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Filtered Search Results
eMolecules 1191062-85-7 | (5-Methyl-6-morpholinopyridin-3-yl)boronic acid | ChemScene | MFCD10566507 | 222.050 | C10H15BN2O3 | 98.000 | Cc1cc(cnc1N1CCOCC1)B(O)O | 100mg | 712787972
(5-Methyl-6-morpholinopyridin-3-yl)boronic acid | ChemScene | 1191062-85-7 | MFCD10566507 | 222.050 | C10H15BN2O3 | 98.000 | Cc1cc(cnc1N1CCOCC1)B(O)O | 100mg | 712787972
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Medchemexpress LLC Pegaptanib sodium | 222716-86-1 | 90.51% | 50000 (Approximately) | 500 MG
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Pegaptanib sodium is an RNA aptamer with polyethylene glycol modifications, directed against vascular endothelial growth factor (VEGF)-165. It can be used for the study of neovascular age-related macular degeneration (AMD).
- Solid appearance.
- White to off-white color.
- Inhibits VEGF165-mediated phosphorylation of VEGFR2 and phospholipase Cγ.
- Inhibits VEGF165-induced calcium mobilization in human umbilical vein endothelial cells.
- Targets vascular endothelial growth factor-165.
- Suitable for the study of neovascular age-related macular degeneration.
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Medchemexpress LLC Nimbin | 5945-86-8 | 5 MG
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Nimbin is an orally active intermediate limonoid found in Azadirachta. It prevents tau aggregation, increases cell viability, and effectively inhibits the envelope protein of the dengue virus. It possesses anti-inflammatory, antipyretic, antifungal, antihistamine, antiseptic, antioxidant, anti-cancer, and anti-viral properties, showing promise for research into neurodegenerative diseases and viral infections.
- Orally active intermediate limonoid
- Prevents tau aggregation and increases cell viability
- Effective inhibitor of the dengue virus envelope protein
- Anti-inflammatory, antipyretic, antifungal, antihistamine, antiseptic, antioxidant, anti-cancer, and anti-viral properties
- Promising for research of neurodegenerative diseases and viral infections
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Medchemexpress LLC Spaglumic acid | 3106-85-2 | MFCD00133559 | 98.0% | 304.25 g·mol⁻¹ | C11H16N2O8 | 100 MG
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Spaglumic acid (N-acetylaspartylglutamic acid, NAAG) is a naturally occurring neuropeptide found in brain tissue. Supplied as a solid analytical standard, it is intended for biochemical, neurochemical, and analytical applications that require a characterized NAAG reference material.
- Analytical standard for neuropeptide and biochemical research.
- High purity (98.0%) suitable for analytical use.
- Molecular weight 304.25 g·mol⁻¹; formula C11H16N2O8.
- Supplied as a solid, white to off-white material.
- Available in small quantities including 100 mg for research use.
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Medchemexpress LLC Ker047 (ALK2-IN-4) | 2248154-85-8 | 98.8% | 475.56 | 100 MG
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Ker047 (ALK2-IN-4) is a potent activin receptor-like kinase-2 (ALK2) inhibitor. It is utilized in the research of metabolic diseases, including fibrodysplasia ossificans progressiva (FOP).
- High purity of 98.8%
- Soluble in DMSO at 10 mg/mL
- Stable as powder for up to 3 years at -20°C
- Stable in solvent for up to 2 years at -80°C
- Documentation available for data, safety, and handling
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Medchemexpress LLC D5D-IN-326 | 1236767-85-3 | 99.9% | 473.27 | C17H11F8N3O4 | 5 MG
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D5D-IN-326 is a selective, orally active delta-5 desaturase (D5D) inhibitor (CAS 1236767-85-3) with reported nanomolar potency in enzymatic and cell-based assays and demonstrated activity in preclinical metabolic disease models. The compound is supplied for research use in multiple formats and sizes and is characterized by high purity and defined storage stability.
- Selective inhibitor of delta-5 desaturase with nanomolar potency.
- Reduces insulin resistance and body weight in preclinical models.
- High purity (99.9%) for reliable experimental results.
- Available as powder and solution formats for flexible dosing.
- Stable under recommended storage conditions for long-term use.
- Supplied in small research quantities suitable for in vitro and in vivo studies.
