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Filtered Search Results
Medchemexpress LLC Sulfadimethoxine | 122-11-2 | 99.1% | 10 MM * 1 ML
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Sulfadimethoxine is a sulfonamide antibiotic effective against various infections, including those affecting the respiratory, urinary tract, enteric, and soft tissue. It is intended for research use only.
- Sulfonamide antibiotic
- Treats respiratory, urinary tract, enteric, and soft tissue infections
- Exhibits antibacterial properties
- Intended for research use only
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eMolecules 578-39-2 | 4-hydroxy-2-methylbenzoic acid | Pharmablock | MFCD02182261 | 152.149 | C8H8O3 | 97.000 | Cc1cc(O)ccc1C(O)=O | 25mg | 642185362
4-hydroxy-2-methylbenzoic acid | Pharmablock | 578-39-2 | MFCD02182261 | 152.149 | C8H8O3 | 97.000 | Cc1cc(O)ccc1C(O)=O | 25mg | 642185362
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eMolecules 103986-79-4 | 1-HYDROXY-1,2,3,4-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID | AstaTech | MFCD07190036 | 192.214 | C11H12O3 | 95.000 | OC1C(CCc2ccccc12)C(O)=O | 0.1g | 713698051
1-HYDROXY-1,2,3,4-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID | AstaTech | 103986-79-4 | MFCD07190036 | 192.214 | C11H12O3 | 95.000 | OC1C(CCc2ccccc12)C(O)=O | 0.1g | 713698051
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Medchemexpress LLC Cefquinome sulfate | 118443-89-3 | 50 MG
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Cefquinome sulfate is a broad-spectrum cephem antibiotic that inhibits various Gram-positive and Gram-negative bacteria, including Staphylococci, Streptococci, Pseudomonas, and Enterobacteriaceae. It functions by binding to penicillin-binding proteins (PBPs), thereby inhibiting the synthesis of bacterial cell walls.
- Inhibits methicillin susceptible S. aureus, Streptococcus spp., Enterococci, E. coli, Salmonella spp., Klebsiella spp., S. marcescens, Enterobacter spp., Citrobacter spp., P. mirabilis, Indole-positive Proteus spp., and P. aeruginosa
- Shows in vivo anti-infectious activity against Klebsiella pneumoniae in a rat pneumonia model
- Reduces lung inflammatory cell infiltration and lung tissue damage
- Inhibits expression of inflammatory factors (TNF-α, IL-1β, IL-8)
- Promotes expression of anti-inflammatory factors (IL-4, IL-10, IL-13)
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=O | 100mg | 601097988](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502421426.JPG-250.jpg)
eMolecules 107757-06-2 | 3-Methyl-5-nitrobenzaldehyde | Ambeed | MFCD18399644 | 165.148 | C8H7NO3 | 98.000 | Cc1cc(C=O)cc(c1)[N+]([O-])=O | 100mg | 601097988
3-Methyl-5-nitrobenzaldehyde | Ambeed | 107757-06-2 | MFCD18399644 | 165.148 | C8H7NO3 | 98.000 | Cc1cc(C=O)cc(c1)[N+]([O-])=O | 100mg | 601097988
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Medchemexpress LLC S2116 | 2262489-89-2 | 98.1% | 437.91 | 50 MG
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S2116 is an N-alkylated tranylcypromine (TCP) derivative and a potent lysine-specific demethylase 1 (LSD1) inhibitor. It enhances H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2116 can induce apoptosis in TCP-resistant T-cell acute lymphoblastic leukemia (T-ALL) cells by suppressing the transcription of NOTCH3 and TAL1 genes and has been shown to significantly slow the growth of T-ALL cells in xenotransplanted mice.
