Furans
![Aobchem B-[4-[(Tetrahydro-2-furanyl)methoxy]phenyl]boronic acid | 95% | CAS 938443-41-5 | C11H15BO4 | 250mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Aobchem B-[4-[(Tetrahydro-2-furanyl)methoxy]phenyl]boronic acid | 95% | CAS 938443-41-5 | C11H15BO4 | 250mg
B-[4-[(Tetrahydro-2-furanyl)methoxy]phenyl]boronic acid | 95% | CAS 938443-41-5 | C11H15BO4 | 250mg
Aobchem 2-[(Tetrahydro-3-furanyl)oxy]-4-pyridinecarboxylic acid | 95% | CAS 1211533-45-7 | C10H11NO4 | 500mg
2-[(Tetrahydro-3-furanyl)oxy]-4-pyridinecarboxylic acid | 95% | CAS 1211533-45-7 | C10H11NO4 | 500mg
Aobchem 2-(5-Methyl-2-furanyl)benzaldehyde | ≥95% | CAS 400746-82-9 | C12H10O2 | 500mg
2-(5-Methyl-2-furanyl)benzaldehyde | ≥95% | CAS 400746-82-9 | C12H10O2 | 500mg
![Aobchem 2-[(Tetrahydro-3-furanyl)oxy]-3-pyridinecarboxylic acid | ≥95% | CAS 1343106-79-5 | C10H11NO4 | 250mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000972843.png-250.jpg)
Aobchem 2-[(Tetrahydro-3-furanyl)oxy]-3-pyridinecarboxylic acid | ≥95% | CAS 1343106-79-5 | C10H11NO4 | 250mg
2-[(Tetrahydro-3-furanyl)oxy]-3-pyridinecarboxylic acid | ≥95% | CAS 1343106-79-5 | C10H11NO4 | 250mg
Medchemexpress LLC Etiocholanolone (5β-Androsterone) | 53-42-9 | 99.5% | 290.44 | 10 MG
Etiocholanolone (5β-Androsterone) is an excreted metabolite of testosterone with anticonvulsant activity. It is also described as a less potent neurosteroid positive allosteric modulator (PAM) of the GABAA receptor compared to its enantiomer form.
- Excreted metabolite of testosterone
- Anticonvulsant activity
- Neurosteroid positive allosteric modulator (PAM) of the GABAA receptor
Medchemexpress LLC BMS-911172 25mg | 1644248-18-9 | 339.34 g/mol | C16H19F2N3O3 | 25 MG
BMS-911172 is a small-molecule, brain-penetrant inhibitor of adaptor protein 2-associated kinase 1 (AAK1) used as a research compound to investigate AAK1-mediated signaling and neuropathic pain mechanisms. Chemical formula C16H19F2N3O3; molecular weight 339.34 g/mol; reported AAK1 activity in the low-nanomolar range.
- Potent AAK1 inhibition with low-nanomolar activity.
- Brain-penetrant small molecule suitable for in vivo models.
- High purity appropriate for biochemical and cellular assays.
- Available in small research quantities for laboratory studies.
Medchemexpress LLC ATH686 | 853299-52-2 | 99.5% | 515.53 | 50 MG
ATH686 is a potent, selective, and ATP-competitive FLT3 inhibitor. It targets mutant FLT3 protein kinase activity, inhibiting the proliferation of cells harboring FLT3 mutants by inducing apoptosis and cell cycle inhibition. It has demonstrated antileukemic effects.
- Potent, selective, and ATP-competitive FLT3 inhibitor.
- Targets mutant FLT3 protein kinase activity.
- Induces apoptosis and cell cycle inhibition.
- Inhibits proliferation of cells harboring FLT3 mutants.
- Demonstrates antileukemic effects.
- For research use only.
