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Células - tronco e Derivados

Células - tronco e Derivados

Os inibidores de células-tronco são compostos que visam especificamente as vias de sinalização e proteínas envolvidas na manutenção, diferenciação e proliferação de células-tronco. Esses inibidores são cruciais para compreender a biologia das células-tronco e para desenvolver estratégias para manipular células-tronco para fins terapêuticos, como medicina regenerativa e tratamento do câncer. Ao controlar o destino das células-tronco, esses inibidores podem ajudar a orientar a diferenciação das células-tronco em tipos celulares específicos ou prevenir o crescimento celular indesejado. Na CymitQuimica, oferecemos uma seleção de inibidores de células-tronco de alta qualidade para apoiar sua pesquisa em biologia de células-tronco, biologia do desenvolvimento e medicina regenerativa.

Subcategorias de "Células - tronco e Derivados"

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Foram encontrados 695 produtos de "Células - tronco e Derivados"

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  • Cardiogenol C
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    Cardiogenol C

    CAS:
    <p>Cardiogenol C is a cardiomyogenesis inducer in embryonic stem cells.</p>
    Fórmula:C13H16N4O2
    Pureza:98.46%
    Cor e Forma:Solid
    Peso molecular:260.29

    Ref: TM-T2161

  • LY3200882
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    LY3200882

    CAS:
    <p>LY3200882 is a highly selective inhibitor of TGF-β receptor type 1 (TGFβRI).</p>
    Fórmula:C24H29N5O3
    Pureza:99.46% - 99.63%
    Cor e Forma:Solid
    Peso molecular:435.52

    Ref: TM-T5125

  • WAY 316606
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    WAY 316606

    CAS:
    <p>WAY 316606 is an inhibitor of the secreted protein sFRP-1, an endogenous antagonist of the secreted glycoprotein Wnt.</p>
    Fórmula:C18H19F3N2O4S2
    Pureza:99.65%
    Cor e Forma:Solid
    Peso molecular:448.48

    Ref: TM-T4468

  • BDP5290
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    BDP5290

    CAS:
    <p>BDP5290 is a potent inhibitor of both ROCK and MRCK(IC50s of 5 nM, 50 nM, 10 nM and 100 nM for ROCK1, ROCK2, MRCKα and MRCKβ, respectively.)</p>
    Fórmula:C17H18ClN7O
    Pureza:97.22%
    Cor e Forma:Solid
    Peso molecular:371.82

    Ref: TM-T7301

  • AZD1080
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    AZD1080

    CAS:
    <p>AZD1080 is a selective, orally active, brain permeable GSK3 inhibitor.</p>
    Fórmula:C19H18N4O2
    Pureza:97.72% - 99.75%
    Cor e Forma:Solid
    Peso molecular:334.37

    Ref: TM-T1741

  • IMR-1A
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    IMR-1A

    CAS:
    <p>IMR-1A is the metabolite of IMR-1 which is a novel class of Notch inhibitors targeting the transcriptional activation with IC50 of 6 μMol/L.</p>
    Fórmula:C13H11NO5S2
    Pureza:97.1% - 99.76%
    Cor e Forma:Solid
    Peso molecular:325.36

    Ref: TM-T3540

  • BD750
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    BD750

    CAS:
    <p>BD750 is an effective immunosuppressant and a JAK3/STAT5 inhibitor, inhibits IL-2-induced JAK3/STAT5-dependent T cell proliferation(IC50 of 1.5 μM and 1.1 μM in</p>
    Fórmula:C14H13N3OS
    Pureza:99.02%
    Cor e Forma:Solid
    Peso molecular:271.34

    Ref: TM-T8546

  • WHI-P154
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    WHI-P154

    CAS:
    <p>WHI-P154 (Jak3 inhibitor ii) is a potent JAK3 inhibitor.</p>
    Fórmula:C16H14BrN3O3
    Pureza:98% - 99.67%
    Cor e Forma:Solid
    Peso molecular:376.2

    Ref: TM-T1985

  • Teplinovivint
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    Teplinovivint

    CAS:
    <p>Teplinovivint is a potent inhibitor of the Wnt/β-catenin signaling pathway, demonstrating anti-inflammatory properties with potential utility in tendinopathy</p>
    Fórmula:C25H26N6O2
    Pureza:97.21%
    Cor e Forma:Solid
    Peso molecular:442.51

