Fluorobenzenes

Organic compounds considered aryl halides that consist of a phenyl group with a fluorine atom substitution in the following structure: C₆H₅F.

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2,731 – 2,745 of 4,403 results

2,731

Medchemexpress LLC GW-870086 | 827319-43-7 | 99.6% | 559.64 | C31H39F2NO6 | 5 MG

GW-870086 is a synthetic glucocorticoid receptor agonist used in research to probe anti-inflammatory signaling. It inhibits NF-κB activity in A549 cells with a reported pIC50 of 10.1 and is supplied with high purity for in vitro pharmacology and cell-based assays.

Potent glucocorticoid receptor agonist active in cell-based NF-κB assays.
Reported pIC50 of 10.1 in A549 NF-κB assay.
High purity (99.59%) suitable for in vitro pharmacology.
Available as powder in multiple mg scales and as a 10 mM solution in DMSO for convenience.
Stable storage recommendations provided for powder and solvent solutions.
Molecular formula C31H39F2NO6; molecular weight 559.64.

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2,732

Medchemexpress LLC CCR2 antagonist 4 (hydrochloride) | 1313730-14-1 | 99.9% | 476.32 g/mol | C21H22Cl2F3N3O2 | 50 MG

CCR2 antagonist 4 hydrochloride is a potent, selective CCR2 receptor antagonist supplied as the hydrochloride salt for biochemical and cell-based research. The compound shows activity against CCR2b and inhibits MCP-1-induced chemotaxis in cellular assays.

Hydrochloride salt suitable for research use.
Molecular formula C21H22Cl2F3N3O2; molecular weight 476.32 g/mol.
Purity 99.9% (as supplied).
Available in small research pack sizes, including 50 mg.
Reported CCR2b and chemotaxis inhibitory activity in cell-based assays.

Pricing & Availability

2,733

eMolecules 586379-66-0 | Medchem Express | PH-797804 | 5mg | 446258469 | HY-10403 | MFCD18251426 | 477.306 | C22H19BrF2N2O3

Medchem Express | PH-797804 | 5mg | 446258469 | HY-10403 | 586379-66-0 | MFCD18251426 | 477.306 | C22H19BrF2N2O3

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2,734

eMolecules 59729-32-7 | Medchem Express | Citalopram (hydrobromide) | 10mg | 446273785 | HY-B1287 | MFCD02101306 | 405.311 | C20H22BrFN2O

Medchem Express | Citalopram (hydrobromide) | 10mg | 446273785 | HY-B1287 | 59729-32-7 | MFCD02101306 | 405.311 | C20H22BrFN2O

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2,735

eMolecules 451492-95-8 | N-(4-((3-Chloro-4-fluorophenyl)amino)-7-(3-methyl-3-(4-methylpiperazin-1-yl)but-1-yn-1-yl)quinazolin-6-yl)acrylamide | MFCD16038939 | 50mg

ChemScene | 5-Bromoisoquinoline-1-carbonitrile | 100mg | 559780268 | CS-0100538 | 956003-76-2 | MFCD17215757 | 233.068 | C10H5BrN2

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2,736

eMolecules 844439-00-5 | 3-Bromo-2,4,6-trifluorobenzotrifluoride | Apollo Scientific | MFCD28140547 | 278.979 | C7HBrF6 | 95.000 | Fc1cc(F)c(c(F)c1Br)C(F)(F)F | 1g | 562441853

3-Bromo-2,4,6-trifluorobenzotrifluoride | Apollo Scientific | 844439-00-5 | MFCD28140547 | 278.979 | C7HBrF6 | 95.000 | Fc1cc(F)c(c(F)c1Br)C(F)(F)F | 1g | 562441853

Pricing & Availability

2,737

eMolecules 35474-99-8 | 1-Monoarachidin (solution in ACN) | Broadpharm | MFCD00673487 | 378.553 | C23H38O4 | 0.000 | CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OCC(O)CO | 5mg | 784455233

1-Monoarachidin (solution in ACN) | Broadpharm | 35474-99-8 | MFCD00673487 | 378.553 | C23H38O4 | 0.000 | CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OCC(O)CO | 5mg | 784455233

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2,738

eMolecules 2741870-03-9 | ChemScene | (S)-3-(1-Aminoethyl)benzonitrile hydrochloride | 100mg | 603128881 | CS-0173269 | MFCD11101269 | 182.65 | C9H11ClN2

Medchem Express | (S)-Ketorolac | 5mg | 482204526 | HY-B0580A | 66635-92-5 | MFCD00871493 | 255.273 | C15H13NO3

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2,739

eMolecules 283173-83-1 | 4-Bromo-2-fluorophenyl-1-(pyrrolidinomethyl)benzene | Combi-Blocks | MFCD09749655 | 258.134 | C11H13BrFN | 95.000 | Fc1cc(Br)ccc1CN1CCCC1 | 1g | 117549777

