Top Suppliers:I want be here


173388-20-0

173388-20-0 structure
173388-20-0 structure
  • Name: TEI-9647
  • Chemical Name: (1S,3R,5Z,7E,23S)-1,3-Dihydroxy-23,26-epoxy-9,10-secocholesta-5,7 ,10,25(27)-tetraen-26-one
  • CAS Number: 173388-20-0
  • Molecular Formula: C27H38O4
  • Molecular Weight: 426.58800
  • Catalog: Signaling Pathways Vitamin D Related VD/VDR
  • Create Date: 2017-09-04 05:00:32
  • Modify Date: 2024-01-13 17:53:43
  • TEI-9647 is a first and potent VDR/vitamin D-responsive element (DRE)-mediated genomic actions antagonist. TEI-9647 is a 1α,25-dihydroxyvitamin D3-26,23-lactone (1α,25-lactone) analogue[1].

Name (1S,3R,5Z,7E,23S)-1,3-Dihydroxy-23,26-epoxy-9,10-secocholesta-5,7 ,10,25(27)-tetraen-26-one
Description TEI-9647 is a first and potent VDR/vitamin D-responsive element (DRE)-mediated genomic actions antagonist. TEI-9647 is a 1α,25-dihydroxyvitamin D3-26,23-lactone (1α,25-lactone) analogue[1].
Related Catalog
Target

VDR[1]

In Vitro TEI-9647 (100 nM; 24 hours; HL-60 cells) treatment clearly suppresses p21WAF1,CIP1 gene expression induced by 1α,25(OH)2D3[1]. TEI-9647 blocks both 1α,25(OH)2D3-mediated HL-60 cell differentiation and also activation of the luciferase reporter in COS-7 cells that has been transfected with the cDNA containing the DRE of the rat 25(OH)D3-24-hydroxylase gene and cDNA of the human vitamin D nuclear receptor[1]. RT-PCR[1] Cell Line: HL-60 cells Concentration: 100 nM Incubation Time: 24 hours Result: Clearly suppressed p21WAF1,CIP1 gene expression induced by 1α,25(OH)2D3.
References

[1]. Miura D, et al. Antagonistic action of novel 1alpha,25-dihydroxyvitamin D3-26, 23-lactone analogs on differentiation of human leukemia cells (HL-60) induced by 1alpha,25-dihydroxyvitamin D3. J Biol Chem. 1999 Jun 4;274(23):16392-9.

Boiling Point 618.492ºC at 760 mmHg
Molecular Formula C27H38O4
Molecular Weight 426.58800
Flash Point 204.543ºC
Exact Mass 426.27700
PSA 66.76000
LogP 5.02530
Vapour Pressure 0mmHg at 25°C
Index of Refraction 1.567