Date published: 2026-2-4

1-800-457-3801

SCBT Portrait Logo
Seach Input

Benproperine phosphate (CAS 19428-14-9)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Benproperinephosphate
CAS Number:
19428-14-9
Purity:
≥95%
Molecular Weight:
407.44
Molecular Formula:
C21H30NO5P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Benproperine phosphate is a compound that is extensively studied in the field of biochemistry and molecular biology, primarily for its inhibitory effects on certain biochemical pathways. Researchers exploring the mechanisms of action of various enzymes and transporters often use Benproperine phosphate as a tool to better understand these complex biological processes. In molecular biology applications, this compound is employed to study gene expression regulation, as it can influence transcriptional activity. Additionally, Benproperine phosphate is of interest in the investigation of membrane dynamics and cellular signaling due to its interaction with phospholipid bilayers. Its role in modulating ion channels and receptors is another area where Benproperine phosphate provides valuable insights into the function and regulation of these proteins.


Benproperine phosphate (CAS 19428-14-9) References

  1. [Determination of benproperine phosphate tablets by high performance liquid chromatography].  |  Yang, XJ. and Yang, XY. 2000. Se Pu. 18: 566-7. PMID: 12541753
  2. Anti-tussive activity of benproperine enantiomers on citric-acid-induced cough in conscious guinea-pigs.  |  Chen, S., et al. 2004. J Pharm Pharmacol. 56: 277-80. PMID: 15005888
  3. Identification of some benproperine metabolites in humans and investigation of their antitussive effect.  |  Li, Y., et al. 2005. Acta Pharmacol Sin. 26: 1519-26. PMID: 16297353
  4. Vancomycin degradation products as potential chiral selectors in enantiomeric separation of racemic compounds.  |  Ghassempour, A. and Aboul-Enein, HY. 2008. J Chromatogr A. 1191: 182-7. PMID: 17950744
  5. Resonance light scattering study on the interaction of benproperine phosphate with eriochrome blue black R in the presence of sodium dodecylbenzene sulphonate and its analytical application.  |  Feng, S., et al. 2009. Luminescence. 24: 67-72. PMID: 18800357
  6. Cough Headache Presenting with Reversible Cerebral Vasoconstriction Syndrome.  |  Kato, Y., et al. 2018. Intern Med. 57: 1459-1461. PMID: 29321411
  7. Unravelling the binding mechanism of benproperine with human serum albumin: A docking, fluorometric, and thermodynamic approach.  |  Wu, D., et al. 2018. Eur J Med Chem. 146: 245-250. PMID: 29407954
  8. Benproperine, an ARPC2 inhibitor, suppresses cancer cell migration and tumor metastasis.  |  Yoon, YJ., et al. 2019. Biochem Pharmacol. 163: 46-59. PMID: 30710516
  9. Clofazimine Reduces the Survival of Salmonella enterica in Macrophages and Mice.  |  Nagy, TA., et al. 2020. ACS Infect Dis. 6: 1238-1249. PMID: 32272013
  10. Repurposing antitussive benproperine phosphate against pancreatic cancer depends on autophagy arrest.  |  Zhang, H., et al. 2021. Mol Oncol. 15: 725-738. PMID: 33226737
  11. Repurposing drugs in autophagy for the treatment of cancer: From bench to bedside.  |  Bu, F., et al. 2022. Drug Discov Today. 27: 1815-1831. PMID: 34808390
  12. Rab11a promotes the malignant progression of ovarian cancer by inducing autophagy.  |  Wang, Y., et al. 2022. Genes Genomics. 44: 1375-1384. PMID: 36125654
  13. S-Benproperine, an Active Stereoisomer of Benproperine, Suppresses Cancer Migration and Tumor Metastasis by Targeting ARPC2.  |  Jang, HJ., et al. 2022. Pharmaceuticals (Basel). 15: PMID: 36558913

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Benproperine phosphate, 10 g

sc-337556
10 g
$560.00