TGF-β / Smad Signaling
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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.
Research Areas
Products Related to TGF-β / Smad Signaling(358)
- GC81672Senkyunolide BCAS: 93236-67-0Purity: >98%
Senkyunolide B is a phthalide found in Angelica sinensis.
- GC81880OSU-2S TFAPurity: >98.00%
OSU-2S TFA is a non-immunosuppressive derivative of Fingolimod hydrochloride (FTY720).
- GC81892Vevorisertib tetrahydrochloridePurity: >98.00%
Vevorisertib tetrahydrochloride (ARQ 751 tetrahydrochloride) is an orally active allosteric AKT inhibitor that blocks AKT phosphorylation.
- GC90543EGFR Peptide (human, mouse) (myristoylated) (trifluoroacetate salt)Purity: >95.00%
A PKC inhibitor
- GD096703,3-Dimethyl-1-butanolCAS: 624-95-3Purity: >99.50%
3,3-Dimethyl-1-butanol is an oral inhibitor that inhibits the production of trimethylamine (TMA) by microorganisms and suppresses different microbial TMA lyases.
- GN10378OxymatrineCAS: 16837-52-8Purity: >98.00%
Oxymatrine is a quinolizidine alkaloid extracted from the roots of Sophora flavescens.
- GN10534AsiaticosideCAS: 16830-15-2Purity: >98.00%
Asiaticoside is a pentacyclic triterpenoid glycoside extracted from Centella asiatica .
- GC11499Enzastaurin (LY317615)CAS: 170364-57-5Purity: >99.50%
Enzastaurin (LY317615) is an ATP-competitive and selective inhibitor of PKCβ with an IC 50 value of 6nM.
- GC15431GF 109203X (Bisindolylmaleimide I)CAS: 133052-90-1Purity: >99.00%
GF 109203X is a selective inhibitor of protein kinase C, selective for the α and β1 isoforms with IC 50 values of 0.0084, 0.0180, 0.210, 0.132, and 5.8μM for α, β1, δ, ε and ζ isoforms of protein kinase C respectively.
- GC15520Sotrastaurin (AEB071)CAS: 425637-18-9Purity: >99.50%
Sotrastaurin (AEB071) is a potent and orally-active pan-protein kinase C (PKC) inhibitor, with Ki values of 0.22nM, 0.64nM, 0.95nM, 1.8nM, 2.1nM and 3.2nM for PKCθ, PKCβ, PKCα, PKCη, PKCδ and PKCε, respectively.
- GC14701Zoledronic AcidCAS: 118072-93-8Purity: >99.00%
Zoledronic Acid is a third-generation nitrogen-containing bisphosphonate bone resorption inhibitor.
- GC12790PirfenidoneCAS: 53179-13-8Purity: >98.00%
Pirfenidone (AMR69) is an orally active antifibrotic drug that attenuates the production of chemokines CCL2 and CCL12 in fibrocytes .
- GC10496Midostaurin (PKC412)CAS: 120685-11-2Purity: >98.00%
Midostaurin (PKC412) is an oral, multi-targeted tyrosine kinase inhibitor that inhibits multiple kinases, including FLT3, KIT, PDGFR, and VEGFR (IC 50 = 22-500nM).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC81672 | Senkyunolide B | 93236-67-0 | >98% | |
Senkyunolide B is a phthalide found in Angelica sinensis. | ||||
| GC81880 | OSU-2S TFA | - | >98.00% | |
OSU-2S TFA is a non-immunosuppressive derivative of Fingolimod hydrochloride (FTY720). | ||||
| GC81892 | Vevorisertib tetrahydrochloride | - | >98.00% | |
Vevorisertib tetrahydrochloride (ARQ 751 tetrahydrochloride) is an orally active allosteric AKT inhibitor that blocks AKT phosphorylation. | ||||
| GC90543 | EGFR Peptide (human, mouse) (myristoylated) (trifluoroacetate salt) | - | >95.00% | |
A PKC inhibitor | ||||
| GD09670 | 3,3-Dimethyl-1-butanol | 624-95-3 | >99.50% | |
3,3-Dimethyl-1-butanol is an oral inhibitor that inhibits the production of trimethylamine (TMA) by microorganisms and suppresses different microbial TMA lyases. | ||||
| GN10336 | Daphnetin | 486-35-1 | >99.00% | |
| GN10378 | Oxymatrine | 16837-52-8 | >98.00% | |
Oxymatrine is a quinolizidine alkaloid extracted from the roots of Sophora flavescens. | ||||
| GN10444 | 12-O-tetradecanoyl phorbol-13-acetate | 16561-29-8 | >98.00% | |
A PKC activator | ||||
| GN10463 | Chelerythrine | 34316-15-9 | >98% | |
| GN10534 | Asiaticoside | 16830-15-2 | >98.00% | |
Asiaticoside is a pentacyclic triterpenoid glycoside extracted from Centella asiatica . | ||||
| GC11499 | Enzastaurin (LY317615) | 170364-57-5 | >99.50% | |
Enzastaurin (LY317615) is an ATP-competitive and selective inhibitor of PKCβ with an IC 50 value of 6nM. | ||||
| GC15281 | K-252c | 85753-43-1 | >99.00% | |
Protein kinase inhibitor | ||||
| GC15420 | ICP 103 | - | >98% | |
Protein kinase inhibitor | ||||
| GC15431 | GF 109203X (Bisindolylmaleimide I) | 133052-90-1 | >99.00% | |
GF 109203X is a selective inhibitor of protein kinase C, selective for the α and β1 isoforms with IC 50 values of 0.0084, 0.0180, 0.210, 0.132, and 5.8μM for α, β1, δ, ε and ζ isoforms of protein kinase C respectively. | ||||
| GC15520 | Sotrastaurin (AEB071) | 425637-18-9 | >99.50% | |
Sotrastaurin (AEB071) is a potent and orally-active pan-protein kinase C (PKC) inhibitor, with Ki values of 0.22nM, 0.64nM, 0.95nM, 1.8nM, 2.1nM and 3.2nM for PKCθ, PKCβ, PKCα, PKCη, PKCδ and PKCε, respectively. | ||||
| GC16907 | Go 6983 | 133053-19-7 | >99.00% | |
Go 6983 is a pan-PKC inhibitor that acts on PKCα, PKCβ, PKCγ, PKCδ, andPKCμ with IC 50 values of 7nM, 7nM, 6nM, 10nM, and 20μM, respectively. | ||||
| GC14701 | Zoledronic Acid | 118072-93-8 | >99.00% | |
Zoledronic Acid is a third-generation nitrogen-containing bisphosphonate bone resorption inhibitor. | ||||
| GC17936 | GSK269962A | 850664-21-0 | >99.50% | |
ROCK inhibitor | ||||
| GC12790 | Pirfenidone | 53179-13-8 | >98.00% | |
Pirfenidone (AMR69) is an orally active antifibrotic drug that attenuates the production of chemokines CCL2 and CCL12 in fibrocytes . | ||||
| GC16354 | Dequalinium Chloride | 522-51-0 | >98.00% | |
anti-tumor agent and PKC inhibitor | ||||
| GC17322 | Ro 31-8220 | 125314-64-9 | >98% | |
pan-PKC inhibitor | ||||
| GC10496 | Midostaurin (PKC412) | 120685-11-2 | >98.00% | |
Midostaurin (PKC412) is an oral, multi-targeted tyrosine kinase inhibitor that inhibits multiple kinases, including FLT3, KIT, PDGFR, and VEGFR (IC 50 = 22-500nM). | ||||
