Name | Teprenone |
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Synonyms |
6,10,14,18-tetramethyl-nonadeca-5t,9t,13t,17-tetraen-2-one
E-0671 6,10,14,18-Tetramethyl-nonadeca-5t,9t,13t,17-tetraen-2-on (5E,9E,13E)-6,10,14,18-Tetramethyl-5,9,13,17-nonadecatetren-2-one (5E,9E,13E)-6,10,14,18-tetramethyl-nonadeca-5,9,13,17-tetraen-2-one 5,9,13,17-Nonadecatetraen-2-one,6,10,14,18-tetramethyl-,(E,E,E) 2-Oxo-6,10,14,18-tetramethyl-nonadecatetraen-(5.9.13.17) (E,E,E)-geranylgeranylacetone E,E,E-geranylgeranylacetyl |
Description | (5E,9E,13E)-Teprenone ((5E,9E,13E)-Geranylgeranylacetone) is an isomer of Teprenone with antiulcer activity. (5E,9E,13E)-Teprenone induces transcriptional activation of HSP genes that may increase gastric mucosal defense at conditions of stress[1]. |
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Related Catalog | |
In Vitro | (5E,9E,13E)-Teprenone might transiently activate the transcription of HSP70 gene[1]. The heat shock element–binding activity reflects the activation of heat shock factor 1 in response to (5E,9E,13E)-Teprenone[1]. |
In Vivo | (5E,9E,13E)-Teprenone induces hat sock proteins accumulations in rat gastric mucosa[1]. Animal Model: Male Wister strain rats (≈250 g)[1] Dosage: 200 mg/kg Administration: Oral administration Result: Caused accumulations of all of HSP90, HSP70, HSC70 and HSP60 within 60 minutes. |
References |
Density | 0.871g/cm3 |
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Boiling Point | 438.2ºC at 760 mmHg |
Molecular Formula | C23H38O |
Molecular Weight | 661.09400 |
Flash Point | 166.5ºC |
Exact Mass | 660.58500 |
PSA | 34.14000 |
LogP | 15.00260 |
Index of Refraction | 1.482 |
Precursor 10 | |
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DownStream 1 | |