Phenols
Medchemexpress LLC JNJ-47117096 hydroch | 1610536-69-0 | 50MG
JNJ-47117096 hydrochloride is potent and selective MELK inhibitor with an IC50 of 23 nM also effectively inhibits Flt3 with an IC50 of 18 nM
Medchemexpress LLC (+)-Norfenfluramine hydrochloride | 37936-89-3 | MFCD11045299 | 99.8% | 239.67 g/mol | C10H13ClF3N | 25 MG
(+)-Norfenfluramine hydrochloride is the optically active hydrochloride salt of norfenfluramine supplied as a research-grade reagent. It is a major hepatic metabolite of fenfluramine and a selective 5-HT2B receptor agonist used in in vitro pharmacology, receptor binding, and metabolic studies. Available in a small, high-purity pack suitable for analytical and experimental use.
- High purity suitable for analytical and pharmacological studies.
- Hydrochloride salt form for improved solubility in polar solvents.
- Optically active (+) enantiomer for stereoselective research.
- Documented activity as a 5-HT2B receptor agonist for receptor studies.
- Small pack size supports limited-scale experiments and reference standards.
Medchemexpress LLC Minodronic acid hydrate | 155648-60-5 | 99.67% | 340.16 | 100 MG
Minodronic acid hydrate is a third-generation bisphosphonate that directly and indirectly prevents proliferation, induces apoptosis, and inhibits metastasis of various types of cancer cells. It also acts as an antagonist of purinergic P2X2/3 receptors, which are involved in pain.
- Directly prevents cell proliferation.
- Induces apoptosis in cancer cells.
- Inhibits metastasis of various cancer cell types.
- Antagonizes purinergic P2X2/3 receptors.
- Involved in pain management.
Medchemexpress LLC 2-Hydroxybenzimidazole | 615-16-7 | 134.14 | 50 G
2-Hydroxybenzimidazole is an inactive compound targeting CYP1A1. It is mainly used as a control compound in the structure-activity relationship study of benzimidazole derivatives. It does not induce CYP1A1 expression like its thiol or amino substituted derivatives. This product is for research use only and not for sale to patients.
- Targets CYP1A1 as an inactive compound
- Used as a control in benzimidazole derivative studies
- Does not induce CYP1A1 expression
- For research use only
Medchemexpress LLC 6-(5-((MeSO2Et-amino)methyl)furan-2-yl)-N-(3-methyl-4-triazolopyridin-7-yloxyphenyl)quinazolin-4-amine | 937265-83-3 | MFCD22420817 | 99.2% | 569.63 g/mol | C29H27N7O4S | 1 ML
ARRY-380 analog is a research small molecule provided as a ready-to-use solution for cellular and biochemical studies. It has been characterized in cell-based assays for effects on apoptotic pathways and intracellular pathogen replication.
- Supplied as a 10 mM solution in DMSO for ready-to-use experiments.
- Reported to activate caspase-3 and caspase-8 in cell-based studies.
- Shown to inhibit Salmonella replication in cellular assays.
- High reported purity (~99.2%) suitable for research applications.
- Molecular weight 569.63 g/mol and formula C29H27N7O4S.
- MFCD22420817 and CAS 937265-83-3 available for database cross-reference.
Alkali Scientific Agarose, Low EEO, 100 G
Agarose, Low EEO, 100 G is a molecular biology grade agarose that features a low electroendosmosis (EEO) property, which helps to minimize the migration of ions in the gel during electrophoresis. This makes it an ideal choice for applications that require low background interference, such as high-resolution gel electrophoresis. The 100g package is perfect for mid-sized laboratories that require a moderate volume of agarose for regular gel preparations. The low EEO property ensures better band clarity and sharper separation of nucleic acids and proteins, making it ideal for applications where precision is essential, such as in nucleic acid analysis and protein assays.
Medchemexpress LLC Norcyclizine (1-(diphenylmethyl)piperazine) | 841-77-0 | 99.7% | 252.35 | 100 G
Norcyclizine is a piperazine compound used for the synthesis of antimicrobial agents. 1-Benzhydrylpiperazine derivatives, including Norcyclizine, have been shown to enhance the antibacterial activity of β-lactam antibiotics against Methicillin-resistant Staphylococcus aureus (MRSA). This enhancement is believed to occur through the inhibition of the allosteric site of PBP2a. Additionally, 1-Benzhydrylpiperazine can function as a pharmacological scaffold for the synthesis of anticancer agents.
- Can be used for the synthesis of antimicrobial agents.
- Enhances the antibacterial activity of β-lactam antibiotics against Methicillin-resistant Staphylococcus aureus (MRSA) by inhibiting the allosteric site of PBP2a.
- Can serve as a pharmacological scaffold for the synthesis of anticancer agents.
Medchemexpress LLC (+)-norfenfluramine hydrochloride | 37936-89-3 | MFCD00871809 | 99.8% | 239.67 g/mol | C10H13ClF3N | 10 MG
(+)-Norfenfluramine hydrochloride is the chiral hydrochloride salt of norfenfluramine, a hepatic metabolite of fenfluramine, provided as a high-purity research reagent for receptor pharmacology and analytical applications.
- Provides high-purity reference material for receptor and metabolic studies.
- Acts as a selective 5-HT2B receptor agonist for pharmacological assays.
- Supplied as a small research-scale quantity suitable for analytical and preparative use.
- Solid white to off-white form that is stable under recommended storage conditions.
Alkali Scientific Doripenem, 250 Mg
Doripenem is a potent carbapenem antibiotic used in laboratory research to investigate bacterial resistance and the effectiveness of antimicrobials. The 250mg dose is used for testing in microbiological studies, including bacterial culture and antibiotic susceptibility assays. Doripenem works by inhibiting bacterial cell wall synthesis, which makes it highly effective against a broad spectrum of bacteria. This compound is essential for studying the mechanisms of resistance, particularly in pathogens resistant to other classes of antibiotics. The product is widely used in clinical microbiology and pharmaceutical research, helping to develop strategies for combating multi-drug resistant bacteria.