LY 294002 HYDROCHLORIDE

LY 294002 HYDROCHLORIDE Basic information
Product Name:LY 294002 HYDROCHLORIDE
Synonyms:LY 294002;LY 294002 HYDROCHLORIDE;2-[4-MORPHOLINYL]-8-PHENYL-1[4H]-BENZOPYRAN-4-ONE;2-(4-MORPHOLINYL)-8-PHENYL-4H-1-BENZOPYRAN-4-ONE;2-(4-MORPHOLINYL)-8-PHENYL-4H-1-BENZOPYRAN-4-ONE HYDROCHLORIDE;2-(4-MORPHOLINO)-8-PHENYL-4H-1-BENZOPYRAN-4-ONE;LY 294002, 99+%;LY294002HCl
CAS:154447-36-6
MF:C19H17NO3
MW:307.34
EINECS:1312995-182-4
Product Categories:Inhibitors;Inhibitor;Anti-cancer&immunity;PI3K/Akt/mTOR;Akt;mTOR;PI3K;Cell Cycle Regulation;apis;Signalling;Lipid signaling;PI3K/Akt Signaling
Mol File:154447-36-6.mol
LY 294002 HYDROCHLORIDE Structure
LY 294002 HYDROCHLORIDE Chemical Properties
Melting point 183-185℃
Boiling point 494.6±45.0 °C(Predicted)
density 1.266
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility DMSO: >5 mg/mL
form solid
pka0.55±0.20(Predicted)
color white to off-white
Water Solubility Soluble in DMSO at 5mg/ml. Insoluble in water
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 4 months.
InChIKeyCZQHHVNHHHRRDU-UHFFFAOYSA-N
CAS DataBase Reference154447-36-6
Safety Information
Safety Statements 24-25
WGK Germany 3
HS Code 29349990
MSDS Information
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SigmaAldrichEnglish
LY 294002 HYDROCHLORIDE Usage And Synthesis
DescriptionLY294002 is a selective phosphatidylinositol 3-kinase (PI3K) inhibitor with a 2.7-fold greater potency than quercetin. LY294002 inhibits purified PI3K with an IC50 of 1.4 μM.
UsesLY 294002 Hydrochloride is a highly selective inhibitor of Phosphatidylinositol 3-kinase (PI3K). It is a salt analogue of LY 294002 (L486590).
UsesLY 294002 is a Phosphatidylinositol 3-kinase (PI3K) inhibitor which has shown to block the formation of tumor tissues in bone marrow cavity an abolish multiple myeloma (MM) induced osteoclast formation and osteolysis in SCID mice.
UsesLY294002 is a selective phosphatidylinositol 3-kinase (PI3K) inhibitor with a 2.7-fold greater potency than quercetin. LY294002 inhibits purified PI3K with an IC50 of 1.4 μM.
UsesA potent blocker of PI 3-kinase/Akt signaling.
DefinitionChEBI: A chromone substituted with a phenyl group at position 8 and a morpholine group at position 2.
Biological ActivityA highly selective inhibitor of phosphatidylinositol 3-kinase (IC 50 values are 0.31, 0.73, 1.06 and 6.60 μ M for PI3K β , PI3K α , PI3K δ and PI3K γ respectively). Inhibits proliferation and induces apoptosis in human colon cancer cells in vitro and in vivo .
targetp110α
References1) Vlahos et al. (1994) A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY 294002); J. Biol. Chem., 269 5241
LY 294002 HYDROCHLORIDE Preparation Products And Raw materials
Raw materials4H-1-Benzopyran-4-one, 8-hydroxy-2-(4-morpholinyl)-–>1-(2-hydroxybiphenyl-3-yl)-3-morpholinopropane-1,3-dione–>N-Acetylmorpholine–>Trifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl ester–>methyl 2-hydroxy-3-phenyl-benzoate–>methyl 2,3-dihydroxybenzoate–>Methyl 3-methoxysalicylate–>2,3-Dihydroxybenzoic acid–>3-Methoxysalicylic acid–>Phenylboronic acid

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