Furans
![Medchemexpress LLC 4-fluoro-N-[1-[1-(oxane-4-carbonyl)-2,3-dihydroindol-5-yl]ethyl]benzamide | 2166616-74-4 | ≥98% | 396.45 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC 4-fluoro-N-[1-[1-(oxane-4-carbonyl)-2,3-dihydroindol-5-yl]ethyl]benzamide | 2166616-74-4 | ≥98% | 396.45 | 100 MG
LY-3381916 (IDO1-IN-5) is a potent, selective, and brain-penetrant inhibitor of IDO1 activity. It functions by binding to apo-IDO1, which lacks heme, rather than to mature heme-bound IDO1.
- Potent IDO1 inhibitor
- Selective IDO1 inhibitor
- Brain-penetrant IDO1 inhibitor
- Binds to apo-IDO1 lacking heme
- Does not show obvious agonism of aryl hydrocarbon receptor (AHR) at concentrations up to 100 μM.
Medchemexpress LLC 1-Aminohydantoin | 6301-02-6 | MFCD02093080 | >=98% | 115.09 | 250 MG
1-Aminohydantoin | 6301-02-6 | MFCD02093080 | >=98% | 115.09 | 250 MG
Medchemexpress LLC Nitrofurazone (Nitrofural) | 59-87-0 | 99.96% | 5 G
Nitrofurazone (Nitrofural) is a broad-spectrum antibiotic with oral activity. It is a nitro-aromatic drug active against both Gram-positive and Gram-negative bacteria. This product is for research use only.
- Broad-spectrum antibiotic
- Oral activity
- Nitro-aromatic drug
- Active against both Gram-positive and Gram-negative bacteria
Medchemexpress LLC Eprazinone dihydrochloride | 10402-53-6 | 99.1% | 100 MG
Eprazinone dihydrochloride is an agent possessing mucolytic, secretolytic, antitussive, and bronchial antispasmodic properties. It acts as a neurokinin 1 receptor (NK1R) ligand. This compound shows potential for treating chronic bronchitis by improving pulmonary function and arterial partial pressure of oxygen.
- Functions as a neurokinin 1 receptor (NK1R) ligand.
- Exhibits mucolytic properties.
- Possesses secretolytic characteristics.
- Acts as an antitussive agent.
- Displays bronchial antispasmodic effects.
- Potential to improve pulmonary function.
- Potential to improve arterial partial pressure of oxygen.
Medchemexpress LLC ATH686 | 853299-52-2 | 99.54% | 515.53 | 5 MG
ATH686 is a potent, selective, and ATP-competitive FLT3 inhibitor that targets mutant FLT3 protein kinase activity. It inhibits the proliferation of cells harboring FLT3 mutants by inducing apoptosis and cell cycle inhibition, also exhibiting antileukemic effects.
- Potently inhibits cell proliferation (IC50 around 0.001 μM) in FLT3-ITD-Ba/F3 cells and D835Y-Ba/F3 cells
- Induces apoptosis
- Inhibits autophosphorylation of mutant FLT3
- Exhibits antileukemic effects
Medchemexpress LLC 2,4-dihydro-5-(4-nitrophenyl)-2-phenyl-3H-pyrazol-3-one | 34320-83-7 | MFCD00506084 | 99.7% | 281.27 | C15H11N3O3 | 10 MG
TCS PrP Inhibitor 13 is a small-molecule antiprion agent that inhibits cellular prion protein (PrPC) and reduces protease-resistant prion accumulation. It is supplied as a solid for research use and shows potent activity in cellular assays (IC50 3 nM).
- Chemical formula: C15H11N3O3.
- Molecular weight: 281.27.
- Purity: 99.7%.
- Appearance: solid, white to yellow.
- Storage conditions: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Reported activity: IC50 3 nM in ScN2a and F3 cells.
- Biological effect: induces apoptosis in schwannoma cells.
