TGF-beta/Smad
Gli inibitori del percorso TGF-beta/Smad sono composti che interferiscono con la via di segnalazione TGF-beta (Transforming Growth Factor-beta), mediata dalle proteine Smad. Questa via è coinvolta nella regolazione della crescita cellulare, della differenziazione, dell'apoptosi e della funzione delle cellule staminali. La disfunzione della segnalazione TGF-beta/Smad è associata al cancro, alla fibrosi e ad altre malattie. Gli inibitori di questa via sono strumenti importanti per studiare queste condizioni e sviluppare potenziali terapie. Presso CymitQuimica, forniamo inibitori di TGF-beta/Smad per supportare la tua ricerca nella segnalazione cellulare, in oncologia e nella riparazione dei tessuti.
Trovati 60 prodotti di "TGF-beta/Smad"
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
TGFβ-IN-5
CAS:TGFβ-IN-5 (WAY-641966) is a potent TGFβ inhibitor with anti-prion activity for the study of fibroproliferative diseases associated with TGF-β signaling.Formula:C20H16N4Purezza:99.29% - 99.62%Colore e forma:SolidPeso molecolare:312.37Myristoyl tetrapeptide-12
CAS:Myristoyl Tetrapeptide-12 activates SMAD2 and facilitates the association of SMAD3 with DNA, promoting eyelash hair growth [1] [2].Formula:C32H63N7O5Purezza:98%Colore e forma:SolidPeso molecolare:625.89TP0427736
CAS:TP0427736: ALK5 inhibitor, IC50=2.72 nM, 300x > ALK3 selectivity; counters TGF-β in human cells, extends anagen in mice.Formula:C14H10N4S2Purezza:97.26%Colore e forma:SolidPeso molecolare:298.39CDD-1431
CAS:<p>CDD-1431 is a highly selective BMPR2 kinase inhibitor with a Kiapp of 20.6 nM. It inhibits BRE reporter gene activity, exhibiting an IC50 of 4.87 μM. BMPs regulate cellular processes across various tissue types such as the kidneys, skeletal muscle, heart, and reproductive organs, and can induce ectopic bone formation.</p>Formula:C33H38N8O5SColore e forma:SolidPeso molecolare:658.77TGFβ1-IN-1
CAS:TGFβ1-IN-1 is a TGF-β1 inhibitor that inhibits the production of TGF-β1-induced fibrosis markers (α-SMA and fibronectin) and can be used in cancer research.Formula:C22H24N2O3Purezza:99.89% - 99.89%Colore e forma:SolidPeso molecolare:364.438Ref: TM-T61389
1mg52,00€5mg111,00€10mg180,00€25mg359,00€50mg588,00€100mg944,00€200mg1.264,00€1mL*10mM (DMSO)124,00€Kartogenin sodium
CAS:Kartogenin (KGN) sodium acts as an inducer of chondrogenic tissue formation (EC 50: 100 nM). It promotes chondrogenesis by binding to fibrin A, disrupting its interaction with the transcription factor core binding factor beta subunit (CBFβ), and modulating the CBFβ-RUNX1 transcriptional program. Additionally, Kartogenin sodium aids tendon-bone junction (TBJ) wound healing by stimulating collagen synthesis. It is extensively utilized in cell-free therapies for cartilage regeneration and protection, tendon-bone healing, wound healing, and limb development. The compound is also vital for cartilage repair, coordinating limb development, and osteoarthritis (OA) research [1] [2] [3] [4].Formula:C20H14NNaO3Peso molecolare:339.32(+)-ITD-1
CAS:(+)-ITD-1 is an inhibitor of TGF-β, effectively inhibiting TGF-β2 with an IC50 of 0.46 μM. It promotes the degradation of the TGF-β type II receptor (TGFBR2) and the differentiation of cardiomyocytes. Additionally, it suppresses the formation of the mesoderm during the early differentiation of mouse embryonic stem cells (mESCs).Formula:C27H29NO3Colore e forma:SolidPeso molecolare:415.52TGFβRI-IN-3
CAS:TGFβRI-IN-3 inhibits TGFβR1 with an IC 50 of 0.79 nM with 2000-fold selectivity against MAP4K4.Formula:C28H23N3O2SPurezza:99.85%Colore e forma:SoildPeso molecolare:465.57Ref: TM-T9523
1mg88,00€5mg187,00€10mg298,00€25mg582,00€50mg908,00€100mg1.301,00€500mg2.593,00€1mL*10mM (DMSO)187,00€Luspatercept
CAS:Luspatercept (ACE-536), a recombinant modified ActRIIB fusion protein, selectively binds to transforming growth factor β superfamily ligands, thereby enhancing erythrocyte production and advancing the maturation of erythroid precursors. Moreover, by binding with GDF11, it inhibits Smad2/3 signaling. This compound is instrumental in anemia research [1].Colore e forma:LiquidDCN1-IN-2
CAS:<p>DCN1-IN-2, a DCN1 inhibitor, exhibits potent activity with an IC 50 of 2.96 nM. It effectively mitigates Ang II/TGFβ-induced activation of cardiac fibroblasts and diminishes ISO-induced cardiac fibrosis and remodeling in mice through the selective inhibition of cullin 3.</p>Formula:C18H14ClF3N4OSColore e forma:SolidPeso molecolare:426.84
