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1-(2-Amino-3-methylphenyl)ethanol
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1-(2-Amino-3-methylphenyl)ethanol
Catalog Number:
(102654-110)
Supplier:
American Radiolabeled Chemicals
Description:
Synonyms: Valium [N-methyl-3H]; Ro 5-2807 [N-methyl-3H]
Supplier:
Thermo Scientific Chemicals
Description:
Xylenecyanol FF, Electrophoresis Reagent, dye content 70%
Supplier:
Spectrum Chemicals
Description:
Sodium Hydroxide, Pellets, FCC is used in the chemical washing and peeling of fruits and vegetables and as a thickening agent. The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.
Catalog Number:
(102988-314)
Supplier:
Adipogen
Description:
Mycotoxin
Supplier:
Adipogen
Description:
Gefitinib is a selective, orally available epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. In NR6wtEGFR and NR6W cells, it inhibits Tyr1173, Tyr992, Tyr1173 and Tyr992 with IC(50) values of 37nM, 37nM, 26nM and 57nM, respectively.
Supplier:
Adipogen
Description:
GDC-0980 (RG7422) is a selective, dual PI3 Kinase and mTOR Kinase inhibitor with IC(50) values of 5, 27, 7, and 14nM for PI3Kalpha-delta respectively. It inhibits mTOR with a Ki of 17nM.
Supplier:
Adipogen
Description:
Shows strong gastrointestinal motor stimulating (GMS) activity. Motilin receptor agonist. Stimulates smooth muscle cell contraction. Stimulates cholinergic neurons in a non-vagal pathway. Enhances gastrointestinal contractile activity and accelerates gastric emptying. Shows orexigenic activity with affinity for the growth-hormone secretagogue receptor (GHS-R, ghrelin receptor).
Supplier:
Adipogen
Description:
Cytotoxic. Melanogenesis inhibitor without cytotoxicity.
Supplier:
Adipogen
Description:
NVP-BSK805 is a potent and selective quinoxaline JAK2 inhibitor with IC(50) values of 0.48, 0.56 and 0.58nM for JAK2 JH1, FL JAK (V617F) and FL JAK2 wt, respectively.
Catalog Number:
(101828-208)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 029464-500MG , MDL Number: MFCD00018894
Catalog Number:
(102988-090)
Supplier:
Adipogen
Description:
Antibiotic
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-Methylbenzophenone 97%
Supplier:
AMBEED, INC
Description:
4-Methylbenzophenone 95%
Catalog Number:
(101914-548)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 058304-500MG , MDL Number: MFCD00155304
Supplier:
TCI America
Description:
CAS Number: 36635-61-7
MDL Number: MFCD00000005 Molecular Formula: C9H9NO2S Molecular Weight: 195.24 Purity/Analysis Method: >98.0% (HPLC,N) Form: Crystal Color: Slightly Pale Yellow Melting point (°C): 110
Supplier:
MP Biomedicals
Description:
Arachidonic Acid is an essential fatty acid. Occurs in liver, brain, glandular organs, and depot fats of animals, in small amounts in human depot fats, and is a constituent of animal phosphatides.
Arachidonic Acid is a precursor in the biosynthesis of prostaglandins, thromboxanes, and leukotrienes. Arachidonic acid plays a key role in cellular regulation and is controlled through multiple interconnected pathways. Arachidonic acid (AA) is an unsaturated ω6 fatty acid constituent of the phospholipids of cell membranes. Phospholipase A2 releases AA from the membrane phospholipids in response to inflammation. AA is subsequently metabolized to prostaglandins and thromboxanes by at least two cyclooxygenase (COX) isoforms, to leukotrienes and lipoxins by lipoxygenases, and to epoxyeicosatrienoic acids via cytochrome p450-catalyzed metabolism. AA and its metabolites play important roles in a variety of biological processes, including signal transduction, smooth muscle contraction, chemotaxis, cell proliferation and differentiation, and apoptosis. AA has been demonstrated to bind to the a subunit of G protein and inhibit the activity of Ras GTPase-activating proteins (GAPs). Cellular uptake of AA is energy dependent and involves protein-facilitated transport across the plasma membrane. If ethanol is undesirable, arachidonic acid may be dissolved in acetonitrile, DMF, or DMSO. Simply evaporate the ethanol under a gentle stream of nitrogen (be certain not to evaporate the material to dryness) and redissolve the arachidonic acid in the solvent of choice.Just prior to use, make dilutions of the stock solution into aqueous buffer or isotonic saline to bring the arachidonic acid to the desired concentration. Ensure that the residual amount of organic solvent is insignificant, since organic solvents may have physiologic effects at low concentrations. A control using the solvent in the absence of the prostaglandin will address this potential variable. We do not recommend storing the aqueous solution for more than one day. It is difficult to obtain aqueous solutions of arachidonic acid directly. However, an organic solvent free solution of arachidonic acid can be prepared using concentrated basic buffers (pH > 8.0 and ionic strength not less than 0.1 M). Add 400 μL of cold buffer (0 °C) per mg of arachidonic acid and agitate vigorously and/or ultrasonicate.
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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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