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Filtered Search Results
Medchemexpress LLC Methenamine hippurate | 5714-73-8 | MFCD00072147 | >95.0% | 319.36 g/mol | C15H21N5O3 | 10 MG
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Methenamine hippurate is the analytical reference standard of methenamine hippurate supplied for research and analytical use. The compound is the hippurate salt of methenamine, an orally active urinary antiseptic that releases formaldehyde under acidic conditions; supplied as a dry solid and handled per SDS storage recommendations.
- Analytical reference standard suitable for research and quality control.
- CAS number 5714-73-8; molecular weight 319.36 g/mol.
- Purity reported by suppliers as ≥95% (HPLC) to ≥98%; check lot-specific certificate.
- Recommended storage: 4°C sealed and dry; in solution -80°C (6 months) or -20°C (1 month).
- Provided as a solid for analytical preparation and formulation testing.
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Medchemexpress LLC KG-655 | 349-58-6 | 99.9% | 230.11 | 25 G
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KG-655 is a small molecule compound that binds to the β-folded surface and internal cavity of ARNT PAS-B, interfering with its binding to the transcriptional coactivator TACC3. It can promote the homodimerization of ARNT PAS-B and has the potential to regulate multiple ARNT-mediated signaling pathways.
- Target: ARNT
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Medchemexpress LLC 2,1,3-benzothiadiazole | 273-13-2 | MFCD00005809 | 98.0% | 136.18 g/mol | C6H4N2S | 25 G
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2,1,3-Benzothiadiazole is a bicyclic heterocyclic organic compound (C6H4N2S) used as a biochemical reagent and synthetic building block in life-science and materials research. It finds application in organic synthesis, agrochemical studies, and optoelectronic materials due to its thiadiazole ring, conjugated aromatic system, and thermal stability.
- Bicyclic heterocycle with an electron-withdrawing thiadiazole ring.
- Useful building block for organic synthesis and derivatization.
- Applicable in agrochemical and optoelectronic materials research.
- Available in high-purity grades for research use (commonly ~98%).
- Solid at ambient conditions and stable under typical laboratory storage.
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Medchemexpress LLC Tetraglycine | 637-84-3 | MFCD00008129 | 98.1% | 246.22 | C8H14N4O5 | 25 G
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Tetraglycine is an oligopeptide composed of four glycine monomers, used in biochemical research to enrich glycine pools in plasma and tissues. It is supplied as a high-purity powder for laboratory research with storage recommendations to preserve stability and activity.
- Oligopeptide of four glycine residues.
- Molecular weight 246.22 g/mol.
- CAS number 637-84-3.
- Purity 98.1%.
- Available in powder packages up to 25 g.
- Recommended storage: powder sealed, away from moisture and light; -80°C for long term, -20°C for up to one year.
- For research use only.
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Medchemexpress LLC 2-Methylanisole | 578-58-5 | MFCD00008373 | 99.8% | 122.17 g/mol | C8H10O | 50 G
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2-Methylanisole is a monomethoxybenzene used as a chemical intermediate in the preparation of compounds containing a methylhydroquinone core. It is supplied as a high-purity liquid in multiple pack sizes for research and synthetic applications.
- High purity (99.8%).
- Molecular weight 122.17 g/mol.
- Molecular formula C8H10O.
- Suitable as a chemical intermediate for organic synthesis.
- Supplied as a liquid in multiple pack sizes, including 50 g.
- Supporting documentation available: datasheet, SDS, COA.
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Medchemexpress LLC (4R)-4-[(1S)-1-fluoroethyl]-3-[2-[[(1S)-1-[4-methyl-5-[2-(trifluoromethyl)-4-pyridinyl]... | 1628805-46-8 | MFCD31630851 | 99.2% | 490.45 g·mol⁻¹ | C23H22F4N6O2 | 1 ML
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IDH-305 is an orally available, mutant-selective, brain-penetrant inhibitor of isocitrate dehydrogenase 1 (IDH1) that targets R132 mutations. It is provided for research use in biochemical and cellular assays and is supplied as a 10 mM solution in DMSO (1 mL) or as solid quantities.
- Potent, mutant-selective inhibition of IDH1 (R132).
- Brain-penetrant, enabling central nervous system studies.
- Supplied as 10 mM solution in DMSO and as solid packs for flexibility.
- High purity for research-grade applications.
- Defined storage conditions to preserve stability.
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Medchemexpress LLC Eprodisate (70% in water) | 21668-77-9 | 98.0% | 1 ML
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Eprodisate (70% in water) is an amyloid inhibitor that interferes with the interaction between amyloidogenic proteins and glycosaminoglycans. It is intended for research use only.
- Inhibits aggregation of amyloid fibrils
- Inhibits deposition of fibrils in tissues
- Slows progression of renal disease associated with AA amyloidosis
- May be useful for other types of amyloidosis
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Medchemexpress LLC Ethambutol dihydrochloride | 1070-11-7 | 99.9% | 1 G
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Ethambutol dihydrochloride is an antimycobacterial compound that prevents cell wall formation by inhibiting arabinosyltransferase activity. It can be used to establish animal models of hyperuricemia and optic neuropathy.
