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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 436 produtos para "Células - tronco e Derivados".

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  • SPL-707

    CAS:
    SPL-707 is an effective and selective signal peptide peptidase-like 2a inhibitor (IC50: 80 nM).
    Fórmula:C27H28FN5O4
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:505.54

    Ref: TM-T16921

    25mg
    2.718,00€
    50mg
    3.582,00€
    100mg
    4.950,00€
  • γ-Secretase modulator 10

    CAS:
    γ-Secretase modulator 10 is a novel γ-secretase modulator.
    Fórmula:C25H23F3N4O2
    Cor e Forma:Solid
    Peso molecular:468.48

    Ref: TM-T40315

    5mg
    873,00€
  • 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
  • LSKL TFA

    CAS:
    LSKL TFA (H-Leu-Ser-Lys-Leu-NH2 TFA) is a TGF-尾1 antagonist that inhibits TSP-1 binding to LAP and reduces renal interstitial fibrosis and liver fibrosis.
    Fórmula:C23H43F3N6O7
    Pureza:99.33%
    Cor e Forma:Solid
    Peso molecular:572.62

    Ref: TM-TP2147

    1mg
    43,00€
    5mg
    85,00€
    10mg
    109,00€
    25mg
    208,00€
    50mg
    309,00€
    100mg
    447,00€
  • Axltide

    CAS:
    Axltide mimics mouse Insulin receptor substrate 1, amino acids 979-989 with sequence KKSRGDYMTMQIG.
    Fórmula:C63H107N19O20S2
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:1514.77

    Ref: TM-TP1713

    100mg
    A consultar
    500mg
    A consultar
  • Povorcitinib phosphate

    CAS:
    Povorcitinib phosphate is a selective JAK1 inhibitor and can be used in studies about the treatment of cutaneous lupus erythematosus and Lichen planus.
    Fórmula:C23H25F5N7O5P
    Pureza:99.57%
    Cor e Forma:Solid
    Peso molecular:605.45

    Ref: TM-T39113L

    1mg
    46,00€
    5mg
    96,00€
    1mL*10mM (DMSO)
    128,00€
    10mg
    145,00€
    25mg
    236,00€
    50mg
    339,00€
    100mg
    460,00€
    200mg
    622,00€
  • Myostatin inhibitory peptide 2 TFA


    Myostatin Inhibitory Peptide 2 (compd 2) TFA is a potent inhibitor of muscle growth suppressant with a dissociation constant (Kd) of 35.9 nM. It is utilized in the study of muscle atrophy diseases.
    Cor e Forma:Odour Solid

    Ref: TM-TP2890

    10mg
    A consultar
    50mg
    A consultar
  • YAP-IN-1


    YAP-IN-1 (Compound (+)-1) is an autophagy inhibitor specifically targeting YAP1. It binds to the Hippo pathway transcription factor YAP1 with a Kd of 9.13 μM, promoting its degradation through the chaperone-mediated autophagy (CMA) pathway. This process inhibits the Rab7-mediated fusion of autophagosomes with lysosomes and decreases autophagy levels without affecting lysosomal function. YAP-IN-1 shows potential for cancer research, including in hepatocellular carcinoma and breast cancer.
    Cor e Forma:Odour Solid

    Ref: TM-T206234

    10mg
    A consultar
    50mg
    A consultar
  • 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
    Cor e Forma:Solid
    Peso molecular:548.67

    Ref: TM-T205385

    10mg
    A consultar
    50mg
    A consultar
  • PROTAC TYK2 degradation agent1

    CAS:
    PROTAC TYK2 Agent1 selectively degrades TYK2, with a 14 nM DC50, for autoimmune research.
    Fórmula:C55H69N13O7S
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:1056.28

    Ref: TM-T75026

    5mg
    A consultar
    50mg
    A consultar
  • Tyrosine Kinase Inhibitor Library


    A unique collection of xnum HIF-1 related small chemicals can be used for drug discovery in ischemic disease and cancer and related mechanism studies;
    Cor e Forma:Odour Solid

    Ref: TM-L2200

    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
  • JAK2-IN-10

    CAS:
    JAK2-IN-10 is a potent inhibitor of JAK2v617f, with an IC50 value of ≤10 nM.
    Fórmula:C33H33D3FN9O2
    Cor e Forma:Solid
    Peso molecular:612.71

    Ref: TM-T88297

    25mg
    3.213,00€
    50mg
    4.033,00€
    100mg
    5.310,00€
  • Tubastatin

    CAS:
    Tubastatin inhibits TGF-β1-induced S6K phosphorylation, HIF-1α expression and VEG F expression.
    Fórmula:C21H22N2O2
    Pureza:98.53%
    Cor e Forma:Solid
    Peso molecular:334.41

    Ref: TM-T29023

    1mg
    46,00€
    5mg
    94,00€
    10mg
    123,00€
    25mg
    197,00€
    50mg
    295,00€
    100mg
    440,00€
    500mg
    982,00€
  • TEAD-IN-16


    TEAD-IN-16 (compound BC-011) is a potent inhibitor of TEAD, with an IC50 of 72.43 μM. This compound plays a significant role in cancer research.
    Fórmula:C16H14F3NO3
    Cor e Forma:Solid
    Peso molecular:325.09258

    Ref: TM-T210264

    10mg
    A consultar
    50mg
    A consultar
  • Kinase Inhibitor Library


    A unique collection of xnum kinase inhibitors/regulators for high throughput screening and high content screening for drug discovery in kinase related diseases;
    Cor e Forma:Odour Solid

    Ref: TM-L1600

    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
  • 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
    Cor e Forma: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
  • PSEN1-IN-2


    PSEN1-IN-2 (Compound 13K) is a potent inhibitor of both PSEN1-APH1A and PSEN1-APH1B complexes, exhibiting IC50 values of 6.9 nM and 2.4 nM, respectively.
    Fórmula:C20H18ClFN2O3S
    Cor e Forma:Solid
    Peso molecular:420.88

    Ref: TM-T79680

    5mg
    A consultar
    50mg
    A consultar
  • 5β-Cholanic acid

    CAS:
    5β-Cholanic acid (5beta-Cholanic acid) is a potent γ-secretase modulator used in Alzheimer's disease research.
    Fórmula:C24H40O2
    Pureza:98.91% - 99.89%
    Cor e Forma:White Solid
    Peso molecular:360.57

    Ref: TM-T88859

    5mg
    42,00€
    1mL*10mM (DMSO)
    44,00€
    10mg
    60,00€
    25mg
    86,00€
  • Epigenetics Compound Library


    A collection of xnum wine components, suitable for high-throughput and high-content screening.
    Cor e Forma: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