Chemical Company

IKK2 Inhibitor VI, Purity >/=95%, CAS 354811-10-2, MF: C12H11N3O2S, MW: 261.3, Synonyms: 5-Phenyl-2-ureidothiophene-3-carboxylic Acid Amide, 2-[(aminocarbonyl)amino]-5-phenyl-3-thiophenecarboxamide, Formulation: A crystalline solid, Storage: -20C, Size: 1mg

Supplier: ABCAM INC CA

Matrix metalloproteinase inhibitor of MMP-2/MMP-9. Synergizes with TNF-α to induce apoptosis in cancer cells. Active in vitro.

Supplier: Thermo Scientific Chemicals

A cell-permeable, potent, and selective inhibitor of GSK-3beta

Supplier: Enzo Life Sciences

Potent, dual site (ATP domain and substrate-binding domain) Src and Lck kinase inhibitor (IC50=44 and 88nM respectively). VEGFR2 IC50=0.32μM; c-fms IC50=30μM.

Supplier: TCI America

2-(3,4-Dimethoxybenzamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide, Purity: >98%(HPLC), CAS: 301305-73-7, MF: C18H20N2O4S, MW: 360.43, Synonyms: Flt-3 Inhibitor, TCS 359, Form: Crystal-Powder, Size: 100MG