4-Bromo-2-fluorophenyl-1-(pyrrolidinomethyl)benzene | Combi-Blocks | 283173-83-1 | MFCD09749655 | 258.134 | C11H13BrFN | 95.000 | Fc1cc(Br)ccc1CN1CCCC1 | 1g | 117549777

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2,740

Apexbio Technology LLC TAK-632 1228591-30-7 5mg

TAK-632 (CAS 1228591-30-7) is a selective inhibitor of RAF kinase isoforms including BRAF CRAF and the mutant BRAF-V600E exhibiting IC50 values of 8 3 nM 1 4 nM and 2 4 nM respectively By targeting the RAF family of serine/threonine kinases TAK-632 disrupts the RAS-RAF-MEK-ERK signaling pathway implicated in MAPK cascade regulation In cellular assays TAK-632 promotes BRAF-CRAF dimerization and demonstrates potent antiproliferative effects in A375 and SK-MEL-2 melanoma cell lines with GI50 values of 6 nM and 11 nM respectively In vivo oral administration in SK-MEL-2 xenograft models inhibits ERK phosphorylation and tumor growth without notable toxicity TAK-632 is suitable for investigating RAF-driven signaling and drug resistance in oncogenic pathway studies

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2,741

eMolecules 1400220-51-0 | Ambeed | 2-(3-Bromo-2-fluorophenyl)-4455-tetramethyl-132-dioxaborolane | 1g | 525140931 | A230987 | MFCD22192539 | 300.96 | C12H15BBrFO2

ChemScene | Amino-PEG10-Boc | 100mg | 632318510 | CS-0114548 | 1818294-42-6 | MFCD26127812 | 585.732 | C27H55NO12

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2,742

eMolecules 139911-27-6 | 3-Methyl-4-fluorophenylboronic acid | Ambeed | MFCD01863527 | 153.950 | C7H8BFO2 | 98.000 | Cc1cc(ccc1F)B(O)O | 1g | 552536964

3-Methyl-4-fluorophenylboronic acid | Ambeed | 139911-27-6 | MFCD01863527 | 153.950 | C7H8BFO2 | 98.000 | Cc1cc(ccc1F)B(O)O | 1g | 552536964

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2,743

eMolecules 727-31-1 | N-(4-Fluorophenyl)-4-methylbenzene-1-sulfonamide | Oakwood Chemical | MFCD00595010 | 265.300 | C13H12FNO2S | 98.000 | Cc1ccc(cc1)S(=O)(=O)Nc1ccc(F)cc1 | 100mg | 537708541

N-(4-Fluorophenyl)-4-methylbenzene-1-sulfonamide | Oakwood Chemical | 727-31-1 | MFCD00595010 | 265.300 | C13H12FNO2S | 98.000 | Cc1ccc(cc1)S(=O)(=O)Nc1ccc(F)cc1 | 100mg | 537708541

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2,744

Echelon Biosciences Research Labs BAM 3200 Bovine Adrenal Medulla Peptide E - 1 mg, CAS#: 78355-50-7

BAM 3200 Bovine Adrenal Medulla Peptide E - 1mg , Tyr-Gly-Gly-Phe-Met-Arg-Arg-Val-Gly-Arg-Pro-Glu-Trp-Trp-Met-Asp-Tyr-Gln-Lys-Arg-Tyr-Gly-Gly-Phe-Leu-OH This item is non returnable

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2,745

Apexbio Technology LLC Mequinol 150-76-5 50mg

Mequinol (150-76-5) is a small-molecule inhibitor targeting tyrosinase It is designed to inhibit tyrosinase activity thereby modulating melanogenesis pathways related to skin pigmentation Mequinol exerts its biological activity primarily through inhibition of tyrosinase and displays antioxidant properties cooperating with other phenolic antioxidants to intervene in oxidative mechanisms potentially related to carcinogenesis In addition Mequinol activates human estrogen receptor (hER )-dependent molecular chaperone proteins indicating estrogen-like activities Based on these pharmacological properties Mequinol holds research potential in studies on melanin biosynthesis regulation anti-oxidative cellular responses and estrogen signaling pathway exploration

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Fluorobenzenes

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Medchemexpress LLC GW-870086 | 827319-43-7 | 99.6% | 559.64 | C31H39F2NO6 | 5 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC CCR2 antagonist 4 (hydrochloride) | 1313730-14-1 | 99.9% | 476.32 g/mol | C21H22Cl2F3N3O2 | 50 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC GW-870086 | 827319-43-7 | 99.6% | 559.64 | C31H39F2NO6 | 5 MG

Medchemexpress LLC CCR2 antagonist 4 (hydrochloride) | 1313730-14-1 | 99.9% | 476.32 g/mol | C21H22Cl2F3N3O2 | 50 MG