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Filtered Search Results
Medchemexpress LLC Atuliflapon (AZD5718) | 2041075-86-7 | 99.0% | 25 MG
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Atuliflapon (AZD5718) is a small-molecule, orally active inhibitor of 5-lipoxygenase activating protein (FLAP) used in preclinical and clinical research to modulate leukotriene biosynthesis and investigate cardiovascular inflammation.
- Inhibits FLAP with low-nanomolar potency in clinical studies.
- Demonstrates target engagement via reduced LTB4 and LTE4 biomarkers.
- Suitable for in vitro human and translational studies; species-dependent activity limits some animal models.
- Provided as a solid powder with high purity for research use.
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eMolecules Ambeed / 3-(Bromomethyl)benzo[d]isoxazole / 100mg / 552734335 / A466071 / / 37924-85-9 / MFCD03701148 / 212.046 / C8H6BrNO
Ambeed / 3-(Bromomethyl)benzo[d]isoxazole / 100mg / 552734335 / A466071 / / 37924-85-9 / MFCD03701148 / 212.046 / C8H6BrNO
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eMolecules Medchem Express / Nav1.1 activator 1 / 5mg / 552386578 / HY-126429 / / 2332897-85-3 / [null] / 440.470 / C24H23F3N4O
Medchem Express / Nav1.1 activator 1 / 5mg / 552386578 / HY-126429 / / 2332897-85-3 / [null] / 440.470 / C24H23F3N4O
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Medchemexpress LLC 4-hydroxy-2-methyl-1,1-dioxo-N-(1,3-thiazol-2-yl)-1λ6,2-benzothiazine-3-carboxamide | 34042-85-8 | MFCD00866053 | 100.0% | 337.37 g/mol | C13H11N3O4S2 | 25 MG
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Sudoxicam is a reversible, orally active cyclooxygenase (COX) antagonist and a non-steroidal anti-inflammatory compound of the enol-carboxamide class supplied for research and analytical use only. It demonstrates anti-inflammatory, anti-edema, and antipyretic activity and is provided as a solid and in DMSO solution formulations for laboratory studies.
- Reversible, orally active COX antagonist.
- High reported purity suitable for analytical work.
- Chemical formula C13H11N3O4S2 and molecular weight 337.37 g/mol.
- Soluble in DMSO; ultrasonic warming may improve solubility.
- Stable as powder at -20°C for long-term storage; in solvent storage guidelines provided.
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Medchemexpress LLC Cadrofloxacin 100mg | 153808-85-6 | 100 MG
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Cadrofloxacin is an orally active fluoroquinolone antibiotic research chemical with activity against aerobic and anaerobic Gram-positive and Gram-negative bacteria. It is supplied as a powder for laboratory research and analytical applications.
- High purity: 98.2%.
- Molecular weight: 411.38 g/mol.
- Chemical formula: C19H20F3N3O4.
- CAS number: 153808-85-6.
- Supplied as a powder, stable at -20°C for long-term storage.
- Available in 100 MG quantity for research use.
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Medchemexpress LLC 4-N,6-N-bis[(4-fluoro-3-methylphenyl)methyl]pyrimidine-4,6-dicarboxamide | 544678-85-5 | MFCD09878513 | 99.2% | 410.42 g/mol | C22H20F2N4O2 | 1MG
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DB04760 is a potent, highly selective, non-zinc-chelating inhibitor of matrix metalloproteinase-13 (MMP-13) with a reported biochemical IC50 of 8 nM. Preclinical studies show the compound reduces paclitaxel-induced neurotoxicity and exhibits anticancer activity. The material is supplied as a light yellow to yellow solid with high purity and recommended storage conditions for powder and solution forms.
