Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 185144 | Pocapavir | 146949-21-5 | >98% |  |
| Pocapavir, also known as SCH-48973 and V-073, is a potent, selective, antienterovirus | ||||
| 185143 | PSMA617 TFA | 1702967-37-0 | >98% |  |
| PSMA-617 is a ligand used to make 177Lu-PSMA-617, which is a radioactive molecule to | ||||
| 185142 | Pyridostatin TFA salt | 1472611-44-1 | >98% |  |
| Pyridostatin stabilizes G-quadruplexes (G4s) in cells and elicits a DNA damage respon | ||||
| 18544 | PF-06260933 | 1811510-56-1 | >98% |  |
| PF-06260933 is a potent and highly selective inhibitor of MAP4K4. | ||||
| 184286 | PHA-767491 HCl | 942425-68-5 | >98% |  |
| PHA-767491, also known as CAY10572, is a potent, ATP-competitive dual cdc7/cdk9 inhib | ||||
| 184285 | PLX51107 | 1627929-55-8 | >98% |  |
| PLX51107 is a potent and selective BRD4 inhibitor or BET inhibitor with novel in vitr | ||||
| 184284 | PD 158780 | 171179-06-9 | >98% |  |
| PD 158780 is a potent in vitro inhibitor of the tyrosine kinase activity of the epide | ||||
| 184162 | PZM21 | 1997387-43-5 | >98% |  |
| PZM21 is a potent Gi activator with exceptional selectivity for μOR and minimal β-a | ||||
| 184107 | PF-9366 | 72882-78-1 | >98% |  |
| PF-9366 is a novel inhibitor of human methionine adenosyltransferase 2A (Mat2A), the | ||||
| 184106 | PFI-2 hydrochloride | 1627607-87-7 | >98% |  |
| PFI-2 is a potent inhibitor of SETD7 with IC50 2 nM and 1000-fold selectivity over ot | ||||
| 184101 | PCI-29732 | 330786-25-9 | >98% |  |
| PCI-29732 is a BTK inhibitor. It acts by blocking B cell antigen receptor (BCR)-media | ||||
| 184318 | PF-0684000 | 198474-05-4 | >98% |  |
| PF-0684000, also known as EOS200271, is potent IDO-1 inhibitor (IC50 0.15 μM). PF-06 | ||||
| 18434 | PF-06409577 | 1467057-23-3 | >98% |  |
| PF-06409577 is a potent and selective activator of 5′ adenosine monophosphate-activ | ||||
| 17101614 | PRN-1371 | 1802929-43-6 | >98% |  |
| PRN-1371 is a covalent, irreversible, highly selective FGFR1, 2, 3 and 4 inhibitor. P | ||||
| 17101612 | PF-5006739 | 1293395-67-1 | >98% |  |
| PF-5006739 is a Potent CK1δ/ε inhibitor. PF-5006739 attenuates opioid drug-seeking | ||||
| 17101611 | PF-04628935 | 1383719-97-8 | >98% |  |
| PF-04628935 is a potent antagonist/inverse agonist of the ghrelin receptor, growth ho | ||||
| 1710134 | PIM447 | 1210608-43-7 | >98% |  |
| PIM447, also known as LGH447, is a potent Moloney murine leukemia (PIM) 1, 2, and 3 k | ||||
| 179302 | PF-562271 HCl | 939791-41-0 | >98% |  |
| PF-562271, also known as PF-562,271 and PF-271, is an orally bioavailable small molec | ||||
| 179221 | Pemafibrate | 848259-27-8 | >98%; EE>98% |  |
| (1)Pemafibrate, also known as K-877 and (R)-K 13675, is a PPAR alpha agonist. (R)-K-1 | ||||
| 1791517 | Pyridostatin TFA salt | 179474-81-8 | 98.0% |  |
| Pyridostatin stabilizes G-quadruplexes (G4s) in cells and elicits a DNA damage respon | ||||
| 1791516 | Prucalopride Succinate | 179474-85-2 | 98.0% |  |
| Prucalopride, also known as R-108512, is a selective, high affinity serotonin (5-HT4) | ||||
| 1791515 | PRT4165 | 31083-55-3 | 98.0% |  |
| PRT4165 is a small molecule inhibitor of polycomb repressive complex 1, which inhibit | ||||
| 1791510 | Pramipexole HCl | 104632-25-9 | 98.0% |  |
| Pramipexole Dihydrochloride is an agonist of the Gαi-linked dopamine receptors D2, D | ||||
| 1791312 | PF-06281355 | 1435467-38-1 | 98.0% |  |
| PF-06281355, also known as PF-1355, is an orally available, selective and potent mech | ||||
| 1791310 | Puromycin Aminonucleoside | 58-60-6 | 98.0% |  |
| Puromycin Aminonucleoside, also known as PAN, NSC3056, is useful in the study of huma | ||||
| 179116 | P7C3-OMe | 1235481-43-2 | 98.0% |  |
| P7C3-OMe, also known as (R)-P7C3-OMe, is an analogue of P7C3 and P3C3-A20. P7C3 Atten | ||||
| 179113 | PF-CBP1 free base | 1962928-21-7 | 98.0% |  |
| PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b | ||||
| 179112 | PF-CBP1 HCl | 2070014-93-4 | 98.0% |  |
| PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b | ||||
| 17988 | PF-06650833 | 1817626-54-2 | 98.0% |  |
| PF-06650833 is an inhibitor of Interleukin-1 receptor associated kinase 4 (IRAK4). RA | ||||
| 17986 | Prexasertib mesylate | 1234015-55-4 | 98.0% |  |
| Prexasertib, also known as LY2606368, is a potent and selective Chk1/Chk2 inhibitor. | ||||