Tetrahydrofuran
Medchemexpress LLC Bifenthrin | 82657-04-3 | MFCD00143694 | 99.8% | 422.87 | C23H22ClF3O2 | 10 MG
Bifenthrin is a synthetic pyrethroid insecticide supplied as an analytical standard for research and analytical applications. It is intended for use as a reference material in qualitative and quantitative analysis, method development, and instrument calibration for chromatographic and mass spectrometric techniques.
- Analytical standard suitable for HPLC, GC, and MS.
- High purity (99.8% by LCMS).
- Molecular formula C23H22ClF3O2; molecular weight 422.87.
- Off-white to white solid physical form.
- Store under recommended conditions shown on the certificate of analysis.
![Medchemexpress LLC D-serine, N-[[2-[(3-cyanophenyl)methoxy]-4-...]] hydrochloride | 2113650-04-5 | 98.0% | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000232072.png-250.jpg)
Medchemexpress LLC D-serine, N-[[2-[(3-cyanophenyl)methoxy]-4-...]] hydrochloride | 2113650-04-5 | 98.0% | 100 MG
BMS-1001 hydrochloride is a small-molecule inhibitor of the PD-1/PD-L1 interaction supplied as the hydrochloride salt for research use. It shows potent binding activity and is intended for in vitro studies of immune checkpoint pathways.
- Orally active PD-1/PD-L1 inhibitor with low cellular toxicity.
- IC50 of 2.25 nM in HTRF binding assay.
- Molecular weight 631.11 and formula C35H35ClN2O7.
- High purity (98.0%) suitable for research applications.
- Provided as a hydrochloride salt to aid solubility in assay buffers.
Medchemexpress LLC 2-methoxyethyl 4-((4-(4-chlorophenoxy)-3,5-difluorophenyl)sulfonyl)-3-(hydroxycarbamoyl)piperaz... | 1224964-36-6 | 98.3% | 548.92 | C21H21ClF2N3O8S | 10 MG
XL-784 is a small-molecule selective matrix metalloproteinase (MMP) inhibitor provided for research use. It exhibits potent activity across multiple MMP isoforms and is applied in studies of extracellular matrix remodeling, tumor invasion, and metastasis.
- Selective inhibition of multiple MMPs with reported IC50s in the subnanomolar to micromolar range (e.g., MMP-13 0.56 nM, MMP-2 0.81 nM).
- Suitable for biochemical and cell-based studies of extracellular matrix and cancer biology.
- High purity (98.3%) for reliable experimental outcomes.
- Provided as a solid and as a DMSO solution for flexible dosing.
- Molecular weight 548.92 g/mol; CAS number 1224964-36-6.
Medchemexpress LLC Naz2329 | 2809469-05-2 | 99.0% | 501.56 g·mol⁻¹ | C21H18F3NO4S3 | 50 MG
NAZ2329 is a small-molecule research inhibitor that allosterically and preferentially inhibits receptor-type protein tyrosine phosphatases PTPRZ and PTPRG. It is supplied as a solid for laboratory research and is characterized by high purity and established solubility in DMSO.
- Allosterically inhibits PTPRZ and PTPRG (reported IC50: PTPRZ 7.5 μM, PTPRG 4.8 μM).
- Cas number 2809469-05-2.
- Purity 99.02%.
- Molecular formula C21H18F3NO4S3.
- Molecular weight 501.56 g·mol⁻¹.
- Appearance solid, white to off-white.
- Soluble in DMSO (~100 mg/mL).
- Pack size 50 mg.
- Storage: powder -20°C (up to 3 years) or 4°C (up to 2 years).
Medchemexpress LLC D-α-tocopherylquinone | 7559-04-8 | MFCD00135657 | 98.9% | 446.71 | C29H50O3 | 10 MG
- Oxidation product of α-tocopherol with quinone structure.
- Exhibits antioxidant and anticoagulant activity.
- Reduces oxidative damage from oxidized lipids.
- Interacts with glutathione-S-transferase (GST).
- Used in reactive oxygen species (ROS) and lipid peroxidation research.
- Molecular formula C29H50O3; MW 446.71 Da.
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran anhydrous
Tetrahydrofuran (THf) is a saturated cyclic ether mainly used as an organic solvent. On long term storage it forms organic peroxides. This process can be suppressed by adding butylated hydroxytoluene (BHT) as a stabilizer. BHT removes the free radicals required for the peroxide formation. It constitutes the key fragment of various natural products (polyether antibiotics). THf forms double hydrate with hydrogen sulfide crystal structure of this double hydrate has been investigated by three-dimensional single-crystal studies.
Medchemexpress LLC Mpt0b392 | 1346169-92-3 | 99.6% | 404.44 g/mol | C19H20N2O6S | 10 MG
MPT0B392 is a research-grade microtubule-depolymerizing agent for preclinical studies of tubulin dynamics and cancer drug resistance. It is an orally active quinoline derivative that inhibits tubulin polymerization, activates c-Jun N-terminal kinase (JNK), induces mitotic arrest, and promotes apoptosis. Supplied as a solid or as a 10 mM solution in DMSO for in vitro and in vivo research use.