- Antimycobacterial compound
- Prevents cell wall formation
- Inhibits arabinosyltransferase activity
- Useful for establishing animal models of hyperuricemia and optic neuropathy
- For research use only
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Medchemexpress LLC Dibenzothiophene | 132-65-0 | MFCD00004969 | 99.9% | 25 G
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Dibenzothiophene is an orally active and noncompetitive CYP1A inhibitor, primarily used for studying developmental toxicity mechanisms. It inhibits CYP1A-mediated EROD activity with a Km of 0.592 μM and interacts with the AHR pathway. This compound enhances the embryotoxicity of β-naphthoflavone and shows acute toxicity in mice.
- Orally active and noncompetitive CYP1A inhibitor
- Inhibits CYP1A-mediated EROD activity
- Interacts with the AHR pathway
- Enhances embryotoxicity of β-naphthoflavone
- Used for studying mechanisms of developmental toxicity
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Medchemexpress LLC MSX-122 | 897657-95-3 | 98.2% | 292.34 | 1 ML
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MSX-122 is an orally active partial antagonist of CXCR4, inhibiting CXCR4/CXCL12 actions with an IC50 of approximately 10 nM. This compound demonstrates anti-inflammatory and anti-metastatic activity. It is intended for research use only.
- Orally active partial antagonist of CXCR4
- Inhibits CXCR4/CXCL12 actions
- Exhibits anti-inflammatory activity
- Exhibits anti-metastatic activity
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Medchemexpress LLC Anethole | 104-46-1 | 98.9% | 25 G
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Anethole is an orally active aromatic compound found widely in nature, primarily used as a flavoring agent. It demonstrates a range of biological effects, including anticancer, anti-inflammatory, antioxidant, and antimicrobial properties. It is also noted for its anesthetic, estrogenic, central nervous system depressant, hypnotic, insecticidal, and gastroprotective activities. This product is for research use only.
- Exhibits anticancer properties
- Anti-inflammatory effects
- Antioxidant activity
- Antibacterial and antifungal properties
- Anesthetic and hypnotic effects
- Central nervous system depressant
- Gastroprotective properties
- Used in studies related to oxidative stress-related skin diseases
- Applicable in prostate cancer research
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Medchemexpress LLC Ethambutol dihydrochloride | 1070-11-7 | 99.9% | 5 G
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Ethambutol dihydrochloride is an antimycobacterial compound that prevents cell wall formation by inhibiting arabinosyltransferase activity. It can be used to establish animal models of hyperuricemia and optic neuropathy.
- Antimycobacterial compound
- Prevents cell wall formation
- Inhibits arabinosyltransferase activity
- Used to establish animal models of hyperuricemia
- Used to establish animal models of optic neuropathy
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Cinchophen | 132-60-5 | 99.97% | 100 G
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Cinchophen is a potent and orally active non-steroidal anti-inflammatory agent that possesses analgesic and antimicrobial effects. It can be utilized in research pertaining to arthritis and certain liver diseases.
- Potent and orally active non-steroidal anti-inflammatory agent
- Exhibits analgesic effects
- Possesses antimicrobial effects
- Useful for research on arthritis and some liver diseases
- High purity of 99.97%
- Available in both solid and solution forms
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Medchemexpress LLC Nafcillin sodium monohydrate | 7177-50-6 | 98.10% | 1 G
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Nafcillin sodium monohydrate is an antibiotic that acts as a reversible inhibitor of β-lactamase, primarily used for research related to staphylococcal infections. This compound appears as a white to off-white solid with a molecular weight of 454.47 and a chemical formula of C21H23N2NaO6S. It exhibits bactericidal activity against methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA) in vivo.
- Reversible inhibitor of β-lactamase
- Used for research of staphylococcal infections
- 98.10% Purity
- White to off-white solid appearance
- Soluble in H2O (5.83 mg/mL)
- Storage at 4°C in sealed conditions, away from moisture
- In solvent storage at -80°C for 6 months or -20°C for 1 month in sealed conditions, away from moisture
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Medchemexpress LLC Ozagrel (sodium) | 189224-26-8 | 99.8% | 1 ML
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Ozagrel sodium is a highly selective and orally active thromboxane A2 (TXA2) synthase inhibitor with an IC50 of 11 nM. It exerts anti-platelet aggregation, vasodilation, and anti-inflammatory effects by inhibiting the production of TXA2 and increasing the production of prostacyclin (PGI2).
- Highly selective and orally active
- Inhibits thromboxane A2 (TXA2) synthase
- Exerts anti-platelet aggregation effects
- Promotes vasodilation
- Possesses anti-inflammatory properties
- Increases prostacyclin (PGI2) production
- Suitable for research on ischemic stroke, asthma, and thromboembolic diseases
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