CymitQuimica logo
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"

Exibir 2 mais subcategorias

Foram encontrados 694 produtos de "Células - tronco e Derivados"

Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
produtos por página.
  • Ruxolitinib
    Targetmol
    + Info

    Ruxolitinib

    CAS:
    <p>Ruxolitinib (INCB018424) is a JAK1/2 inhibitor (IC50=3.3/2.8 nM) that is potent and selective.</p>
    Fórmula:C17H18N6
    Pureza:99.4% - >99.99%
    Cor e Forma:Solid
    Peso molecular:306.36

    Ref: TM-T1829

  • Stafia-1
    Targetmol
    + Info

    Stafia-1

    CAS:
    <p>Stafia-1 is a potent STAT5a inhibitor ( IC50=22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members.</p>
    Fórmula:C24H27O10P
    Pureza:98.08%
    Cor e Forma:Solid
    Peso molecular:506.44

    Ref: TM-T9339

  • (E)-SIS3
    Targetmol
    + Info

    (E)-SIS3

    CAS:
    <p>(E)-SIS3 (SIS3) is a Smad3 inhibitor (IC50=3 μM) selective.inhibits the differentiation of fibroblasts into myofibroblasts via TGF-β1. High-Quality, Low-Cost!</p>
    Fórmula:C28H27N3O3·HCl
    Pureza:95.64% - 98%
    Cor e Forma:Solid
    Peso molecular:489.99

    Ref: TM-T3636

  • MSAB
    Targetmol
    + Info

    MSAB

    CAS:
    <p>MSAB inhibits Wnt/β-catenin by binding to β-catenin and inducing its breakdown.</p>
    Fórmula:C15H15NO4S
    Pureza:99.76%
    Cor e Forma:Solid
    Peso molecular:305.35

    Ref: TM-T8710

  • Ritlecitinib tosylate
    Targetmol
    + Info

    Ritlecitinib tosylate

    CAS:
    <p>Ritlecitinib (PF-06651600) is a potent, selective JAK3 inhibitor with proven in vivo efficacy, low clearance, and has undergone clinical trials.</p>
    Fórmula:C22H27N5O4S
    Cor e Forma:Solid
    Peso molecular:457.549

    Ref: TM-T69822

  • WAY-262611
    Targetmol
    + Info

    WAY-262611

    CAS:
    <p>WAY262611 is a Wnt/β-catenin agonist and an inhibitor of Dkk1. It increases bone formation rate with EC50 of 0.63 μM in TCF-luciferase assay.</p>
    Fórmula:C20H22N4
    Pureza:98.09% - 99.09%
    Cor e Forma:Solid
    Peso molecular:318.42

    Ref: TM-T1971

  • Cardiogenol C
    Targetmol
    + Info

    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

  • PF-04802367
    Targetmol
    + Info

    PF-04802367

    CAS:
    <p>PF-04802367 is a highly selective GSK-3 inhibitor with an IC50 of 2.1 nM based on a recombinant human GSK-3β enzyme assay and 1.1 nM based on ADP-Glo assay.</p>
    Fórmula:C16H16ClN5O3
    Pureza:98.76%
    Cor e Forma:Solid
    Peso molecular:361.78

    Ref: TM-T9611

  • Y-27632 dihydrochloride
    Targetmol
    + Info

    Y-27632 dihydrochloride

    CAS:
    <p>View and buy Y-27632 dihydrochloride from TargetMol.Y-27632 is a selective inhibitor of ROCKs.Cited in 10 publications.</p>
    Fórmula:C14H21N3O·2HCl
    Pureza:97.96% - 99.98%
    Cor e Forma:Solid
    Peso molecular:320.26

    Ref: TM-T1725

  • S3I-201
    Targetmol
    + Info

    S3I-201

    CAS:
    <p>S3I-201 (S3I-201) is a selective Stat3 inhibitor (IC50: 86±33 μM) and low effect towards STAT1/5.</p>
    Fórmula:C16H15NO7S
    Pureza:97.83%
    Cor e Forma:Solid
    Peso molecular:365.36

    Ref: TM-T2505

  • (E/Z)-GO289
    Targetmol
    + Info

    (E/Z)-GO289

    CAS:
    <p>(E/Z)-GO289, which strongly lengthened circadian period, is a potent and selective inhibitor of CK2.</p>
    Fórmula:C17H15BrN4O2S
    Pureza:98.1%
    Cor e Forma:Solid
    Peso molecular:419.3

    Ref: TM-T9356

  • IHR-1
    Targetmol
    + Info

    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>
    Fórmula:C20H12Cl4N2O2
    Pureza:97.02%
    Cor e Forma:Solid
    Peso molecular:454.13

    Ref: TM-T24159

  • TDZD-8
    Targetmol
    + Info

    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

  • ETC-159
    Targetmol
    + Info

    ETC-159

    CAS:
    <p>ETC-159 (ETC-1922159) is a potent, orally available PORCN inhibitor. It inhibits β-catenin reporter activity with an IC50 of 2.9 nM.</p>
    Fórmula:C19H17N7O3
    Pureza:96.87% - 99.30%
    Cor e Forma:Solid
    Peso molecular:391.38

    Ref: TM-T4043

  • LH846
    Targetmol
    + Info

    LH846

    CAS:
    <p>LH846 is a selective inhibitor of CK1δ (IC50 values are 290 nM, 1.3 uM and 2.5 uM for CK1δ, ε and α); exhibits no inhibitory activity at CK2.</p>
    Fórmula:C16H13ClN2OS
    Pureza:90% - 98.26%
    Cor e Forma:Solid
    Peso molecular:316.81

    Ref: TM-T1877

  • Avagacestat
    Targetmol
    + Info

    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>
    Fórmula:C20H17ClF4N4O4S
    Pureza:98.87% - 99.73%
    Cor e Forma:Solid
    Peso molecular:520.89

    Ref: TM-T6249

  • MRT-14
    Targetmol
    + Info

    MRT-14

    CAS:
    <p>MRT-14 is a potent Smo antagonist and can be used in several types of cancers linked to abnormal Hh signaling studies.</p>
    Fórmula:C24H24N4O5
    Pureza:99.54%
    Cor e Forma:Solid
    Peso molecular:448.47

    Ref: TM-T9531

  • BML-284 hydrochloride
    Targetmol
    + Info

    BML-284 hydrochloride

    CAS:
    <p>BML-284 hydrochloride (Wnt agonist 1 HCL) is a potent, selective Wnt canonical signaling activator and tubulin polymerization inhibitor.</p>
    Fórmula:C19H19ClN4O3
    Pureza:99.80%
    Cor e Forma:Solid
    Peso molecular:386.84

    Ref: TM-T8820

  • BDP5290
    Targetmol
    + Info

    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

  • SAR-20347
    Targetmol
    + Info

    SAR-20347

    CAS:
    <p>SAR-20347 is an inhibitor of TYK2, JAK1/2/3 (IC50: 0.6/23/26/41 nM).</p>
    Fórmula:C21H18ClFN4O4
    Pureza:98.99% - 99.77%
    Cor e Forma:Solid
    Peso molecular:444.84

    Ref: TM-T4210