Signaling Pathways
Signaling Pathways(信号通路)
- Proteases(63)
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- Metabolism(420)
- MAPK Signaling(32)
- Tyrosine Kinase(97)
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- Neuroscience(462)
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- Peptide Inhibitors and Substrate(1)
- Other Signal Transduction(141)
- Immunology/Inflammation(1111)
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- Vitamin D Related
- Antibody-drug Conjugate/ADC Related
- PROTAC(254)
- Ox Stress Reagents(25)
- Others(1718)
- Antiparasitics(21)
- Toxins(90)
Signaling Pathways 相关产品(35130)
- GC14703Oxybutynin chlorideCAS: 1508-65-2纯度: >98.00%
An antagonist of muscarinic acetylcholine receptors
- GC14726Mianserin HClCAS: 21535-47-7纯度: >99.50%
Mianserin HCl是一种四环类化合物,对5-HT6受体的K i 值为0.056 ± 0.012μM。
- GC14745Plerixafor (AMD3100)CAS: 110078-46-1纯度: >98.00% / >99.00%
Plerixafor(AMD3100) 是 CXCR4 和 CXCL12 介导的趋化作用的小分子抑制剂,IC50 值分别为 44 nM 和 5.7 nM 。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC14682 | PCI-24781 (CRA-024781) | 783355-60-2 | >98.50% | |
An HDAC inhibitor | ||||
| GC14683 | Sunitinib malate | 341031-54-7 | >99.00% | |
A multi-kinase inhibitor | ||||
| GC14693 | CMK | 821794-90-5 | >99.50% | |
CMK 是一种 RSK2 激酶抑制剂,与 FMK 相比,具有相似的效力,但化学稳定性较低。 | ||||
| GC14695 | CO-1686 (AVL-301) | 1374640-70-6 | >99.50% | |
A selective inhibitor of mutant EGFR | ||||
| GC14703 | Oxybutynin chloride | 1508-65-2 | >98.00% | |
An antagonist of muscarinic acetylcholine receptors | ||||
| GC14704 | Levonorgestrel | 797-63-7 | >99.00% / >98.00% | |
Levonorgestrel是一种口服有效的孕酮抑制剂。 | ||||
| GC14709 | AZD1152 | 722543-31-9 | >99.50% | |
AZD1152是一种高度选择性的Aurora B激酶(AURKB)抑制剂,IC 50 值为0.37nM。AZD1152是一种前体药物,在体内转化为活性形式AZD1152-hydroxyquinazoline pyrazol anilide(AZD1152-hQPA),主要用于研究与治疗急性髓系白血病等恶性肿瘤。 | ||||
| GC14715 | AZ 12080282 dihydrochloride | - | >98.00% | |
刺猬抑制剂 | ||||
| GC14720 | Zalcitabine | 7481-89-2 | >99.50% | |
A nucleoside reverse transcriptase inhibitor | ||||
| GC14726 | Mianserin HCl | 21535-47-7 | >99.50% | |
Mianserin HCl是一种四环类化合物,对5-HT6受体的K i 值为0.056 ± 0.012μM。 | ||||
| GC14729 | (R)-Crizotinib | 877399-52-5 | >99.50% | |
A c-MET and ALK receptor tyrosine kinase inhibitor | ||||
| GC14732 | PLX-4720 | 918505-84-7 | >99.50% | |
An orally-available inhibitor of the B-raf mutant B-Raf V600E | ||||
| GC14733 | SU14813 | 627908-92-3 | >98.50% | |
A dual VEGFR and PDGFR family kinase inhibitor | ||||
| GC14743 | WY 45233 succinate | 448904-47-0 | - | |
serotonin and noradrenalin reuptake inhibitor | ||||
| GC14745 | Plerixafor (AMD3100) | 110078-46-1 | >98.00% / >99.00% | |
Plerixafor(AMD3100) 是 CXCR4 和 CXCL12 介导的趋化作用的小分子抑制剂,IC50 值分别为 44 nM 和 5.7 nM 。 | ||||
| GC14746 | Meropenem | 96036-03-2 | >98.00% | |
美罗培南是一种碳青霉烯类抗菌剂。 | ||||
| GC14751 | Malotilate | 59937-28-9 | >99.50% | |
A hepatoprotective agent | ||||
| GC14759 | Fenoldopam | 67227-56-9 | - | |
An agonist of dopamine D 1A and D 1B receptors | ||||
| GC14764 | Lamotrigine | 84057-84-1 | >99.50% | |
An anticonvulsant | ||||
| GC14769 | Carvedilol | 72956-09-3 | >99.50% / >98.00% | |
Carvedilol是一种非选择性α1和β-肾上腺素能受体(Ars)的拮抗剂。 | ||||
| GC14783 | Trilostane | 13647-35-3 | >99.50% | |
A 3β-hydroxysteroid dehydrogenase inhibitor | ||||
| GC14785 | Alvelestat | 848141-11-7 | >99.50% | |
An inhibitor of neutrophil elastase | ||||
| GC14787 | Curcumin | 458-37-7 | >98.00% | |
A yellow pigment with diverse biological activities | ||||
| GC14788 | Tianeptine | 66981-73-5 | >98.00% | |
An atypical antidepressant | ||||
