Quinolines and derivatives
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Filtered Search Results
Medchemexpress LLC 1-tert-Butyl-3-ethoxybenzene | 133073-81-1 | 95.0% | C12H18O | 500 MG
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1-tert-Butyl-3-ethoxybenzene is a drug intermediate for the synthesis of various active compounds. This product is intended for research use only and is not for human or medical applications.
- A drug intermediate for the synthesis of various active compounds.
- For research use only.
- Appearance: Liquid.
- Color: Light yellow to light brown.
- Chemically stable under recommended storage conditions.
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Medchemexpress LLC 7-PPD | 3081-01-4 | 98.28% | 282.42 | 25 G
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7-PPD (DMPPD) is a rubber antioxidant that scavenges free radicals and inhibits the oxidative degradation of rubber chains. It shows promise for research in tire manufacturing and rubber product processing.
- Scavenges free radicals.
- Inhibits oxidative degradation of rubber chains.
- Potential for use in tire manufacturing.
- Suitable for rubber product processing research.
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Medchemexpress LLC 4',7-Dimethoxyisoflavone | 1157-39-7 | 10 MM 1 ML
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4',7-Dimethoxyisoflavone, also known as Dimethoxydaidzein, is a natural compound isolated from the leaves of Albizzia lebbeck. It exhibits antifungal activity against various plant pathogenic fungi and is intended for research use only.
- Isolated from Albizzia lebbeck
- Exhibits antifungal activity
- For research use only
- High purity (98.20%)
- White to off-white solid appearance
- Soluble in DMSO
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Medchemexpress LLC STF-31 | 724741-75-7 | 99.79% | 423.53 | 25 MG
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STF-31 is a selective inhibitor of glucose transporter 1 (GLUT1) with an IC50 of 1 μM. It also functions as a NAMPT inhibitor, inhibiting glucose uptake in renal cell carcinoma (RCC) 4 cells.
- Selective inhibitor of glucose transporter 1 (GLUT1)
- Functions as a NAMPT inhibitor
- Inhibits glucose uptake in renal cell carcinoma (RCC) 4 cells
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Medchemexpress LLC STF-31 | 724741-75-7 | 97.0% | 423.53 | 10 MM 1 ML
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STF-31 is a selective inhibitor of glucose transporter 1 (GLUT1) with an IC50 of 1 μM. It also functions as a NAMPT inhibitor and inhibits glucose uptake in renal cell carcinoma (RCC) 4 cells.
- Targets GLUT
- Targets Autophagy
- Used in cancer research
- Cited in over 15 publications
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eMolecules 2-CHLORO-6,7-DIMETHOXY-QUINAZOLINE | 94644-47-0 | MFCD06249130 | 1g
AstaTech | 2-CHLORO-6,7-DIMETHOXY-QUINAZOLINE | 1g | 112525127 | 57469 | 97.000 | 94644-47-0 | MFCD06249130 | 224.640 | C10H9ClN2O2
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eMolecules 2-Methylpyrazolo[1,5-a]quinazolin-5(4h)-one | 25468-50-2 | MFCD02696475 | 1g
Combi-Blocks | 2-Methylpyrazolo[1,5-a]quinazolin-5(4h)-one | 1g | 117564271 | SS-7721 | 98.000 | 25468-50-2 | MFCD02696475 | 199.213 | C11H9N3O
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Medchemexpress LLC Ro 31-9790 | 145337-55-9 | 99.4% | 315.41 g/mol | C15H29N3O4 | 1 ML
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Ro 31-9790 is a synthetic metalloproteinase (MMP) inhibitor used in biochemical and cell-based research. It blocks L-selectin shedding and modulates cytokine shedding in immune cells, displaying submicromolar to micromolar potency across different cell types. The compound is provided as a concentrated solution for laboratory assays and requires appropriate storage and handling.
- Inhibits L-selectin and TNF-α shedding in immune cells.
- Potent activity with IC50 values as low as 0.3 μM.
- Supplied as a 10 mM solution in DMSO for ready-to-use dosing.
- High purity suitable for research applications.
- High DMSO solubility (50 mg/mL) with warming or sonication if needed.
- Stable in solvent when stored at -80°C for long-term preservation.
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Medchemexpress LLC 5'-O-(4,4'-dimethoxytrityl)-2'-O-methyluridine | 103285-22-9 | MFCD00274123 | 98.0% | 560.59 | C31H32N2O8 | 5 G
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5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyluridine is a DMT-protected uridine analog used as a nucleoside building block and intermediate for the synthesis of modified oligonucleotides. It is supplied as a light-yellow solid with defined purity and storage specifications suited for research and preparative oligonucleotide chemistry.
- DMT protected at the 5' hydroxyl for selective chain assembly.
- 2'-O-methyl modification supports increased nuclease resistance in oligonucleotides.
- High purity material suitable for synthesis and analytical workflows.
- Available in gram-scale pack sizes to accommodate different synthesis scales.
- Stable under recommended storage conditions to preserve quality over time.
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Ambeed Palladium II acetate
Palladium(II) acetate, 3375-31-3, 99.9%
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Ambeed Benzyl 3oxocyclobutyl carbama
Benzyl (3-oxocyclobutyl)carbamate, 130369-36-7, 97%
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Ambeed R 4Benzyl2oxazolidinone
(R)-4-Benzyl-2-oxazolidinone, 102029-44-7, 98%
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Accela Chembio Inc 2-ethoxy-1-ethoxycarbonyl-1 | 2-dihydroquinoline (eedq) | 100g | 16357-59-8 | MFCD00006703 | 97+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
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2-ethoxy-1-ethoxycarbonyl-1 | 2-dihydroquinoline (eedq) | 100g | 16357-59-8 | MFCD00006703 | 97+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
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Medchemexpress LLC TL02-59 | 1315330-17-6 | 99.9% | 609.64 | 25 MG
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TL02-59 is an orally active, selective Src-family kinase Fgr inhibitor with an IC50 of 0.03 nM. It also inhibits Lyn and Hck with IC50s of 0.1 nM and 160 nM, respectively. This compound potently suppresses the growth of acute myelogenous leukemia (AML) cells.
- Selectively targets the Src-family kinase Fgr with high potency (IC50 of 0.03 nM).
- Also shows inhibitory activity against Lyn (IC50 of 0.1 nM) and Hck (IC50 of 160 nM).
- Potently suppresses acute myelogenous leukemia (AML) cell growth.
- Induces growth arrest and apoptosis of AML cell lines at single-digit nM potency and induces growth arrest in primary AML bone marrow samples.
- Completely eliminates AML cells from the spleen and peripheral blood, and dramatically suppresses bone marrow involvement in a mouse model of AML.
- Has good oral bioavailability with a t1/2 of 5.7 h by i.v injection and 6.5 h by p.o. administration.
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eMolecules POTASSIUM TRANS-2-ETHOX 250MG
5000190575 POTASSIUM TRANS-2-ETHOX 250MG
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