≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Desiccated,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
TRV120027 TFA, a β-arrestin-1 -biased agonist of the angiotensin II receptor type 1 (AT1R) , engages ß-arrestins while blocking G-protein signaling. TRV120027 TFA induces acute catecholamine secretion through cation channel subfamily C3 (TRPC3) coupl
Appearance:Solid
IC50& Target:IC50: the angiotensin II receptor type 1 (AT1R)
In Vitro:TRV120027 TFA (100 nM) significantly increases the AT1R and TRPC3 association with the immunoprecipitated β-arrestin-1 in HEK293 cells co-transfected with Flag-AT1R-cherry, HA-β-arrestin-1 and TRPC3-GFP. TRV120027 TFA (100 nM) induces an [Ca 2+ ]i in
In Vivo:TRV120027 TFA (intravenous injection; 0.3 or 1.5 µg/kg per minute; infusion rate, 0.5 mL/min) when added to furosemide decreases cardiac preload and afterload, systemic and renal vascular resistances, and left ventricular external work while increasing ca
Biological Activity:TRV120027 TFA, a β-arrestin-1 -biased agonist of the angiotensin II receptor type 1 (AT1R) , engages ß-arrestins while blocking G-protein signaling . TRV120027xa0TFA inducesxa0acutexa0catecholaminexa0secretionxa0through cation channel subfamily C3 (TR
| Molecular Weight | 1040.1 |
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Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| Solubility | DMSO : 100 mg/mL (96.14 mM; Need ultrasonic) |
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