Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 101903 | 2-Pyrimidineacetonitrile (9CI) | 59566-45-9 | 98% | -cas-59566-45-9.png) |
| Coming soon! | ||||
| 101601 | PF06447475 | 1527473-33-1 | 98% |  |
| PF-06447475 is a highly potent, selective, brain penetrant LRRK2 inhibitor with IC0 o | ||||
| 100502 | Pluripotin(SC-1) | 839707-37-8 | 98% by HPLC | -cas-839707-37-8.png) |
| SC1 (Pluripotin) was identified in a cell-based chemical library screen for small mol | ||||
| 92302 | PTP1B-IN-1 | 612530-44-6 | 98% |  |
| Coming soon! | ||||
| 92301 | Piboserod | 152811-62-6 | 98% |  |
| Piboserod , also known as SB-207266, is a selective 5-HT4 receptor antagonist which w | ||||
| 92206 | Pyrrolidin-1-yl-acetic acid hydrochloride | 6628-74-6 | 98% |  |
| Coming soon! | ||||
| 91806 | phenyl 2-(benzyloxy)-3-(dibenzylamino)-5-fluoro-6-methylbenzoate | 1253799-29-9 | 98% | -3-(dibenzylamino)-5-fluoro-6-methylbenzoate-cas-1253799-29-9.png) |
| Coming soon! | ||||
| 91409 | 3-Piperazinobenzisothiazole Hydrochloride | 144010-02-6 | 98% |  |
| The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3 | ||||
| 91408 | 3-(1-Piperazinyl)-1,2-Benzisothiazole | 87691-87-0 | 98% | -12-Benzisothiazole-cas-87691-87-0.png) |
| The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3 | ||||
| 90709 | 3-(4-phenoxyphenyl)propanoic acid | 20062-91-3 | 98% | propanoicacid-cas-20062-91-3.png) |
| Coming soon! | ||||
| 82406 | PFI-4 | 900305-37-5 | 98% |  |
| PFI-4 is a potent and selective BRPF1 bromodomain inhibitor (IC50 = 80 nM). Exhibits | ||||
| 81821 | Piperazin-2-ylmethanol dihydrochloride | 122323-87-9 | 98% |  |
| Coming soon! | ||||
| 81817 | Piperazine-2-Carboxylic Acid Methyl Ester Dihydrochloride | 122323-88-0 | 98% |  |
| Coming soon! | ||||
| 81814 | Piperazine-2-carboxylic acid dihydrochloride | 3022-15-9 | 98% |  |
| Coming soon! | ||||
| 81302 | Pimecrolimus | 137071-32-0 | 98% |  |
| Pimecrolimus is an immunophilin ligand, which binds specifically to the cytosolic rec | ||||
| 81301 | Pitavastatin Calcium | 147526-32-7 | 98% |  |
| Pitavastatin is a member of the blood cholesterol lowering medication class of statin | ||||
| 73109 | PKI-587 | 1197160-78-3 | 97% |  |
| PKI-587 is a potent inhibitor to PI3K-, PI3K-, and mTOR (FRAP) with IC50 of 0.4 nM, 5 | ||||
| 52824 | PFK-015 | 4382-63-2 | 98% |  |
| PFK-015 is an effective inhibitor of PFKFB3 with IC50 of 110 nM (recombinant PFKFB3) | ||||
| 52817 | Pramiracetam | 68497-62-1 | 98% |  |
| Pramiracetam is a nootropic drug derived from piracetam, and is more potent. Pramirac | ||||
| 52816 | PF-573228 | 869288-64-2 | 98% |  |
| PF-573228 is a potent and selective FAK inhibitor with IC50 of 4 nM for inhibiton of | ||||
| 52815 | Paromomycin Sulfate | 1263-89-4 | 98% |  |
| Paromomycin Sulfate is an aminoglycoside antibiotics inhibiting protein synthesis in | ||||
| 52756 | PLX647 | 873786-09-5 | 98% | |
| PLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM respe | ||||
| 52753 | Pexidartinib | 1029044-16-3 | 98% |  |
| pexidartinib is acapsule formulation containing a small-molecule receptor tyrosine ki | ||||
| 52740 | PF-543 | 1415562-82-1 | 98% |  |
| PF-543 is a novel cell-permeant inhibitor of SphK1 with a Ki of 3.6 nM, PF-543 is sph | ||||
| 52718 | PSI-7977 | 1190307-88-0 | 98% |  |
| PSI-7977(sofosbuvir) is an investigational nucleotide analog for treatment of chronic | ||||
| 52701 | Pirfenidone | 53179-13-8 | 98% |  |
| Pirfenidone(AMR69) is an inhibitor for TGF- production and TGF- stimulated collagen p | ||||
| 52634 | Poziotinib | 1092364-38-9 | 98% | |
| Poziotinib(NOV120101; HM781-36B) is an irreversible Pan-HER inhibitor with IC50s of 3 | ||||
| 52631 | PF-4708671 | 1255517-76-0 | 98% |  |
| PF-4708671 is a novel cell-permeable inhibitor of S6K1 (p70 ribosomal S6 kinase 1), w | ||||
| 52613 | Perifosine | 157716-52-4 | 98% |  |
| Perifosine (KRX-0401; D-21266; NSC 639966) is a novel Akt inhibitor with IC50 of 4.7 | ||||
| 52603 | Plinabulin | 714272-27-2 | 98% |  |
| Plinabulin (NPI-2358) is a vascular disrupting agents (VDA) against tubulin-depolymer | ||||