Fluorobenzenes

Fluconazole, USP, 98-102%, Spectrum™ Chemical

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CAS: 86386-73-4 Molecular Formula: C13H12F2N6O Molecular Weight (g/mol): 306.28 InChI Key: RFHAOTPXVQNOHP-UHFFFAOYSA-N IUPAC Name: 2-(2,4-difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol SMILES: OC(CN1C=NC=N1)(CN1C=NC=N1)C1=CC=C(F)C=C1F

eMolecules​ 3-(2-Fluorophenyl)-4,5,6,7-tetrahydro-2H-pyrazolo [4,3-c]pyridine | 916423-12-6 | MFCD09258791 | 250mg

Oakwood Chemical | 3-(2-Fluorophenyl)-4,5,6,7-tetrahydro-2H-pyrazolo [4,3-c]pyridine | 250mg | 537693788 | 046437 | | 916423-12-6 | MFCD09258791 | 217.247 | C12H12FN3

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eMolecules​ ChemScene / 2-(4-Fluorophenyl)-67-dihydro-5H-pyrrolo[12-a]imidazole / 100mg / 711935230 / CS-0160040 / 0.000 / 111883-62-6 / MFCD27941578 / 202.232 / C12H11FN2

ChemScene / 2-(4-Fluorophenyl)-67-dihydro-5H-pyrrolo[12-a]imidazole / 100mg / 711935230 / CS-0160040 / 0.000 / 111883-62-6 / MFCD27941578 / 202.232 / C12H11FN2

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eMolecules​ AstaTech / 2-(4-FLUOROPHENYL)-88-DIMETHYL-78-DIHYDROIMIDAZO[12-A]PYRAZIN-6(5H)-ONE / 0.1g / 696739587 / 69248 / 95.000 / 1261118-04-0 / MFCD22690264 / 259.284 / C14H14FN3O

AstaTech / 2-(4-FLUOROPHENYL)-88-DIMETHYL-78-DIHYDROIMIDAZO[12-A]PYRAZIN-6(5H)-ONE / 0.1g / 696739587 / 69248 / 95.000 / 1261118-04-0 / MFCD22690264 / 259.284 / C14H14FN3O

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Accela Chembio Inc (8r | 9s | 10r | 13s | 14s)-10 | 13-dimethylspiro[7 | 8 | 9 | 11 | 12 | 13 | 15 | 16-octahydro-6h-cyclopenta[a]phenanthrene-6 | 2'-oxirane]-3 | 17(10h | 14h)-dione | 1g | 184972-12-1 | MFCD19442795 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4

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(8r | 9s | 10r | 13s | 14s)-10 | 13-dimethylspiro[7 | 8 | 9 | 11 | 12 | 13 | 15 | 16-octahydro-6h-cyclopenta[a]phenanthrene-6 | 2'-oxirane]-3 | 17(10h | 14h)-dione | 1g | 184972-12-1 | MFCD19442795 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4

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Accela Chembio Inc (8r | 9s | 10r | 13s | 14s)-10 | 13-dimethyl-7 | 8 | 9 | 11 | 12 | 13 | 15 | 16-octahydro-10h-cyclopenta[a]phenanthrene-3 | 6 | 17(14h)-trione | 1g | 72648-46-5 | MFCD19442767 | 95+% | Shelf Life: 1440 Days | Light Sensitive/+4

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(8r | 9s | 10r | 13s | 14s)-10 | 13-dimethyl-7 | 8 | 9 | 11 | 12 | 13 | 15 | 16-octahydro-10h-cyclopenta[a]phenanthrene-3 | 6 | 17(14h)-trione | 1g | 72648-46-5 | MFCD19442767 | 95+% | Shelf Life: 1440 Days | Light Sensitive/+4

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Medchemexpress LLC IK1 inhibitor PA-6 | 500715-03-7 | 99.3% | 492.61 | 50 MG

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IK1 inhibitor PA-6, a pentamidine analogue, is a selective and potent IK1 (KIR2.x ion-channel-carried inward rectifier current) inhibitor. It has IC50 values of 12-15 nM for human and mouse KIR2.x currents and elevates KIR2.1 protein expression, inducing intracellular KIR2.1 accumulation. This inhibitor has the potential to treat atrial fibrillation and arrhythmia.

• Selective and potent IK1 inhibitor
• IC50 values of 12-15 nM for human and mouse KIR2.x currents
• Elevates KIR2.1 protein expression
• Induces intracellular KIR2.1 accumulation
• Potential to treat atrial fibrillation
• Potential to treat arrhythmia

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Medchemexpress LLC IK1 inhibitor PA-6 | 500715-03-7 | 99.3% | 492.61 | 10 MG

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IK1 inhibitor PA-6, a pentamidine analogue, is a selective and potent IK1 (KIR2.x ion-channel-carried inward rectifier current) inhibitor, with IC50 values of 12-15 nM for human and mouse KIR2.x currents. It elevates KIR2.1 protein expression and induces intracellular KIR2.1 accumulation. This product has the potential to treat atrial fibrillation and arrhythmia.

