Azobenzenes
![eMolecules 57805-85-3 | Ambeed | Methyl 3-amino-2-benzo[b]furancarboxylate | 250mg | 525177991 | A301059 | MFCD00466275 | 191.186 | C10H9NO3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502436930.JPG-250.jpg)
eMolecules 57805-85-3 | Ambeed | Methyl 3-amino-2-benzo[b]furancarboxylate | 250mg | 525177991 | A301059 | MFCD00466275 | 191.186 | C10H9NO3
Ambeed | Methyl 3-amino-2-benzo[b]furancarboxylate | 250mg | 525177991 | A301059 | 57805-85-3 | MFCD00466275 | 191.186 | C10H9NO3
eMolecules 136087-85-9 | Medchem Express | Fidarestat | 1mg | 489862920 | HY-105185 | MFCD00919183 | 279.227 | C12H10FN3O4
Ambeed | 2-Aminopent-4-ynoic acid hydrochloride | 250mg | 517262008 | A420478 | 16900-57-5 | MFCD11113137 | 149.570 | C5H8ClNO2
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Medchemexpress LLC Hydrastinine | 6592-85-4 | 99.92% | 5 MG
Hydrastinine is a major alkaloid constituent in goldenseal (Hydrastis canadensis) and can be used as a haemostatic agent. Goldenseal has been used for the treatment of various ailments including gastrointestinal disturbances, urinary tract disorders, and inflammation. The five major alkaloid constituents in goldenseal are Berberine, Palmatine, Hydrastine, Hydrastinine, and Canadine.
- Molecular weight: 207.23
- Formula: C11H13NO3
- Appearance: Solid
- Color: Off-white to light brown
- Structure classification: Alkaloids, Isoquinoline Alkaloids
- Initial source: Plants, Ranunculaceae
Medchemexpress LLC 4-mmpb | 928853-86-5 | 98.5% | 313.42 | C16H19N5S | 10 MG
4-MMPB is a research-grade small molecule that selectively inhibits 15-lipoxygenase and is provided for biochemical and cell-based studies of lipid metabolism and cancer-related pathways.
- Selective inhibitor of 15-lipoxygenase with a reported IC50 of ≈18 μM.
- High reported purity, suitable for biochemical assays (≈98.5%).
- Molecular formula C16H19N5S and molecular weight 313.42 g/mol.
- Supplied as a solid 10 MG and available in larger quantities; also offered as a 10 mM solution in DMSO.
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC Orismilast (LEO-32731) | 1353546-86-7 | 99.9% | 510.29 | C19H15Cl2F2NO7S | 50 MG
Orismilast is an orally active, selective phosphodiesterase 4 (PDE4) inhibitor provided as a solid research reagent for in vitro and in vivo studies of inflammatory and dermatological disease pathways. It is supplied with high purity and characterized physical data for laboratory use only.
- Selective PDE4 inhibitor for inflammatory research.
- High purity (99.88%) solid suitable for analytical and biological assays.
- Molecular weight 510.29 and formula C19H15Cl2F2NO7S for precise dosing and calculations.
- Available in small-scale packages including 50 mg for preclinical studies.
- Stable when stored frozen; follow manufacturer storage recommendations.
Medchemexpress LLC DB04760 | 544678-85-5 | 99.2% | 410.42 g·mol⁻¹ | C22H20F2N4O2 | 50MG
DB04760 is a potent, highly selective, non-zinc-chelating MMP-13 inhibitor (IC50 = 8 nM) used as a research reagent in preclinical studies. It has been reported to reduce paclitaxel-induced neurotoxicity and to exhibit anticancer activity. The compound has formula C22H20F2N4O2, molecular weight 410.42 g·mol⁻¹, and is supplied in solid and solution forms with high purity suitable for biological assays.
- Potent MMP-13 inhibition with IC50 = 8 nM.
- Non-zinc-chelating mechanism for selective target studies.
- Shown to reduce paclitaxel-induced neurotoxicity in models.
- Reported anticancer activity in preclinical research.
- Available as solid and as 10 mM solution in DMSO for assay flexibility.
- High purity (~99%) appropriate for biological testing.