Medchemexpress LLC 7-TFA-ap-7-Deaza-dA | 178420-75-2 | 98.8% | 399.32 | 50 MG
7-TFA-ap-7-Deaza-dA is a modified nucleoside that can be utilized in the synthesis of deoxyribonucleic acid or nucleic acid. It functions as a click chemistry reagent due to its Alkyne group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Modified nucleoside for nucleic acid synthesis
- Functions as a click chemistry reagent
- Contains an alkyne group for CuAAc reactions
- Related to nucleoside analogs and adenosine
- Applicable in cancer research and cell cycle/DNA damage studies
Medchemexpress LLC 1-aminohydantoin hydrochloride | 2827-56-7 | MFCD02181047 | >98.0% | 151.55 g/mol | C3H6ClN3O2 | 100mg
1-Aminohydantoin hydrochloride (Standard) is the analytical standard of 1-Aminohydantoin hydrochloride (HY-Y0469) This product is intended for research and analytical applications 1-Aminohydantoin hydrochloride is a major metabolite of Nitrofurantoin (HY-A0090) in animal tissues and can be used as a standard for the determination of residues of veterinary agents in meat milk et al 1-Aminohydantoin hydrochloride covalently binds to tissue proteins and is released from the tissues under slightly acidic conditions and derivatized with 2-nitrobenzaldehyde to form nitrophenyl derivatives of 1-Aminohydantoin hydrochloride before detection[1][2]
Medchemexpress LLC Selank diacetate 25mg | 25MG
Selank (Selanc) acetate is a synthetic peptide derived from tuftsin Selank acetate has anxiolytic activity and is a nootropic neuropsychotropic antidepressant and antistress compound[1
Alkali Scientific Nitrofurantoin, 5 G
Nitrofurantoin, 5g, is a laboratory-grade antibiotic used to study bacterial resistance, particularly in the context of urinary tract infections (UTIs). It is effective against a broad spectrum of Gram-positive and Gram-negative bacteria by disrupting their protein synthesis, DNA replication, and overall metabolism. The 5g quantity is ideal for use in antimicrobial susceptibility testing, such as Minimum Inhibitory Concentration (MIC) assays, disk diffusion, and other microbiological tests. Nitrofurantoin is also used in research settings to better understand antimicrobial resistance mechanisms, including the development of resistance in UTI pathogens.
Medchemexpress LLC 1-aminohydantoin hydrochloride | 2827-56-7 | MFCD02181047 | ≥98.0% | 151.55 | C3H6ClN3O2 | 25g
1-Aminohydantoin hydrochloride is a major metabolite of Nitrofurantoin (HY-A0090) in animal tissues and can be used as a standard for the determination of residues of veterinary agents in meat milk et al 1-Aminohydantoin hydrochloride covalently binds to tissue proteins and is released from the tissues under slightly acidic conditions and derivatized with 2-nitrobenzaldehyde to form nitrophenyl derivatives of 1-Aminohydantoin hydrochloride before detection[1][2]
Medchemexpress LLC Selank diacetate 50mg | 50MG
Selank (Selanc) acetate is a synthetic peptide derived from tuftsin Selank acetate has anxiolytic activity and is a nootropic neuropsychotropic antidepressant and antistress compound[1
Medchemexpress LLC B022 | 1202764-53-1 | 99.4% | 100 MG
B022 is a selective NF-κB-inducing kinase (NIK) inhibitor research compound commonly used in biochemical and cellular studies targeting NF-κB signaling pathways. It is provided as a high-purity small-molecule suitable for in vitro experiments.
- Selective inhibition of NF-κB-inducing kinase with low nanomolar potency (Ki ≈ 4.2 nM, IC50 ≈ 15.1 nM).
- High purity: 99.37% as listed by supplier.
- Molecular formula C19H16ClN5OS; molecular weight 397.88 g·mol⁻¹.
- Available in small-molecule research sizes, including 100 MG.
- Recommended storage: powder at -20°C (up to 3 years) or 4°C (up to 2 years).
- Suitable for studies of inflammation, oxidative stress, and liver injury models.
Medchemexpress LLC DMA-135 hydrochloride | 2237925-62-9 | 98.0% | C16H18ClN7O | 50 MG
DMA-135 hydrochloride is an inhibitor targeting enterovirus 71 (EV71) IRES-dependent translation and replication. It binds to the EV71 SLII domain with moderately high affinity (KD= 520 nM) and shows no significant toxicity in cell-based studies. It induces conformational changes in the RNA structure and stabilizes the ternary complex DMA135-RNA-AUF1, inhibiting the translation and replication of EV71 with an IC50 of 7.54 μM.
- Targets enterovirus 71 (EV71) IRES-dependent translation and replication.
- Binds to the EV71 SLII domain with moderately high affinity.
- Induces conformational changes in RNA structure.
- Stabilizes the ternary complex DMA135-RNA-AUF1.
- Inhibits translation and replication of EV71 with an IC50 of 7.54 μM.
- Demonstrates no significant toxicity in cell-based studies.