产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 16122785 | PRI-724 | 847591-62-2 | 98% |  |
| PRI-724 is a potent, specific inhibitor of the canonical Wnt signaling pathway in can | ||||
| 16122777 | PLX7904 | 1393465-84-3 | 98% |  |
| PLX7904, also known as PB04, is a potent and selective paradox-breaker RAF inhibitor. | ||||
| 16122774 | Pamapimod (R-1503, Ro4402257) | 449811-01-2 | 98% | -cas-449811-01-2.png) |
| Pamapimod (R-1503, Ro4402257) is a novel, selective inhibitor of p38 mitogen-activate | ||||
| 16122770 | PRIMA-1 | 5608-24-2 | 98% |  |
| PRIMA-1 is a mutant p53 reactivator. It induces apoptosis and inhibits growth of huma | ||||
| 16122714 | Picolinamide | 1452-77-3 | 98% |  |
| Picolinamide is found to be a strong inhibitor of poly (ADP-ribose) synthetase of nuc | ||||
| 16122710 | PD0166285 | 185039-89-8 | 98% | |
| PD0166285 is a potent Wee1 and Chk1 inhibitor with activity at nanomolar concentratio | ||||
| 16122707 | Peficitinib (ASP015K, JNJ-54781532) | 944118-01-8 | 98% | |
| Peficitinib (ASP015K, JNJ-54781532) is an orally bioavailable JAK inhibitor. Phase 3. | ||||
| 6111525 | PF-543 Citrate | 1415562-83-2 | 98% |  |
| PF-543 Citrate is a novel cell-permeant inhibitor of SphK1 with a K(i) of 3.6 nM, PF- | ||||
| 61115 | Pasireotide | 396091-73-9 | 98% |  |
| Pasireotide(SOM 230) is a stable cyclohexapeptide somatostatin mimic that exhibits un | ||||
| 6111020 | PFI-3 | 1819363-80-8 | 98% |  |
| PFI-3 | ||||
| 611943 | PF-2771 | 98% |  | |
| PF-2771 is a potent, selective CENP-E inhibitor, PF-2771 inhibits CENP-E motor activi | ||||
| 611939 | PF-04929113 Mesylate | 1173111-67-5 | 98% | |
| PF-04929113 Mesylate is a potent and selective Hsp90 inhibitor with an IC50 of median | ||||
| 611908 | PI4KIIIbeta-IN-9 | 1429624-84-9 | 98% | |
| PI4KIII-IN-9 is a potent PI4KIII inhibitor (IC50 of 7 nM) and is >140-fold selecti | ||||
| 611907 | PI4KIIIbeta-IN-10 | 1881233-39-1 | 98% | |
| PI4KIIIbeta-IN-10 is the most potent PI4KIII inhibitor currently reported, with very | ||||
| 611903 | PI3Kα inhibitor 1 | 1235449-52-1 | 98% | |
| PI3Kα inhibitor 1 is a PI3Kα inhibitor extracted from patent US/20120088764A1, comp | ||||
| 611902 | PF-04979064 | 1220699-06-8 | ≧98.0% |  |
| PF-04979064 is a potent and selective PI3K/mTOR dual kinase inhibitor with an IC(50) | ||||
| 611821 | PQR620 | 98% |  | |
| PRQ620 is a highly potent and selective mTORC1/2 inhibitor, shows anti-tumor effects | ||||
| 161009011 | PP121 | 1092788-83-4 | 98% by HPLC |  |
| PP121 blocks the proliferation of tumor cells by direct inhibition of oncogenic tyros | ||||
| 161009002 | PF-4989216 | 1276553-09-3 | 98% by HPLC |  |
| PF-4989216 inhibits the phosphorylation of PI3K downstream molecules and subsequently | ||||
| 160926013 | PIK-294 | 900185-02-6 | 98% by HPLC |  |
| PIK-294 is a highly selective inihibitor of the phosphoinositide 3-kinase (PI3K) p110 | ||||
| 160926010 | PIK-90 | 677338-12-4 | 98% by HPLC |  |
| PIK-90 is a potent PI3K inhibitor with potential anticancer activity. | ||||
| 160926009 | PIK-93 | 593960-11-3 | 98% by HPLC |  |
| PIK-93 is a potent PI3K inhibitor. PIK93 selectively inhibits the type III PI 4-kinas | ||||
| 160926002 | PI-103 | 371935-74-9 | 97% by HPLC |  |
| It inhibits ATR and ATM only at much higher concentrations (IC50= 850 and 920 nM, res | ||||
| 16071409 | PNU-159682 | 202350-68-3 | 98% by HPLC |  |
| PNU-159682 is a major active metabolite of nemorubicin (MMDX) in human liver microsom | ||||
| 16071408 | Pevonedistat | 905579-51-3 | 98% by HPLC |  |
| Pevonedistat, also known as MLN-4924 and TAK-924, is a small molecule inhibitor of Ne | ||||
| 16071114 | PRX-08066 | 866206-54-4 | 98% by HPLC |  |
| PRX-08066 is a a novel 5-hydroxytryptamine receptor 2B antagonist, reduces monocrotal | ||||
| 16071111 | PS 48 | 1180676-32-7 | 98% by HPLC |  |
| PS 48 has been shown to be a PKB Kinase (phosphoinositide-dependent protein kinase-1, | ||||
| 16071030 | Panulisib | 1356033-60-7 | 98% by HPLC |  |
| Panulisib, also known as AK151761, is a potent and selective imidazoquinoline based P | ||||
| 16071028 | Piclidenoson | 152918-18-8 | 98% by HPLC |  |
| Piclidenoson, also known as CF101, is a specific agonist to the A3 adenosine receptor | ||||
| 16070806 | Pirarubicin | 72496-41-4 | 98% by HPLC |  |
| Pirarubicin is an anthracycline drug. An analogue of the anthracycline antineoplastic | ||||