Name | (1S,3R,5Z,7E,23S)-1,3-Dihydroxy-23,26-epoxy-9,10-secocholesta-5,7 ,10,25(27)-tetraen-26-one |
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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]. |
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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 |
Boiling Point | 618.492ºC at 760 mmHg |
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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 |