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1-(2-Amino-3-methylphenyl)ethanol
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1-(2-Amino-3-methylphenyl)ethanol
Supplier:
Adipogen
Description:
TG-46 is an inhibitor of JAK2, FLT3, RET, JAK3 with IC(50) values of 6nM, 25nM, 17nM, 169nM respectively.
Supplier:
Adipogen
Description:
TG-89 is a JAK inhibitor. It has IC(50) values of 6, 25, 17 and 169nM against JAK2, FLT3, RET and JAK3 respectively.
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Xylenol orange tetrasodium salt ACS
Supplier:
Adipogen
Description:
PD173955 is an ATP-competitive, dual Src/Bcr-Abl kinase inhibitor. It is a potent inhibitor of Bcr-Abl with an IC(50) of 1-2nM in kinase inhibition assays. In cellular growth assays it inhibits Bcr-Abl-dependent substrate tyrosine phosphorylation. PD173955 also inhibits Src kinase activity in vitro with an IC(50) of 22nM and could represent a novel class of anti-mitotic drug.
Supplier:
Adipogen
Description:
PCI-32765 (Ibrutinib) is a potent and highly selective Btk inhibitor with an IC(50) of 0.5nM.
Catalog Number:
(10082-150)
Supplier:
Proteintech
Description:
ADH5, also named as ADHX, FDH FALDH GSH-FDH ADH3 and GSNOR, belongs to the zinc-containing alcohol dehydrogenase family and Class-III subfamily. It is remarkably ineffective in oxidizing ethanol, but it readily catalyzes the oxidation of long-chain primary alcohols and the oxidation of S-(hydroxymethyl) glutathione. ADH5 mediates multiple cardiovascular functions. It plays in regulating heterocellular communication in the artery wall.
Supplier:
Adipogen
Description:
CX-4945 is a first-in-class, orally active, potent and selective inhibitor of the protein kinase CK2, with an IC(50) of 1nM.
Catalog Number:
(10282-048)
Supplier:
Bioss
Description:
ADH6 (alcohol dehydrogenase 6), also known as ADH-5, is a 368 amino acid member of the class V zinc-containing alcohol dehydrogenase family. This family of enzymes functions to metabolize a wide variety of substrates such as retinol, hydroxysteroids, ethanol, aliphatic alcohols and lipid peroxidation products. Localized to the cytoplasm and expressed in the stomach and liver, ADH6 catalyzes the reversible oxidation of alcohols to their corresponding aldehydes or ketones and is able to bind two zinc ions as cofactors. ADH6 contains a glucocorticoid response element upstream of its 5' UTR which is thought to be a steroid binding site, suggesting that expression of ADH6 may be under hormonal control. Multiple isoforms of ADH6 exist due to alternative splicing events.
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Xylenol orange tetrasodium salt, water soluble, pure
Catalog Number:
(IC15034310)
Supplier:
MP Biomedicals
Description:
4-Aminoantipyrine is a reagent for determination of chlorinated phenols, phenylglycosidase, and glucose in the presence of phenol and peroxidase.
Supplier:
AMBEED, INC
Description:
Xylenol orange tetrasodium salt indicator
Supplier:
Adipogen
Description:
PF-562,271 is a potent, ATP-competitive, reversible inhibitor of FAK and Pyk2 catalytic activity with a IC(50) of 1.5 and 14nM, respectively. In addition, PF-562,271 displayed robust inhibition in an inducible cell-based assay measuring phospho-FAK with an IC(50) of 5nM. PF-562,271 was evaluated against multiple kinases and displays <gt/>100x selectivity against a long list of nontarget kinases. In tests, PF-562,271 inhibits FAK phosphorylation in vivo in a dose-dependent fashion with a calculated EC50 of 93ng/mL using injections.
Supplier:
AMBEED, INC
Description:
1-(4-(Diisobutylamino)-2'-(2H-tetrazol-5-yl)-[1,1'-biphenyl]-3-yl)-3-(p-tolyl)urea, Purity: 98+%, CAS Number: 1668565-74-9, Appearance: White to off white powder or crystals, Storage: Sealed in dry, Store in freezer, under -20 C, Size: 1mg
Supplier:
Adipogen
Description:
PP242 exhibits potent selectivity for mTOR over other PI3K family kinases such as p110 alpha - delta and DNA-PK, with IC(50) of 1.96µM, 2.2µM, 1.27µM, 0.102µM, and 0.408µM, respectively.
Supplier:
Adipogen
Description:
CYC116 is an orally active small molecule multi-kinase inhibitor with anti-neoplastic activity. CYC116 inhibits Aurora kinases A/B and vascular endothelial growth factor receptor 2 (VEGFR2), resulting in disruption of the cell cycle, rapid cell death, and the inhibition of angiogenesis.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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