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eMolecules Medchem Express / DB04760 / 1mg / 536984011 / HY-125166 / / 544678-85-5 / MFCD09878513 / 410.425 / C22H20F2N4O2
Medchem Express / DB04760 / 1mg / 536984011 / HY-125166 / / 544678-85-5 / MFCD09878513 / 410.425 / C22H20F2N4O2
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eMolecules Medchem Express / Orismilast / 5mg / 719836725 / HY-117960 / / 1353546-86-7 / [null] / 510.290 / C19H15Cl2F2NO7S
Medchem Express / Orismilast / 5mg / 719836725 / HY-117960 / / 1353546-86-7 / [null] / 510.290 / C19H15Cl2F2NO7S
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Sigma Aldrich Fine Chemicals Biosciences 4-(Phenylazo)diphenylamine 97% | 101-75-7 | MFCD00003023 | 25G
4-(Phenylazo)diphenylamine 97% | Purity: 97% | Mol Wt: 273.33 | 101-75-7 | MFCD00003023 | 25G
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Medchemexpress LLC 4H,8H-Benzo[1,2-b:3,4-b']dipyran-4-one, 9,10-dihydro-3,5-dihydroxy-2-(4-methoxyphenyl)-8,8-dimethyl | 38226-86-7 | 368.38 | 5 MG
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β-Anhydroicaritin is isolated from Boswellia carterii Birdware and possesses important biological and pharmacological effects. It ameliorates the degradation of periodontal tissue, inhibits the synthesis and secretion of TNF-α and MMP-3 in diabetic rats, and decreases the overproduction of NO, IL-10, TNF-α, MCP-1, and IL-6 in peritonitis mice. Additionally, it inhibits the elevation of intracellular Ca2+ and markedly decreases iNOS protein expression.
- Antiosteoporosis properties
- Estrogen regulation properties
- Antitumor properties
- Ameliorates the degradation of periodontal tissue
- Inhibits the synthesis and secretion of TNF-α and MMP-3 in diabetic rats
- Decreases the overproduction of NO, IL-10, TNF-α, MCP-1, and IL-6 in peritonitis mice
- Inhibits the elevation of intracellular Ca2+
- Markedly decreases iNOS protein expression
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eMolecules AstaTech / 15-DIHYDROXYPENTAN-3-ONE / 0.25g / 297085484 / 20750 / 95.000 / 4254-85-7 / MFCD06658431 / 118.132 / C5H10O3
AstaTech / 15-DIHYDROXYPENTAN-3-ONE / 0.25g / 297085484 / 20750 / 95.000 / 4254-85-7 / MFCD06658431 / 118.132 / C5H10O3
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Medchemexpress LLC Iclepertin | 1421936-85-7 | 512.42 | 50 MG
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Iclepertin (BI-425809) is a potent, selective, and orally active glycine transporter 1 (GlyT1) inhibitor. It is inactive against GlyT2 and is used for research into Alzheimer's disease and schizophrenia. It inhibits GlyT1 in rat primary neurons and human SK-N-MC cells, and a single oral administration has shown to increase glycine CSF levels in rats.
- Potent, selective, and orally active glycine transporter 1 (GlyT1) inhibitor
- Inactive against GlyT2
- Used for Alzheimer's disease research
- Used for schizophrenia research
- Increases glycine cerebrospinal fluid (CSF) levels
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eMolecules 3,3',5,5'-Azobenzene tetracarboxylic acid, TazbH4, 97% | 365549-33-3 | MFCD30738344 | 1g
Strem Chemicals | 3,3',5,5'-Azobenzene tetracarboxylic acid, TazbH4, 97% | 1g | 432919857 | 08-0125 | 97.000 | 365549-33-3 | MFCD30738344 | 358.262 | C16H10N2O8
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Medchemexpress LLC 4-methyl-2-(4-methylpiperazinyl)pyrimido[4,5-b]benzothiazine | 928853-86-5 | 98.5% | 313.42 | C16H19N5S | 100 MG
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4-MMPB (CAS 928853-86-5) is a small-molecule research compound that selectively inhibits 15-lipoxygenase and has been used in studies of cancer biology. It is provided as a high-purity research reagent with characterized activity and recommended storage conditions for long-term stability.
- Selective 15-lipoxygenase inhibitor with reported IC50 ≈ 18 μM.
- High purity suitable for research (≈98.5%).
- Available in small pack sizes for laboratory use, including solid and solution formats.
- Recommended storage: powder at -20°C (up to 3 years) or 4°C (up to 2 years); in solvent at -80°C (up to 6 months) or -20°C (up to 1 month).
- Molecular formula C16H19N5S and molecular weight 313.42, suitable for analytical characterization.
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eMolecules 4-Aminoazobenzene hydrochloride | 287481-35-0 | MFCD00012994 | 1g
Combi-Blocks | 4-Aminoazobenzene hydrochloride | 1g | 439372908 | QC-5473 | 95.000 | 287481-35-0 | MFCD00012994 | 233.700 | C12H12ClN3
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