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Filtered Search Results
Pfaltz & Bauer P-ACETOPHENETIDIDE 97% 250G
p-Acetophenetidide 97% 250G CAS# 62-44-2
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Medchemexpress LLC Leflunomide | 75706-12-6 | 99.8% | C12H9F3N2O2 | 1 ML
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Leflunomide is a pyrimidine synthesis inhibitor that acts by inhibiting dihydroorotate dehydrogenase (DHODH), functioning as a disease-modifying antirheumatic agent. It is an immunomodulatory drug that prevents the expansion of activated and autoimmune lymphocytes by interfering with cell cycle progression due to inadequate rUMP production and by utilizing mechanisms involving p53. This product is for research use only.
- Inhibits dihydroorotate dehydrogenase (DHODH)
- Functions as a disease-modifying antirheumatic agent
- Inhibits proliferation of mononuclear and T-cells
- Inhibits several protein tyrosine kinases
- Prevents expansion of activated and autoimmune lymphocytes
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Medchemexpress LLC Leflunomide | 75706-12-6 | C12H9F3N2O2 | 500 MG
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Leflunomide is a pyrimidine synthesis inhibitor, primarily functioning by inhibiting dihydroorotate dehydrogenase (DHODH), and is recognized as a disease-modifying antirheumatic agent. This prodrug inhibits the proliferation of mononuclear and T-cells and acts as an inhibitor of several protein tyrosine kinases, with IC50 values ranging from 30 mM to 100 mM in in vitro assays. It also interferes with cell cycle progression and utilizes p53-dependent mechanisms to prevent the expansion of activated and autoimmune lymphocytes.
- Inhibits dihydroorotate dehydrogenase (DHODH)
- Acts as a disease-modifying antirheumatic agent
- Inhibits proliferation of mononuclear and T-cells
- Functions as an inhibitor of several protein tyrosine kinases
- Inhibits p59fyn and p56lck activity in tyrosine kinase assays
- Inhibits calcium mobilization in Jurkat cells
- Prevents expansion of activated and autoimmune lymphocytes
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Medchemexpress LLC ANIMAL-FREE NAP-2/CX 10UG
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5000178081 ANIMAL-FREE NAP-2/CX 10UG
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Medchemexpress LLC N-[2-methyl-3-[[4-[4-[[4-(trifluoromethoxy)phenyl]methoxy]piperidin-1-yl]-1,3,5-triazin-2-yl]amino]phenyl]acetamide | 1211866-85-1 | MFCD22123242 | 99.7% | 516.52 g/mol | C25H27F3N6O3 | 25 MG
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TC-N 1752 is a small-molecule research compound that inhibits Nav1.7 (voltage-gated sodium) channels and is used in pharmacology and electrophysiology studies of sodium channel function and pain signaling. The substance is identified by CAS 1211866-85-1, has molecular formula C25H27F3N6O3 and a molecular weight of about 516.5 g/mol. It is supplied as a solid with DMSO solubility and is accompanied by analytical data supporting its stated purity.
- Potent Nav1.7 inhibitory activity useful for sodium channel research.
- High reported purity suitable for biochemical assays.
- Characterized chemical identity with CAS and molecular formula available.
- Soluble in DMSO for preparation of experimental solutions.
- Available in multiple pack sizes to accommodate different study scales.
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Selleck Chemical LLC HC-067047-5mg
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HC-067047 is a selective TRPV4 channel antagonist with IC50 values of 48 nM,133 nM,and 17 nM for human, rat, and mouse TRPV4 orthologs,respectively.
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Medchemexpress LLC Imatinib 10Mm/1Ml In Dmso | HY-15463-1ML
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Imatinib 10Mm/1Ml In Dmso
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Medchemexpress LLC 2-chloro-N-(4'-chloro[1,1'-biphenyl]-2-yl)-3-pyridinecarboxamide | 188425-85-6 | 99.8% | 500 MG
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Boscalid is a broad-spectrum carboxamide fungicide and succinate dehydrogenase (SDH) inhibitor supplied as a solid analytical standard for research and analytical applications. Typical pack contains 500 MG with a listed purity of 99.8%.
- High purity of 99.8% suitable for analytical use.
- Formula C18H12Cl2N2O with molecular weight 343.21 g·mol⁻¹.
- Solid powder appearance for easy handling and formulation.
- Storage: powder stable at -20°C (up to 3 years) or 4°C (up to 2 years); in solvent store at -80°C (6 months) or -20°C (1 month).
