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IGF-1R Inhibitor, PPP (CAS 477-47-4)

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Alternate Names:
IGF-1R Inhibitor, PPP is also known as Picropodophyllin.
Application:
IGF-1R Inhibitor, PPP is a non-competitive inhibitor of IGF-1R and apoptosis inducer, with antineoplastic activity.
CAS Number:
477-47-4
Purity:
≥96%
Molecular Weight:
414.40
Molecular Formula:
C22H22O8
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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IGF-1R Inhibitor, PPP is an insulin-like, cell-permeable cis-cyclolignan compound that acts as a non-competitive, potent, and specific inhibitor of IGF-1Rα/β (growth factor-I receptor kinase - IC50 = 1 nM in cell-free kinase assay ≤ 60 nM for cell viability and receptor autophosphorylation in melanoma cell lines). IGF-1R Inhibitor, PPP exhibits little effect towards IR, FGFR, PDGFR and EGFR, and exerts no effects on microtubules and DNA topoisomerase II. IGF-1R Inhibitor, PPP is the first inhibitor reported to discriminate between IGF-1R and IR, and has shown promising in vivo effects in SCID mice (complete inhibition of IGF-1R-dependent tumor cell growth at 20 mg/kg/12 hr i.p. in SCID mice) with minimum toxic effect (LD50 > 500 mg/kg). IGF-1R Inhibitor, PPP has an IC50 of 1 nM.


IGF-1R Inhibitor, PPP (CAS 477-47-4) References

  1. Cyclolignans as inhibitors of the insulin-like growth factor-1 receptor and malignant cell growth.  |  Girnita, A., et al. 2004. Cancer Res. 64: 236-42. PMID: 14729630
  2. IGF-1 receptor tyrosine kinase inhibition by the cyclolignan PPP induces G2/M-phase accumulation and apoptosis in multiple myeloma cells.  |  Strömberg, T., et al. 2006. Blood. 107: 669-78. PMID: 16166596
  3. Activation of a novel calcineurin-mediated insulin-like growth factor-1 receptor pathway, altered metabolism, and tumor cell invasion in cells subjected to mitochondrial respiratory stress.  |  Guha, M., et al. 2007. J Biol Chem. 282: 14536-46. PMID: 17355970
  4. Structure and in vitro replication of DNA templates containing 7,8-dihydro-8-oxoadenine.  |  Guschlbauer, W., et al. 1991. Nucleic Acids Res. 19: 1753-8. PMID: 1851559
  5. Determination of picropodophyllin and its isomer podophyllotoxin in human serum samples with electrospray ionization of hexylamine adducts by liquid chromatography-tandem mass spectrometry.  |  Rönquist-Nii, Y., et al. 2011. J Chromatogr B Analyt Technol Biomed Life Sci. 879: 326-34. PMID: 21251888
  6. Picropodophyllin inhibits tumor growth of human nasopharyngeal carcinoma in a mouse model.  |  Yin, SC., et al. 2013. Biochem Biophys Res Commun. 439: 1-5. PMID: 23973483
  7. Picropodophyllin and sorafenib synergistically suppress the proliferation and motility of hepatocellular carcinoma cells.  |  Tomizawa, M., et al. 2014. Oncol Lett. 8: 2023-2026. PMID: 25289088
  8. Picropodophyllin inhibits proliferation and survival of diffuse large B-cell lymphoma cells.  |  Strömberg, T., et al. 2015. Med Oncol. 32: 188. PMID: 26021470
  9. Picropodophyllin (PPP) is a potent rhabdomyosarcoma growth inhibitor both in vitro and in vivo.  |  Tarnowski, M., et al. 2017. BMC Cancer. 17: 532. PMID: 28793874
  10. Picropodophyllin inhibits type I endometrial cancer cell proliferation via disruption of the PI3K/Akt pathway.  |  Dong, L., et al. 2019. Acta Biochim Biophys Sin (Shanghai). 51: 753-760. PMID: 31168597
  11. Rehmannia glutinosa Libosch Extracts Prevent Bone Loss and Architectural Deterioration and Enhance Osteoblastic Bone Formation by Regulating the IGF-1/PI3K/mTOR Pathway in Streptozotocin-Induced Diabetic Rats.  |  Gong, W., et al. 2019. Int J Mol Sci. 20: PMID: 31443143
  12. N-cadherin upregulation mediates adaptive radioresistance in glioblastoma.  |  Osuka, S., et al. 2021. J Clin Invest. 131: PMID: 33720050
  13. Trimetazidine attenuates dexamethasone-induced muscle atrophy via inhibiting NLRP3/GSDMD pathway-mediated pyroptosis.  |  Wang, L., et al. 2021. Cell Death Discov. 7: 251. PMID: 34537816
  14. Picropodophyllin inhibits the growth of pemetrexed-resistant malignant pleural mesothelioma via microtubule inhibition and IGF-1R-, caspase-independent pathways.  |  Sun, R., et al. 2022. Transl Lung Cancer Res. 11: 543-559. PMID: 35529797
  15. Picropodophyllin Inhibits the Proliferation of Human Prostate Cancer DU145 and LNCaP Cells via ROS Production and PI3K/AKT Pathway Inhibition.  |  Zhu, X., et al. 2022. Biol Pharm Bull. 45: 1027-1035. PMID: 35908886

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

IGF-1R Inhibitor, PPP, 1 mg

sc-204008A
1 mg
$138.00

IGF-1R Inhibitor, PPP, 10 mg

sc-204008
10 mg
$203.00

IGF-1R Inhibitor, PPP, 100 mg

sc-204008B
100 mg
$895.00

Could I get a quote for this reagent (1mg), including shipping costs via email?  The shipping address is Macquarie University in NSW, Australia. 

Asked by: Sunny An
Thank you for contacting Santa Cruz Biotechnology. For a price quote and ship date please email cc@scbt.com.
Answered by: BlakeJ
Date published: 2025-03-07

How long dose is safe to storage at +4 degree as powder status ?

Asked by: nemmy
Thank you for your question. It would be helpful if you could call us directly at 800-457-3801 ext. 1, allowing for a more interactive discussion of this and other related questions.
Answered by: Blake J
Date published: 2023-12-05

What is the appearance of the compound?

Asked by: two2igm05
Thank you for your question. IGF-1R Inhibitor, PPP, sc-204008, is in white powder form.
Answered by: Chemical Support 4
Date published: 2017-04-25

Does sc-204008 contain any biological? In other words, it is derived from living organisms?

Asked by: ChemSynth123
Thank you for your question. IGF-1R Inhibitor, PPP (CAS 477-47-4); sc-204008 is derived from a synthetic source and contains no biological substance.
Answered by: Chemical Support 7
Date published: 2017-03-01
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Rated 5 out of 5 by from OthmanOthman, E.M. et al. (PubMed 24355212) used product sc-204008 (IGF-1R Inhibitor) to determine if the signaling pathway of insulin-mediated genotoxicity begins with activation of IGF-1R. In the presence of sc-204008 genomic damage was significantly reduced in a hyperinsulinemia environment. -SCBT Publication Review
Date published: 2015-07-02
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IGF-1R Inhibitor, PPP is rated 5.0 out of 5 by 1.
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