Basic information Uses Safety Supplier Related

5,15-DIPHENYL-21H,23H-PORPHINE

Basic information Uses Safety Supplier Related

5,15-DIPHENYL-21H,23H-PORPHINE Basic information

Product Name:
5,15-DIPHENYL-21H,23H-PORPHINE
Synonyms:
  • 5,15-DIPHENYL-21H,23H-PORPHINE
  • 5,15-DIPHENYLPORPHINE
  • 5, 15-BIS-(PHENYL)PORPHYRINS
  • 5,15-Diphenylporphyrin
  • STAT3 Inhibitor VIII, 5,15-DPP - CAS 22112-89-6 - Calbiochem
  • 10,20-diphenyl-21,22-dihydroporphyrin
  • 5,15-Bis-(phenyl)-21H,23H-porphyrins
  • 5,15-DPP
CAS:
22112-89-6
MF:
C32H22N4
MW:
462.54
Product Categories:
  • Biochemistry
  • Porphyrins
Mol File:
22112-89-6.mol
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5,15-DIPHENYL-21H,23H-PORPHINE Chemical Properties

Melting point:
>200℃
Boiling point:
912.3±65.0 °C(Predicted)
Density 
1.285±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
solubility 
≤2mg/ml in dimethyl formamide
form 
Deep blue to deep purple solid
color 
Red to Dark blue to Black
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Safety Information

WGK Germany 
3
HS Code 
2933.99.8290
HazardClass 
IRRITANT
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5,15-DIPHENYL-21H,23H-PORPHINE Usage And Synthesis

Uses

5,15-Diphenylporphyrin (cas# 22112-89-6) is a useful research chemical.

Biological Activity

5,15-diphenylporphyrin (5,15-dpp) is a selective stat3-sh2 antagonist [1].stat3 is constitutively activated in many human cancers. stat3 functions as a critical mediator of oncogenic signaling through transcriptional activation of genes encoding apoptosis inhibitors, cell-cycle regulators and inducers of angiogenesis [2]. aberrant stat3 activity has been associated with transforming mechanisms induced by oncogenic tyrosine kinases [1].

in vitro

5,15-dpp directly bound to stat3 and antagonized the function of stat3-sh2. 5,15-dpp selectively antagonized stat3-sh2 with an ic50 of 0.28 μm over the other sh2-containing proteins stat1 and grb2[1]. the estimated kd values for the 5,15-dpp binding to stat3 was 880 nm. treatment with 5,15-dpp suppressed the dna binding activity of stat3 in a concentration-dependent manner. 5,15-dpp poorly inhibited stat1 with an ic50 of 10 μm and showed no effect grb2 [1].

References

[1] uehara y, mochizuki m, matsuno k, et al. novel high-throughput screening system for identifying stat3–sh2 antagonists[j]. biochemical and biophysical research communications, 2009, 380(3): 627-631.
[2] jing n, tweardy d j. targeting stat3 in cancer therapy[j]. anti-cancer drugs, 2005, 16(6): 601-607.

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