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Cellule staminali

Cellule staminali

Gli inibitori delle cellule staminali sono composti che mirano specificamente alle cellule staminali e alle loro vie di segnalazione, influenzando la loro capacità di autorinnovarsi e differenziarsi. Questi inibitori sono cruciali nella ricerca focalizzata sul controllo del comportamento delle cellule staminali, sulla comprensione dei processi di sviluppo e sullo sviluppo di terapie per malattie come il cancro, dove si ritiene che le cellule staminali svolgano un ruolo chiave. Presso CymitQuimica, offriamo una varietà di inibitori delle cellule staminali per supportare la tua ricerca in medicina rigenerativa, biologia dello sviluppo e oncologia.

Trovati 470 prodotti di "Cellule staminali"

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  • 1(R),2(S)-epoxy Cannabidiol

    CAS:
    <p>1(R),2(S)-epoxy Cannabidiol (Compound 2a) is a structural analog of phytocannabinoids, exhibiting significant inhibitory activity on the Wnt/β-catenin pathway. It holds potential for research as a neuroprotective agent.</p>
    Formula:C21H30O3
    Colore e forma:Solid
    Peso molecolare:330.46
  • STAT3-IN-31


    <p>STAT3-IN-31 (compound K2071), derived from STATtic, acts as an inhibitor of both STAT3 and mitotic processes. This compound interrupts mitotic progression and impacts the formation of the mitotic spindle. Additionally, STAT3-IN-31 hampers migration in glioblastoma cells, suppresses cellular proliferation within tumor spheroids, induces senescence in glioblastoma, and inhibits the growth of Temozolomide-resistant cells while reducing the secretion of the pro-inflammatory cytokine monocyte chemoattractant protein (MCP-1).</p>
    Formula:C16H15NO3S
    Colore e forma:Solid
    Peso molecolare:301.36
  • LP-922056

    CAS:
    <p>LP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.</p>
    Formula:C11H9ClN2O2S2
    Purezza:99.84%
    Colore e forma:Solid
    Peso molecolare:300.78
  • Super-TDU (1-31) (TFA)


    Super-TDU (1-31) TFA, a peptide, inhibits YAP-TEAD; it has strong anti-tumor effects in gastric cancer models.
    Formula:C141H218N40O48·C2HF3O2
    Colore e forma:Solid
    Peso molecolare:3355.5
  • Foxy-5 Ammonium Salt


    Foxy-5 Ammonium Salt, a WNT5A mimetic, blocks epithelial cancer cell migration without β-catenin impact and curbs prostate cancer spread.
    Formula:C26H46N7O12S2
    Purezza:97.70%
    Colore e forma:Solid
    Peso molecolare:712.26
  • WAY-656935

    CAS:
    WAY-656935 inhibits ROCK.
    Formula:C20H28ClN3O3S
    Purezza:97%
    Colore e forma:Solid
    Peso molecolare:425.97
  • ABC99

    CAS:
    ABC99 irreversibly inhibits wnt-deacylating enzyme NOTUM (IC50: 13 nM) with high serine hydrolase family selectivity.
    Formula:C22H21ClN4O5
    Purezza:99.89%
    Colore e forma:Soild
    Peso molecolare:456.88
  • Linavonkibart

    CAS:
    <p>Linavonkibart (SRK181) is a humanized antibody targeting TGFβ1 that blocks the release of TGF-β1 protein by specifically binding latent TGF-β1.</p>
    Purezza:97.4% (SDS-PAGE); 99.4% (SEC-HPLC) - 97.4% (SDS-PAGE); 99.4% (SEC-HPLC)
    Colore e forma:Liquid
  • Casein kinase 1δ-IN-6

    CAS:
    CK1δ-IN-6: potent, selective CK-1δ inhibitor, IC50 23 nM, neuroprotective, anti-inflammatory, for neurodegenerative research.
    Formula:C16H10ClF3N2OS
    Purezza:99.87%
    Colore e forma:Soild
    Peso molecolare:370.78
  • Cirevetmab

