Furans
Selleck Chemical LLC 4E1RCat-5mg
4E1RCat is a dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction, and inhibits the binding of eIF4G to eIF4E.
Selleck Chemical LLC Mometasone furoate S1987-50mg
Mometasone Furoate (SCH-32088 mometasone 17-furoate) is a glucocorticoid receptor agonist used topically to reduce inflammation of the skin or in the airways
Selleck Chemical LLC Wortmannin S2758-20mg
Wortmannin is the first described PI3K inhibitor with IC50 of 3 nM in a cell-free assay with little selectivity within the PI3K family Wortmannin blocks autophagosome formation and potently inhibits DNA-PK/ATM with IC50 of 16 nM and 150 nM in cell-free assays Wortmannin also inhibits PLK1 activity
Selleck Chemical LLC 1-Aminohydantoin Hydrochloride S4891-25mg
1-Aminohydantoin Hydrochloride is a pharmaceutical and pesticide intermediate
Selleck Chemical LLC Dantrolene sodium
Dantrolene sodium(F 440) acts as a postsynaptic muscle relaxant by inhibiting Ca2 ions release from sarcoplasmic reticulum stores by antagonizing ryanodine receptors
Selleck Chemical LLC Mometasone furoate S1987-200mg
Mometasone Furoate (SCH-32088 mometasone 17-furoate) is a glucocorticoid receptor agonist used topically to reduce inflammation of the skin or in the airways
Selleck Chemical LLC Mometasone Furoate Hydrate
Mometasone Furoate (SCH 32088) Hydrate is a synthetic glucocorticoid with anti-inflammatory activity
Selleck Chemical LLC Nitrofurantoin S4536-100mg
Nitrofurantoin (Macrodantin Furadantine Furadonine) is an antibiotic used to treat bladder infections It inhibits bacterial DNA RNA and cell wall protein synthesis
Selleck Chemical LLC Furazolidone S4528-100mg
Furazolidone(Furoxone) is a synthetic nitrofuran derivative with bactericidal or bacteriostatic activity when used against Gram-positive and Gram-negative bacteria Furazolidone can be used to induce animal models of Cardiomyopathy
Selleck Chemical LLC Dantrolene sodium
Dantrolene sodium(F 440) acts as a postsynaptic muscle relaxant by inhibiting Ca2 ions release from sarcoplasmic reticulum stores by antagonizing ryanodine receptors
Medchemexpress LLC DS08210767 | 2376334-75-5 | 99.4% | 513.67 | C31H39N5O2 | 5MG
DS08210767 is a small-molecule, orally bioavailable antagonist of the parathyroid hormone receptor 1 (PTHR1) with a reported IC50 of 90 nM. It is supplied for research use only and is provided as a light yellow solid intended for laboratory applications.
- Orally bioavailable PTHR1 antagonist with an IC50 of 90 nM.
- High chemical purity of 99.4%.
- Molecular weight 513.67 and chemical formula C31H39N5O2.
- Supplied as a light yellow solid suitable for laboratory research.
- Provided in a 5 mg quantity for experimental use.
Medchemexpress LLC 3-(4-nitrophenyl)-1-phenyl-2-pyrazolin-5-one | 34320-83-7 | 99.7% | 281.27 g/mol | C15H11N3O3 | 5 MG
TCS PrP Inhibitor 13 is a small-molecule antiprion compound that inhibits accumulation of protease-resistant prion protein in cellular assays. It has been reported to show potent cellular activity and is used as a research reagent for studies of prion biology and for screening antiprion compounds.
- Potent antiprion activity with reported cellular IC50 ~3 nM.
- High chemical purity (99.7%).
- Chemical formula C15H11N3O3 and molecular weight 281.27 g/mol.
- Suitable for prion biology research and antiprion compound screening.
- Provided in milligram quantities for laboratory studies.
Medchemexpress LLC Lobenzarit | 63329-53-3 | MFCD00866065 | 99.4% | 291.69 g/mol | C14H10ClNO4 | 5MG
Lobenzarit is a small-molecule immunomodulator and benzoic acid derivative provided for research applications. It is used in in vitro and preclinical studies to investigate immunomodulatory pathways and antioxidant-related effects. The compound has the chemical formula C14H10ClNO4, a molecular weight of approximately 291.69 g/mol, and is typically supplied at high purity for biochemical assays. Intended for research use only; not for human or veterinary use.
- High purity (≈99.4%) suitable for biochemical assays.
- Defined chemical identity and molecular weight for reproducible studies.
- Applicable to in vitro immunomodulation and antioxidant research.
- Useful for pharmacological mechanism-of-action investigations.
- Documentation available for quality verification, including COA and SDS.
Medchemexpress LLC Lycoramine | 21133-52-8 | 99.8% | 289.37 g/mol | C17H23NO3 | 10 MG
Lycoramine is a dihydro-derivative of galanthamine isolated from Lycoris radiata. It functions as a potent acetylcholinesterase (AChE) inhibitor and is supplied for research use in biochemical and pharmacological studies. Refer to the manufacturer's documentation for COA and SDS.
- Potent acetylcholinesterase inhibitor used in in vitro assays.
- Available as a solid powder suitable for solution preparation.
- High purity (~99.8%), with certificate of analysis available.
- Applicable to neuroscience and cholinergic pathway research.
- Documented chemical identifiers: CAS 21133-52-8; formula C17H23NO3.
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.