- Potent lysine-specific demethylase 1 (LSD1) inhibitor
- Effective for T-ALL cell lines with IC50 values ranging from 1.1 μM to 6.8 μM
- Induces apoptosis and down-regulates NOTCH3 and TAL1 protein expression in T-ALL cells
- Significantly reduces subcutaneous tumor size in xenotransplanted mice
- Exhibits favorable pharmacokinetic properties in mice with a T1/2 of 3.76 hours
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eMolecules 61291-21-2 | 5-Methylthiazole-2-carboxylic acid | Ambeed | MFCD08060736 | 143.160 | C5H5NO2S | 95.000 | Cc1cnc(s1)C(O)=O | 250mg | 524990445
5-Methylthiazole-2-carboxylic acid | Ambeed | 61291-21-2 | MFCD08060736 | 143.160 | C5H5NO2S | 95.000 | Cc1cnc(s1)C(O)=O | 250mg | 524990445
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eMolecules 42438-89-1 | Medchem Express | Pinostilbene | 5mg | 599151211 | HY-N3059 | MFCD12407153 | 242.274 | C15H14O3
AstaTech | 3-PHENYLPROPIOLONITRILE | 1g | 233627790 | 36388 | 95.000 | 935-02-4 | MFCD19300770 | 127.146 | C9H5N
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eMolecules 214139-26-1 | Ambeed | 1-(Boc-amino)-1-indanecarboxylic Acid | 250mg | 506391265 | A547721 | MFCD00800596 | 277.32 | C15H19NO4
Ambeed | N-(4-(4455-Tetramethyl-132-dioxaborolan-2-yl)phenyl)acrylamide | 1g | 595930997 | A1372127 | 434898-99-4 | 273.140 | C15H20BNO3
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eMolecules 612-20-4 | ChemScene | 2-Hydroxymethyl benzoic acid | 5g | 536779344 | CS-0028786 | MFCD02151998 | 152.149 | C8H8O3
ChemScene | 2-Hydroxymethyl benzoic acid | 5g | 536779344 | CS-0028786 | 612-20-4 | MFCD02151998 | 152.149 | C8H8O3
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eMolecules 446866-87-1 | Ambeed | 3-Morpholinobenzaldehyde | 100mg | 624121189 | A446045 | MFCD07772811 | 191.23 | C11H13NO2
ChemScene | 5-Bromo-4-methyl-1H-benzo[d]imidazole | 100mg | 582640735 | CS-W022329 | 952511-48-7 | MFCD18642426 | 211.062 | C8H7BrN2
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![eMolecules 123524-53-8 | ChemScene | [11-Binaphthalene]-44-dicarboxylic acid | 100mg | 601109945 | CS-0146252 | 342.35 | C22H14O4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502434996.JPG-250.jpg)
eMolecules 123524-53-8 | ChemScene | [11-Binaphthalene]-44-dicarboxylic acid | 100mg | 601109945 | CS-0146252 | 342.35 | C22H14O4
Ambeed | 9-Ethynylanthracene | 100mg | 717401480 | A277906 | 13752-40-4 | MFCD00183717 | 202.256 | C16H10
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![eMolecules 37663-44-8 | Ambeed | 3H-Spiro[isobenzofuran-14-piperidine] hydrochloride | 100mg | 521456653 | A167510 | MFCD02179146 | 225.72 | C12H16ClNO](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502435647.JPG-250.jpg)
eMolecules 37663-44-8 | Ambeed | 3H-Spiro[isobenzofuran-14-piperidine] hydrochloride | 100mg | 521456653 | A167510 | MFCD02179146 | 225.72 | C12H16ClNO
Ambeed | (E)-3-(6-((E)-3-(Pyrrolidin-1-yl)-1-(p-tolyl)prop-1-en-1-yl)pyridin-2-yl)acrylic acid | 1mg | 761012450 | A158908 | 87848-99-5 | MFCD00869830 | 348.446 | C22H24N2O2
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eMolecules 287118-97-2 | Medchem Express | NCX4040 | 5mg | 784543586 | HY-103385 | MFCD08062164 | 331.28 | C16H13NO7
ChemScene | 57-Dimethyl-[124]triazolo[15-a]pyrimidin-2-ylamine | 100mg | 718356394 | CS-0033788 | 7135-02-6 | MFCD00227025 | 163.184 | C7H9N5
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Medchemexpress LLC (E)-2-(((5-bromothiophen-2-yl)methylene)amino)benzamide | 304456-62-0 | 98.0% | 309.18 | C12H9BrN2OS | 5MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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BTYNB is a small-molecule research inhibitor of IMP1 (IGF2BP1) that disrupts IMP1 binding to c-Myc mRNA, resulting in reduced c-Myc expression and decreased proliferation in IMP1-positive cancer cell lines. The compound is supplied as a solid reagent in multiple sizes and as a 10 mM solution in DMSO for convenient stock preparation, and is reported with high purity for in vitro applications.
- Inhibits IMP1 binding to c-Myc mRNA with reported IC50 ≈ 5 μM.
- High reported purity suitable for in vitro research applications.
- Available in multiple solid pack sizes and a 10 mM solution format in DMSO.
- Soluble in DMSO for preparation of concentrated stock solutions.
- Used to study RNA-protein interactions and cancer cell proliferation.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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