All ProductsDisplaying Products Alphabetically by Name (F)
| Cat. No. | Product Name / Activity |
|---|---|
| 6253 | F 127 (20% solution in DMSO) |
| Nonionic detergent | |
| 0523 | 4F 4PP oxalate |
| Selective 5-HT2A antagonist | |
| 3414 | FAK Inhibitor 14 |
| Selective FAK inhibitor | |
| 7287 | FAM-DEALA-Hyp-YIPD |
| Fluorescent HIF-1α peptide; can be used to evaluate the effect of VHL binding on degradation activity | |
| 7452 | FAM-DEALAHypYIPMDDDFQLRSF |
| Fluorescent HIF-1α peptide; can be used to evaluate the effect of VHL binding on degradation activity | |
| 7306 | FC 11 |
| Highly potent focal adhesion kinase (FAK) Degrader (PROTAC®) | |
| 0453 | FCCP |
| Oxidative phosphorylation uncoupler | |
| 5200 | FFN 102 mesylate |
| Selective fluorescent substrate of DAT and VMAT2 | |
| 5911 | FFN 200 dihydrochloride |
| Selective fluorescent VMAT2 substrate | |
| 5043 | FFN 206 dihydrochloride |
| Fluorescent VMAT2 substrate | |
| 6717 | FFN 270 |
| Fluorescent substrate for NET and VMAT2 | |
| 3878 | FFN 511 |
| Fluorescent substrate for VMAT2 | |
| 0554 | FG 7142 |
| Benzodiazepine inverse agonist | |
| 0658 | FGIN-1-27 |
| Potent, specific ligand for mitochondrial DBI receptor | |
| 5254 | FH 1 |
| Enhances iPSC-derived hepatocyte differentiation and maturation | |
| 4344 | FH 535 |
| Inhibitor of Wnt/β-catenin signaling | |
| 7644 | FHT 1015 |
| Potent and selective SMARCA4/2 inhibitor | |
| 7645 | FHT 2344 |
| Potent SMARCA2/4 inhibitor | |
| 5304 | FICZ |
| High affinity aryl hydrocarbon receptor (AhR) agonist | |
| 4002 | FIIN 1 hydrochloride |
| Potent, irreversible FGFR inhibitor | |
| 6280 | FIN 56 |
| Ferroptosis activator | |
| 3600 | FIPI |
| Phospholipase D inhibitor | |
| 5440 | FITC |
| Green fluorescent dye | |
| 7627 | FITC-labelled Keap1-Nrf2 probe |
| Fluorescent Keap1-Nrf2 peptide | |
| 6859 | FITM |
| Potent and selective negative allosteric modulator of mGlu1 receptors | |
| 3515 | FK 228 |
| Potent and selective class I histone deacetylase inhibitor; antitumor | |
| 3631 | FK 506 |
| Potent calcineurin inhibitor; immunosuppressant | |
| 8072 | FK 866 New |
| Potent and non-competitive NAMPT inhibitor; induces apoptosis and autophagy | |
| 2400 | FK 888 |
| High affinity NK1 antagonist | |
| 6653 | FM19G11 |
| HIF α-subunit inhibitor | |
| 7158 | FMF-04-159-2 |
| Potent covalent CDK14 and CDK16 inhibitor; also inhibits other TAIRE kinase family members | |
| 7159 | FMF-04-159-R |
| Potent CDK14 and CDK16 inhibitor; displays reversible inhibition of CDK14 | |
| 7373 | FNIR-Tag, NHS |
| Near-infrared fluorescent dye for labeling of amines; supplied as NHS ester | |
| 2926 | FPA 124 |
| Akt/PKB inhibitor | |
| 1403 | FPL 64176 |
| Potent CaV1.x activator | |
| 6237 | FPS ZM1 |
| High affinity antagonist of RAGE | |
| 1507 | FR 122047 hydrochloride |
| Cyclooxygenase (COX-1) inhibitor | |
| 3643 | FR 171113 |
| PAR1 antagonist | |
| 3706 | FR 180204 |
| Selective ERK inhibitor | |
| 5190 | FRAX 486 |
| Potent PAK inhibitor; brain penetrant and orally bioavailable | |
| 6029 | FRAX 597 |
| Potent group I PAK inhibitor | |
| 4751 | FSLLRY-NH2 |
| PAR2 peptide antagonist | |
| 6784 | FTBMT |
| Potent and selective GPR52 agonist; orally bioavailable and BBB permeable | |
| 5000 | FTIDC |
| Potent and selective negative allosteric modulator of mGlu1 receptors; also mGlu1 inverse agonist | |
| 6176 | FTY 720 |
| Potent S1P receptor agonist; also immunosuppressant | |
| 2220 | FURA-2AM |
| Fluorescent Ca2+ indicator | |
| 6323 | FX 1 |
| Bcl-6 inhibitor; 10-fold more potent than endogenous Bcl-6 corepressors | |
| 7290 | Famotidine |
| Potent and high affinity H2 biased inverse agonist | |
| 6100 | Fasentin |
| GLUT1/GLUT4 inhibitor; also Fas-sensitizer | |
| 0541 | Fasudil hydrochloride |
| Inhibitor of cyclic nucleotide dependent- and Rho-kinases | |