![eMolecules 1797409-86-9 | Ambeed | 2H-Pyrazolo[43-d]pyrimidin-7(6H)-one | 100mg | 714087621 | A651037 | MFCD28392134 | 136.114 | C5H4N4O](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502514576.JPG-250.jpg)
eMolecules 1797409-86-9 | Ambeed | 2H-Pyrazolo[43-d]pyrimidin-7(6H)-one | 100mg | 714087621 | A651037 | MFCD28392134 | 136.114 | C5H4N4O
Ambeed | rel-Methyl (4aS7aS)-6-benzylhexahydropyrano[23-c]pyrrole-7a(2H)-carboxylate | 100mg | 672522902 | A1492658 | 2696257-57-3 | 550.696 | C32H42N2O6
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Medchemexpress LLC 4-hydroxytolbutamide | 5719-85-7 | MFCD00144466 | 99.7% | 286.35 g/mol | C12H18N2O4S | 5 MG
4-Hydroxytolbutamide is a hydroxylated metabolite of the sulfonylurea tolbutamide, used as a reference compound in studies of drug metabolism and cytochrome P450 enzyme activity. It is employed to investigate biotransformation pathways mediated by CYP2C8 and CYP2C9.
- Suitable as a reference standard for CYP2C8 and CYP2C9 metabolism studies.
- High purity (>99%) for analytical and bioanalytical applications.
- Solid powder form for ease of handling and storage.
- Stored at -20°C in powder; in solvent store at -80°C for long-term stability.
- Chemical formula C12H18N2O4S; molecular weight 286.35 g/mol.
eMolecules 1643354-85-1 | Ambeed | Methyl 23-dichloroquinoxaline-5-carboxylate | 50mg | 600840331 | A435754 | MFCD27922608 | 257.07 | C10H6Cl2N2O2
Ambeed | 2-(Pyrrolidin-1-yl)pyrimidine-4-carboxylic acid hydrochloride | 100mg | 672838295 | A1496655 | 2361643-61-8 | 229.660 | C9H12ClN3O2
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Medchemexpress LLC Oxypeucedanin hydrate | 2643-85-8 | 50 MG
Oxypeucedanin hydrate | 2643-85-8 | 50 MG
Medchemexpress LLC Orismilast | 1353546-86-7 | 99.9% | 510.29 g·mol⁻¹ | C19H15Cl2F2NO7S | 5 MG
Orismilast is an orally active, selective phosphodiesterase 4 (PDE4) inhibitor used in preclinical research on inflammatory diseases. It demonstrates potent activity against PDE4B and PDE4D subtype splice variants and is supplied as a high-purity research compound.
- Selective phosphodiesterase 4 (PDE4) inhibitor.
- Orally active compound suitable for inflammatory disease research.
- Potent inhibition of PDE4B and PDE4D subtype splice variants.
- High purity solid supplied in a 5 mg package.
- Molecular weight 510.29 g·mol⁻¹; formula C19H15Cl2F2NO7S.
Medchemexpress LLC Manool | 596-85-0 | 290.48 | 100 MG
Manool is a diterpene derived from *Salvia officinalis*. It selectively induces cytotoxicity in cancer cells and arrests them at the G(2)/M phase of the cell cycle. For research use only.
- Diterpene from *Salvia officinalis*.
- Induces selective cytotoxicity in cancer cells.
- Arrests cancer cells at the G(2)/M phase of the cell cycle.
- Exhibits higher cytotoxic activity against HeLa (IC50=6.7 μg/mL) and U343 (IC50=6.7 μg/mL) cells.
- Shows a protective effect against chromosome damage induced by MMS in HepG2 cells.
Medchemexpress LLC Nimbin | 5945-86-8 | 5 MG
Nimbin is an orally active intermediate limonoid found in Azadirachta. It prevents tau aggregation, increases cell viability, and effectively inhibits the envelope protein of the dengue virus. It possesses anti-inflammatory, antipyretic, antifungal, antihistamine, antiseptic, antioxidant, anti-cancer, and anti-viral properties, showing promise for research into neurodegenerative diseases and viral infections.
- Orally active intermediate limonoid
- Prevents tau aggregation and increases cell viability
- Effective inhibitor of the dengue virus envelope protein
- Anti-inflammatory, antipyretic, antifungal, antihistamine, antiseptic, antioxidant, anti-cancer, and anti-viral properties
- Promising for research of neurodegenerative diseases and viral infections