Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 18445 | Fonadelpar | 515138-06-4 | >98% |  |
| Fonadelpar is a potent and selective peroxisome proliferator activated receptor δ (P | ||||
| 18436 | FM-381 | unknown | >98% |  |
| FM-381 is a Chemical Probe For JAK3 and JAK3 specific reversible covalent inhibitor. | ||||
| 18431 | Fmoc-Val-Ala-PAB | 1394238-91-5 | >98% |  |
| Fmoc-Val-Ala-PAB，也称为Fmoc-Val-Ala-PAB-OH，是一种有效的药物结合剂， | ||||
| 184210 | Ferrostatin-1 | 347174-05-4 | >98% |  |
| Ferrostatin-1 (fe -1)是一种亲脂的抗氧化剂，有效地阻断了铁蛋白的形 | ||||
| 1712155 | Fostemsavir | 864953-29-7 | >98% |  |
| Fostemsavir, also known as BMS-663068, is a oral, safe and effective HIV-1 attachment | ||||
| 179156 | Farampator | 211735-76-1 | 98.0% |  |
| Farampator, also known as Org-24448; CX-691, is an AMPA receptor positive allosteric | ||||
| 1791315 | FRAX1036 | 1432908-05-8 | 98.0% |  |
| FRAX1036 is a potent and selective PAK1 inhibitor. | ||||
| 17989 | FITM | 932737-65-0 | 98.0% |  |
| FITM is a potent mGlu1 inhibitor. | ||||
| 178309 | Fluralaner | 864731-61-3 | 98.0% |  |
| Fluralaner, also known as AH252723, is a systemic insecticide and acaricide that is a | ||||
| 521191 | 4-fluoro-2-Methoxy-5-nitroaniline | 1075705-01-9 | >96% |  |
| AZD9291 drug intermediate-1 | ||||
| 178225 | 4-FORMYL-2-METHOXY-3-NITROPHENYL ACETATE | 2698-69-3 | 96.0% |  |
| 4-FORMYL-2-METHOXY-3-NITROPHENYL ACETATE | ||||
| 178221 | 1-(3-Fluorophenyl)-cyclohexanamine HCl | 125802-18-8 | 98.0% | -cyclohexanamineHCl-cas-125802-18-8.png) |
| 1-(3-Fluorophenyl)-cyclohexanamine HCl | ||||
| 16123002 | FPS-ZM1 | 945714-67-0 | 98% |  |
| FPS-ZM1 is a high-affinity RAGE-specific blocker that inhibits amyloid- binding to RA | ||||
| 16123001 | Flutamide | 13311-84-7 | 98% |  |
| Flutamide, also known as SCH13521, is a toluidine derivative and nonsteroidal antiand | ||||
| 16122947 | Fluoxymesterone | 76-43-7 | 98% |  |
| Fluoxymesterone is an anabolic steroid with strong androgenic properties that has bee | ||||
| 16122946 | Firategrast | 402567-16-2 | 98% |  |
| Firategrast, also known as SB-683699 or T-0047, is an orally bioavailable alpha4 beta | ||||
| 16122945 | FIIN-3 | 1637735-84-2 | 98% |  |
| FIIN-3 is a potent, selective, irreversible and the next-generation covalent FGFR inh | ||||
| 16122813 | FGFR4-IN-1 | 1708971-72-5 | 98% | |
| FGFR4-IN-1 is a potent and selective FGFR4 inhibitor. FGFR4 may be a novel therapeuti | ||||
| 16122812 | FG-2216 | 223387-75-5 | 98% |  |
| FG-2216, also known as YM311, is orally bioavailable HIF-prolyl hydroxylase inhibitor | ||||
| 16122788 | FH535 | 108409-83-2 | 98% |  |
| FH535 is a Wnt/-catenin signaling inhibitor and also a dual PPAR and PPAR antagonist. | ||||
| 16122709 | FLLL32 | 1226895-15-3 | 98% | |
| FLLL32 is a potent JAK2/STAT3 inhibitor with IC50 of <5 M.In MDA-MB-231 breast and | ||||
| 90102 | Fevipiprant ( NVP-QAW039 ) | 872365-14-5 | ≧98.0% |  |
| Fevipiprant (QAW039; NVP-QAW039) is a selective, potent, reversible competitive CRTh2 | ||||
| 16071102 | Filanesib | 885060-09-3 | 98% by HPLC |  |
| Filanesib, also known as ARRY-520, is a synthetic, small molecule targeting the kines | ||||
| 1662306 | FK866(APO866,Daporinad) | 658084-64-1 | 98% by HPLC/HNMR | -cas-658084-64-1.png) |
| FK866 is a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltra | ||||
| 16062117 | FIIN-2 | 1633044-56-0 | 98% by HPLC |  |
| FIIN-2 is a potent, selective, irreversible and the next-generation covalent FGFR inh | ||||
| 032513 | FPH2 | 957485-64-2 | 98% |  |
| Coming soon! | ||||
| 021901 | Fludarabine | 21679-14-1 | 98% |  |
| Fludarabine, a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment | ||||
| 122910 | Fumagillin | 23110-15-8 | 98% |  |
| Fumagillin is a complex biomolecule and used as an antimicrobial agent. | ||||
| 122807 | Falnidamol | 196612-93-8 | 98% |  |
| Falnidamol is a pyrimido-pyrimidine with antitumor activity. | ||||
| 122306 | Fedratinib ( TG-101348 ) | 936091-26-8 | 98% |  |
| Fedratinib ( TG-101348 ) is a selective inhibitor of JAK2 with IC50 of 3 nM, 35- and | ||||