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Phenylpropaniods are organic compounds characterized by having an aromatic ring and a three-carbon propene tail. Polyketides are compounds characterized by having two or more carbonyl functional groups connected with a single carbon atom.
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PI3K/AKT-IN-1 is an effective dual inhibitor of PI3K and AKT, exhibiting anticancer activity by inhibiting the PI3K/AKT axis and inducing caspase 3-dependent apoptosis. This compound has high cytotoxic activity against leukemia K562 and breast cancer MCF-7 cell lines, and is intended for research use only.
Demonstrates high cytotoxic activity, particularly against leukemia cell line K562 (IC50=2.62 μM) and breast cancer cell line MCF-7 (IC50=3.22 μM)
Promotes S-phase cell cycle arrest and induces apoptosis in K562 cells
Significantly reduces the expression of PI3K, p-PI3K, AKT, p-AKT, Cyclin D1, and NF-κB
Found to be non-toxic and well-tolerated in animal studies, with an LD50 greater than 2000 mg/kg
Soluble in DMSO at 50 mg/mL
Solid, off-white to light yellow appearance
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(-)-Epicatechin (CAS 490-46-0) is a flavonoid compound known for inducing pancreatic -cell regeneration and modulating nitric oxide (NO) metabolism It inhibits nitric oxide-related nitrite formation induced by interferon- and lipopolysaccharide in mouse macrophages and reduces peroxynitrite-mediated tyrosine nitration in HL-60 human leukemia cells Additionally in human endothelial cells (HUVECs) it enhances NO production displaying vasodilatory properties In diabetic rat models (alloxan-induced) (-)-epicatechin administration promotes -cell recovery reduces hyperglycemia and prevents -cell necrosis This profile underscores its research relevance for diabetes and vascular biology investigations
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Oxytetracycline hydrochloride is an antibiotic that belongs to the tetracycline class. It is a potent inhibitor of both Gram-negative and Gram-positive bacteria. This compound acts as a protein synthesis inhibitor by preventing the binding of aminoacyl-tRNA to the m-ribosomal RNA complex. Additionally, Oxytetracycline hydrochloride exhibits anti-HSV-1 activity. Oxytetracycline is a bacterial aromatic polyketide, synthesized by a type II polyketide synthase which generates its poly-beta-ketone backbone through successive decarboxylative condensation of malonyl-CoA extender units, followed by modifications from cyclases, oxygenases, transferases, and other tailoring enzymes.
Antibiotic belonging to the tetracycline class
Potent inhibitor of Gram-negative and Gram-positive bacteria
Functions as a protein synthesis inhibitor
Prevents aminoacyl-tRNA binding to the m-ribosomal RNA complex
Possesses anti-HSV-1 activity
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool<|a>
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N-Fmoc-2,3-difluoro-D-phenylalanine is a Amino Acid reagent (Subcategory: Phe) sold by WuXi TIDES. Offered in 25 g. Store at 4 °C. SDS available for reference.
Specifications - CAS: 1260609-30-0 - MDL: No data - InChIKey: MNEDJBJASVXQIC-OAQYLSRUSA-N - Molecular Weight: 423.416 - Molecular Formula: C24H19F2NO4 - Purity: ≥95% - Container Type: 125 mL HDPE - Pack Size: 25 g - Net Weight: 25 g - Gross Weight: 54.3 g - Commodity Code: 29242970 - Country Of Origin: China - IUPAC: (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,3-difluorophenyl)propanoic acid - SMILES: O=C(OCC1C2=CC=CC=C2C3=CC=CC=C31)N[C@@H](C(O)=O)CC4=CC=CC(F)=C4F
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A coumarin with diverse biological activities; inhibits 15-LO-1 (IC50 = 9.5 µM); scavenges DPPH radicals in a cell-free assay (IC50 = 0.61 mM); inhibits lipid peroxidation in vitro (IC50 = 69.07 mM); protective against UVB-induced embryotoxicity in sea urchins
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