Tetrahydrofuran
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Filtered Search Results
eMolecules 3-Oxotetrahydrofuran | Combi-Blocks | 22929-52-8 | MFCD07778393 | 86.090 | C4H6O2 | 98.000 | O=C1CCOC1 | 25g | 213791601
3-Oxotetrahydrofuran | Combi-Blocks | 22929-52-8 | MFCD07778393 | 86.090 | C4H6O2 | 98.000 | O=C1CCOC1 | 25g | 213791601
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Medchemexpress LLC D-serine, N-[[2-[(3-cyanophenyl)methoxy]-4-...]] hydrochloride (1:1) | 2113650-04-5 | 98.0% | 50 MG
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BMS-1001 hydrochloride is a small-molecule inhibitor of the PD-1/PD-L1 interaction supplied as the hydrochloride salt for research use. It is described as orally active and exhibits low cellular toxicity, and is provided as a solid with high purity suitable for cellular assays and interaction studies.
- Orally active PD-1/PD-L1 interaction inhibitor.
- High purity (98.0%).
- Molecular weight 631.11 g·mol⁻1.
- Solid appearance; store sealed and away from moisture.
- Storage in solvent: -80°C up to 6 months, -20°C up to 1 month.
- Available in small milligram pack sizes for research use.
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Medchemexpress LLC Rhodojaponin III | 26342-66-5 | MFCD01714943 | 99.8% | 368.46 | C20H32O6 | 10 MG
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Rhodojaponin III is a grayanane-type diterpenoid isolated from the leaves of Rhododendron molle. It is supplied as a high-purity research reagent for in vitro studies of anti-inflammatory activity and related biochemical research. For research use only; not for human or clinical use.
- High purity suitable for research applications.
- Reported anti-inflammatory biological activity.
- Available in small quantities for assay development and screening.
- Provided as a solid powder for laboratory handling.
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Medchemexpress LLC 1-(1-(3-methoxyphenyl)-7-propoxyindolizin-3-yl)ethanone | 1693766-04-9 | MFCD30186082 | 99.5% | 323.39 | C20H21NO3 | 50 MG
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GSK8573 is a small-molecule inactive control compound used in epigenetic reader-domain research and biochemical assays. Supplied as a solid for research use only, it is intended for use as a control in binding studies and compound screening. Store and handle according to the supplier safety data sheet and batch certificate of analysis.
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Medchemexpress LLC Vebicorvir (ABI-H0731) | 2090064-66-5 | 99.7% | 467.44 g·mol^-1 | C19H12F3N3O4S2 | 5 MG
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Vebicorvir (ABI-H0731) is a research-grade small-molecule inhibitor of the hepatitis B virus (HBV) core protein. It functions as a core protein allosteric modulator that suppresses formation of covalently closed circular DNA (cccDNA) in cellular infection models. For research use only.
- Inhibits HBV core protein via allosteric modulation.
- Suppresses cccDNA formation in cellular models (reported EC50 1.84-7.3 μM).
- High chemical purity suitable for biochemical and cellular assays.
- Molecular formula C19H12F3N3O4S2; molecular weight 467.44 g·mol^-1.
- Supplied as a solid, soluble in common organic solvents.
- For research use only; not for human or clinical use.
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Medchemexpress LLC Liensinine perchlorate | 2385-63-9 | MFCD09953798 | 99.7% | 711.20 g/mol | C37H42N2O6·xHClO4 | 10 MG
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Liensinine perchlorate is the perchlorate salt of liensinine, an alkaloid from Nelumbo nucifera supplied as a research reagent. It is used in vitro for biological studies and has reported anti-hypertensive and anti-cancer activities, including induction of apoptosis in colorectal cancer cells. Sold for research use only.
- High purity (99.67%).
- Available in small milligram quantities for screening and mechanistic studies.
- Perchlorate salt form improves solubility for biological assays.
- Identified by CAS number 2385-63-9 for unambiguous chemical reference.
- Handle with appropriate laboratory safety precautions; not for clinical use.
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Medchemexpress LLC Benzobicyclon | 156963-66-5 | MFCD09751259 | 98.0% | 446.97 | C22H19ClO4S2 | 10 MG
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Benzobicyclon analytical standard is supplied for research and analytical applications as a reference material. It is a 4-HPPD inhibitor herbicide that hydrolyzes in water to form the active herbicidal species, producing bleaching and death in susceptible plants. The material is provided at high purity for accurate analytical and testing use.
- Intended for research and analytical applications.
- High purity suitable for reference and analytical workflows.
- Hydrolyzes in water to form the active herbicide.
- Effective against grass, sedge, and broadleaf weeds.
- Suitable for analytical quantification and method development.
