Date published: 2026-3-19

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MY-5445 (CAS 78351-75-4)

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Application:
MY-5445 is a selective cGMP phosphodiesterase inhibitor
CAS Number:
78351-75-4
Purity:
99%
Molecular Weight:
331.8
Molecular Formula:
C20H14ClN3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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MY-5445, also known as 1-(3-chloroanilino)-4-phenylphthalazine, is an inhibitor of platelet aggregation via an increase in cyclic GMP. Mechanistic studies suggest that this compound affects cyclic GMP phosphodiesterase, therefore preventing metabolism of cyclic GMP in platelets. Experiments show that MY-5445 does not have any impact on cyclic AMP content, and has the potential to cause relaxation of rat aorta.


MY-5445 (CAS 78351-75-4) References

  1. cAMP modulates cGMP-mediated cerebral arteriolar relaxation in vivo.  |  Xu, HL., et al. 2004. Am J Physiol Heart Circ Physiol. 287: H2501-9. PMID: 15271668
  2. Cyclic nucleotides and neuroblastoma differentiation.  |  Messina, E., et al. 2004. Nucleosides Nucleotides Nucleic Acids. 23: 1551-4. PMID: 15571296
  3. Up-regulation of microglial CD11b expression by nitric oxide.  |  Roy, A., et al. 2006. J Biol Chem. 281: 14971-80. PMID: 16551637
  4. Phosphodiesterase type 5 is highly expressed in the hypertrophied human right ventricle, and acute inhibition of phosphodiesterase type 5 improves contractility.  |  Nagendran, J., et al. 2007. Circulation. 116: 238-48. PMID: 17606845
  5. Peripheral analgesia and activation of the nitric oxide-cyclic GMP pathway.  |  Durate, ID., et al. 1990. Eur J Pharmacol. 186: 289-93. PMID: 1981187
  6. Role of selective cyclic GMP phosphodiesterase inhibition in the myorelaxant actions of M&B 22,948, MY-5445, vinpocetine and 1-methyl-3-isobutyl-8-(methylamino)xanthine.  |  Souness, JE., et al. 1989. Br J Pharmacol. 98: 725-34. PMID: 2480168
  7. Design and synthesis of 3-aminophthalazine derivatives and structural analogues as PDE5 inhibitors: anti-allodynic effect against neuropathic pain in a mouse model.  |  Bollenbach, M., et al. 2019. Eur J Med Chem. 177: 269-290. PMID: 31158744
  8. MY-5445, a phosphodiesterase type 5 inhibitor, resensitizes ABCG2-overexpressing multidrug-resistant cancer cells to cytotoxic anticancer drugs.  |  Wu, CP., et al. 2020. Am J Cancer Res. 10: 164-178. PMID: 32064159
  9. STIMULATION OF THE CYCLIC AMP/GMP SIGNALLING ENHANCES THE RELAXATION OF ISOLATED HUMAN DETRUSOR SMOOTH MUSCLE ACHIEVED BY PHOSPHODIESTERASE INHIBITORS.  |  Rahardjo, HE., et al. 2021. Georgian Med News. 7-12. PMID: 34103422
  10. Suppression of Proliferation of Human Glioblastoma Cells by Combined Phosphodiesterase and Multidrug Resistance-Associated Protein 1 Inhibition.  |  Kopanitsa, L., et al. 2021. Int J Mol Sci. 22: PMID: 34575827
  11. Antiallodynic action of phosphodiesterase inhibitors in a mouse model of peripheral nerve injury.  |  Megat, S., et al. 2022. Neuropharmacology. 205: 108909. PMID: 34875284
  12. Effect of 1-(3-chloroanilino)-4-phenylphthalazine (MY-5445), a specific inhibitor of cyclic GMP phosphodiesterase, on human platelet aggregation.  |  Hagiwara, M., et al. 1984. J Pharmacol Exp Ther. 228: 467-71. PMID: 6141286
  13. Inhibitory effects of natriuretic peptides on vasopressin neurons mediated through cGMP and cGMP-dependent protein kinase in vitro.  |  Akamatsu, N., et al. 1993. J Neuroendocrinol. 5: 517-22. PMID: 8680419

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

MY-5445, 10 mg

sc-201195
10 mg
$153.00