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Stem Cell

Research Areas

Products Related to Stem Cell(471)

  • GC17840 structure
    GC17840Cardiogenol C hydrochloride
    CAS: 1049741-55-0
    Purity: >99.50%

    Induces differentiation of mouse embryonic stem cells (ESCs) into cardiomyocytes

  • GC17907 structure
    GC179073-Deazaneplanocin A (DZNep) hydrochloride
    CAS: 120964-45-6
    Purity: >99.50%

    3-Deazaneplanocin A (DZNep) hydrochloride is an adenosine analogue and is a competitive S-adenosylhomocysteine hydrolase inhibitor with a Ki of 50 pM in cell-free tests.

  • GC18107 structure
    GC18107Salinomycin sodium salt
    CAS: 55721-31-8
    Purity: >98.00%

    Salinomycin sodium salt is a macrocyclic polyether ionophore antibiotic produced by the fermentation of Streptomyces albus .

  • GC18291 structure
    GC18291PKF118-310
    CAS: 84-82-2
    Purity: >99.00%

    PKF118-310 (Xanthothricin) is an antagonist of transcription factor 4 (TCF4)/β-catenin complex, also acts as an inhibitor of KDM4A, with antitumor activity.

  • GC18475 structure
    GC18475Robotnikinin
    CAS: 1132653-79-2
    Purity: >98%

    Sonic hedgehog (Shh) is the most widely characterized of the three vertebrate Hedgehog homologs, and is essential for proper embryonic development.

  • GC18533 structure
    GC18533ZLDI-8
    CAS: 667880-38-8
    Purity: >98.50%

    Temiverine hydrochloride is a synthesized drug that is expected to have anticholinergic action.

  • GC18595 structure
    GC18595G244-LM
    CAS: 1563007-08-8
    Purity: >98%

    An inhibitor of Wnt signaling

  • GC18599 structure
    GC18599PF-05274857 (hydrochloride)
    CAS: 1613439-62-5
    Purity: >98%

    PF-05274857 (hydrochloride) is a potent, selective, orally active and brain-penetrant antagonist of Smo, with an IC50 of 5.8 nM and Ki of 4.6 nM. PF-05274857 (hydrochloride) has potential for research of tumor types including brain tumors and brain metastasis driven by an activated Hh pathway.

  • GC18616 structure
    GC18616MMP-8 Inhibitor I
    CAS: 236403-25-1
    Purity: >98.00%

    MMP-8 Inhibitor I is a potent matrix metalloproteinase-8 (MMP-8) inhibitor with low oral bioavailability.

  • GC18734 structure
    GC18734JS-K
    CAS: 205432-12-8
    Purity: >95.00%

    JS-K is a nitric oxide (NO) donor that reacts with glutathione to generate NO at physiological pH.

  • GC18875 structure
    GC18875GSK3β Inhibitor XVIII
    CAS: 1139875-74-3
    Purity: >98%

    An inhibitor of GSK3β

  • GC19144 structure
    GC19144ETC-159
    CAS: 1638250-96-0
    Purity: >98.00%

    ETC-159 is a potent, orally available PORCN inhibitor.

  • GC19198 structure
    GC19198iCRT3
    CAS: 901751-47-1
    Purity: >99.00%

    iCRT3 is an inhibitor of both Wnt and β-catenin-responsive transcription.

  • GC19216 structure
    GC19216KYA1797K
    CAS: 1956356-56-1
    Purity: >98.00%

    A potent and selective Wnt/β-catenin inhibitor

  • GC19260 structure
    GC19260NCB-0846
    CAS: 1792999-26-8
    Purity: >98.00%

    NCB-0846 is an orally available TNIK inhibitor with an IC50 of 21 nM.

  • GC19299 structure
    GC19299Porcupine-IN-1
    CAS: 2036044-77-4
    Purity: >99.00%

    Porcupine-IN-1 is potent porcupine inhibitor with an IC50 of 0.5±0.2 nM.

  • GC19336 structure
    GC19336SR-3029
    CAS: 1454585-06-8
    Purity: >99.00%

    SR-3029 is a potent and ATP competitive CK1δ and CK1ε inhibitor, with IC50s of 44 nM and 260 nM, respectively, and Kis of 97 nM for both kinases.

  • GC25603 structure
    GC25603M2912
    CAS: 1460286-21-8
    Purity: >98%

    M2912 (MSC2504877) is a very potent TNKS1/TNKS2 inhibitor (IC50=0.6 nM for TNKS1) with exquisite selectivity over other PARP family enzymes and favorable compound properties. This inhibitor potently modulates the Wnt/β-catenin pathway by elevating the levels of axin2 (EC50=17 nM) and tankyrase in DLD1 cells in a dose-dependent manner resulting in reduced cellular Wnt reporter activity.

  • GC26049 structure
    GC26049WAY-119064
    CAS: 1198098-03-1
    Purity: >98%

    WAY-119064 is a potent glycogen synthase kinase-3β (GSK-3β) inhibitor with an IC50 value of 80.5 nM.

  • GC26088 structure
    GC26088YAP-TEAD Inhibitor 1 (Peptide 17)
    CAS: 1659305-78-8
    Purity: >98%

    YAP-TEAD Inhibitor 1 (Peptide 17) is a YAP-TEAD protein-protein interaction inhibitor which has potential usage in treatment of YAP-involved cancers with IC50 of 25 nM.

  • GC30276 structure
    GC30276Casein Kinase II Inhibitor IV
    CAS: 863598-09-8
    Purity: >98.00%

    Casein Kinase II Inhibitor IV is a potent, ATP-competitive of casein kinase II inhibitor with an IC50 of 9 nM.

  • GC30767 structure
    GC30767Heparan Sulfate
    CAS: 9050-30-0

    Heparan Sulfate is a complex polyanionic polysaccharide, regulates important developmental processes in invertebrates and vertebrates.

  • GC31268 structure
    GC31268tCFA15
    CAS: 220757-88-0
    Purity: >99.00%

    tCFA15 is a trimethyl cyclohexenonic long chain fatty alcohol containing 15 carbon atoms on the side chain, promotes the differentiation of neurons, and may regulates Notch signaling.

  • GC31663 structure
    GC31663Adavivint (SM04690)
    CAS: 1467093-03-3
    Purity: >99.00%

    Adavivint (SM04690) (SM04690; Lorecivivint) is a potent and selective inhibitor of canonical Wnt signaling, with an EC50 of 19.5 nM via a high-throughput TCF/LEF-reporter assay in SW480 colon cancer cells.