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Células madre y Derivados

Células madre y Derivados

Los inhibidores de células madre son compuestos que se dirigen específicamente a las vías de señalización y proteínas involucradas en el mantenimiento, diferenciación y proliferación de células madre. Estos inhibidores son cruciales para comprender la biología de las células madre y para desarrollar estrategias que permitan manipularlas con fines terapéuticos, como en la medicina regenerativa y el tratamiento del cáncer. Al controlar el destino de las células madre, estos inhibidores pueden ayudar a guiar la diferenciación de células madre en tipos celulares específicos o prevenir el crecimiento celular no deseado. En CymitQuimica, ofrecemos una selección de inhibidores de células madre de alta calidad para apoyar su investigación en biología de células madre, biología del desarrollo y medicina regenerativa.

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Se han encontrado 431 productos para "Células madre y Derivados".

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  • JAK-IN-15

    CAS:
    JAK-IN-15 is a JAK inhibitor. WO2016119700A1 (Compound 15).
    Fórmula:C22H23FN4O3S
    Forma y color:Solid
    Peso molecular:442.51

    Ref: TM-T39400

    5mg
    873,00€
  • Notch 1 TFA


    Notch 1 TFA encodes a member of the NOTCH family of proteins.
    Fórmula:C64H98N15F3O25S3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1614.81

    Ref: TM-T19483

    100mg
    A consultar
    500mg
    A consultar
  • 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
    Forma y color:Odour Solid

    Ref: TM-L1200

    1mg
    A consultar
    10μL*10mM (DMSO)
    A consultar
    20μL*10mM (DMSO)
    A consultar
    30μL*10mM (DMSO)
    A consultar
    50μL*10mM (DMSO)
    A consultar
    100μL*10mM (DMSO)
    A consultar
    250μL*10mM (DMSO)
    A consultar
  • SJ1008030

    CAS:
    SJ1008030, a JAK2 PROTAC, degrades JAK2; EC50: 5.4 nM, IC50: 32.09 nM in MHH-CALL-4 cells for leukemia research.
    Fórmula:C42H43N13O7S
    Forma y color:Solid
    Peso molecular:873.94

    Ref: TM-T74580

    5mg
    A consultar
    50mg
    A consultar
  • FRM-024

    CAS:
    FRM-024 is a powerful gamma secretase modulator with the ability to penetrate the central nervous system (CNS), designed specifically for the treatment of
    Fórmula:C22H22ClN5O2
    Forma y color:Solid
    Peso molecular:423.9

    Ref: TM-T39492

    5mg
    873,00€
  • LY2382770


    LY2382770 is a human monoclonal antibody (mAb) that specifically targets TGFB1. It is utilized in the study of diabetic nephropathy.

    Ref: TM-T9901A-1687

    1mg
    A consultar
    5mg
    A consultar
  • Tyrosine Protein Kinase JAK 2 (Phospho-Tyr8, 9)

    CAS:
    Tyrosine Protein Kinase JAK 2 (Phospho-Tyr8, 9) is a peptide derived from mouse JAK2, specifically composed of amino acids 475 to 491.
    Fórmula:C88H138N20O34P2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2082.1

    Ref: TM-TP1269

    1mg
    92,00€
    5mg
    288,00€
    10mg
    454,00€
  • LH168


    LH168 is a potent and selective probe for WDR5, with a SPR Kd value of 13 nM.
    Fórmula:C29H31F3N6O2S
    Forma y color:Solid
    Peso molecular:584.66

    Ref: TM-T205103

    10mg
    A consultar
    50mg
    A consultar
  • MMT3-72

    CAS:
    MMT3-72 is a weak JAK1 inhibitor with superior efficacy and reduced p-STAT3 in DSS-induced colitis [1].
    Fórmula:C40H42N8O9S
    Peso molecular:810.87

    Ref: TM-T86914

    10mg
    A consultar
    50mg
    A consultar
  • Wnt/Hedgehog/Notch Compound Library


    A unique collection of 237 Wnt/Hedgehog/Notch signaling targeted compounds for high throughput and high content screening;

    Forma y color:Odour Solid

    Ref: TM-L4300

    1mg
    A consultar
  • Depiperazine-DM3189

    CAS:
    Depiperazine-DM3189 inhibits the phosphorylation of SMAD 1/5/8 induced by bone morphogenetic protein 4 and can be used in biochemical experiments .
    Fórmula:C21H14N4
    Pureza:99.69%
    Peso molecular:322.36

