GLPBio

JAK/STAT Signaling

Research Areas

Products Related to JAK/STAT Signaling(493)

  • GC79466 structure
    GC79466STAT6-IN-9
    CAS: 3092076-15-5
    Purity: >98.00%

    STAT6-IN-9 is a potent STAT6 inhibitor with an EC 50 value of 4 nM.

  • GC79467 structure
    GC79467ortho-Topolin riboside
    CAS: 50868-58-1
    Purity: >98%

    ortho-Topolin riboside is a naturally occurring cytokinin secreted from Populus x robusta leaves after sunrise.

  • GC79468 structure
    GC79468ZDZ-553
    Purity: >99.50%

    ZDZ-553 is an orally active STAT1 inhibitor with an IC 50 value of 0.87 μM.

  • GC79469 structure
    GC79469STAT6-IN-10
    CAS: 3092076-19-9
    Purity: >98.50%

    STAT6-IN-10 is a STAT6 (signal transducer and activator of transcription 6) inhibitor with an EC 50 of 2 nM.

  • GC79470 structure
    GC79470S3I-1757
    CAS: 1456602-51-9
    Purity: >99.50%

    S3I-1757 is a STAT3 inhibitor.

  • GC79471 structure
    GC79471STAT6-IN-8
    CAS: 3033741-50-0
    Purity: >98.50%

    STAT6-IN-8 is a STAT6 inhibitor with an IC 50 of 0.45 μmol/L.

  • GC79472 structure
    GC79472INCA033989
    Purity: >98.00%

    INCA033989 is a fully human IgG1 monoclonal antibody targeting mutCALR ( K D = 1.75 nM for mutCALR del52; K D = 6.78 nM for mutCALR ins5 ).

  • GC79477 structure
    GC79477KZ-02
    CAS: 1801756-14-8
    Purity: >98.00%

    KZ-02 is an orally active dual MEK1 / Pim-1 kinase inhibitor, with an IC 50 of 1.07 nM against MEK1 and an IC 50 of 1.34 μM against Pim-1.

  • GC79757 structure
    GC79757ALOX5 stabilizer-1 TFA
    Purity: >98.00%

    ALOX5 stabilizer-1 TFA is an arachidonate 5-lipoxygenase ( ALOX5 ) stabilizer with a K d of 7.26 μM.

  • GC80468 structure
    GC80468Peficitinib-d 3
    Purity: >98%

    Peficitinib -d 3 (ASP015K-d 3 ) is the deuterium labeled Peficitinib.

  • GC80858 structure
    GC80858Firmonertinib-d 3 mesylate
    Purity: >99.00%

    Firmonertinib-d 3 (Alflutinib-d 3 ) mesylate is the deuterium labeled Firmonertinib mesylate.

  • GC80946 structure
    GC80946PROTAC JAK1/2 degrader-1
    Purity: >99.00%

    PROTAC JAK1/2 degrader-1 is an orally active JAK1 / JAK2 PROTAC degrader, with DC 50 values of 1.4 μM and 0.92 μM against JAK1 and JAK2, respectively.

  • GC80947 structure
    GC80947JAK1/2 ligand 1
    CAS: 1026028-96-5
    Purity: >99.50%

    JAK1/2 ligand 1 is a ligand for the PROTAC target protein of JAK1/2, which can be used to synthesize PROTAC JAK1/2 degrader-1.

  • GC80949 structure
    GC80949PROTAC STAT6 degrader-3
    CAS: 3077385-98-6
    Purity: >98.00%

    PROTAC STAT6 degrader-3 is a potent STAT6 PROTAC degrader with a DC 50 of less than 1 nM.

  • GC81026 structure
    GC81026PROTAC SKP2 Degrader-1
    CAS: 3120650-15-6
    Purity: >99.50%

    PROTAC SKP2 Degrader-1 is a PROTAC degrader targeting SKP2, with a K d value of 6.28 μM.

  • GC81323 structure
    GC81323PDGFRA/CAIX/XII-IN-1
    Purity: >98.00%

    PDGFRA/CAIX/XII-IN-1 is an inhibitor of PDGFRA, CA IX and CA XII, with an IC 50 of 20 nM against PDGFRA, a K i of 93.3 nM against CA IX, and a K i of 80.0 nM against CA XII.

  • GC81428 structure
    GC81428Rolditamig
    CAS: 3038136-62-5
    Purity: >95.00%

    Rolditamig (TQB2102 Antibody) is a recombinant humanized anti-human epidermal growth factor receptor 2 ( HER2 ) antibody.

  • GC81496 structure
    GC81496TAVO101
    Purity: >96.50%

    TAVO101 is a humanized anti- TSLP antibody with an EC 50 of 0.19 nM against hTSLP.

  • GC81497 structure
    GC81497Vadalentamig
    CAS: 3030203-93-8
    Purity: >95.00%

    Vadalentamig is a human-derived bispecific antibody targeting NKG2D/CD314 & ERBB1/EGFR/HER1 [1] .

  • GC81732 structure
    GC81732iAfaPhos1
    Purity: >98%

    iAfaPhos1 is a FKBP12F36V epimer ligand.

  • GF17531 structure
    GF175318-Epixanthatin
    CAS: 30890-35-8
    Purity: >98.00%

    8-Epixanthatin is a light-induced growth inhibitor that regulates the phototropic curvature in sunflower hypocotyls.

  • GN10115 structure
    GN10115Diosgenin
    CAS: 512-04-9
    Purity: >98.00%

    Diosgenin is a naturally occurring steroidal sapogenin that can inhibit the STAT3 signaling pathway and acts as an activator of Pdia3/ERp57, possessing a variety of important pharmacological activities.

  • GN10164 structure
    GN10164Saikosaponin D
    CAS: 20874-52-6
    Purity: >98.50%

    Saikosaponin D is a triterpenoid saponin derivative with antioxidant, antipyretic, and anti-inflammatory properties.

  • GN10282 structure
    GN10282Vitexicarpin (Casticin)
    CAS: 479-91-4
    Purity: >99.50%

    Vitexicarpin (Casticin), a non-isotopic tetramethoxyflavone with three phenyl rings, is a phosphatidylinositol 3-kinase (PI3K) inhibitor with high cytotoxicity.