| 4444 | Fatostatin A |
| Cell permeable inhibitor of SREBP activation | |
| 7225 | Favipiravir |
| Viral RNA polymerase inhibitor | |
| 4427 | Febuxostat |
| Xanthine oxidase inhibitor | |
| 6407 | Fendiline Hydrochloride |
| Inhibits KRas localization to the plasma membrane; also L-type calcium channel blocker | |
| 2386 | Fenobam |
| Potent and selective mGlu5 negative allosteric modulator (NAM) | |
| 4113 | Fenofibrate |
| PPARα agonist | |
| 1659 | Fenoldopam hydrochloride |
| Selective D1-like partial agonist | |
| 6926 | Fenoprofen calcium |
| Positive allosteric modulator of MC3 receptors; exhibits biased signaling | |
| 1396 | Fenretinide |
| Synthetic retinoid; antiproliferative and antioxidant | |
| 5180 | Ferrostatin 1 |
| Selective inhibitor of erastin induced ferroptosis | |
| 2563 | Fexaramine |
| Potent, selective farnesoid X receptor (FXR) agonist | |
| 6250 | Filipin III |
| Fluorescent cholesterol stain; also polyene antibiotic | |
| 3293 | Finasteride |
| Type II 5α-reductase inhibitor | |
| 5016 | Fisetin |
| Naturally occuring flavonoid and antioxidant; neuroprotective | |
| 3094 | Flavopiridol hydrochloride |
| Cdk inhibitor; potently inhibits cdk2 and cdk9 | |
| 1470 | Flecainide acetate |
| Cardiac Na+ channel blocker. Antiarrhythmic | |
| 3764 | Fluconazole |
| Triazole antifungal agent | |
| 3495 | Fludarabine |
| Purine analog; inhibits DNA synthesis | |
| 4522 | Flufenamic acid |
| Calcium-activated chloride channel blocker; NSAID. Also activates TRPC6 | |
| 1328 | Flumazenil |
| Benzodiazepine antagonist | |
| 6255 | Fluo-4 AM |
| Cell-permeable, fluorescent Ca2+ indicator | |
| 6456 | Fluorescein Tyramide |
| Green fluorescent reagent widely used for signal amplification in IHC and FISH | |
| 6574 | Fluorescein-NAD+ |
| Fluorescent NAD+; substrate for ADP-ribosylation for use in PARP assays | |
| 3257 | 5-Fluorouracil |
| Thymidylate synthetase inhibitor | |
| 0927 | Fluoxetine hydrochloride |
| 5-HT reuptake inhibitor | |
| 4057 | Flupenthixol dihydrochloride |
| Dopamine antagonist | |
| 2867 | Flupirtine maleate |
| KV7 channel activator; also GABAA modulator and indirect NMDA antagonist | |
| 0478 | Flurofamide |
| Urease inhibitor | |
| 4094 | Flutamide |
| Non-steroidal androgen receptor antagonist | |
| 2226 | Flutax 1 |
| Fluorescent taxol derivative; microtubule stain | |
| 6254 | Flutax 2 |
| Green fluorescent taxol derivative; binds microtubules | |
| 2007 | Fluticasone propionate |
| Selective high affinity glucocorticoid receptor agonist | |
| 3309 | Fluvastatin sodium |
| Potent HMG-CoA reductase inhibitor | |
| 1033 | Fluvoxamine maleate |
| 5-HT reuptake inhibitor | |
| 4690 | Fmk |
| Irreversible ribosomal S6 kinase 1/2 inhibitor | |
| 1448 | Formoterol hemifumarate |
| Potent and selective β2 agonist | |
| 1921 | N-Formyl-Met-Leu-Phe |
| Endogenous FPR1 agonist | |
| 1099 | Forskolin |
| Adenylyl cyclase activator | |
| TB1099-RMU | Forskolin |
| Forskolin synthesized to Ancillary Material Grade | |
| 1840 | Fostriecin sodium salt |
| Potent PP2A and PP4 inhibitor | |
| 5461 | Foxy 5 |
| Wnt5a peptide mimetic | |
| 2876 | Fumitremorgin C |
| Inhibitor of BCRP-mediated multidrug resistance | |
| 3103 | Fumonisin B1 |
| Inhibitor of sphingosine N-acyltransferase | |
| 0926 | β-Funaltrexamine hydrochloride |
| Irreversible and selective μ antagonist | |
| 5202 | Furamidine dihydrochloride |
| Selective PRMT1 inhibitor | |
| 3109 | Furosemide |
| Na+/2Cl-/K+ (NKCC) symporter inhibitor; also GABAA antagonist | |
| 3015 | 2-Furoyl-LIGRLO-amide |
| Potent and selective PAR2 agonist | |
| 6961 | FzM1.8 |
| Frizzled 4 allosteric agonist; exhibits biased signaling; preserves stemness |
Tocris Products by Catalog Number
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