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Filtered Search Results
Selleck Chemical LLC Rosiglitazone maleate S2505-10mM/1mL
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Rosiglitazone maleate a member of the thiazolidinedione class of antihyperglycaemic agents is a high-affinity selective agonist of the peroxisome proliferator-activated receptor- (PPAR- ) with IC50 of 42 nM Rosiglitazone maleate also modulates TRP channels and induces autophagy Rosiglitazone prevents ferroptosis
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Medchemexpress LLC BGT226 (maleate) | 1245537-68-1 | MFCD22124895 | 99.9% | 650.60 g/mol | C32H29F3N6O6 | 5 MG
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BGT226 maleate is a small-molecule PI3K/mTOR dual inhibitor used for research into PI3K signaling and oncology. It shows low-nanomolar potency against PI3K isoforms and mTOR and is used in cell-based and preclinical studies to evaluate antiproliferative and apoptotic effects.
- Inhibits PI3Kα, PI3Kβ, PI3Kγ, and mTOR.
- Exhibits low nanomolar potency in enzymatic assays.
- Demonstrates growth-inhibitory activity in cancer cell models.
- Supplied as the maleate salt for stability.
- High purity suitable for biochemical and cellular assays.
- Available in multiple small pack sizes for research use.
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Medchemexpress LLC NB-598 Maleate | 155294-62-5 | 99.4% | 565.74 | 25 MG
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NB-598 Maleate | 155294-62-5 | 99.4% | 565.74 | 25 MG
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Medchemexpress LLC (S)-Timolol maleate | 26921-17-5 | 99.9% | 432.49 | 100 MG
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(S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic β-adrenoceptor blocker. It is widely used as a standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. This compound can also be used for hypertension, angina pectoris, and myocardial infarction.
- Non-cardioselective hydrophilic β-adrenoceptor blocker
- Used as standard medication for intraocular pressure (glaucoma)
- Prevents the production of aqueous humor
- Can be used for hypertension, angina pectoris, and myocardial infarction
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Medchemexpress LLC Filgotinib (maleate) | 1802998-75-9 | 99.88% | 541.58 | 100 MG
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Filgotinib maleate is a selective, orally available JAK1 inhibitor with anti-inflammatory and antiviral activities. It inhibits the activities of JAK1, JAK2, JAK3, and TYK2. It also inhibits HIV-1 driven gene transcription and reduces the proliferation of HIV-1 infected cells. It is used in the study of rheumatoid arthritis and inflammatory bowel disease.
- Selectively inhibits JAK1 with high potency
- Demonstrates anti-inflammatory and antiviral properties
- Inhibits Th2 and Th1 cell differentiation in a dose-dependent manner
- Produces dose-dependent bone damage protection in rat models of collagen-induced arthritis
- Reduces inflammatory cell infiltration and protects articular cartilage and bone
- Reduces serum levels of inflammatory cytokines and chemokines
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(C)OCCCBr | 5g | 386413511](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502438151.JPG-250.jpg)
eMolecules 89031-84-5 | (3-BROMOPROPOXY)-TERT-BUTYLDIMETHYLSILANE | AstaTech | MFCD00216589 | 253.255 | C9H21BrOSi | 95.000 | CC(C)(C)[Si](C)(C)OCCCBr | 5g | 386413511
(3-BROMOPROPOXY)-TERT-BUTYLDIMETHYLSILANE | AstaTech | 89031-84-5 | MFCD00216589 | 253.255 | C9H21BrOSi | 95.000 | CC(C)(C)[Si](C)(C)OCCCBr | 5g | 386413511
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Medchemexpress LLC Vtp50469 (fumarate) | 2169919-29-1 | 99.8% | 804.93 | 50 MG
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Vtp50469 (fumarate) | 2169919-29-1 | 99.8% | 804.93 | 50 MG
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TARGETMOL CHEMICALS INC AVITINIB MALEATE 10MG
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Also available in 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Avitinib maleate is a pyrrolopyrimidine-based irreversible epidermal growth factor receptor (EGFR) inhibitor. purity: 99%
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Electron Microscopy Sciences DMA N, N-Dimethylaminoethyl Methacrylate 450 ML
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CAS #2867-47-2 C₈H₁₅NO₂ F.W. 157.21
Boiling point: 76°C
A water soluble monomer.
