Other Apoptosis
Other Apoptosis(其他细胞凋亡)
Other Apoptosis 相关产品(883)
- GC168537,8-DihydroxyflavoneCAS: 38183-03-8纯度: >99.50% / >98.00%
7,8-Dihydroxyflavone(7,8-二羟基黄酮)是一种高亲和力酪氨酸激酶受体B(TrkB)激动剂,IC 50 值为0.26μM 。
- GC17030AZD6244(Selumetinib)CAS: 606143-52-6纯度: >99.00%
AZD6244(Selumetinib)是一种口服小分子特异性MEK1/2蛋白ATP非竞争性抑制剂,IC 50 值为14.1± 0.79nM。
- GC17107PluriSIn #1 (NSC 14613)CAS: 91396-88-2纯度: >99.50%
A selective inhibitor of stearoyl-CoA desaturase
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC16827 | ELR510444 | 1233948-35-0 | >98.00% | |
An inhibitor of tubulin polymerization | ||||
| GC16835 | LY2228820 | 862507-23-1 | >99.50% | |
A potent inhibitor of p38α MAP kinase | ||||
| GC16843 | Hydroxyurea | 127-07-1 | >97.00% / >98.00% | |
An antineoplastic agent | ||||
| GC16853 | 7,8-Dihydroxyflavone | 38183-03-8 | >99.50% / >98.00% | |
7,8-Dihydroxyflavone(7,8-二羟基黄酮)是一种高亲和力酪氨酸激酶受体B(TrkB)激动剂,IC 50 值为0.26μM 。 | ||||
| GC16868 | Sulfasalazine | 599-79-1 | >99.00% / >98.00% | |
Sulfasalazine是一种磺胺类药物。 | ||||
| GC16869 | Ixabepilone | 219989-84-1 | >99.50% | |
A broad-spectrum anticancer agent | ||||
| GC16875 | FLLL32 | 1226895-15-3 | >99.50% | |
An inhibitor of JAK2/STAT3 signaling | ||||
| GC16880 | Flurbiprofen | 5104-49-4 | >99.50% | |
A non-selective COX inhibitor | ||||
| GC16893 | ICG 001 | 780757-88-2 | >99.50% / >98.00% | |
ICG001 是一种靶向 Wnt/β-catenin 通路的小分子抑制剂。 | ||||
| GC16922 | Kobe0065 | 436133-68-5 | >99.50% | |
A selective Ras inhibitor | ||||
| GC16948 | Valinomycin | 2001-95-8 | >98.00% / >95.00% | |
缬霉素Valinomycin是一种十二肽抗生素,从几种链霉菌菌株中获得。 | ||||
| GC16976 | Mitotane (Lsodren) | 53-19-0 | >99.50% | |
An inhibitor of steroidogenesis | ||||
| GC16991 | PQ 401 | 196868-63-0 | >99.50% | |
An inhibitor of IGF-1R | ||||
| GC17023 | HLCL-61 | 1158279-20-9 | >99.50% | |
A PRMT5 inhibitor | ||||
| GC17030 | AZD6244(Selumetinib) | 606143-52-6 | >99.00% | |
AZD6244(Selumetinib)是一种口服小分子特异性MEK1/2蛋白ATP非竞争性抑制剂,IC 50 值为14.1± 0.79nM。 | ||||
| GC17045 | AXL1717 | 477-47-4 | >99.50% | |
AXL1717是一种具有口服活性和高效选择性的胰岛素样生长因子1受体(IGF-1R)抑制剂,IC 50 值为1nM。 | ||||
| GC17050 | CYT387 | 1056634-68-4 | >98.50% | |
A potent inhibitor of JAK1 and JAK2 | ||||
| GC17054 | Thalidomide | 50-35-1 | >99.50% | |
Thalidomide是一种非成瘾性、非巴比妥类镇静剂,可抑制cereblon蛋白,具有抗炎和抗血管生成特性。 | ||||
| GC17057 | Lithocholic Acid | 434-13-9 | >98.00% / >99.50% | |
A toxic secondary bile acid | ||||
| GC17067 | LDC000067 | 1073485-20-7 | >98.50% | |
A Cdk9 inhibitor | ||||
| GC17074 | Tadalafil | 171596-29-5 | >99.50% | |
Tadalafil是一种有效、可逆且具有选择性的磷酸二酯酶5(PDE5)小分子抑制剂,IC 50 为1.8nM。Tadalafil还能够抑制PDE11(IC 50 为11nM)。 | ||||
| GC17094 | Acitretin | 55079-83-9 | >99.00% | |
A retinoid | ||||
| GC17096 | STF-118804 | 894187-61-2 | >99.00% | |
A Nampt inhibitor | ||||
| GC17107 | PluriSIn #1 (NSC 14613) | 91396-88-2 | >99.50% | |
A selective inhibitor of stearoyl-CoA desaturase | ||||
