Furans
Medchemexpress LLC Camelliaside A | 135095-52-2 | 5 MG
Camelliaside A is a phytochemical that acts as a HER2 ligand. It has been shown to lack antifungal activity against *Rhizoctonia solani* and is applicable to breast cancer-related research.
- Phytochemical and HER2 ligand
- Shows no inhibitory effect on mycelial growth of *Rhizoctonia solani*
- Applicable to breast cancer-related research
- Off-white to light yellow solid appearance
- Purity of 99.65%
- Store at 4°C, protect from light. In solvent: -80°C for 6 months; -20°C for 1 month (protect from light).
- Soluble in DMSO (100 mg/mL)
Medchemexpress LLC Nitrofurantoin (Standard) | 67-20-9 | 99.7% | C8H6N4O5 | 50 MG
Nitrofurantoin (Standard) is the analytical standard of Nitrofurantoin. It is a potent and orally active broad-spectrum beta-lactamase antimicrobial agent, primarily used for research and analytical applications. This antibiotic is suitable for the study of urinary tract infections (UTIs), including cystitis and kidney infections.
- Analytical standard for qualitative, quantitative, and methodological research
- Used in HPLC, GC, and MS experiments
- Potent and orally active broad-spectrum antimicrobial agent
- Acts as an antibiotic
- Suitable for studying urinary tract infections, including cystitis and kidney infections
Medchemexpress LLC Nitrofurantoin (Standard) | 67-20-9 | 99.74% | C8H6N4O5 | 25 MG
Nitrofurantoin (Standard) is an analytical standard primarily intended for research and analytical applications. This potent, orally active, broad-spectrum beta-lactamase antimicrobial agent functions as an antibiotic, making it suitable for the study of urinary tract infections (UTIs), including cystitis and kidney infections.
- Analytical standard for research and analytical applications
- Potent and orally active
- Broad-spectrum beta-lactamase antimicrobial agent
- Effective as an antibiotic
- Useful for studying urinary tract infections (UTIs), including cystitis and kidney infections
Medchemexpress LLC BMS-911172 100mg | 1644248-18-9 | 339.34 | C16H19F2N3O3 | 100 MG
BMS-911172 is a small-molecule inhibitor of adaptor-associated kinase 1 (AAK1) with a reported IC50 of 35 nM; it is supplied for laboratory research use only.
- Inhibits AAK1 with IC50 of 35 nM
- Reported purity 99.49%
- Available in multiple solid sizes and 10 mM DMSO solutions
- Suitable for in vitro and preclinical research; not for human use
- Molecular weight 339.34 g/mol; formula C16H19F2N3O3
- Certificate of analysis and safety data sheet available
Medchemexpress LLC Linperlisib | 1702816-75-8 | MFCD31544346 | 98.9% | 588.69 g·mol⁻¹ | C28H37FN6O5S | 25 MG
Linperlisib is a potent, orally bioavailable, and selective inhibitor of phosphoinositide 3-kinase delta (PI3Kδ) developed for research applications. It demonstrates an IC50 of approximately 6.4 nM against PI3Kδ and is supplied as a high-purity solid suitable for in vitro and preclinical studies.
- Potent, selective inhibitor of PI3Kδ (IC50 ≈ 6.4 nM).
- Orally bioavailable profile useful for in vivo studies.
- Supplied as a high-purity solid (≈98.9%).
- Suitable for in vitro and preclinical research applications.
- Available in multiple small-scale quantities for laboratory use.
- Recommended storage at low temperatures to preserve stability.
Medchemexpress LLC Tovinontrine (IMR-687) | 2062661-53-2 | 99.8% | 394.47 | 1 ML
Tovinontrine (IMR-687) | 2062661-53-2 | 99.8% | 394.47 | 1 ML
Medchemexpress LLC PF-06456384 trihydrochloride | 1834610-75-1 | 99.4% | 829.18 g/mol | C35H35Cl3F3N7O3S2 | 50 MG
PF-06456384 trihydrochloride is the trihydrochloride salt of a highly potent and selective NaV1.7 inhibitor developed for preclinical pharmacology and pain model research. The compound has been profiled in vitro and in vivo and is supplied as a high-purity research sample.
- Salt form: trihydrochloride.
- Target: voltage-gated sodium channel NaV1.7.
- Potency: IC50 = 0.01 nM against NaV1.7.
- Purity: 99.38% by HPLC (supplier specification).
- Molecular weight: 829.18 g/mol (trihydrochloride salt).
- Molecular formula: C35H35Cl3F3N7O3S2.
- Intended use: preclinical pharmacology and formalin pain model research.
- Supplied quantity: 50 mg research sample.
Medchemexpress LLC 2-isopropylphenyl (2-(naphthalen-2-yl)ethyl)carbamate | 1354359-53-7 | MFCD20926355 | 99.5% | 333.42 g/mol | C22H23NO2 | 50 MG
JW480 is a potent, selective small-molecule inhibitor of the serine hydrolase KIAA1363 (AADACL1) used in biochemical and cell-based research to probe enzyme function and related pathways. This compound is supplied for research use only.
- Potent, selective inhibitor of KIAA1363.
- Intended for research use only.
- High purity: 99.54%.
- Chemical formula: C22H23NO2.
- Molecular weight: 333.42 g/mol.
- CAS number: 1354359-53-7.
- Supplied as a 50 mg quantity.
Medchemexpress LLC Gunagratinib | 2211082-53-8 | 98.5% | 423.47 g·mol⁻¹ | C22H25N5O4 | 5 MG
Gunagratinib is a covalent, orally active pan-FGFR inhibitor supplied as a purified research compound for preclinical studies. It irreversibly inhibits FGFR signaling through covalent binding and is provided in multiple small-scale pack sizes and formats for use in in vitro and in vivo research.
- Covalent pan-FGFR inhibitor with irreversible binding.
- Orally active compound suitable for preclinical studies.
- High purity (98.5%) for research applications.
- Molecular formula C22H25N5O4; molecular weight 423.47 g·mol⁻¹.
- Available in small pack sizes (including 5 mg) as solid or DMSO solution.
- Supplied for laboratory research use only.