    CAS:
    Cirevetmab (ZTS-00521426), a caninized monoclonal antibody targeting Canis lupus familiaris TGFB1, is classified as an immunoglobulin G2-kappa.
    Colore e forma:Liquid
  • LX-7101 hydrochloride

    CAS:
    <p>LX-7101 hydrochloride is a potent LIMK and ROCK2 inhibitor with antihypertensive activity, inhibits LIMK1/2, ROCK, PKA, and can be used to study glaucoma.</p>
    Formula:C23H29N7O3xHCl
    Purezza:98.96%
    Colore e forma:Solid
    Peso molecolare:487.99
  • Lerdelimumab

    CAS:
    <p>Lerdelimumab (CAT-152) is an IgG4 monoclonal antibody targeting TGF-β2, used in glaucoma scarring research.</p>
    Colore e forma:Liquid
  • BAY 593

    CAS:
    BAY 593 functions as an inhibitor of geranylgeranyltransferase-I (GGTase-I), effectively preventing the activation of Rho-GTPases and consequently inactivating YAP1/TAZ signaling pathways. It has been shown to inhibit tumor growth dose-dependently in xenograft mouse models, exhibiting IC50 values of 38.4 nM in MT-1080 cells and 564 nM in MDA-MB-231 cells, as well as in PXF 541 xenografts.
    Formula:C26H32ClF3N2O3
    Colore e forma:Solid
    Peso molecolare:512.99
  • Prafnosbart

    CAS:
    Prafnosbart (DS-6016A) is a humanized IgG1-kappa monoclonal antibody targeting ACVR1 (activin A receptor type 1, ACVRLK2, ALK2, ACVR1A, SKR1), utilized in
    Colore e forma:Liquid
  • TEAD-IN-19


    TEAD-IN-19 (Compound 1l) is a transcriptional inhibitor of TEAD, showing inhibition rates of 38.5%, 36.2%, 57.8%, and 71.3% for TEAD1, TEAD2, TEAD3, and TEAD4, respectively, at 10 μM. It exhibits strong antiproliferative and antimigratory effects on prostate cancer cell lines and significantly reduces the expression of TEAD-regulated downstream genes. TEAD-IN-19 holds potential for research in the field of cancer therapeutics.
    Colore e forma:Odour Solid
  • Fresolimumab

    CAS:
    <p>Fresolimumab (GC1008) is a human monoclonal antibody targeting active TGFβ1, TGFβ2, TGFβ3, studied for cancer and focal segmental glomerulosclerosis.</p>
    Purezza:> 95% - > 95%
    Colore e forma:Liquid
    Peso molecolare:144.4 kDa
  • WAY-297174

    CAS:
    <p>WAY-297174 is a human protein kinase CK2 inhibitor with IC50 of &gt; 33 μM.</p>
    Formula:C11H12N2O2S2
    Purezza:99.53%
    Colore e forma:Soild
    Peso molecolare:268.36
  • RBPJ Inhibitor-1

    CAS:
    <p>RBPJ Inhibitor-1 (RIN1), a compound that impedes the functional interaction between RBPJ and SHARP, effectively inhibits NOTCH-dependent tumor cell</p>
    Formula:C17H14FN3O2
    Purezza:99.58%
    Colore e forma:Soild
    Peso molecolare:311.31
  • YAP-IN-1


    YAP-IN-1 (Compound (+)-1) is an autophagy inhibitor specifically targeting YAP1. It binds to the Hippo pathway transcription factor YAP1 with a Kd of 9.13 μM, promoting its degradation through the chaperone-mediated autophagy (CMA) pathway. This process inhibits the Rab7-mediated fusion of autophagosomes with lysosomes and decreases autophagy levels without affecting lysosomal function. YAP-IN-1 shows potential for cancer research, including in hepatocellular carcinoma and breast cancer.
    Colore e forma:Odour Solid
  • Epigenetics Compound Library


    Well-chosen 953 compounds related to epigenetic regulation for research in epigenetics, high throughput screening (HTS) and high content screening (HCS) for new
    Colore e forma:Odour Solid