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IGF-1R

IGF-1R

IGF-1R inhibitors are compounds that specifically target and inhibit the Insulin-like Growth Factor 1 Receptor (IGF-1R), a receptor tyrosine kinase involved in cellular growth, development, and survival. IGF-1R signaling plays a significant role in cancer progression, making these inhibitors valuable in oncology research. At CymitQuimica, we offer IGF-1R inhibitors to support your research in cancer biology, endocrinology, and targeted therapy development.

Found 119 products for "IGF-1R".

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  • Picropodophyllin

    CAS:
    Picropodophyllin (PPP) is a selective IGF-1R inhibitor with IC50 of 1 nM, not affecting other growth factor receptors.
    Formula:C22H22O8
    Purity:98.38% - 99.83%
    Color and Shape:White Solid
    Molecular weight:414.41
  • AZ7550

    CAS:
    AZ7550, an active metabolite of AZD9291, inhibits the activity of IGF1R (IC50: 1.6 μM).
    Formula:C27H31N7O2
    Purity:97.07% - 99.75%
    Color and Shape:Solid
    Molecular weight:485.5807
  • NVP-TAE 226

    CAS:
    NVP-TAE 226: Potent FAK inhibitor, IC50=5.5nM, stronger vs Pyk2, IC50=3.5nM, weaker against IGF-1R, InsR, c-Met, ALK.
    Formula:C23H25ClN6O3
    Purity:98.07% - 98.78%
    Color and Shape:Solid
    Molecular weight:468.936
  • GSK1838705A

    CAS:
    GSK1838705A: IGF-1R inhibitor (IC50=2.0nM), IR (1.6nM), ALK (0.5nM), minimal other kinase impact.
    Formula:C27H29FN8O3
    Purity:98.89% - >99.99%
    Color and Shape:Yellow Solid
    Molecular weight:532.57
  • NVP-AEW541

    CAS:
    NVP-AEW541 (AEW541), a potent inhibitor of IGF-1R(IC50=150 nM) and InsR(IC50=140 nM), exhibits excellent efficiency and specificity for IGF-1R in a cell-based
    Formula:C27H29N5O
    Purity:98.7% - 99.86%
    Color and Shape:White Solid
    Molecular weight:439.5521
  • NVP-ADW742

    CAS:
    NVP-ADW742 (ADW) is an IGF-1R inhibitor with IC50 of 0.17 μM, >16-fold more potent against IGF-1R than InsR; little activity to HER2, PDGFR, VEGFR-2, Bcr-Abl
    Formula:C28H31N5O
    Purity:96.14% - 98.70%
    Color and Shape:White Solid
    Molecular weight:453.58
  • NT157

    CAS:
    NT157, a small tyrphostin, inhibits IRS, IGF-1R, and STAT3 in TME, reducing cancer cell survival.
    Formula:C16H14BrNO5S
    Purity:99.64%
    Color and Shape:Solid
    Molecular weight:412.255
  • Ginsenoside Rg5

    CAS:
    Ginsenoside Rg5 shows promise for Alzheimer's, reduces inflammation, and aids vascular health without side effects.
    Formula:C42H70O12
    Purity:98% - 99.65%
    Color and Shape:White Solid
    Molecular weight:766.998
  • Insulin (cattle)

    CAS:
    Insulin(cattle) is a peptide hormone that promotes glycogen synthesis. Insulin) has hypoglycemic activity. Cost-effective and quality-assured.
    Formula:C254H377N65O75S6
    Purity:98%
    Color and Shape:White Solid
    Molecular weight:5800 (Approximately)
  • NBI-31772 hydrate


    NBI-31772 hydrate blocks IGF and IGFBPs binding, freeing IGF-I with Ki 1-24 nM; it has anxiolytic and antidepressant effects.
    Formula:C17H13NO8
    Color and Shape:Solid
    Molecular weight:372.82
  • Linsitinib

    CAS:
    OSI-906 (Linsitinib) is an oral inhibitor of IGF-1R with anti-cancer properties, potentially halting tumor growth and inducing cell death.
    Formula:C26H23N5O
    Purity:98.31% - ≥95%
    Color and Shape:Solid
    Molecular weight:421.49
  • AZD-3463

    CAS:
    AZD-3463 (ALK/IGF1R inhibitor) , an orally bioavailable ALK inhibitor (Ki: 0.75 nM), can inhibit IGF1R with equivalent potency.
    Formula:C24H25ClN6O
    Purity:99.13% - 99.97%
    Color and Shape:Cyan Solid
    Molecular weight:448.948
  • AG1024

    CAS:
    AG1024 (Tyrphostin) suppresses IGF-1R autophosphorylation(IC50=7 μM), and is less potent for IR(IC50=57 μM).
    Formula:C14H13BrN2O
    Purity:98% - 99.37%
    Color and Shape:Solid
    Molecular weight:305.17
  • MID-1

    CAS:
    MID-1 is an inhibitor of MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) interaction.
    Formula:C12H11N3O4S
    Purity:99.39%
    Color and Shape:Solid
    Molecular weight:293.298
  • BRD7552

    CAS:
    BRD7552 is an inducer of transcription factor PDX1, which increases insulin expression. BRD7552 increases PDX1 expression in mouse αTC cells but not βTC cells.
    Formula:C33H33N3O15
    Purity:99.03% - ≥98%
    Color and Shape:Solid
    Molecular weight:711.63
  • Sari 59-801

    CAS:
    Sari 59-801 is a novel, orally effective hypoglycemic compound that appears to act largely by stimulation of insulin release.
    Formula:C18H23N3O2
    Purity:99.92%
    Color and Shape:Solid
    Molecular weight:313.3941
  • Glymidine

    CAS:
    Glycodiazine, a sulfadiazine derivative, reduces blood sugar by boosting insulin release and sensitivity.
    Formula:C13H15N3O4S
    Color and Shape:Solid
    Molecular weight:309.34
  • GIP (1-30) amide, porcine acetate


    GIP (1-30) amide, porcine is a GIP receptor agonist that stimulates insulin and mildly inhibits gastric acid.
    Formula:C164H249N41O49S
    Purity:98.50%
    Color and Shape:Solid
    Molecular weight:3611.04
  • Glymidine sodium

    CAS:
    Glymidine sodium is a sulfonamide hypoglycemic agent which stimulates insulin secretion.
    Formula:C13H14N3NaO4S
    Purity:98.19%
    Color and Shape:Solid
    Molecular weight:331.32
  • PQ401 hydrochloride


    PQ401 inhibits autophosphorylation of IGF-1R domain with IC50 of <1 μM.
    Formula:C18H17Cl2N3O2
    Purity:99.67%
    Color and Shape:Solid
    Molecular weight:378.25