Azobenzenes
Chemscene ChemScene | 4-Bromo-1,8-naphthalic anhydride | 100G | CS-0015910 | 0.97 | 81-86-7| MFCD00006927 | 277.073
ChemScene | 4-Bromo-1,8-naphthalic anhydride | 100G | CS-0015910 | 0.97 | 81-86-7| MFCD00006927 | 277.073
eMolecules 302799-86-6 | Medchem Express | TCS 46b | 5mg | 791205920 | HY-107707 | MFCD09971137 | 345.446 | C22H23N3O
Ambeed | 2-Chloro-4-methyl-56-dihydro-7H-cyclopenta[b]pyridin-7-one | 100mg | 490540447 | A234844 | 745075-82-5 | MFCD18255919 | 181.620 | C9H8ClNO
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Medchemexpress LLC Cadrofloxacin 100mg | 153808-85-6 | 100 MG
Cadrofloxacin is an orally active fluoroquinolone antibiotic research chemical with activity against aerobic and anaerobic Gram-positive and Gram-negative bacteria. It is supplied as a powder for laboratory research and analytical applications.
- High purity: 98.2%.
- Molecular weight: 411.38 g/mol.
- Chemical formula: C19H20F3N3O4.
- CAS number: 153808-85-6.
- Supplied as a powder, stable at -20°C for long-term storage.
- Available in 100 MG quantity for research use.
eMolecules ChemScene / 1-(2-Isopropoxypyridin-3-yl)ethanone / 100mg / 582634293 / CS-0042760 / 0.000 / 1551553-85-5 / MFCD27974420 / 179.219 / C10H13NO2
ChemScene / 1-(2-Isopropoxypyridin-3-yl)ethanone / 100mg / 582634293 / CS-0042760 / 0.000 / 1551553-85-5 / MFCD27974420 / 179.219 / C10H13NO2
eMolecules 138500-85-3 | 2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | Ambeed | MFCD02179493 | 297.000 | C13H18BBrO2 | 97.000 | CC1(C)OB(OC1(C)C)c1ccc(CBr)cc1 | 1g | 525123326
2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | Ambeed | 138500-85-3 | MFCD02179493 | 297.000 | C13H18BBrO2 | 97.000 | CC1(C)OB(OC1(C)C)c1ccc(CBr)cc1 | 1g | 525123326
![Medchemexpress LLC 4H,8H-Benzo[1,2-b:3,4-b']dipyran-4-one, 9,10-dihydro-3,5-dihydroxy-2-(4-methoxyphenyl)-8,8-dimethyl | 38226-86-7 | 368.38 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000416426.png-250.jpg)
Medchemexpress LLC 4H,8H-Benzo[1,2-b:3,4-b']dipyran-4-one, 9,10-dihydro-3,5-dihydroxy-2-(4-methoxyphenyl)-8,8-dimethyl | 38226-86-7 | 368.38 | 5 MG
β-Anhydroicaritin is isolated from Boswellia carterii Birdware and possesses important biological and pharmacological effects. It ameliorates the degradation of periodontal tissue, inhibits the synthesis and secretion of TNF-α and MMP-3 in diabetic rats, and decreases the overproduction of NO, IL-10, TNF-α, MCP-1, and IL-6 in peritonitis mice. Additionally, it inhibits the elevation of intracellular Ca2+ and markedly decreases iNOS protein expression.
- Antiosteoporosis properties
- Estrogen regulation properties
- Antitumor properties
- Ameliorates the degradation of periodontal tissue
- Inhibits the synthesis and secretion of TNF-α and MMP-3 in diabetic rats
- Decreases the overproduction of NO, IL-10, TNF-α, MCP-1, and IL-6 in peritonitis mice
- Inhibits the elevation of intracellular Ca2+
- Markedly decreases iNOS protein expression
Medchemexpress LLC Vacuolin-1 | 351986-85-1 | MFCD00321410 | 98.5% | 577.42 | C26H24IN7O | 5 MG
Vacuolin-1 (CAS 351986-85-1) is a cell-permeable small molecule that inhibits PIKfyve and blocks Ca2+-dependent lysosomal exocytosis. It impairs lysosomal maturation, inhibits late-stage autophagy, and induces vacuole formation, making it useful for studying endosomal/lysosomal trafficking and membrane dynamics in cell biology research.
- Potent, cell-permeable PIKfyve inhibitor.
- Blocks Ca2+-dependent lysosomal exocytosis in cells.
- Impairs lysosomal maturation and inhibits late-stage autophagy.
- Induces vacuole formation and alters endosomal/lysosomal trafficking.
- Provided at high purity for research applications.
Medchemexpress LLC Triptonine B | 168009-85-6 | 1 MG
Triptonine B is a sesquiterpene pyridine alkaloid. It functions as an inhibitor of HIV replication, specifically in H9 lymphocytes, demonstrating an EC50 value of less than 0.10 μg/mL. This compound is intended for research use only and is characterized as a white to off-white solid with a high purity of 99.83%. It has a molecular weight of 967.87 and a chemical formula of C46H49NO22. Triptonine B is classified within the terpenoid and sesquiterpene categories and is naturally sourced from plants of the Celastraceae family, particularly *Tripterygium wilfordii Hook. f.*
- Inhibits HIV replication in H9 lymphocytes
- EC50 value of less than 0.10 μg/mL
- High purity of 99.83%
- Molecular weight of 967.87
- Chemical formula C46H49NO22
- Derived from *Tripterygium wilfordii Hook. f.*
Medchemexpress LLC 4-hydroxy-2-methyl-1,1-dioxo-N-(1,3-thiazol-2-yl)-1λ6,2-benzothiazine-3-carboxamide | 34042-85-8 | MFCD00866053 | 100.0% | 337.37 g·mol⁻1 | C13H11N3O4S2 | 10 MG
Sudoxicam is a non-steroidal anti-inflammatory drug (NSAID) of the enol-carboxamide class that acts as a reversible, orally active cyclooxygenase (COX) antagonist. Provided as a research-grade chemical for in vitro and analytical use.
