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Stem Cell and Derivatives

Stem Cell and Derivatives

Stem cell inhibitors are compounds that specifically target signaling pathways and proteins involved in the maintenance, differentiation, and proliferation of stem cells. These inhibitors are crucial for understanding stem cell biology and for developing strategies to manipulate stem cells for therapeutic purposes, such as regenerative medicine and cancer treatment. By controlling stem cell fate, these inhibitors can help guide stem cell differentiation into specific cell types or prevent unwanted cell growth. At CymitQuimica, we offer a selection of high-quality stem cell inhibitors to support your research in stem cell biology, developmental biology, and regenerative medicine.

Subcategories of "Stem Cell and Derivatives"

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Found 693 products of "Stem Cell and Derivatives"

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  • Afuresertib hydrochloride
    Targetmol
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    Afuresertib hydrochloride

    CAS:
    <p>Afuresertib hydrochloride is an inhibitor of Akt kinase (Kis of 0.08/2/2.6 nM for Akt1/Akt2/Akt3 respectively)</p>
    Formula:C18H18Cl3FN4OS
    Purity:99.96%
    Color and Shape:Solid
    Molecular weight:463.8

    Ref: TM-T7885

  • BP-1-102
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    BP-1-102

    CAS:
    <p>BP-1-102 is an orally active, effective and specific STAT3 inhibitor.</p>
    Formula:C29H27F5N2O6S
    Purity:99.25% - 99.44%
    Color and Shape:Solid
    Molecular weight:626.59

    Ref: TM-T3708

  • Belumosudil
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    Belumosudil

    CAS:
    <p>Belumosudil (Rezurock) is an orally available, and specific ROCK2 inhibitor (IC50/Ki: 60/41 nM).</p>
    Formula:C26H24N6O2
    Purity:97.64% - 98.59%
    Color and Shape:Solid
    Molecular weight:452.51

    Ref: TM-T6867

  • iCRT 14
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    iCRT 14

    CAS:
    <p>iCRT 14 is a novel potent inhibitor of β-catenin-responsive transcription (CRT)(IC50= 40.3 nM in assays of Wnt pathway activity).</p>
    Formula:C21H17N3O2S
    Purity:99.8% - 99.97%
    Color and Shape:Solid
    Molecular weight:375.44

    Ref: TM-T4486

  • 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>
    Formula:C30H42O7
    Purity:96.69% - 99.8%
    Color and Shape:Solid
    Molecular weight:514.65

    Ref: TM-TQ0196

  • 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>
    Formula:C48H60F3N9O9
    Purity:>99.99%
    Color and Shape:Solid
    Molecular weight:964.05

    Ref: TM-TP1433

  • URMC-099
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    URMC-099

    CAS:
    <p>URMC-099: oral, brain-accessible MLK/LRRK2 inhibitor; IC50 – MLK1/2/3/DLK: 19/42/14/150 nM, LRRK2: 11 nM.</p>
    Formula:C27H27N5
    Purity:99.32% - 99.98%
    Color and Shape:Solid
    Molecular weight:421.54

    Ref: TM-T6057

  • 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>
    Formula:C15H14FN3
    Purity:99.93%
    Color and Shape:Solid
    Molecular weight:255.29

    Ref: TM-T9696

  • 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>
    Formula:C25H26N6O2
    Purity:97.21%
    Color and Shape:Solid
    Molecular weight:442.51

    Ref: TM-T9151

  • WHI-P154
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    WHI-P154

    CAS:
    <p>WHI-P154 (Jak3 inhibitor ii) is a potent JAK3 inhibitor.</p>
    Formula:C16H14BrN3O3
    Purity:98% - 99.67%
    Color and Shape:Solid
    Molecular weight:376.2

    Ref: TM-T1985

  • XMU-MP-1
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    XMU-MP-1

    CAS:
    <p>XMU-MP-1 is a reversible and selective MST1/2 kinase inhibitor, IC50 values for MST1 and MST2 are 71.1 nM and 38.1 nM, respectively. High-Quality, Low-Cost!</p>
    Formula:C17H16N6O3S2
    Purity:99.68% - 99.79%
    Color and Shape:Solid
    Molecular weight:416.48

    Ref: TM-T4212

  • BMS-911543
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    BMS-911543

    CAS:
    <p>BMS-911543 is a potent and selective inhibitor of JAK2 with IC50 of 1.1 nM, ~350-, 75- and 65-fold selective to JAK1, JAK3 and TYK2, respectively. Phase 1/2.</p>
    Formula:C23H28N8O
    Purity:97.69% - 99.98%
    Color and Shape:Solid
    Molecular weight:432.52

    Ref: TM-T6790

  • Avagacestat
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    Avagacestat

    CAS:
    <p>Avagacestat (BMS-708163) (BMS-708163) is a potent, selective, orally bioavailable γ-secretase inhibitor of Aβ40 and Aβ42 with IC50 of 0.3 nM and 0.27 nM,</p>
    Formula:C20H17ClF4N4O4S
    Purity:98.87% - 99.73%
    Color and Shape:Solid
    Molecular weight:520.89

    Ref: TM-T6249

  • SAR407899 hydrochloride
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    SAR407899 hydrochloride

    CAS:
    <p>SAR407899 hydrochloride is a selective, potent and ATP-competitive ROCK inhibitor, with an IC50 of 135 nM for ROCK-2, and Kis of 36 nM and 41 nM for human and</p>
    Formula:C14H17ClN2O2
    Purity:99.15%
    Color and Shape:Solid
    Molecular weight:280.75

    Ref: TM-T23308

  • Cardiogenol C
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    Cardiogenol C

    CAS:
    <p>Cardiogenol C is a cardiomyogenesis inducer in embryonic stem cells.</p>
    Formula:C13H16N4O2
    Purity:98.46%
    Color and Shape:Solid
    Molecular weight:260.29

    Ref: TM-T2161

  • Upadacitinib
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    Upadacitinib

    CAS:
    <p>Upadacitinib (ABT-494), a selective JAK1 inhibitor, is researched for autoimmune diseases; IC50: 43 nM.</p>
    Formula:C17H19F3N6O
    Purity:98.96% - 99.94%
    Color and Shape:Solid
    Molecular weight:380.37

    Ref: TM-T7503

  • AZD1080
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    AZD1080

    CAS:
    AZD1080 is a selective, orally active, brain permeable GSK3 inhibitor.
    Formula:C19H18N4O2
    Purity:97.72% - 99.75%
    Color and Shape:Solid
    Molecular weight:334.37

    Ref: TM-T1741

  • IMR-1A
    Targetmol
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    IMR-1A

    CAS:
    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.
    Formula:C13H11NO5S2
    Purity:97.1% - 99.76%
    Color and Shape:Solid
    Molecular weight:325.36

    Ref: TM-T3540

  • IHR-1
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    IHR-1

    CAS:
    <p>IHR-1, a Smo inhibitor (IC50 7.6 nM), blocks Hedgehog pathway, not Wnt/Notch, and prevents Smo in primary cilium.</p>
    Formula:C20H12Cl4N2O2
    Purity:97.02%
    Color and Shape:Solid
    Molecular weight:454.13

    Ref: TM-T24159

  • (E/Z)-GO289
    Targetmol
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    (E/Z)-GO289

    CAS:
    <p>(E/Z)-GO289, which strongly lengthened circadian period, is a potent and selective inhibitor of CK2.</p>
    Formula:C17H15BrN4O2S
    Purity:98.1%
    Color and Shape:Solid
    Molecular weight:419.3

    Ref: TM-T9356