Signaling Pathways
Signaling Pathways(信号通路)
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Signaling Pathways 相关产品(35130)
- GC13441CyclopamineCAS: 4449-51-8纯度: >99.50%
Cyclopamine是一种天然存在的Hedgehog (Hh)特异性小分子信号甾体生物碱抑制剂,对肿瘤生长具有深远的抑制作用,在人乳腺癌细胞中具有显著的抗侵袭、抗增殖和抗雌激素活性。
- GC134514-Methylumbelliferone (4-MU)CAS: 90-33-5纯度: >99.50%
4-Methylumbelliferone是一种已知的合成透明质酸(HA)抑制剂。增殖试验的IC 50 值为0.65±0.04mM。
- GC13508Trametinib (GSK1120212)CAS: 871700-17-3纯度: >98.00% / >99.00%
Trametinib (GSK1120212, JTP-74057) 是第二代 MEK 激酶小分子抑制剂。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13426 | CPPHA | 693288-97-0 | - | |
A positive allosteric modulator of the mGluR5 | ||||
| GC13428 | Mosapride | 112885-41-3 | - | |
A 5-HT 4 receptor agonist | ||||
| GC13432 | Adenine | 73-24-5 | >99.50% / >98.50% | |
腺嘌呤(6-氨基嘌呤)是一种嘌呤,是DNA核酸中的四种核碱基之一。腺嘌呤是DNA和RNA的化学成分。腺嘌呤还在涉及细胞呼吸、ATP 和辅因子(NAD 和 FAD)的形式以及蛋白质合成的生物化学中发挥重要作用。 | ||||
| GC13433 | AZ 960 | 905586-69-8 | >98.00% | |
A JAK2 inhibitor | ||||
| GC13435 | KD 5170 | 940943-37-3 | - | |
An inhibitor of class I and II HDACs | ||||
| GC13437 | ZLN005 | 49671-76-3 | >99.50% | |
ZLN005是一种强效且具有细胞特异性的过氧化物酶体增殖激活受体-γ辅激活因子-1α(PGC-1α)转录激活剂。 | ||||
| GC13441 | Cyclopamine | 4449-51-8 | >99.50% | |
Cyclopamine是一种天然存在的Hedgehog (Hh)特异性小分子信号甾体生物碱抑制剂,对肿瘤生长具有深远的抑制作用,在人乳腺癌细胞中具有显著的抗侵袭、抗增殖和抗雌激素活性。 | ||||
| GC13443 | Doxazosin Mesylate | 77883-43-3 | >99.50% | |
An α 1 -AR antagonist | ||||
| GC13447 | Doxazosin | 74191-85-8 | - | |
An α 1 -AR antagonist | ||||
| GC13449 | Rocuronium Bromide | 119302-91-9 | >98.00% | |
A non-depolarizing muscle relaxant | ||||
| GC13451 | 4-Methylumbelliferone (4-MU) | 90-33-5 | >99.50% | |
4-Methylumbelliferone是一种已知的合成透明质酸(HA)抑制剂。增殖试验的IC 50 值为0.65±0.04mM。 | ||||
| GC13452 | 2'-Deoxycytidine hydrochloride | 3992-42-5 | >99.50% | |
A deoxyribonucleoside | ||||
| GC13456 | Doxycycline hyclate | 24390-14-5 | >98.00% | |
Doxycycline hyclate是四环素的衍生物,具有抗炎和抗菌活性。 | ||||
| GC13467 | PMPA (NAALADase inhibitor) | 173039-10-6 | >98.00% | |
A potent inhibitor of GCP II/NAALADase | ||||
| GC13468 | BI-D1870 | 501437-28-1 | >99.00% | |
An inhibitor of RSK1-4 | ||||
| GC13476 | AM966 | 1228690-19-4 | >98.50% | |
A potent and selective LPA 1 receptor antagonist | ||||
| GC13478 | Pizotifen Malate | 5189-11-7 | - | |
A triptan | ||||
| GC13486 | Cimetidine | 51481-61-9 | >98.00% | |
A histamine H 2 receptor antagonist | ||||
| GC13487 | ARP 100 | 704888-90-4 | >99.00% / >98.00% | |
A selective inhibitor of MMP-2 | ||||
| GC13488 | R8-T198wt | 2305815-72-7 | - | |
R8-T198wt 是一种细胞可渗透的羧基末端 p27Kip1 肽,通过抑制 Pim-1 激酶表现出抗肿瘤活性。 | ||||
| GC13495 | Trequinsin hydrochloride | 78416-81-6 | >99.50% | |
An inhibitor of PDE3 | ||||
| GC13501 | VUF 10166 | 155584-74-0 | - | |
A 5-HT 3 receptor antagonist | ||||
| GC13508 | Trametinib (GSK1120212) | 871700-17-3 | >98.00% / >99.00% | |
Trametinib (GSK1120212, JTP-74057) 是第二代 MEK 激酶小分子抑制剂。 | ||||
| GC13512 | glucagon receptor antagonists 3 | 202917-17-7 | >98.50% | |
胰高血糖素受体拮抗剂 3 是一种高效的胰高血糖素受体拮抗剂。 | ||||