- Reversible COX antagonist for inflammation research.
- Analytical-grade solid with molecular formula C13H11N3O4S2 and molecular weight 337.37 g·mol⁻¹.
- High purity (99.96%), suitable for research and analytical applications.
- Available in small package sizes (1 mg, 5 mg, 10 mg) for assay and method development.
- Storage: powder - -20°C (3 years), 4°C (2 years); in solvent - -80°C (6 months), -20°C (1 month).
![Medchemexpress LLC Urea, N-[3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-N' | 1166393-85-6 | 98.6% | 445.52 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000387730-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Urea, N-[3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-N' | 1166393-85-6 | 98.6% | 445.52 | 50 MG
PF-4618433 is a potent and selective PYK2 inhibitor, with an IC50 of 637 nM. It may be suitable for the research of osteoporosis, craniofacial and appendicular skeletal defects, and for targeted bone regeneration.
- Potent and selective PYK2 inhibitor with an IC50 of 637 nM.
- Promotes osteogenesis of hMSC cultures, increasing alkaline phosphatase (ALP) activity and mineralization.
- Enhances osteoblast proliferation.
- Enhances calcium deposition.
- Increases cell proliferation activity in murine bone marrow-derived mesenchymal stem cells (BMSC).
Medchemexpress LLC Voacamine | 3371-85-5 | 10 MG
Voacamine is an indole alkaloid with cannabinoid 1 (CB1) antagonistic activity. It inhibits nuclear translocation and enhances the effect of Doxorubicin by interfering with P-glycoprotein (P-gp) function. It promotes apoptosis-independent autophagic cell death in human osteosarcoma cells, activates the mitochondrial-associated apoptosis signaling pathway, and inhibits the PI3K/Akt/mTOR signaling pathway to suppress breast cancer progression. Voacamine also inhibits EGFR to exert oncogenic activity against colorectal cancer.
- High purity of 99.64%
- Inhibits nuclear translocation
- Enhances Doxorubicin efficacy by interfering with P-gp function
- Promotes apoptosis-independent autophagic cell death
- Suppresses breast cancer progression via PI3K/Akt/mTOR pathway inhibition
- Exerts oncogenic activity against colorectal cancer by inhibiting EGFR
eMolecules 287481-35-0 | 4-Aminoazobenzene hydrochloride | Combi-Blocks | MFCD00012994 | 233.700 | C12H12ClN3 | 95.000 | Cl.Nc1ccc(cc1)\N=N\c1ccccc1 | 1g | 439372908
4-Aminoazobenzene hydrochloride | Combi-Blocks | 287481-35-0 | MFCD00012994 | 233.700 | C12H12ClN3 | 95.000 | Cl.Nc1ccc(cc1)\N=N\c1ccccc1 | 1g | 439372908
Medchemexpress LLC Cadrofloxacin 5mg | 153808-85-6 | 411.38 g·mol⁻1 | C19H20F3N3O4 | 5 MG
Cadrofloxacin is a fluoroquinolone antibiotic supplied for research use. It is provided as a solid for experimental assays, with manufacturer guidance for solubilization and storage to preserve activity.
- Purity 98.21% as reported by the manufacturer.
- Molecular weight 411.38 g·mol⁻1.
- Soluble in DMSO at about 10 mg/mL with warming and pH adjustment.
- Store powder at -20°C for long-term stability; aliquot solutions to avoid freeze-thaw cycles.
- Suitable for in vitro antibacterial research and assay development.
Medchemexpress LLC GSK1702934A | 924377-85-5 | 99.1% | 395.52 | 1 MG
GSK1702934A is a selective TRPC3 agonist that modulates cardiac contractility and arrhythmogenesis by activating TRPC3. In vitro, it induces TRPC3/6-currents in HEK293 cells and promotes NCX currents in TRPC3-overexpressing myocytes. In vivo, it transiently increases blood pressure in Sprague Dawley rats.
- Modulates cardiac contractility and arrhythmogenesis
- Induces TRPC3/6-currents in HEK293 cells
- Promotes NCX currents in TRPC3-overexpressing myocytes
- Increases blood pressure in rats
- Suitable for research use only
Medchemexpress LLC Manool | 596-85-0 | 290.48 | 50 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. Manool has shown higher cytotoxic activity against HeLa (IC50=6.7 μg/mL) and U343 (IC50=6.7 μg/mL) cells. Additionally, it exhibits a protective effect against chromosome damage induced by MMS in HepG2 cells.
- Diterpene from Salvia officinalis.
- Induces selective cytotoxicity in cancer cells.
- Arrests cancer cells at the G(2)/M phase of the cell cycle.
- Exhibits protective effect against chromosome damage.