Tetrahydrofuran

Medchemexpress LLC Methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate | 173436-66-3 | 99.8% | 50MG

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Methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate | 173436-66-3 | 99.8% | 50MG

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Medchemexpress LLC Methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate | 173436-66-3 | ≥95.0% | 10MG

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Methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate | 173436-66-3 | ≥95.0% | 10MG

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eMolecules​ Ambeed / (3aR3bS7aR8aR)-2255-Tetramethyltetrahydro-7H-[13]dioxolo[4545]furo[32-d][13]dioxine / 5g / 572926723 / A181940 / / 20881-04-3 / MFCD00063224 / 230.260 / C11H18O5

Ambeed / (3aR3bS7aR8aR)-2255-Tetramethyltetrahydro-7H-[13]dioxolo[4545]furo[32-d][13]dioxine / 5g / 572926723 / A181940 / / 20881-04-3 / MFCD00063224 / 230.260 / C11H18O5

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Medchemexpress LLC BMS-1001 hydrochloride | 2113650-04-5 | 98.0% | 25 MG

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A small-molecule hydrochloride salt developed as an orally active inhibitor of the PD-1/PD-L1 immune checkpoint. Intended for preclinical research applications, it is supplied at research-grade purity with batch-specific documentation.

• Orally active PD-1/PD-L1 inhibitor for immunology research.
• Hydrochloride salt form to improve solubility.
• High purity suitable for preclinical studies (≈98.0%).
• Available in small-scale quantities for screening and assays.
• Supplied with certificate of analysis and batch data.

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Medchemexpress LLC Cil62 | 117593-36-9 | 97.0% | C23H26O5 | 10MG

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CIL62 is a small-molecule research compound that induces caspase-3/7-independent cell death through a necrostatin-1-dependent pathway. It is supplied as a purified powder for laboratory research use only; consult the datasheet and SDS for handling, stability, and safety information.

• Induces caspase-3/7-independent cell death via a necrostatin-1-dependent mechanism.
• Molecular formula C23H26O5; molecular weight 382.45 g/mol.
• Purity 97.0% by HPLC.
• Available as a powder in multiple package sizes for laboratory research.
• Recommended storage: powder at -20°C for long-term, 4°C for short-term.

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Medchemexpress LLC GW406108X 100mg | 1644443-92-4 | 100 MG

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GW406108X is a small-molecule research inhibitor that targets Kif15 (Kinesin-12) and ULK1, reported to inhibit autophagy via ATP-competitive inhibition of ULK1. Supplied as a solid, light yellow to yellow powder for laboratory research use only.

• Potent autophagy inhibitor: ULK1 pIC50 6.37 (≈427 nM); Kif15 ATPase IC50 0.82 μM.
• Specified purity: 98.0%.
• Molecular weight: 400.21 and formula C20H11Cl2NO4.
• Appearance: light yellow to yellow solid.
• Recommended storage: powder at -20°C for long term; in solvent, -80°C for up to 6 months.
• Available in multiple pack sizes including 100 mg.

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Medchemexpress LLC AZD5423 100mg | 1034148-04-3 | 100MG

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AZD5423 is an inhaled potent selective and non-steroidal glucocorticoid receptor (GR) modulator (SGRM)[1 AZD5423 effectively reduces allergen-induced responses in subjects with mild allergic asthma[2

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Medchemexpress LLC Resorcinolnaphthalein | 41307-63-5 | 99.9% | 100 MG

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Resorcinolnaphthalein (CAS 41307-63-5) is a synthetic spiro dye used as a biochemical reagent for colorimetric and enzymatic assays. Supplied as a dry solid, it is intended for analytical and research applications; handle according to the SDS and COA.

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Medchemexpress LLC 1-(1-ethylpiperidin-4-yl)sulfonyl-3-(1,2,3,5,6,7-hexahydro-s-indacen-4-yl)urea | 2260969-36-4 | MFCD34579587 | 99.5% | C20H29N3O3S | 10MG

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Selnoflast is an orally active, potent, selective, and reversible small-molecule inhibitor of the NLRP3 inflammasome for research use. It is supplied as a white to off-white solid with high reported purity, and the manufacturer provides solubility and storage guidance for preparation and stability in in vitro and preclinical workflows.