    Ref: TM-T9151

  • I3MT-3
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    I3MT-3

    CAS:
    <p>I3MT-3 (HMPSNE) is a selective inhibitor of 3MST, targeting active site cysteine residues and permeating cell membranes.</p>
    Fórmula:C17H14N2O2S
    Pureza:99.76%
    Cor e Forma:Solid
    Peso molecular:310.37

    Ref: TM-T8851

  • CMD178 TFA
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    CMD178 TFA

    <p>CMD178 (TFA) is a lead peptide that consistently reduces the expression of Foxp3 and STAT5 induced by IL-2/s IL-2Rα signaling.</p>
    Fórmula:C48H60F3N9O9
    Pureza:>99.99%
    Cor e Forma:Solid
    Peso molecular:964.05

    Ref: TM-TP1433

  • ML116
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    ML116

    CAS:
    <p>ML116 is a potent and selective STAT3 inhibitor.</p>
    Fórmula:C18H19N3S
    Pureza:99.49%
    Cor e Forma:Solid
    Peso molecular:309.43

    Ref: TM-T8597

  • Cucurbitacin I
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    Cucurbitacin I

    CAS:
    <p>Cucurbitacin I (JSI-124), a natural compound, is a selective inhibitor of JAK2/STAT3 with anti-cancer activity.</p>
    Fórmula:C30H42O7
    Pureza:96.69% - 99.8%
    Cor e Forma:Solid
    Peso molecular:514.65

    Ref: TM-TQ0196

  • β-catenin-IN-2
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    β-catenin-IN-2

    CAS:
    <p>β-catenin-IN-2 is a potent inhibitor of β-catenin that can be used in colorectal cancer research.</p>
    Fórmula:C15H14FN3
    Pureza:99.93%
    Cor e Forma:Solid
    Peso molecular:255.29

    Ref: TM-T9696

  • GLPG0634 analog
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    GLPG0634 analog

    CAS:
    <p>GLPG0634 analog (GLPG0634 analogue) is a specific JAK1 inhibitor with IC50 of 10/28/810/116 nM for JAK1/2/3 and TYK2, respectively.</p>
    Fórmula:C23H18N6O2
    Pureza:99.52% - >99.99%
    Cor e Forma:Solid
    Peso molecular:410.43

    Ref: TM-T3076

  • TTP 22
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    TTP 22

    CAS:
    <p>TTP 22: ATP-competitive CK2 inhibitor; IC50/Ki: 0.1 μM/40 nM; &gt;250x selective over JNK3, ROCK1, MET.</p>
    Fórmula:C16H14N2O2S2
    Pureza:97.08% - 97.78%
    Cor e Forma:Solid
    Peso molecular:330.42

    Ref: TM-T1828

  • SH-4-54
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    SH-4-54

    CAS:
    <p>SH-4-54 is a most potent, small molecule, nonphosphorylated STAT3 inhibitor.</p>
    Fórmula:C29H27F5N2O5S
    Pureza:98% - 99.12%
    Cor e Forma:Solid
    Peso molecular:610.59

    Ref: TM-T6669

  • TDZD-8
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    TDZD-8

    CAS:
    <p>TDZD-8 (NP 01139) is an inhibitor of GSK-3β, with an IC50 of 2 μM; minimal inhibitory effect observed on CDK1, casein kinase II, PKA and PKC.</p>
    Fórmula:C10H10N2O2S
    Pureza:97.13% - 99.61%
    Cor e Forma:White Solid
    Peso molecular:222.26

    Ref: TM-T6187

  • JI130
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    JI130

    CAS:
    <p>JI130 hinders Hes1 transcription repression; notably shrinks pancreatic tumor volume in mice.</p>
    Fórmula:C23H24N2O3
    Pureza:99.61%
    Cor e Forma:Solid
    Peso molecular:376.45

    Ref: TM-T9588

  • GS87
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    GS87

    CAS:
    <p>GS87 is a highly specific inhibitor of GSK3 (glycogen synthase kinase 3) that induces extensive differentiation of AML cells.</p>
    Fórmula:C16H11N5O2S
    Pureza:98.86%
    Cor e Forma:Solid
    Peso molecular:337.36

    Ref: TM-T8605