• It is a selective and potent IK1 inhibitor.
• It has IC50 values of 12-15 nM for human and mouse KIR2.x currents.
• It elevates KIR2.1 protein expression.
• It induces intracellular KIR2.1 accumulation.
• It has the potential to treat atrial fibrillation and arrhythmia.

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Medchemexpress LLC Vitexin-2"-O-rhamnoside | 64820-99-1 | MFCD29913069 | 578.52 | 5 MG

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Vitexin-2"-O-rhamnoside is an orally active flavonoid glycoside that inhibits Apoptosis, increases the phosphorylation levels of PI3K/Akt, inhibits caspase-3, SOD activity, and promotes cytokine (IL-2, IL-6, and IL-12) secretion. It strongly inhibits DNA synthesis in MCF-7 cells with an IC50 of 17.5 μM, enhances immune function, improves the absorption of active compounds, and has antioxidant activity. It is used in the study of cardiovascular disease and immune-related diseases.

• Inhibits apoptosis.
• Increases phosphorylation levels of PI3K/Akt.
• Inhibits caspase-3 and SOD activity.
• Promotes cytokine (IL-2, IL-6, and IL-12) secretion.
• Strongly inhibits DNA synthesis in MCF-7 cells with an IC50 of 17.5 μM.
• Enhances immune function.
• Improves absorption of active compounds.
• Has antioxidant activity.
• Used in the study of cardiovascular disease and immune-related diseases.

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Medchemexpress LLC STING agonist-12 | 2259624-71-8 | MFCD34676739 | 98.3% | 490.88 g/mol | C25H19ClF4N2O2 | 5 MG

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STING agonist-12 is a non-nucleotide, orally active small-molecule activator of human STING intended for research use. It demonstrates potent STING activation in cell-based assays and is provided as a high-purity solid suitable for in vitro and in vivo studies.

• Activates human STING (EC50 185 nM).
• Orally active small molecule suitable for in vivo studies.
• High purity: 98.3%.
• Molecular weight 490.88 g/mol; formula C25H19ClF4N2O2.
• Soluble in DMSO at 250 mg/mL; ultrasonic assistance recommended.
• Store protected from light; short-term 4°C; in solvent: -80°C for 6 months, -20°C for 1 month.
• Supplied in mg-scale quantities for research applications.

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Medchemexpress LLC Dp-c-4 (EGFR PARP dual-targeting PROTAC) | 00-00-0 | 98.2% | 1450.93 | C72H78ClF2N15O14 | 5 MG

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DP-C-4 is a Cereblon-based dual PROTAC that induces simultaneous degradation of EGFR and PARP in vitro, showing dose-dependent effects in cellular assays (1-50 μM; 24 h). It is intended for research into targeted protein degradation and dual-target therapeutic strategies, supplied as a high-purity solid with specific storage and solubility recommendations.

• High purity: 98.15%.
• Dual-target activity: degrades EGFR and PARP simultaneously.
• Validated in cell assay: dose-dependent degradation in SW1990 cells (1-50 μM; 24 h).
• Appearance: light yellow to green yellow solid.
• Solubility: DMSO 12 mg/mL; may require ultrasonic agitation.
• Storage: -80°C under nitrogen; stock solution stable up to 6 months.

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Medchemexpress LLC IK1 inhibitor PA-6 | 500715-03-7 | 99.3% | 492.61 g/mol | C31H32N4O2 | 5 MG

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IK1 inhibitor PA-6 is a selective and potent inhibitor of inward rectifier potassium (IK1) currents used in electrophysiology and ion-channel research. Supplied as an off-white to light yellow solid, the compound includes detailed solubility and storage specifications for both in vitro and in vivo studies.

• Selective inhibitor of inward rectifier potassium currents with IC50 ≈ 12-15 nM.
• High purity (99.29%).
• Molecular formula C31H32N4O2; molecular weight 492.61 g/mol.
• Off-white to light yellow solid appearance.
• Soluble in DMSO at 125 mg/mL; in vivo formulations ≥ 2.08 mg/mL using recommended vehicle protocols.
• Recommended storage: powder at -20°C (3 years) or 4°C (2 years); solutions at -80°C (2 years) or -20°C (1 year).
• For research use only; not intended for human or diagnostic use.

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Medchemexpress LLC STING Agonist-12 | 2259624-71-8 | 98.3% | 490.88 | 50 MG

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STING agonist-12 is a potent, orally active human STING activator with an EC50 of 185 nM. It demonstrates excellent pan-polymorph activity across STING proteins in HEK293T cells. This compound is well-absorbed in animal models, exhibiting a short terminal half-life. For research use only.

• Potent, orally active human STING activator
• EC50 of 185 nM against STING
• Excellent pan-polymorph activity
• Not active at mouse STING
• Well-absorbed in animal models
• Short terminal half-life
• Appearance: Solid, light yellow to yellow
• Shipping: Room temperature (continental US)
• Storage: 4°C, protect from light (solid)
• Storage in solvent: -80°C for 6 months; -20°C for 1 month (protect from light)

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