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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 467 prodotti di "Cellule staminali"

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  • Trevogrumab

    CAS:
    Trevogrumab is a human monoclonal antibody that inhibits myostatin (GDF8) to promote muscle growth, and is under research for treating age-related muscle loss (sarcopenia).
    Purezza:95% - 97.6% (SDS-PAGE); 95.9% (SEC-HPLC)
    Colore e forma:Liquid
  • Metelimumab

    CAS:
    Metelimumab (CAT-192) is a humanised monoclonal antibody targeting TGFβ1, which can be used to study diffuse systemic sclerosis (d-SSc).
    Purezza:95%
    Colore e forma:Liquid
  • 1-Azakenpaullone

    CAS:
    1-Azakenpaullone (azakenpaullone) is a potent and selective GSK-3β inhibitor with IC50 of 18 nM, >100-fold selectivity over CDK1/cyclin B and CDK5/p25.
    Formula:C15H10BrN3O
    Purezza:99.73%
    Colore e forma:Tan Solid
    Peso molecolare:328.16
  • VT103

    CAS:
    VT103, an oral TEAD1 palmitoylation inhibitor, shows promise against various cancers by disrupting YAP/TAZ-TEAD interactions.
    Formula:C18H17F3N4O2S
    Purezza:99.58%
    Colore e forma:Solid
    Peso molecolare:410.41
  • TEAD-IN-6

    CAS:
    TEAD-IN-6 (Example 11-1) is a TEAD modulator that inhibits the YAP1/TAZ-TEAD interaction, and has applications in cancer research [1].
    Formula:C19H17F3N4O3S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:438.42
  • TGFβRI-IN-1

    CAS:
    TGFβRI-IN-1 is an oral active and selective inhibitor of TGFβ receptor type I (TGFβRI) kinase(IC50 values of 2 nM and 7.6 μM for TGFβRI and TGFβRII,
    Formula:C20H14D3N5O2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:362.4
  • CK2-IN-4

    CAS:
    CK2-IN-4 is a protein kinase (CK2) inhibitor with an IC50 value of 8.6 µM.
    Formula:C18H11N3O4S
    Purezza:99.65%
    Colore e forma:Solid
    Peso molecolare:365.36
  • CK2α-IN-1

    CAS:
    CK2α-IN-1 is a selective non-ATP-competitive CK2α inhibitor with an IC50 of 7.0 µM and a Ki of 1.6 µM.CK2α-IN-1 exhibits potential anticancer activity and can
    Formula:C16H11N3O4S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:341.34
  • JA310

    CAS:
    JA310 is a highly selective inhibitor of the MST3 kinase, demonstrating significant cellular potency with an EC50 value of 106 nM [1].
    Formula:C17H19N7O
    Colore e forma:Solid
    Peso molecolare:337.38
  • JAK1-IN-4

    CAS:
    JAK1-IN-4 selectively blocks JAK1 (IC50 = 85 nM) over JAK2/JAK3 and halts STAT3 phosphorylation in NCI-H 1975 cells (IC50 = 227 nM).
    Formula:C26H32FN9O2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:521.59
  • ELN318463 racemate

    CAS:
    ELN318463 racemate (ELN 318463 racemate) is the racemate of ELN318463 which is an amyloid precursor protein (APP) selective γ-secretase inhibitor.
    Formula:C19H20BrClN2O3S
    Purezza:99.69%
    Colore e forma:Solid
    Peso molecolare:471.8
  • JAK-IN-11

    CAS:
    JAK-IN-11 (R-348) is a potent and selective inhibitor of JAK, has the potential for the skin disorders treatment.
    Formula:C23H22FN5O4S
    Purezza:99.75%
    Colore e forma:Solid
    Peso molecolare:483.52
  • H-1152

    CAS:
    <p>H-1152 is a potent, specific, ATP-competitive, and cell permeable ROCK inhibitor (Ki = 1.6 nM).</p>
    Formula:C16H21N3O2S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:319.42
  • GSK3-IN-2

    CAS:
    <p>GSK3-IN-2 is a potent GSK3 inhibitor for the treatment of diabetes and neurodegenerative diseases.</p>
    Formula:C17H19N3OS
    Purezza:98.8%
    Colore e forma:Solid
    Peso molecolare:313.42
  • CJJ300

    CAS:
    <p>CJJ300 is a TGF-β inhibitor disrupting TGF-β-TβR complex formation, with an IC50 of 5.3 μM, and halts cell migration.</p>
    Formula:C30H33N3
    Purezza:99.80%
    Colore e forma:Solid
    Peso molecolare:435.6
  • SD-1029

    CAS:
    SD-1029 is a JAK2 inhibitor and a novel Stat3 activation inhibitor that inhibits Stat3 phosphorylation and JAK-STAT signaling.
    Formula:C25H32Br2Cl2N2O3
    Colore e forma:Solid
    Peso molecolare:639.25
  • JAK-IN-30

    CAS:
    <p>JAK-IN-30 (compound 31) is a water-soluble inhibitor of Janus kinases (JAKs), demonstrating inhibitory potency with half-maximal inhibitory concentration (IC50</p>
    Formula:C19H26N8S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:398.53
  • (Rac)-SIS3 free base

    CAS:
    SIS3 free base is a potent and selective Smad3 phosphorylation inhibitor. SIS3 free base inhibits the myofibroblast differentiation of fibroblasts by TGF-β1.
    Formula:C28H27N3O3
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:453.53
  • SB-772077B dihydrochloride

    CAS:
    SB-772077B dihydrochloride is an aminofurazan-based Rho kinase inhibitor (IC50s: 5.6 nM and 6 nM toward ROCK1 and ROCK2, respectively).
    Formula:C15H20Cl2N8O2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:415.28
  • inS3-54-A26

    CAS:
    <p>inS3-54-A26 is an inhibitor of the DNA-binding domain of STAT3. inS3-54-A26 suppresses tumor growth, metastasis and the gene expression of STAT3.</p>
    Formula:C25H19ClN2O2
    Purezza:99.57%
    Colore e forma:Solid
    Peso molecolare:414.88