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Filtered Search Results
Medchemexpress LLC SR9243 | 1613028-81-1 | 99.17% | 626.62 | 200 MG
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SR9243 | 1613028-81-1 | 99.17% | 626.62 | 200 MG
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Medchemexpress LLC PI3K-IN-31 | 50MG
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PI3K-IN-31 | 50MG
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Medchemexpress LLC Poly(oxy-1,2-ethanediyl), α-(2-aminoethyl)-ω-methoxy- | 80506-64-5 | 98.0% | (C2H4O)nC3H9NO | 250 MG
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mPEG-amine (MW 5000) is a modifier that increases the water solubility of long-wavelength voltage-sensitive dyes (VSD) or Pittsburgh (PGH) dyes by replacing the sulfonic acid portion of the dye molecule. It can also form amide bonds with carboxyl groups on the surface of microspheres through EDC and Sulfo-NHS mediation, creating a PEG coating on fluorescent microspheres for large-scale rotational cytoplasmic flow studies. This product is for research use only.
- Increases water solubility of long-wavelength voltage-sensitive dyes (VSD) or Pittsburgh (PGH) dyes
- Replaces the sulfonic acid portion of dye molecules
- Forms amide bonds with carboxyl groups on microsphere surfaces
- Creates a PEG coating on fluorescent microspheres
- Suitable for large-scale rotational cytoplasmic flow studies
- For research use only
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Medchemexpress LLC DC-BPi-03 | 2758411-46-8 | C14H14N4O2S | 200 MG
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DC-BPi-03 is a potent BPTF-BRD inhibitor with an IC50 of 698.3 nM and a Kd of 2.81 μM. This compound is intended for research use only.
- Potent BPTF-BRD inhibitor
- IC50 of 698.3 nM
- Kd of 2.81 μM
- Purity of 99.77%
- White to off-white solid appearance
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Medchemexpress LLC Amino-PEG7-amine | 332941-25-0 | 99.3% | C16H36N2O7 | 250 MG
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Amino-PEG7-amine is a PEG-based PROTAC linker used in the synthesis of Proteolysis Targeting Chimeras (PROTACs). These compounds are designed with two ligands connected by a linker: one targeting an E3 ubiquitin ligase and the other for a target protein. PROTACs utilize the intracellular ubiquitin-proteasome system to achieve selective degradation of target proteins. This product is for research use only.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Utilizes the intracellular ubiquitin-proteasome system
- Designed for selective degradation of target proteins
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371376 POMALIDOMIDE-5-C9-NH 5MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371277 GSK269962A 200MG
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Medchemexpress LLC (Ser8)-GLP-1 (7-36) amide, human | 215777-46-1 | 99.1% | 3313.63 | 25 MG
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(Ser8)-GLP-1 (7-36) amide, human is a glucagon-like peptide 1 amide, which is derived from glucagonogen as a cleavage product of the GLP-1 (1-36) amide peptide. This compound functions as an entero-insulinotropic hormone, meaning it stimulates the glucose-dependent release of insulin from pancreatic β-cells. Additionally, it influences gastrointestinal motility and secretion. These properties make it relevant for research into metabolic diseases and conditions affecting glucose regulation and digestive processes.
- Glucagon-like peptide 1 amide derivative.
- Stimulates glucose-dependent insulin release from pancreatic β-cells.
- Affects gastrointestinal motility and secretion.
- High purity (99.10%).
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Medchemexpress LLC Lenvatinib | 417716-92-8 | 99.8% | 1 G
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Lenvatinib (E7080) is an oral, multi-targeted tyrosine kinase inhibitor. It inhibits VEGFR1-3, FGFR1-4, PDGFR, KIT, and RET, demonstrating potent antitumor activities. This compound shows antiproliferative activity and growth inhibition in various cell lines.
- Inhibits VEGFR2, VEGFR3, and VEGFR1
- Inhibits PDGFRα, PDGFRβ, and FGFR1
- Inhibits KIT and RET
- Demonstrates antiproliferative activity
- Available as a solid form
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Medchemexpress LLC Foliglurax monohydrochloride | 2133294-96-7 | 98.6% | 457.97 | 10 MM 1 ML
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Foliglurax monohydrochloride is a highly selective and potent, brain-penetrant metabotropic glutamate receptor 4 positive allosteric modulator (mGluR4 PAM), with an EC50 of 79 nM. It exhibits an antiparkinsonian effect.
- Highly selective and potent metabotropic glutamate receptor 4 positive allosteric modulator (mGluR4 PAM)
- Brain-penetrant
- EC50 of 79 nM
- Antiparkinsonian effect
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371584 MPEG-AMINE MW 750 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371628 AZD1208 200MG
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Medchemexpress LLC Vebicorvir | 2090064-66-5 | 99.7% | 467.44 | 10 MM 1 ML
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Vebicorvir (ABI-H0731) is a first-generation hepatitis B virus (HBV) core protein inhibitor. It suppresses covalently closed circular DNA (cccDNA) formation in two de novo infection models with EC50s ranging from 1.84 μM to 7.3 μM. In vitro, it inhibits pgRNA, HBeAg, and HBsAg production, and is also an inhibitor of pgRNA encapsidation and rcDNA synthesis. The product appears as a white to off-white solid for research use only.
- Suppresses covalently closed circular DNA (cccDNA) formation
- Inhibits pgRNA, HBeAg, and HBsAg production
- Inhibits pgRNA encapsidation and rcDNA synthesis
- Appears as a white to off-white solid
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Medchemexpress LLC Valbenazine | 1025504-45-3 | 98.6% | 418.57 | 200 MG
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Valbenazine is a vesicular monoamine transporter 2 (VMAT2) inhibitor with a Ki of 110-190 nM. It exhibits VMAT2 binding affinity in rat striatum and human platelets. In vivo, Valbenazine induces ptosis and increases plasma prolactin in rats.
- VMAT2 inhibitor.
- Exhibits VMAT2 binding affinity in rat striatum and human platelets.
- Induces ptosis and increases plasma prolactin in rats.
- Available in solid and solution forms.
- Can be stored long-term as powder at -20°C (3 years) or 4°C (2 years).
- In solvent, stock solutions can be stored at -80°C (2 years) or -20°C (1 year).
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371852 MPEG-AMINE MW 550 500MG
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