Furans
Apexbio Technology LLC MOMETASONE-FUROATE-D3-1MG
Mometasone furoate-d3 (CAS No 83919-23-7) is a deuterated form of the corticosteroid mometasone furoate used primarily in biomedical research particularly in pharmacokinetic studies Originating from the class of synthetic corticosteroids it functions by modulating the activity of glucocorticoid receptors influencing gene transcription to exert anti-inflammatory effects This compound is often used to explore pathways related to inflammation and immune response making it a valuable tool in both in vitro and in vivo studies Its bioactivity is typically observed in the nanomolar to low micromolar range indicating potent efficacy in cellular assays Common applications include studies on asthma allergic reactions and dermatological conditions often using cell models like keratinocytes or animal models such as murine systems Experimental concentrations typically depend on the specific research design allowing flexibility for various investigative needs
Medchemexpress LLC Mometasone furoate | MFCD00866003 | 99.9% | 521.43 g/mol | C27H30Cl2O6 | 5 MG
Mometasone furoate-13C,d6 is an isotopically labeled reference standard of mometasone furoate intended for analytical and research use. It provides a stable, labeled analog for method development and quantitative mass spectrometry studies involving glucocorticoid receptor assays. Parent compound properties: CAS 83919-23-7; formula C27H30Cl2O6; molecular weight 521.43 g/mol.
- Isotopically labeled with 13C and six deuteriums for clear mass separation.
- Suitable as an internal standard for quantitative LC-MS/MS assays.
- Chemically analogous to the parent compound for accurate recovery and matrix matching.
- Intended for analytical, reference, and method development applications.
Medchemexpress LLC Mometasone furoate (Standard) | 83919-23-7 | 99.9% | 521.43 | 50 MG
Mometasone furoate (Standard) is the analytical standard of Mometasone furoate, intended for research and analytical applications. It is a glucocorticoid receptor agonist with anti-inflammatory and anti-allergic activity.
- Acts as a corticosteroid agent
- Used for topical applications in chronic skin eczema and airway inflammation management of asthma in vivo
- Grade of analytical standard, which is the reference standard supplied assay
- Commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS
Selleck Chemical LLC Mometasone furoate S1987-50mg
Mometasone Furoate (SCH-32088 mometasone 17-furoate) is a glucocorticoid receptor agonist used topically to reduce inflammation of the skin or in the airways
![eMolecules 72680-01-4 | 6-Ethoxybenzo[d]thiazol-2(3H)-one | MFCD08459029 | 5g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502143763.JPG-250.jpg)
eMolecules 72680-01-4 | 6-Ethoxybenzo[d]thiazol-2(3H)-one | MFCD08459029 | 5g
WuXi ChemSupply | 6-Ethoxybenzo[d]thiazol-2(3H)-one | 5g | 599169829 | LN02169506 | 95.000 | 72680-01-4 | MFCD08459029 | 195.240 | C9H9NO2S
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Matrix Scientific FURAN-2,5-DICARBOXYLIC ACID-5G
Furan-2,5-dicarboxylic acid, -5g,C6H4O5, MFCD00016582, mw 156.10,
eMolecules 52938-97-3 | 5-Phenyl-2-furoic acid | Combi-Blocks | MFCD00456304 | 188.182 | C11H8O3 | 95.000 | OC(=O)c1ccc(o1)-c1ccccc1 | 5g | 267187633
5-Phenyl-2-furoic acid | Combi-Blocks | 52938-97-3 | MFCD00456304 | 188.182 | C11H8O3 | 95.000 | OC(=O)c1ccc(o1)-c1ccccc1 | 5g | 267187633
eMolecules 551001-79-7 | (5-Methoxybenzofuran-2-yl)boronic acid | MFCD06801701 | 1g
Ambeed | (5-Methoxybenzofuran-2-yl)boronic acid | 1g | 525040408 | A134230 | 551001-79-7 | MFCD06801701 | 191.980 | C9H9BO4
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eMolecules 52938-96-2 | 5-(4-Bromophenyl)-2-furoic acid | Oakwood Chemical | MFCD00194276 | 267.078 | C11H7BrO3 | 95.000 | OC(=O)c1ccc(o1)-c1ccc(Br)cc1 | 1g | 537711364
5-(4-Bromophenyl)-2-furoic acid | Oakwood Chemical | 52938-96-2 | MFCD00194276 | 267.078 | C11H7BrO3 | 95.000 | OC(=O)c1ccc(o1)-c1ccc(Br)cc1 | 1g | 537711364
Medchemexpress LLC Betulin diacetate | 1721-69-3 | MFCD00017378 | 95.0% | 526.79 | 5 MG
Betulin diacetate, a triterpene and derivative of Betulin, is an anti-AID agent and also possesses anti-cancer activity.
- Is a triterpene and derivative of Betulin
- Acts as an anti-AID agent
- Possesses anti-cancer activity
- Shows cytotoxicity against various human cell lines including 518A2, A-375, A2780, A549, HT-29, HeLa, and MCF7
- Induces melanogenesis in mouse B16 2F2 cells
- Inhibits growth in mouse B16 2F2 cells
- Exhibits anti-HIV activity against acutely infected H9 lymphocytes
Medchemexpress LLC Ath686 | 853299-52-2 | MFCD22665713 | 99.5% | 515.53 | C25H28F3N7O2 | 10 MG
ATH686 is a potent, selective, ATP-competitive FLT3 kinase inhibitor used in research to study FLT3-mutant leukemia. It inhibits mutant FLT3 activity, induces apoptosis, and suppresses proliferation in FLT3-mutant cells.
- Potent, selective ATP-competitive FLT3 inhibition.
- Demonstrated induction of apoptosis and cell-cycle arrest in FLT3-mutant cells.
- High purity suitable for biochemical and cellular assays.
- Available as solid and as 10 mM solution in DMSO for convenience.
- Stable under recommended storage conditions for long-term use.
Medchemexpress LLC Ethynodiol diacetate | 297-76-7 | MFCD00083326 | 99.85% | 1 G
Ethynodiol diacetate is a click chemistry reagent that contains an Alkyne group. It can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. It is for research use only and not sold to patients.
- Click chemistry reagent
- Contains an Alkyne group
- Can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups
Medchemexpress LLC Azimilide dihydrochloride | 149888-94-8 | 98.2% | 530.88 | 1 ML
Azimilide dihydrochloride is a class III antiarrhythmic agent that functions by blocking potassium channels in the heart. It is a dual blocker of IKs (IC50 = 2.6 μM) and IKr (IC50 = 1 μM), and also inhibits HERG channels, L-type calcium current (ICa), and sodium current (INa). This compound is used for the study of atrial fibrillation and ventricular fibrillation.
- Class III antiarrhythmic agent
- Blocks potassium channels in the heart
- Dual blocker of IKs and IKr
- Inhibits HERG channel
- Inhibits L-type calcium current (ICa) and sodium current (INa)
- Can be used for the study of atrial fibrillation and ventricular fibrillation
- Purity: 98.17%
Medchemexpress LLC Dantrolene | 7261-97-4 | MFCD00867709 | 98.4% | 314.25 g/mol | C14H10N4O5 | 500MG
Dantrolene is a small-molecule ryanodine receptor antagonist used as a direct-acting skeletal muscle relaxant in research. It is supplied as a solid powder with a reported purity of 98.38% and is offered in multiple pack sizes, including a 500 mg vial. Manufacturer documentation includes a datasheet, certificate of analysis, and safety data sheet to support experimental use and handling.