- Mode of action: succinate dehydrogenase (SDH) inhibitor useful in fungal respiration studies.
- Intended for research and analytical applications; not for human or veterinary use.
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Medchemexpress LLC ANIMAL-FREE NAP-2/CX 50UG
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5000177865 ANIMAL-FREE NAP-2/CX 50UG
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Medchemexpress LLC Animal-free NAP-2/CXCL7 protein, human (His) | >95.0% | 2UG
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Recombinant human NAP-2/CXCL7 protein fragment with an N-terminal 6xHis tag, produced in E. coli and supplied with a certificate of analysis. The preparation corresponds to residues A59-D128 (70 amino acids), has an approximate molecular weight of ~11 kDa, and is ≥95.0% pure by reducing SDS-PAGE. For research use only.
- Recombinant fragment representing residues A59-D128.
- N-terminal 6xHis tag for purification and detection.
- Produced in E. coli for efficient expression.
- Purity ≥95.0% as determined by reducing SDS-PAGE.
- Provided with a certificate of analysis for batch-specific data.
- Suitable for biochemical assays and antibody development.
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Medchemexpress LLC N-[2-methyl-3-[[4-[4-[[4-(trifluoromethoxy)phenyl]methoxy]piperidin-1-yl]-1,3,5-triazin-2-yl]amino]phenyl]... | 1211866-85-1 | MFCD22123242 | 99.7% | 516.52 g/mol | C25H27F3N6O3 | 5 MG
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Potent, orally active Nav1.7 sodium channel inhibitor intended for research use in ion-channel pharmacology and analgesia studies. The compound is a well-characterized small molecule with high reported purity and documented activity across human and rodent NaV subtypes; supplied in solid and solution formats with recommended cold storage.
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Medchemexpress LLC (S)-1,1'-bi-2,2'-naphthol | 18531-99-2 | MFCD00004068 | 100.0% | 286.32 | C20H14O2 | 1 ML
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(S)-1,1'-Bi-2,2'-naphthol is a chiral diol used as a ligand and chiral auxiliary in asymmetric synthesis and catalysis. Supplied as a 10 mM solution in DMSO for research use, it facilitates formation of chiral catalysts, supports enantioselective transformations, and aids method development in organic synthesis.
- Chiral diol useful as a ligand for asymmetric catalysis.
- High chemical purity suitable for research and analytical applications.
- Provided as a 10 mM solution ready for reconstitution or direct use.
- Characterized by supporting analytical data such as COA, 1H NMR, and RP-HPLC.
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Medchemexpress LLC Boscalid | 188425-85-6 | 99.8% | 1 G
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Boscalid is a fungicidal research chemical that inhibits succinate dehydrogenase (SDH), disrupting fungal respiration. It is supplied for research and analytical applications and is available as a solid or as a 10 mM solution in DMSO.
- Provides fungicidal activity as a succinate dehydrogenase inhibitor
- High purity suitable for analytical use (99.8%)
- Molecular formula C18H12Cl2N2O; molecular weight 343.21 g/mol
- Available in solid form and as a 10 mM solution in DMSO; common pack sizes include 50 mg-1 g
- Intended for research use only; not for human or veterinary use
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Medchemexpress LLC NAP-2/CXCL7 Rat CH 2ug
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CXCL7 (also known as neutrophil activating peptide 2 NAP-2) is a platelet-derived growth factor that belongs to the ELR CXC chemokine family functioning as a potent chemoattractant and activator of neutrophils through binding to its receptor CXCR2[1] NAP-2/CXCL7 Protein Rat (CHO) is produced in CHO cells and consists of 62 amino acids (I46-I107)
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Medchemexpress LLC (S)-1,1'-bi-2,2'-naphthol | 18531-99-2 | MFCD00004068 | 100.0% | 286.32 | C20H14O2 | 25 G
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(S)-1,1'-Bi-2,2'-naphthol (S)-BINOL is a chiral diol used widely as a ligand and chiral auxiliary in asymmetric synthesis and catalysis. It is supplied as a white to off-white solid with high purity, intended for research use in organic synthesis, catalyst development, and related life-science applications.
- Chiral ligand for asymmetric catalysis and ligand design.
- High purity suitable for research and synthesis.
- Solid, white to off-white appearance for easy handling.
- Stable under recommended storage conditions for prolonged shelf life.
- Useful as a starting material or chiral auxiliary in academic and industrial research.
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