- Novel microtubule-depolymerizing mechanism supporting tubulin studies.
- Induces JNK activation and mitotic arrest for apoptosis research.
- Available as solid or 10 mM solution in DMSO for flexible dosing.
- High listed purity (99.63%) suitable for biochemical assays.
- Documented molecular weight and formula to aid experimental planning.
Medchemexpress LLC Nateglinide | 105816-04-4 | MFCD00875706 | 99.95% | 100 MG
Nateglinide is a D-phenylalanine derivative that acts as an orally active, short-acting insulinotropic agent and a DPP IV inhibitor. It functions by inhibiting ATP-sensitive K+ channels in pancreatic β-cells and is utilized in the treatment of type 2 (non-insulin-dependent) diabetes mellitus. This product is intended for research use only and is not sold to patients.
- Acts as an orally active, short-acting insulinotropic agent
- Functions as a DPP IV inhibitor
- Inhibits ATP-sensitive K+ channels in pancreatic β-cells
- Used for the treatment of type 2 diabetes mellitus
- Inhibits dinitrophenol-induced KATP currents
- Stimulates human C-peptide secretion
- Improves postprandial glucose concentrations
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran anhydrous
Tetrahydrofuran (THf) is a saturated cyclic ether mainly used as an organic solvent. On long term storage it forms organic peroxides. This process can be suppressed by adding butylated hydroxytoluene (BHT) as a stabilizer. BHT removes the free radicals required for the peroxide formation. It constitutes the key fragment of various natural products (polyether antibiotics). THf forms double hydrate with hydrogen sulfide crystal structure of this double hydrate has been investigated by three-dimensional single-crystal studies.
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran d8 99.5 at
Tetrahydrofuran-d8 (THf-d8 TDf) is a deuterated NMR solvent useful in NMR-based research and analyses. 1H NMR line shape analysis of the exchange rates of proton between methanol and acetic acid dissolved in THf-d8 was reported. It participates as a solvent in the synthesis of deuteriotris[bis(trimethylsilyl)amido]thorium and deuteriotris[bis(trimethylsiiyl)amido]uranium. Dynamic NMR spectroscopic study of 15N 15NAE-dipentadeuterophenylformamidine (DPfA) has been studied in THf-d8.
Medchemexpress LLC Morphiceptin | 74135-04-9 | 99.1% | 521.61 | 10 MG
Morphiceptin is a potent and specific agonist for morphine (μ) receptors. It is a synthetic peptide, an amide of a fragment of the milk protein β-casein. Morphiceptin exhibits morphinelike activities and shows high specificity for morphine (μ) receptors, but not for Enkephalin receptors. It potently inhibits the binding of [3H]dihydromorphine, 125I-labeled FK33824, and [3H]naloxone to rat brain membrane preparations with an IC50 of about 20 nM.
- Potent and specific agonist for morphine (μ) receptors
- Synthetic peptide derived from β-casein
- Exhibits morphinelike activities
- High specificity for morphine (μ) receptors over Enkephalin receptors
- Inhibits binding of [3H]dihydromorphine, 125I-labeled FK33824, and [3H]naloxone to rat brain membrane preparations
Medchemexpress LLC Sonlicromanol | 1541170-75-5 | 99.8% | 25MG
Sonlicromanol | 1541170-75-5 | 99.8% | 25MG
![Medchemexpress LLC 2-((4-(Benzo[d]thiazol-5-ylamino)-6-(tert-butylsulfonyl)quinazolin-7-yl)oxy)ethyl Dihydrogen Phosphate | 99.5% | 612.63 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000439242-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2-((4-(Benzo[d]thiazol-5-ylamino)-6-(tert-butylsulfonyl)quinazolin-7-yl)oxy)ethyl Dihydrogen Phosphate | 99.5% | 612.63 | 50 MG
GSK2983559 is an orally active and potent receptor interacting protein 2 (RIP2) kinase inhibitor. It blocks many proinflammatory cytokine responses in vivo and in human inflammatory bowel disease explant samples.
- Blocks MDP-induced IL-8 in THP-1 cells.
- Inhibits MDP-induced IL-6 in mouse.
Medchemexpress LLC CUR61414 | 334998-36-6 | 99.04% | 550.69 | 100 MG
CUR61414 is a novel, potent, and cell-permeable Hedgehog signaling pathway inhibitor. It is a small-molecule aminoproline compound that selectively binds to smoothened (Smo). This compound can induce apoptosis in cancer cells without affecting neighboring non-tumor cells.
- Potent and cell-permeable Hedgehog signaling pathway inhibitor.
- Selectively binds to smoothened (Smo).
- Induces apoptosis in cancer cells.
- Spares neighboring non-tumor cells.
- Exhibits an IC50 of 100-200 nM.