Date published: 2026-4-29

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PD 150606 (CAS 179528-45-1)

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Alternate Names:
3-(4-Iodophenyl)-2-mercapto-(Z)-2-propenoic Acid; PD 150,606
Application:
PD 150606 is a cell-permeable, non-competitive, selective, non-peptide inhibitor directed at the Ca2+ binding sites of calpain.
CAS Number:
179528-45-1
Molecular Weight:
306.1
Molecular Formula:
C9H7IO2S
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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PD 150606 is a cell-permeable, non-competitive, selective, non-peptide Ca2+ dependent calpain inhibitor for calpain-1 and for calpain-2 directed towards the Ca2+ binding sites of calpain. It may act to decrease hypertrophy and inhibit proteolytic activity at all instances. PD 150606 in vitro treated human metastatic melanoma cells displayed a reduction in both effector caspase 3/7 activation and cellular detachment. It has also been observed to inhibit Ca2+ and calyculin A induced sperm motility of the fowl.


PD 150606 (CAS 179528-45-1) References

  1. Differential effects of calpain inhibitors on hypertrophy of cardiomyocytes.  |  Pollack, JR., et al. 2003. Mol Cell Biochem. 251: 47-50. PMID: 14575303
  2. Effects of calpain and Rho-kinase inhibitors on the acrosome reaction and motility of fowl spermatozoa in vitro.  |  Ashizawa, K., et al. 2006. Reproduction. 131: 71-9. PMID: 16388011
  3. Caspase-dependent and -independent pathways for cadmium-induced apoptosis in cultured kidney proximal tubule cells.  |  Lee, WK., et al. 2006. Am J Physiol Renal Physiol. 291: F823-32. PMID: 16597613
  4. Caspases and calpain are independent mediators of cisplatin-induced endothelial cell necrosis.  |  Dursun, B., et al. 2006. Am J Physiol Renal Physiol. 291: F578-87. PMID: 16622172
  5. Cross-talk between calpain and caspase-3/-7 in cisplatin-induced apoptosis of melanoma cells: a major role of calpain inhibition in cell death protection and p53 status.  |  Del Bello, B., et al. 2007. Oncogene. 26: 2717-26. PMID: 17130844
  6. Overexpression of TRPC3 increases apoptosis but not necrosis in response to ischemia-reperfusion in adult mouse cardiomyocytes.  |  Shan, D., et al. 2008. Am J Physiol Cell Physiol. 294: C833-41. PMID: 18184877
  7. The cytoprotective action of the potassium channel opener BMS-191095 in C2C12 myoblasts is related to the modulation of calcium homeostasis.  |  Malinska, D., et al. 2010. Cell Physiol Biochem. 26: 235-46. PMID: 20798507
  8. Calpain inhibitors exhibit matrix metalloproteinase-2 inhibitory activity.  |  Ali, MA., et al. 2012. Biochem Biophys Res Commun. 423: 1-5. PMID: 22575511
  9. Cleavage of IκBα by calpain induces myocardial NF-κB activation, TNF-α expression, and cardiac dysfunction in septic mice.  |  Li, X., et al. 2014. Am J Physiol Heart Circ Physiol. 306: H833-43. PMID: 24441549
  10. Role of calcium and calpain in the downregulation of voltage-gated sodium channel expression by the pyrethroid pesticide deltamethrin.  |  Magby, JP. and Richardson, JR. 2015. J Biochem Mol Toxicol. 29: 129-34. PMID: 25358543
  11. Targeting microparticle biogenesis: a novel approach to the circumvention of cancer multidrug resistance.  |  Roseblade, A., et al. 2015. Curr Cancer Drug Targets. 15: 205-14. PMID: 25714701
  12. Calpain 1 regulates TGF-β1-induced epithelial-mesenchymal transition in human lung epithelial cells via PI3K/Akt signaling pathway.  |  Tan, WJ., et al. 2017. Am J Transl Res. 9: 1402-1409. PMID: 28386365
  13. The human blood parasite Schistosoma mansoni expresses extracellular tegumental calpains that cleave the blood clotting protein fibronectin.  |  Wang, Q., et al. 2017. Sci Rep. 7: 12912. PMID: 29018227
  14. Lysosomal permeabilization and endoplasmic reticulum stress mediate the apoptotic response induced after photoactivation of a lipophilic zinc(II) phthalocyanine.  |  Chiarante, N., et al. 2018. Int J Biochem Cell Biol. 103: 89-98. PMID: 30130653
  15. Early Deсline in Rat Soleus Passive Tension with Hindlimb Unloading: Inactivation of Cross-bridges or Activation of Calpains?  |  Petrova, IO., et al. 2018. Dokl Biochem Biophys. 481: 205-207. PMID: 30168060

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

PD 150606, 5 mg

sc-222133
5 mg
$118.00

PD 150606, 25 mg

sc-222133A
25 mg
$403.00

Can you please confirm whether or not sc-222133 is light sensitive?

Asked by: ChemSynth123
Thank you for your question. PD 150606 (CAS 179528-45-1): sc-222133 is light sensitive.
Answered by: Chemical Support 7
Date published: 2023-03-11
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Rated 5 out of 5 by from Del Bello et alDel Bello et al. (PubMed ID 17130844) found that PD 150606, a calpain inhibitor, reduced both caspase-3/-7 activity and led to cell detachment in melanoma cells. -SCBT Publication Review
Date published: 2015-07-14
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PD 150606 is rated 5.0 out of 5 by 1.
  • y_2026, m_4, d_24, h_10
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