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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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  • Casein kinase 1δ-IN-7

    CAS:
    <p>Casein kinase 1δ-IN-7 is a Casein kinase 1δ inhibitor for neurodegenerative diseases such as Alzheimer's disease.</p>
    Fórmula:C17H14N4O2S
    Pureza:98.6%
    Cor e Forma:Solid
    Peso molecular:338.38
  • SJ1008030

    CAS:
    <p>SJ1008030, a JAK2 PROTAC, degrades JAK2; EC50: 5.4 nM, IC50: 32.09 nM in MHH-CALL-4 cells for leukemia research.</p>
    Fórmula:C42H43N13O7S
    Cor e Forma:Solid
    Peso molecular:873.94
  • JAK1/TYK2-IN-1

    CAS:
    <p>JAK1/TYK2-IN-1 is a dual inhibitor of TYK2 and JAK1 ( IC 50 = 29 and 41 nM respectively).</p>
    Fórmula:C18H20F3N7O
    Cor e Forma:Solid
    Peso molecular:407.401
  • YAP/TEAD-IN-1


    <p>YAP/TEAD-IN-1 (compound 4) is a potent inhibitor of YAP and TEAD, exhibiting antioxidant properties. It demonstrates antiproliferative effects on tumor cells while showing minimal cytotoxic activity towards normal human cells.</p>
    Fórmula:C32H30N8O
    Cor e Forma:Solid
    Peso molecular:542.634
  • FDA-Approved Kinase Inhibitor Library


    <p>A unique collection of 263 kinase inhibitors/regulators for specific targeting of kinases, ready for high-throughput screening and high-content screening.</p>
    Cor e Forma:Liquid
  • Epigenetics Compound Library


    <p>Well-chosen 953 compounds related to epigenetic regulation for research in epigenetics, high throughput screening (HTS) and high content screening (HCS) for new</p>
    Cor e Forma:Odour Solid
  • CIA-1 (Free base)

    CAS:
    <p>CIA-1, a COUP-TFII inhibitor, has IC50 of 1.2-7.6 μM in prostate cancer cells; inhibits tumor growth in mouse prostate cancer.</p>
    Fórmula:C17H19N3O2S
    Pureza:99%
    Cor e Forma:Solid
    Peso molecular:329.42
  • Tyrosine Kinase Inhibitor Library


    <p>A unique collection of 1016 tyrosine kinase inhibitors for high throughput screening and high content screening for drug discovery in tyrosine kinase related</p>
    Cor e Forma:Odour Solid
  • Kinase Inhibitor Library


    <p>A unique collection of 2720 kinase inhibitors/regulators for high throughput screening and high content screening for drug discovery in kinase related diseases;</p>
    Cor e Forma:Odour Solid
  • YAP-IN-1


    <p>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.</p>
    Cor e Forma:Odour Solid
  • SJ10542

    CAS:
    <p>SJ10542: potent JAK2/3-targeting PG-PROTAC; DC50s: JAK2 - 14 nM, JAK3 - 11 nM, JAK2-fusion ALL - 24 nM; CRBN recruiter.</p>
    Fórmula:C41H46N12O5S
    Cor e Forma:Solid
    Peso molecular:818.95
  • FRM-024

    CAS:
    <p>FRM-024 is a powerful gamma secretase modulator with the ability to penetrate the central nervous system (CNS), designed specifically for the treatment of</p>
    Fórmula:C22H22ClN5O2
    Cor e Forma:Solid
    Peso molecular:423.9
  • 1(R),2(S)-epoxy Cannabidiol

    CAS:
    <p>1(R),2(S)-epoxy Cannabidiol (Compound 2a) is a structural analog of phytocannabinoids, exhibiting significant inhibitory activity on the Wnt/β-catenin pathway. It holds potential for research as a neuroprotective agent.</p>
    Fórmula:C21H30O3
    Cor e Forma:Solid
    Peso molecular:330.46
  • Foxy-5 Ammonium Salt


    <p>Foxy-5 Ammonium Salt, a WNT5A mimetic, blocks epithelial cancer cell migration without β-catenin impact and curbs prostate cancer spread.</p>
    Fórmula:C26H46N7O12S2
    Pureza:97.70%
    Cor e Forma:Solid
    Peso molecular:712.26
  • YAP-TEAD-IN-1 acetate


    <p>YAP-TEAD-IN-1 acetate is an effective and competitive inhibitor of YAP–TEAD interaction with an IC50 of 25 nM.</p>
    Fórmula:C95H148ClN23O23S2
    Pureza:98.11% - 99.57%
    Cor e Forma:Soild
    Peso molecular:2079.92
  • Carboxylesterase-IN-2

    CAS:
    <p>Carboxylesterase-IN-2 is a potent Carboxylesterase Notum inhibitor (IC50 &lt;= 10 nM).Carboxylesterase-IN-2 has potential for the study of cancer diseases.</p>
    Fórmula:C13H12N4OS
    Pureza:99.92%
    Cor e Forma:Soild
    Peso molecular:272.33
  • Fresolimumab

    CAS:
    <p>Fresolimumab (GC1008) is a human monoclonal antibody targeting active TGFβ1, TGFβ2, TGFβ3, studied for cancer and focal segmental glomerulosclerosis.</p>
    Pureza:> 95% - > 95%
    Cor e Forma:Liquid
    Peso molecular:144.4 kDa
  • TEAD-IN-19


    <p>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.</p>
    Cor e Forma:Odour Solid
  • Notch 1 TFA


    <p>Notch 1 TFA encodes a member of the NOTCH family of proteins.</p>
    Fórmula:C64H98N15F3O25S3
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:1614.81
  • LH168


    <p>LH168 is a potent and selective probe for WDR5, with a SPR Kd value of 13 nM.</p>
    Fórmula:C29H31F3N6O2S
    Cor e Forma:Solid
    Peso molecular:584.66