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Cellule staminali e Derivati

Cellule staminali e Derivati

Gli inibitori delle cellule staminali sono composti che bersagliano specificamente le vie di segnalazione e le proteine coinvolte nel mantenimento, nella differenziazione e nella proliferazione delle cellule staminali. Questi inibitori sono cruciali per comprendere la biologia delle cellule staminali e per sviluppare strategie per manipolare le cellule staminali a fini terapeutici, come la medicina rigenerativa e il trattamento del cancro. Controllando il destino delle cellule staminali, questi inibitori possono aiutare a guidare la differenziazione delle cellule staminali in tipi cellulari specifici o a prevenire una crescita cellulare indesiderata. Presso CymitQuimica, offriamo una selezione di inibitori delle cellule staminali di alta qualità per supportare la tua ricerca in biologia delle cellule staminali, biologia dello sviluppo e medicina rigenerativa.

Sottocategorie di "Cellule staminali e Derivati"

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Trovati 693 prodotti di "Cellule staminali e Derivati"

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  • INCB16562

    CAS:
    <p>INCB16562: oral JAK1/2 inhibitor, halts IL-6/STAT3 in myeloma cells, boosts drug efficacy, stunts myeloma in mice.</p>
    Formula:C19H11Cl2N5
    Colore e forma:Solid
    Peso molecolare:380.23
  • OICR-0547

    CAS:
    <p>OICR-0547 is an inactive derivative of OICR-9429 and is commonly used as a negative control for OICR-9429.</p>
    Formula:C28H29F3N4O4
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:542.55
  • CK2α-IN-1

    CAS:
    <p>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</p>
    Formula:C16H11N3O4S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:341.34
  • CK2-IN-4

    CAS:
    <p>CK2-IN-4 is a protein kinase (CK2) inhibitor with an IC50 value of 8.6 µM.</p>
    Formula:C18H11N3O4S
    Purezza:99.72%
    Colore e forma:Solid
    Peso molecolare:365.36
  • JI051

    CAS:
    JI051 has anti-tumor effects and can interact with PHB2 to inhibit the proliferation of HEK293 cells and pancreatic cancer cells.
    Formula:C22H24N2O3
    Purezza:≥98% - ≥98.0%
    Colore e forma:Solid
    Peso molecolare:364.44
  • TGFβRI-IN-1

    CAS:
    <p>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,</p>
    Formula:C20H14D3N5O2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:362.4
  • Povorcitinib

    CAS:
    <p>Povorcitinib is a highly potent and selective JAK1 inhibitor with significant potential for the investigation of cutaneous lupus erythematosus (CLE) and Lichen planus (LP).</p>
    Formula:C23H22F5N7O
    Colore e forma:Solid
    Peso molecolare:507.469
  • JAK-IN-20

    CAS:
    <p>JAK-IN-20: potent oral JAK1,2,3 inhibitor with IC50s 7, 5, 14 nM respectively, good pharmacokinetics, anti-inflammatory in vivo.</p>
    Formula:C28H30FN7O2
    Colore e forma:Solid
    Peso molecolare:515.58
  • FzM1.8

    CAS:
    <p>FzM1.8: allosteric FZD4 agonist, pEC50=6.4; boosts TCF/LEF, activates WNT/β-catenin with no WNT needed.</p>
    Formula:C18H14N2O4
    Purezza:99.89%
    Colore e forma:Solid
    Peso molecolare:322.31
  • Casein kinase 1δ-IN-1

    CAS:
    Casein kinase 1δ-IN-1 (WAY-643895) is an inhibitor of casein kinase 1δ (CK1δ), which inhibits CK1δ.
    Formula:C11H7N3OS
    Purezza:99.89%
    Colore e forma:Solid
    Peso molecolare:229.26
  • Butyzamide

    CAS:
    <p>Butyzamide: oral Mpl activator, non-peptide, antagonizes TPO receptors, boosts hMpl, Ba/F3 cells, and enhances platelets in mice.</p>
    Formula:C29H32Cl2N2O5S
    Purezza:99.51% - 99.83%
    Colore e forma:Soild
    Peso molecolare:591.55
  • GSK-3β inhibitor 2

    CAS:
    <p>GSK-3β inhibitor 2 (5-Thiazolecarboxamide,2-[2-[(cyclopropylcarbonyl)amino]-4-pyridinyl]-4-methoxy-) is a BBB-crossing and selective inhibitor of GSK-3β (IC50</p>
    Formula:C14H14N4O3S
    Purezza:99.08%
    Colore e forma:Solid
    Peso molecolare:318.35
  • TT-10

    CAS:
    <p>TT-10 (TAZ-K) activates YAP-TEAD; useful in heart disease with cardiomyocyte loss research.</p>
    Formula:C11H10FN3OS2
    Purezza:99.29%
    Colore e forma:Solid
    Peso molecolare:283.35
  • Rhodblock 6

    CAS:
    <p>Rhodblock 6 is a Rho kinase inhibitor, blocking phosphorylated MRLC localization by targeting ROCK activity.</p>
    Formula:C12H13N3O
    Purezza:98.27%
    Colore e forma:Solid
    Peso molecolare:215.25
  • XL413 xHCl

    CAS:
    <p>BMS-863233 HCl is an ATP-competitive Cdc7 inhibitor (IC50: 3.4 nM) that is potent and selective.BMS-863233 HCl inhibited CK2 and PIM1 with IC50 values of 215</p>
    Formula:C14H12ClN3O2·xHCl
    Purezza:99.37% - 99.67%
    Colore e forma:Solid
    Peso molecolare:326.18
  • LM-41

    CAS:
    <p>LM-41 is a TEAD binding agent with potential anticancer activity for the study of breast cancer.</p>
    Formula:C19H14FNO2
    Purezza:99.73%
    Colore e forma:Solid
    Peso molecolare:307.32
  • PI-828

    CAS:
    <p>PI-828 (LY 294002), a PI3K inhibitor, researches PI3K function and aids stem cell differentiation into mesoderm.</p>
    Formula:C19H18N2O3
    Purezza:99.95%
    Colore e forma:Solid
    Peso molecolare:322.36
  • FzM1

    CAS:
    <p>FzM1, a negative allosteric modulator (NAM) of the Frizzled receptor FZD4, diminishes WNT5A-dependent WNT responsive element (WRE) activity (log EC50inh=−6.2)</p>
    Formula:C21H16N2O2S
    Purezza:99.37% - 99.89%
    Colore e forma:Solid
    Peso molecolare:360.43
  • Izencitinib

    CAS:
    <p>Izencitinib (JNJ-8398) is a JAK inhibitor with potential anti-inflammatory activity for the study of ulcerative colitis and Crohn;s disease.</p>
    Formula:C22H26N8
    Purezza:99.82%
    Colore e forma:Solid
    Peso molecolare:402.50
  • Rho-Kinase-IN-1

    CAS:
    <p>Rho-Kinase-IN-1: ROCK inhibitor, Ki of 30.5 nM (ROCK1) &amp; 3.9 nM (ROCK2), used in research for diseases linked to cell overgrowth and inflammation.</p>
    Formula:C20H24N4S
    Purezza:99.8%
    Colore e forma:Solid
    Peso molecolare:352.5