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Filtered Search Results
Accela Chembio Inc Trans | trans-dibenzylideneacetone | 100g | 35225-79-7 | MFCD00004790 | 97+% | Shelf Life: 1260 Days | Light Sensitive
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Trans | trans-dibenzylideneacetone | 100g | 35225-79-7 | MFCD00004790 | 97+% | Shelf Life: 1260 Days | Light Sensitive
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Medchemexpress LLC Immunoproteasome inhibitor 1 | 2755772-63-3 | 99.6% | C20H26N2O4 | 1 ML
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Immunoproteasome inhibitor 1 is a potent, reversible, and time-independent inhibitor of both immunoproteasome and proteasome. It exhibits Ki values of 1.18 μM in β5c, 0.27 μM in β1i, and 1.91 μM in β5i subunits. The compound demonstrates high binding affinity for the β1i subunit and good inhibitory properties towards the β5i and β5c subunits. This inhibitor can be utilized for research into certain neoplastic diseases.
- Potent, reversible, and time-independent inhibition
- Targets both immunoproteasome and proteasome subunits (β5c, β1i, β5i)
- High binding affinity for β1i subunit (0.27 μM)
- Useful for research into neoplastic diseases
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Sigma Aldrich Fine Chemicals Biosciences Propenyl guaethol >=99%, FCC, FG | 94-86-0 | MFCD00009283 |
Propenyl guaethol >=99%, FCC, FG | Purity: >=99% | Mol Wt: 178.23 | 94-86-0 | MFCD00009283 |
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Medchemexpress LLC 2-((5-bromo-2-((1-(methylsulfonyl)piperidin-4-yl)amino)pyrimidin-4-yl)amino)-6-fluorobenzamide | 2488892-01-7 | 99.4% | 487.35 g/mol | C17H20BrFN6O3S | 10 MG
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TMX-2039 is a research-grade pan-cyclin-dependent kinase (pan-CDK) inhibitor intended for biochemical and cellular studies of cell cycle and transcriptional CDKs. Supplied as an off-white to light yellow solid with high reported purity, it is suitable for assay development, mechanism-of-action experiments, and probe validation in research settings.
- Pan-CDK activity covering cell cycle and transcriptional CDKs.
- High purity (≈99.4%) suitable for research applications.
- Supplied as a solid powder for flexible formulation and dosing.
- Available in small research-friendly pack sizes, e.g. 10 mg.
- Stable under recommended storage: 4°C under nitrogen; in solvent, -80°C for 6 months or -20°C for 1 month.
- Provides consistent material for biochemical and cellular assays.
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Medchemexpress LLC Gt-653 | 3057627-63-8 | 99.8% | 653.60 | C32H27N7O9 | 10 MG
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GT-653 is a PROTAC degrader that targets lysine-specific demethylase 5B (KDM5B), promoting ubiquitin-proteasome-dependent degradation and modulating H3K4 methylation in cellular models. It is supplied as a white to off-white solid for research use in biochemical and cellular studies of epigenetic regulation.
- PROTAC mechanism targeting KDM5B, a histone demethylase.
- Demonstrated 68.35% degradation of KDM5B at 10 μM in cell assays.
- Upregulates H3K4me3 levels and activates type-I interferon signaling in prostate cancer cells.
- Available as a white to off-white powder suitable for in vitro studies.
- Molecular formula C32H27N7O9; molecular weight 653.60.
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Medchemexpress LLC Styrene-divinylbenzene sulfonated copolymer | 69011-20-7 | 98% | 25 G
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Styrene-divinylbenzene sulfonated copolymer is a strongly acidic resin and a cationic exchange resin. It is made from a microporous styrene/divinylbenzene (DVB) co-polymer with a sulfonic acid group.