    Ref: TM-T204059

    1mg
    175,00€
    5mg
    434,00€
    10mg
    622,00€
    25mg
    973,00€
    50mg
    1.341,00€
  • Baricitinib-D3

    CAS:
    Baricitinib-D3 is the deuterated form of Baricitinib. Baricitinib (T2485) (LY3009104; INCB028050) acts as a selective and orally administered inhibitor of JAK1 and JAK2, with IC50 values of 5.9 nM and 5.7 nM, respectively.
    Fórmula:C16H17N7O2S
    Forma y color:Solid
    Peso molecular:374.44

    Ref: TM-TMID-1196

    10mg
    A consultar
    50mg
    A consultar
  • OPN-9652

    CAS:
    OPN-9652 is a covalent TEAD inhibitor reversing drug resistance in BRAF-mutant tumors.
    Fórmula:C19H15F4NO2
    Pureza:99.78%
    Forma y color:White Solid
    Peso molecular:365.32

    Ref: TM-T212610

    1mg
    175,00€
    5mg
    434,00€
    10mg
    622,00€
    25mg
    973,00€
    50mg
    1.341,00€
    100mg
    1.765,00€
  • P17 Peptide

    CAS:
    P17 Peptide, a human TGF-β1 inhibitory peptide, effectively blocks the activity of woodchuck TGF-β1.
    Fórmula:C95H139N27O21
    Forma y color:Solid
    Peso molecular:1995.29

    Ref: TM-TP2844

    10mg
    A consultar
    50mg
    A consultar
  • SJ10542

    CAS:
    SJ10542: potent JAK2/3-targeting PG-PROTAC; DC50s: JAK2 - 14 nM, JAK3 - 11 nM, JAK2-fusion ALL - 24 nM; CRBN recruiter.
    Fórmula:C41H46N12O5S
    Forma y color:Solid
    Peso molecular:818.95

    Ref: TM-T74429

    2mg
    1.288,00€
  • JAK1/STAT3-IN-1


    JAK1/STAT3-IN-1 (compound 4f) functions as an anti-atopic dermatitis (AD) agent by inhibiting the JAK1/STAT3 signaling pathway. It has an IC50 value of 2.17 μM for inhibiting NO production. Additionally, JAK1/STAT3-IN-1 improves skin conditions in AD-like mice by reducing inflammatory infiltration, suppressing the expression of p-JAK1/JAK1 and p-STAT3/STAT3, and alleviating the hyperimmune response induced by MC903 (Calcipotriol).
    Fórmula:C30H33FN4O3S
    Forma y color:Solid
    Peso molecular:548.67

    Ref: TM-T205385

    10mg
    A consultar
    50mg
    A consultar
  • 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.
    Forma y color:Odour Solid

    Ref: TM-T206604

    10mg
    A consultar
    50mg
    A consultar
  • RBPJ Inhibitor-1

    CAS:
    RBPJ Inhibitor-1 (RIN1), a compound that impedes the functional interaction between RBPJ and SHARP, effectively inhibits NOTCH-dependent tumor cell
    Fórmula:C17H14FN3O2
    Pureza:99.79%
    Forma y color:Solid
    Peso molecular:311.31

    Ref: TM-T35566

    1mg
    38,00€
    2mg
    50,00€
    5mg
    84,00€
    1mL*10mM (DMSO)
    93,00€
    10mg
    130,00€
    25mg
    215,00€
    50mg
    371,00€
    100mg
    537,00€
  • HC-258

    CAS:
    HC-258 is a direct TEAD inhibitor covalent Cys380, and reduces the transcriptional levels and inhibits the migration of CTGF, CYR61, AXL and NF2 MDA-MB-231.
    Fórmula:C20H24N2O2
    Forma y color:Yellow Solid
    Peso molecular:324.42

    Ref: TM-T88390

    1mg
    64,00€
    5mg
    165,00€
    10mg
    255,00€
  • TYD-68


    TYD-68 is a potent and selective CRBN-recruiting TYK2 PROTAC degrader, with a DC50 value of 0.42 nM. This compound effectively inhibits IL-12 and IFN-α-induced phosphorylation of STAT4 and STAT1, thereby blocking TYK2-dependent signaling pathways. TYD-68 is applicable in psoriasis research.
    Forma y color:Odour Solid

    Ref: TM-T206972

    10mg
    A consultar
    50mg
    A consultar