• Potent and selective NLRP3 inflammasome inhibition.
• Reversible small-molecule mechanism enabling temporal studies.
• High reported purity for consistent experimental results.
• Solid form suitable for standard laboratory storage and handling.
• Documented solubility in DMSO and alkaline media with preparation notes.
• Specified storage recommendations for powder and solution stability.
• Multiple pack sizes available to support different study scales.

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Medchemexpress LLC G5-7 25mg | 939681-36-4 | 25 MG

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G5-7 is an orally active, allosteric JAK2 inhibitor used for research applications. It selectively inhibits JAK2-mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3, and has been reported to induce cell cycle arrest, promote apoptosis, and exhibit antiangiogenic effects.

• Allosteric JAK2 inhibitor with oral activity.
• Selective inhibition of JAK2-mediated EGFR and STAT3 phosphorylation.
• Reported to induce cell cycle arrest and apoptosis.
• Exhibits antiangiogenic activity and glioma research relevance.
• Provided as a solid; 25 mg pack available.
• High purity (approximately 99.6%).

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eMolecules​ 2-OXABICYCLO[2.2.1]HEPTANE-5-CARBOXYLIC ACID, 3-OXO-, (1R,4R,5R)-CINCHONIDINE SALT | 1233219-43-6 | | 5g

AstaTech | 2-OXABICYCLO[2.2.1]HEPTANE-5-CARBOXYLIC ACID, 3-OXO-, (1R,4R,5R)-CINCHONIDINE SALT | 5g | 410714116 | P14524 | 95.000 | 1233219-43-6 | | 450.535 | C26H30N2O5

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Medchemexpress LLC Nusinersen | 1258984-36-9 | 98.9% | 7127.3 g/mol | C234H340N61O128P17S17 | 5 MG

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Nusinersen is an antisense oligonucleotide that modulates SMN2 pre-mRNA splicing to increase production of full-length survival motor neuron (SMN) protein. This research-grade material (CAS 1258984-36-9) is supplied as a purified oligonucleotide for laboratory biochemical and cellular studies; typical pack size is 5 mg and reported purity is 98.91%.

• Antisense oligonucleotide for SMN2 splicing modulation.
• High purity (approximately 98.9%) suitable for biochemical assays.
• Supplied as a solid oligonucleotide for in vitro and ex vivo use.
• Applicable to studies of spinal muscular atrophy mechanisms and SMN biology.
• Characterized by defined molecular formula and molecular weight for reproducible experiments.

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Medchemexpress LLC Smyrindioloside | 87592-77-6 | 424.40 | 1 MG

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Smyrindioloside is a natural product isolated from the bark of *Streblus indicus*. It is for research use only and not sold to patients.

• High purity: 99.32%
• White to off-white solid appearance
• Available in various quantities, including 1 mg, 5 mg, 10 mg, and 50 mg
• In-stock availability for 1 mg size
• Detailed documentation available, including data sheet, COA, and SDS

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Medchemexpress LLC Zectivimod | 1623066-63-6 | 99.4% | C28H31Cl2N3O3 | 10MG

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Zectivimod is a sphingosine-1-phosphate (S1P) receptor agonist supplied for preclinical research into immune modulation, autoimmune disorders, and chronic inflammatory disease models. It is provided as a solid research chemical with solubility and formulation guidance for in vitro and in vivo studies.

• Acts as a sphingosine-1-phosphate receptor agonist for immunomodulation studies.
• High purity (≈99.4%) suitable for preclinical research.
• Available in multiple small-scale pack sizes for dosing and formulation work.
• Soluble in DMSO with explicit in vivo formulation protocols available.
• Storage and stability guidance provided for solid and solvent conditions.

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Medchemexpress LLC 24-Methylenecycloartanyl ferulate | 469-36-3 | 10 MG

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24-Methylenecycloartanyl ferulate is a γ-oryzanol compound that promotes parvin-beta expression in human breast cancer cells. It is also identified as a potential ATP-competitive Akt1 inhibitor.

• A γ-oryzanol compound
• Promotes parvin-beta expression in human breast cancer cells
• Functions as a potential ATP-competitive Akt1 inhibitor (EC50 = 33.3 μM)

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