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(C)OC[C@H]1OC(=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 5g | 525162250](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502423099.PNG-250.jpg)
eMolecules 32384-65-9 | 2,3,4,6-Tetra-O-trimethylsilyl-D-glucono-1,5-lactone | Ambeed | MFCD22665922 | 466.868 | C18H42O6Si4 | 95.000 | C[Si](C)(C)OC[C@H]1OC(=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 5g | 525162250
2,3,4,6-Tetra-O-trimethylsilyl-D-glucono-1,5-lactone | Ambeed | 32384-65-9 | MFCD22665922 | 466.868 | C18H42O6Si4 | 95.000 | C[Si](C)(C)OC[C@H]1OC(=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 5g | 525162250
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eMolecules ChemScene / (Chloromethyl)triethoxysilane / 5g / 536799853 / CS-0086574 / 0.000 / 15267-95-5 / MFCD00039354 / 212.750 / C7H17ClO3Si
ChemScene / (Chloromethyl)triethoxysilane / 5g / 536799853 / CS-0086574 / 0.000 / 15267-95-5 / MFCD00039354 / 212.750 / C7H17ClO3Si
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Medchemexpress LLC Monostearyl maleate | 2424-62-6 | MFCD08274815 | 98.0% | 368.55 g·mol⁻1 | C22H40O4 | 250 MG
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Monostearyl maleate (octadecyl fumarate) is a long-chain alkyl ester supplied as a solid analytical reagent for biochemical and metabolic research. It is provided at high purity (≈98%) and is commonly used as an analytical standard or assay reagent in metabolism-related studies. Key identifiers include CAS 2424-62-6, molecular formula C22H40O4, and molecular weight 368.55 g·mol⁻1.
- High purity suitable for analytical use.
- Solid form for convenient handling and storage.
- Used in biochemical and metabolism assay workflows.
- Available in small pack sizes for analytical and standard applications.
- CAS-registered compound for unambiguous identification.
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Medchemexpress LLC Perhexiline maleate | 6724-53-4 | 99.97% | 200 MG
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Perhexiline maleate is an orally active inhibitor of CPT1 and CPT2, which functions to reduce fatty acid metabolism. This compound is known to induce mitochondrial dysfunction and apoptosis in hepatic cells. It can cross the blood-brain barrier and has demonstrated anti-tumor activity, making it relevant for research in cancers and cardiovascular diseases such as angina.
- Reduces fatty acid metabolism.
- Induces mitochondrial dysfunction in hepatic cells.
- Induces apoptosis in hepatic cells.
- Crosses the blood-brain barrier.
- Shows anti-tumor activity.
- Used in research for cancers and cardiovascular disease like angina.
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Medchemexpress LLC Sumanirole (maleate) | 179386-44-8 | 99.8% | C15H17N3O5 | 25 MG
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Sumanirole maleate (U-95666E; PNU-95666E) is a highly selective D2 receptor full agonist with an ED50 of about 46 nM. It plays an important role in the research of Parkinson's disease and restless leg syndrome. Sumanirole is a valuable tool compound for basic research to identify neurobiological mechanisms based on a dopamine D2-linked (vs. D1, D3, D4, and D5-linked) mechanism of action.
- Highly selective D2 receptor full agonist
- ED50 of about 46 nM
- Valuable tool for identifying neurobiological mechanisms
- Used in research for Parkinson's disease
- Used in research for restless leg syndrome
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TARGETMOL CHEMICALS INC Ro 25-6981 Maleate 25MG
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Also available in 1 mL, 1 mg, 5 mg, 10 mg and bulk. Please contact Fisher for quotes. Ro 25-6981 Maleate is a potent and selective activity-dependent NMDA receptor blocker, specifically targeting the NR2B subunit (IC50 values are 0.009 uM for NR1C/NR2B and 52 uM for NR1C/NR2A receptor subunit combinations). Purity 99.42%
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