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Medchemexpress LLC Erk1/2 inhibitor 2 (ASTX-029) | 2095719-92-7 | >98.0% | 584.04 g/mol | C29H31ClFN5O5 | 25MG
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ASTX029 is a dual-mechanism extracellular signal-regulated kinase (ERK) 1/2 inhibitor developed as a clinical candidate. It inhibits ERK catalytic activity and ERK phosphorylation, with reported ERK2 IC50 ≈ 2.7 nM, and has demonstrated antineoplastic activity in preclinical models and early clinical evaluation. Supplied as a crystalline solid for research use, typical vendor-reported purity is ≥98% (CAS 2095719-92-7).
- Potent dual-mechanism ERK inhibitor with low-nanomolar potency.
- Inhibits both catalytic activity and phosphorylation of ERK.
- Demonstrated antineoplastic activity in preclinical and early clinical studies.
- Supplied as a crystalline solid suitable for in vitro and in vivo formulation.
- Typical purity ≥98% by vendor testing.
- CAS number 2095719-92-7 and molecular weight ≈584.04 g/mol.
- For research use only; not for human therapeutic use.
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Medchemexpress LLC 1-(1-(3-methoxyphenyl)-7-propoxyindolizin-3-yl)ethan-1-one | 1693766-04-9 | 99.5% | 323.39 g·mol⁻¹ | C20H21NO3 | 25 MG
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GSK8573 is a small-molecule research reagent used as a structurally related inactive control for acetyl-lysine competitive bromodomain inhibitors. It exhibits measurable binding to BRD9 (Kd ≈ 1.04 μM) and is supplied with characterization data and storage recommendations for reliable use in biochemical and cell-based assays.
- High purity, supporting reproducible experimental results (reported ≈99.5%).
- Validated as an inactive control for bromodomain inhibitor studies.
- Measurable BRD9 binding, useful for target engagement comparisons.
- Available in multiple pack sizes to suit assay throughput needs.
- Detailed solubility and storage guidance for sample preparation and stability.
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Medchemexpress LLC Naz2329 | 2809469-05-2 | 99.0% | 501.56 g·mol⁻¹ | C21H18F3NO4S3 | 50 MG
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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).
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Medchemexpress LLC p-Ethynylphenylalanine hydrochloride | 188640-63-3 | 99.23% | 225.67 | 50 MG
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p-Ethynylphenylalanine hydrochloride (4-Ethynyl-L-phenylalanine hydrochloride) is a potent, selective, reversible, and competitive inhibitor of tryptophan hydroxylase (TPH), with a Ki of 32.6 μM. It is also a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Potent, selective, reversible, and competitive inhibitor of tryptophan hydroxylase (TPH).
- Click chemistry reagent.
- Contains an Alkyne group for CuAAc reactions.
- Selectively and reversibly inhibits the biosynthesis of serotonin.
- Decreases 5-HT and 5-HIAA levels in the rat midbrain (at 30 mg/kg; i.p.).
- Does not inhibit aromatic amino acid decarboxylase.
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Medchemexpress LLC Spiro[1H,3H-naphtho[1,8-cd]pyran-1,9'-[9H]xanthen]-3-one, 3',6'-dihydroxy- | 41307-63-5 | 99.9% | 25 MG
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Resorcinolnaphthalein is a small-molecule research reagent (C24H14O5) used as an ACE2 enhancer in biochemical assays. It is supplied as a high-purity solid suitable for in vitro research.
- Functions as an ACE2 enhancer with reported EC50 of 19.5 μM.
- High purity as measured by LCMS (99.9%).
- Provided as a light yellow to orange solid; available in solid quantities and as a 10 mM solution in DMSO.
- Molecular weight 382.4 g/mol; formula C24H14O5.
- Intended for research use only and not for human use.
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Medchemexpress LLC Mpt0b392 | 1346169-92-3 | 99.6% | 404.44 g/mol | C19H20N2O6S | 10 MG
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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.
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Medchemexpress LLC DS08210767 | 2376334-75-5 | 99.4% | 513.67 | C31H39N5O2 | 25MG
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DS08210767 is a small-molecule antagonist of the parathyroid hormone receptor 1 (PTHR1) for research use. It is reported to be orally bioavailable and shows an in vitro IC50 of 90 nM against PTHR1. The compound is supplied as a light yellow to yellow solid with high reported purity and is intended for biochemical and cellular studies; follow manufacturer storage recommendations.
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eMolecules AstaTech / 25-BIS(BROMOMETHYL)TEREPHTHALONITRILE / 0.1g / 696742362 / D81099 / 95.000 / 64746-04-9 / [null] / 313.980 / C10H6Br2N2
AstaTech / 25-BIS(BROMOMETHYL)TEREPHTHALONITRILE / 0.1g / 696742362 / D81099 / 95.000 / 64746-04-9 / [null] / 313.980 / C10H6Br2N2
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