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 Complement C5-IN-1 | 2365402-67-9 | 99.14% | 50 MG
Complement C5-IN-1 is a selective allosteric inhibitor of complement component protein C5. It inhibits the cleavage of C5 into C5a and C5b, blocking the formation of the membrane attack complex (MAC). This compound demonstrates an IC50 of 0.77 μM in 50% human whole blood and 5 nM in 2% human serum for blocking MAC deposition induced by zymosan. It is valuable for studying diseases associated with complement overactivation, such as paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS). This product is for research use only.
- Selective allosteric inhibitor of complement component protein C5
- Prevents C5 from being cleaved by C5 convertase
- Inhibits cleavage of C5 into C5a and C5b
- Blocks the formation of the membrane attack complex (MAC)
- Supports research into complement overactivation diseases
- Appears as a solid, white to off-white material
Medchemexpress LLC L-proline, L-threonyl-L-lysyl-L-prolyl-L-arginyl-L-prolylglycyl (diacetate) | 00-00-0 | 99.9% | 871.98 | C37H65N11O13 | 10 MG
Selank diacetate is a synthetic peptide derived from tuftsin with reported anxiolytic, nootropic, antidepressant, and antistress activity. It is supplied as a white to off-white solid for laboratory research use only, with documented molecular and purity data to support experimental use. Use appropriate laboratory safety practices and consult the SDS and COA prior to handling.
- High purity suitable for research applications.
- Known amino acid sequence: Thr-Lys-Pro-Arg-Pro-Gly-Pro.
- Supplied as a white to off-white solid.
- High solubility in water with sonication recommended.
- COA and SDS available for quality and safety information.
Medchemexpress LLC BMS-962212 10mg | 1430114-34-3 | C32H28ClFN8O5 | 10 MG
BMS-962212 is a reversible, direct, and selective small-molecule inhibitor of coagulation factor XIa (FXIa) used in research on anticoagulation and thrombosis. It produces dose-dependent increases in activated partial thromboplastin time (aPTT) and reductions in FXI clotting activity; molecular formula C32H28ClFN8O5, molecular weight 659.07 g·mol⁻1.
- Reversible, selective FXIa inhibition for anticoagulation research.
- Demonstrated dose-dependent pharmacodynamic effects on aPTT and FXI activity.
- High reported purity (99.33%).
- Offered in research sample quantities (10 MG).
Selleck Chemical LLC 1-Aminohydantoin Hydrochloride S4891-25mg
1-Aminohydantoin Hydrochloride is a pharmaceutical and pesticide intermediate
Med Vet International Nitrofurantoin 100mg, 100 Capsuls
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Nitrofurantoin is an antibiotic used to treat or prevent certain bladder infections. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections. This medication should not be used in infants younger than 1 month old (see also Precautions section). This drug should not be used to treat infections outside the bladder (e.g., kidney infections such as pyelonephritis or perinephric abscesses).
![Medchemexpress LLC 2H-tetrazole-2-butanoic acid, β-amino-5-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenyl]-, (βS)- | 1799681-85-8 | 98.4% | C16H14ClFN6O3 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000261361.png-250.jpg)
Medchemexpress LLC 2H-tetrazole-2-butanoic acid, β-amino-5-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenyl]-, (βS)- | 1799681-85-8 | 98.4% | C16H14ClFN6O3 | 10MG
LYS006 is a small-molecule inhibitor of leukotriene A4 hydrolase (LTA4H) developed for research into inflammatory and autoimmune disorders. It is reported to have subnanomolar to low-nanomolar potency (IC50 ≈ 2 nM) and is supplied with analytical characterization suitable for laboratory studies.
- Potent leukotriene A4 hydrolase (LTA4H) inhibitor (IC50 ≈ 2 nM).
- High purity suitable for research (≈98.4%).
- Available as solid and as DMSO solution for assay flexibility.
- Characterized by a certificate of analysis with structural confirmation.
- Intended for preclinical and pharmacology studies in inflammation and immunology.