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| Product | Description | |
|---|---|---|
| FX-909 | FX-909 is a covalent peroxisome proliferator-activated receptor gamma ( PPARG ) inverse agonist. FX-909 can be used for the research of cancer [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2924573-90-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153344. |  |
| FXIIIa-IN-1 sodium | C.I.Reactive Black 5 (Technical Grade) is a biological molecule. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Reactive Black 5. CAS No. 17095-24-8. Pack Sizes: 100 mg; 250 mg; 500 mg. Product ID: HY-W783421. | |
| FXR/TGR5 agonist 1 | FXR/TGR5 agonist 1, a dual agonist of FXR and TGR5, can be used to treat fatty liver disease. Synonyms: N-(3-chloro-5-methoxyphenyl)-N-((4-(3-cyano-4-methoxyphenyl)bicyclo[2.2.2]octan-1-yl)methyl)-3-methylisonicotinamide. CAS No. 2677689-72-2. Molecular formula: C31H32ClN3O3. Mole weight: 530.06. |  |
| FY26 (complex) | This active moleculr is a Os(II) anticancer drug candidate. It can generate reactive oxygen species and disrupt the redox balance in cancer cells. Using FY26 and nontoxic doses of L-BSO together allows the potentiation of its anticancer activity and inpartantly, it improves the selectivity for cancer cells versus normal fibroblasts. FY26 can shut down a cancer cell by exploiting weaknesses inherent in their energy generation. Uses: Anti-cancer. Synonyms: FY26; FY-26; FY 26. Osmium(1+)?, [N,?N-dimethyl-4-[2-(2-pyridinyl-κN)?diazenyl-κN1]?benzenamine]?iodo[(1,?2,?3,?4,?5,?6-η)?-1-methyl-4-(1-methylethyl)?benzene]?-, hexafluorophosphate(?1-) (1:1). Grade: 98%. CAS No. 1255143-82-8. Molecular formula: C23H28F6IN4OsP. Mole weight: 822.60. | |
| FYN A, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. |  |
| FYN A active human | recombinant, expressed in baculovirus infected Sf9 cells, ?60% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Fz7-21 | Fz7-21, a peptide antagonist of Frizzled 7 receptor, selectively binds to Frizzled 7 CRD subclass. Synonyms: FZD7 binding peptide; Ac-Leu-Pro-Ser-Asp-Asp-Leu-Glu-Phe-Trp-Cys-His-Val-Met-Tyr-NH2. Grade: ≥97% by HPLC. CAS No. 2247635-23-8. Molecular formula: C83H114N18O23S2. Mole weight: 1796.05. | |
| FzM1 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| FzM1 | FzM1 is a negative allosteric modulator (NAM) of Frizzled receptor FZD4. FzM1 reduces WNT5A-dependent WNT responsive element (WRE) activity (log EC 50inh =-6.2). FzM1 binds to an allosteric binding site located in intracellular loop 3 (ICL3) of FZD4 and alters the conformation of the receptor, ultimately inhibiting the WNT/β-catenin cascade [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1680196-54-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116553. | |
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