- Strongly acidic resin
- Cationic exchange resin
- Made from microporous styrene/divinylbenzene (DVB) co-polymer
- Contains a sulfonic acid group
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Medchemexpress LLC Styrene-divinylbenzene sulfonated copolymer | 69011-20-7 | 98% | 5 G
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Styrene-divinylbenzene sulfonated copolymer is a strongly acidic resin. It is a cationic exchange resin made from a microporous styrene/divinylbenzene (DVB) co-polymer with a sulfonic acid group.
- Strongly acidic resin
- Cationic exchange resin
- Made from a microporous styrene/divinylbenzene (DVB) co-polymer
- Contains a sulfonic acid group
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eMolecules Ambeed / [114141-Quaterphenyl]-44-dicarboxylic acid / 100mg / 599357228 / A974340 / / 143613-17-6 / [null] / 394.426 / C26H18O4
Ambeed / [114141-Quaterphenyl]-44-dicarboxylic acid / 100mg / 599357228 / A974340 / / 143613-17-6 / [null] / 394.426 / C26H18O4
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TARGETMOL CHEMICALS INC ELN318463 RACEMATE 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ELN318463 racemate (ELN 318463 racemate) is the racemate of ELN318463 which is an amyloid precursor protein (APP) selective (gamma)-secretase inhibitor. purity: 99%
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Medchemexpress LLC Styrene-divinylbenzene sulfonated copolymer | 69011-20-7 | 98% | 50 G
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Styrene-divinylbenzene sulfonated copolymer is a strongly acidic resin and a cationic exchange resin. It is manufactured from a microporous styrene/divinylbenzene (DVB) co-polymer that includes a sulfonic acid group.
- Solid appearance
- Light yellow to brown color
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Medchemexpress LLC Methyl isoeugenol | 93-16-3 | 100 MG
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Methyl isoeugenol (MIE) is a natural food flavor isolated from Pimenta pseudocaryophyllus leaf. It shows anxiolytic and antidepressant-like effects and is orally active.
- Natural food flavor
- Isolated from Pimenta pseudocaryophyllus leaf
- Exhibits anxiolytic and antidepressant-like effects
- Orally active
- Liquid appearance, colorless to light yellow
- Purity of 98.11%
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eMolecules trans-4-Phenyl-cyclohexylamine hydrochloride | 5769-08-4 | | 1g
J & W PharmLab LLC | trans-4-Phenyl-cyclohexylamine hydrochloride | 1g | 491379591 | 20R1690S | 96.000 | 5769-08-4 | | 211.730 | C12H18ClN
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TARGETMOL CHEMICALS INC 653-47 hydrochloride 5MG
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Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. 653-47 hydrochloride is a potentiator, significantly potentiates the cAMP-response element binding protein (CREB) inhibitory activity of 666-15. It is also a very weak CREB inhibitor with IC50 of 26.3 uM. Purity 99.65%
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Selleck Chemical LLC NMS-873
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NMS-873 is an allosteric and specific p97 inhibitor with IC50 of 30 nM that demonstrates potent selectivity for VCP/p97 compared to a panel of other AAA ATPases Hsp90 and 53 additional analyzed kinases (IC50s 10 M)
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Medchemexpress LLC K858 racemic | 72926-24-0 | MFCD00181155 | 99.8% | 277.35 g·mol⁻1 | C13H15N3O2S | 10 MG
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K858 (racemic) is a small-molecule ATP-uncompetitive inhibitor of the mitotic kinesin Eg5 with an IC50 of 1.3 μM. Supplied as a solid powder, it is intended for cellular and biochemical research into mitosis, spindle dynamics, and antiproliferative mechanisms. Manufacturer guidance includes solubility and in vivo formulation protocols for experimental use.
- ATP-uncompetitive inhibitor of kinesin Eg5 (IC50 1.3 μM).
- High purity (99.8%).
- Solid powder form suitable for laboratory handling.
- Soluble in DMSO up to 100 mg/mL; ultrasonic assistance recommended.
- Includes in vivo formulation protocols for dosing studies.
- Available in small research quantities for preclinical experiments.
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