Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 20640 | FLAG-003 | 1614235-14-1 | ≧98.0% |  |
| FLAG-003 is a multi-acting, water-soluable small molecule therapeutic designed to tar | ||||
| 20569 | FC-116 | 2417298-29-2 | 98% Min. |  |
| FC-116 is a Tubulin inhibitor that effectively inhibits tumor growth in mice. | ||||
| 20556 | F7H inhibitor | 897109-93-2 | 98% Min. |  |
| F7H is a Frizzled receptor FZD7 antagonist. | ||||
| 237071 | Flavopiridol ( Alvocidib ) | 146426-40-6 | ≧98.0% |  |
| Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst | ||||
| 20471 | FHD-286 | 2671128-05-3 | ≧98.0% |  |
| FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i | ||||
| 20433 | 3-fluoro-6-methoxyquinoline | 426842-85-5 | 98% Min. |  |
| 20420 | 5-Fluoroquinazoline-2,4(1H,3H)-dione | 192570-33-5 | 98% Min. |  |
| 20405 | 4-Fluoro-2-(trifluoromethyl)benzaldehyde | 90176-80-0 | 98% Min. |  |
| 1711225 | Fosgonimeton (ATH-1017) | 2093305-05-4 | ≧98.0% |  |
| Fosgonimeton (ATH-1017) is a small molecule which enhance the activity of hepatocyte | ||||
| L20347 | Fadraciclib free base | 1070790-89-4 | 98% Min. |  |
| Fadraciclib, also known as CYC065, is an orally bioavailable inhibitor of cyclin depe | ||||
| 20315 | F1063-0967 | 613225-56-2 | 98% Min. |  |
| F1063-0967 is a novel inhibitor of dual-specificity phosphatase 26 (DUSP26), inducing | ||||
| 20262 | 1-[6-(4-fluoro-1H-pyrazol-1-yl)-3-pyridinyl]Ethanone | 1980023-94-6 | 96% Min. |  |
| 26188 | Firibastat ( QGC-001 ) | 648927-86-0 | ≧98.0% |  |
| Firibastat, (originally named QGC001) is the first drug candidate of a new class of c | ||||
| 20122201 | FM-381 | 2226521-65-7 | 98% Min. |  |
| FM-381 is a Chemical Probe For JAK3 and JAK3 specific reversible covalent inhibitor. | ||||
| 2091911 | FOY-251 mesylate | 71079-09-9 | 98% Min. |  |
| FOY-251 is a metabolite of Camostat that acts as a pollen protease inhibitor for prev | ||||
| 2091909 | FG-7142 | 78538-74-6 | 98% Min. |  |
| FG-7142 is a benzodiazepine receptor ligand with anxiogenic and proconvulsant propert | ||||
| 2071557 | FT113 | 1630808-89-7 | 98% Min. |  |
| FT113 is a novel potent inhibitor of fatty acid synthase (fasn) | ||||
| 2071514 | Fulacimstat | 1488354-15-9 | 98% Min. |  |
| Fulacimstat, also known as BAY1142524, is a chymase inhibitor and antifibrotic drug c | ||||
| 207102 | FB23-2 | 2243736-45-8 | 98% Min. |  |
| FB23-2 is a potent FTO inhibitor. FB23-2 demonstrated the potent inhibitory impact in | ||||
| 262324 | 2-(3-Fluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 1350426-06-0 | 98% Min. |  |
| 2062015 | 2-fluoro-4-methyl-5-nitrobenzoic acid methyl ester | 753924-48-0 | 98% Min. |  |
| 111897 | FTI-2148 | 251577-09-0 | 98% Min. |  |
| FTI-2148 is a potent farnesyltransferase inhibitor with potential antitumor activity. | ||||
| 193253 | FR-190809 | 215589-63-2 | >98% |  |
| FR-190809 is a potent, nonadrenotoxic, orally efficacious ACAT inhibitor. | ||||
| 192211 | FM19G11 | 329932-55-0 | >98% |  |
| FM19G11 is an inhibitor of Hypoxia Inducible Factors α (HIFα), reported to affect s | ||||
| 188102 | Fmk | 821794-92-7 | >98% |  |
| Potent irreversible RSK1/2 inhibitor (IC50 = 15 nM). Inactivates the C-terminal auto- | ||||
| 18794 | Fluspirilene | 1841-19-6 | >98% |  |
| Fluspirilene is a diphenylbutylpiperidine typical antipsychotic drug, used for the tr | ||||
| 18722 | Fezolinetant | 1629229-37-3 | >98% |  |
| Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which | ||||
| 18721 | FRAX486 | 1232030-35-1 | >98% |  |
| FRAX486 is a potent p21-activated kinase (PAK) inhibitor (IC50 values are 14, 33, 39 | ||||
| 184283 | Fialuridine | 69123-98-4 | >98% |  |
| Fialuridine, also known as FIAU, DRG-0098, is a DNA-directed DNA polymerase inhibitor | ||||
| 18445 | Fonadelpar | 515138-06-4 | >98% |  |
| Fonadelpar is a potent and selective peroxisome proliferator activated receptor δ (P | ||||