TGF-β / Smad Signaling
TGF-β / Smad Signaling(TGF-β / Smad 信号转导)
Transforming growth factor-beta (TGF-beta) is a multifunctional cytokine that regulates proliferation, migration, differentiation, and survival of many different cell types. Deletion or mutation of different members of the TGF-β family have been shown to cause vascular remodeling defect and absence of mural cell formation, leading to embryonic lethality or severe vascular disorders. TGF-β induces smooth muscle differentiation via Notch or SMAD2 and SMAD3 signaling in ES cells or in a neural crest stem cell line. TGF-β binds to TGF-βRI and to induce phosphorylation of SMAD2/3, thereby inhibiting proliferation, tube formation, and migration of endothelial cells (ECs).
TGF-β is a pluripotent cytokine with dual tumour-suppressive and tumour-promoting effects. TGF-β induces the epithelial-to-mesenchymal transition (EMT) leading to increased cell plasticity at the onset of cancer cell invasion and metastasis.
TGF-β / Smad Signaling 相关产品(360)
- GC14363Mitoxantrone HClCAS: 70476-82-3纯度: >98.00%
An inhibitor of DNA topoisomerase IIα and HIV-1 integrase
- GC14716Bisindolylmaleimide IVCAS: 119139-23-0纯度: >98.50% / >97.00%
Bisindolylmaleimide IV 是一种强效的细胞膜透过性蛋白激酶C(PKC)抑制剂,其IC 50 值为0.1-0.55μM。
- GC15148Ionomycin calcium saltCAS: 56092-82-1纯度: >98.00%
Ionomycin calcium salt是一种窄谱抗生素,对革兰氏阳性菌具有活性,由丛生链霉菌(Streptomyces conglobatus)产生。
- GC15345[Ala113]-MBP (104-118)CAS: 99026-78-5
[Ala113]-MBP (104-118) 是一种蛋白激酶 C (PKC) 的非竞争性肽抑制剂,IC50 范围为 28-62 μM。
- GC15446Ionomycin free acidCAS: 56092-81-0纯度: {{1-15}>98.00%}
Ionomycin free acid 是一种选择性的强效钙离子载体,可作为活性 Ca2+ 载体。
- GC15471PKC β pseudosubstrateCAS: 172308-76-8
Selective cell-permeable peptide inhibitor of protein kinase C
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC14349 | SB525334 | 356559-20-1 | >99.50% / >98.00% | |
SB525334已被鉴定为一种高效且选择性的转化生长因子β1(TGF-β1)受体、活化素受体样激酶(ALK5)抑制剂。SB525334对ALK5激酶活性的IC 50 为14.3nM。 | ||||
| GC14363 | Mitoxantrone HCl | 70476-82-3 | >98.00% | |
An inhibitor of DNA topoisomerase IIα and HIV-1 integrase | ||||
| GC14583 | R 59-022 | 93076-89-2 | 不显示 | |
R 59-022是一种二酰甘油激酶抑制剂(IC 50 = 2.8µM)。 | ||||
| GC14592 | KW 2449 | 1000669-72-6 | >99.50% | |
A multi-kinase inhibitor | ||||
| GC14650 | CGP60474 | 164658-13-3 | >98.50% | |
A CDK inhibitor | ||||
| GC14716 | Bisindolylmaleimide IV | 119139-23-0 | >98.50% / >97.00% | |
Bisindolylmaleimide IV 是一种强效的细胞膜透过性蛋白激酶C(PKC)抑制剂,其IC 50 值为0.1-0.55μM。 | ||||
| GC14767 | PF-00562271 | 939791-38-5 | >99.00% | |
A selective FAK/PYK2 inhibitor | ||||
| GC15018 | Hispidin | 555-55-5 | >99.50% | |
A polyphenol with diverse biological activities | ||||
| GC15057 | Kartogenin | 4727-31-5 | >98.00% | |
Kartogenin是软骨样组织形成的诱导剂(EC 50 : 100 nM)。 | ||||
| GC15148 | Ionomycin calcium salt | 56092-82-1 | >98.00% | |
Ionomycin calcium salt是一种窄谱抗生素,对革兰氏阳性菌具有活性,由丛生链霉菌(Streptomyces conglobatus)产生。 | ||||
| GC15170 | SB 772077B dihydrochloride | 607373-46-6 | >98.50% | |
A ROCK1 and ROCK2 inhibitor | ||||
| GC15345 | [Ala113]-MBP (104-118) | 99026-78-5 | - | |
[Ala113]-MBP (104-118) 是一种蛋白激酶 C (PKC) 的非竞争性肽抑制剂,IC50 范围为 28-62 μM。 | ||||
| GC15446 | Ionomycin free acid | 56092-81-0 | {{1-15}>98.00%} | |
Ionomycin free acid 是一种选择性的强效钙离子载体,可作为活性 Ca2+ 载体。 | ||||
| GC15471 | PKC β pseudosubstrate | 172308-76-8 | - | |
Selective cell-permeable peptide inhibitor of protein kinase C | ||||
| GC15564 | Go 6976 | 136194-77-9 | >99.00% / >98.00% | |
Go 6976 是一种有效的蛋白激酶(PKs)抑制剂,对PKC、cGMP依赖性蛋白激酶和肌球蛋白轻链激酶的IC 50 值分别为0.02μM、6.2μM和5.8μM。 | ||||
| GC15567 | K02288 | 1431985-92-0 | >98.00% | |
A BMP signaling inhibitor | ||||
| GC15884 | Dasatinib Monohydrate | 863127-77-9 | - | |
An inhibitor of Abl and Src | ||||
| GC16289 | SAR407899 hydrochloride | 923262-96-8 | >98.00% | |
A ROCK1 and ROCK2 inhibitor | ||||
| GC16405 | Safingol | 15639-50-6 | - | |
A dual inhibitor of PKC and SPHK | ||||
| GC16475 | Afuresertib | 1047644-62-1 | >99.50% | |
A pan-Akt inhibitor | ||||
| GC16510 | ZIP, Biotinylated | - | - | |
ZIP with a biotin moiety covalently attached | ||||
| GC16539 | Butaprost | 69685-22-9 | >98.00% | |
A selective agonist for the EP 2 receptors | ||||
| GC16584 | TCS 21311 | 1260181-14-3 | >95.00% | |
A JAK3 inhibitor | ||||
| GC16678 | UCN-02 | 121569-61-7 | - | |
A PKC inhibitor | ||||