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eMolecules 6750-85-2 | Ambeed | 5-(Methoxycarbonyl)furan-2-carboxylic acid | 100mg | 601095712 | A259026 | MFCD19441220 | 170.12 | C7H6O5
Ambeed | 5-(Methoxycarbonyl)furan-2-carboxylic acid | 100mg | 601095712 | A259026 | 6750-85-2 | MFCD19441220 | 170.120 | C7H6O5
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Medchemexpress LLC Pegaptanib sodium | 222716-86-1 | 90.5% | 50,000 Da (approximately) | 5 MG
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Pegaptanib sodium is a PEGylated 28-mer RNA aptamer that selectively binds vascular endothelial growth factor (VEGF)-165. Supplied as the sodium salt, it is intended for research use in studies of VEGF-mediated angiogenesis and neovascular age-related macular degeneration (AMD). It provides a research-ready reagent for in vitro and in vivo experimental models.
- Selective VEGF-165 binding suitable for anti-angiogenic research.
- PEGylated aptamer structure provides increased molecular weight and stability.
- Supplied as sodium salt with approximate molecular weight 50,000 Da.
- Purity approximately 90.5% as provided by the manufacturer.
- Available as a small research quantity (5 mg) for laboratory studies.
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Medchemexpress LLC Cp-409092 Hydrochlor 50Mg | HY-101639A-50MG
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Cp-409092 Hydrochlor 50Mg
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eMolecules 947669-86-5 | Medchem Express | WWL113 | 5mg | 713704307 | HY-110148 | MFCD28160857 | 466.537 | C29H26N2O4
Medchem Express | WWL113 | 5mg | 713704307 | HY-110148 | 947669-86-5 | MFCD28160857 | 466.537 | C29H26N2O4
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Medchemexpress LLC 3-(benzylthio)-5-(phenoxymethyl)-4-phenyl-4H-1,2,4-triazole | 129544-85-0 | 99.9% | C22H19N3OS | 10MG
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MIND4-19 is a small-molecule SIRT2 inhibitor (IC50 7.0 μM) used as a research tool in studies of neurodegeneration, including Huntington's disease. The compound is a solid, white to off-white material with formula C22H19N3OS and a molecular weight of 373.47 g·mol⁻¹; it is supplied with high purity and storage recommendations to protect activity.
- Potent SIRT2 inhibition (IC50 7.0 μM).
- High chemical purity (>99.9%).
- Solid, white to off-white appearance for easy handling.
- Suitable for neurodegeneration and SIRT2 biology research.
- Storage conditions provided to preserve stability and activity.
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eMolecules 474709-85-8 | 1-(3,4-Difluorophenyl)cyclopropan-1-amine | ChemScene | MFCD09910057 | 169.175 | C9H9F2N | 98.000 | NC1(CC1)c1ccc(F)c(F)c1 | 100mg | 572219114
1-(3,4-Difluorophenyl)cyclopropan-1-amine | ChemScene | 474709-85-8 | MFCD09910057 | 169.175 | C9H9F2N | 98.000 | NC1(CC1)c1ccc(F)c(F)c1 | 100mg | 572219114
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eMolecules 31486-86-9 | Ambeed | Thieno[32-b]thiophene-2-carbaldehyde | 1g | 525077647 | A162309 | MFCD01859924 | 168.23 | C7H4OS2
Ambeed | 3-Methyl-1H-indene | 100mg | 552730613 | A436721 | 767-60-2 | MFCD00674487 | 130.190 | C10H10
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Medchemexpress LLC Atuliflapon (AZD5718) | 2041075-86-7 | 99.0% | 100 MG
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Atuliflapon (AZD5718) is a small-molecule, orally active inhibitor of 5-lipoxygenase activating protein (FLAP) investigated as a research compound for cardiovascular indications such as coronary artery disease. It potently suppresses leukotriene production and has documented preclinical and clinical pharmacology data.
- Oral FLAP inhibitor with potent activity (reported FLAP IC50 ≈ 2 nM).
- Reduces leukotriene production in human whole blood.
- Reported molecular weight 446.50 g·mol⁻¹ and formula C24H26N6O3.
- High purity (about 99.0%), white to off-white solid.
- Soluble in DMSO (≈125 mg/mL); sonication may be required for full dissolution.
- Powder storage: -20°C for long-term stability; in solvent, store at -80°C when possible.
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eMolecules 544678-85-5 | Medchem Express | DB04760 | 1mg | 536984011 | HY-125166 | MFCD09878513 | 410.425 | C22H20F2N4O2
Medchem Express | DB04760 | 1mg | 536984011 | HY-125166 | 544678-85-5 | MFCD09878513 | 410.425 | C22H20F2N4O2
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