(S)-Willardiine Catalog No.:M8448-2 SR9009 was used at 5-10

SR9009 was used at 5-10 µM concentration in vitro and in cellular assays

it was also found that LCZ696 could inhibit cardiac hypertrophy

CAS Number: 2242464-44-2

[2] KD025 ()150 mg/kg

1H-Indole-3-acetic acid

(S)-Willardiine Catalog No.:M8448-2 SR9009 was used at 5-10(S) Willardiine is a potent agonist of AMPA kainate receptors with EC50 of 44. 8 uM. IC50 value: 44. 8 uM(EC50) Target: AMPA kainate receptor agonistin vitro: The (S) but not (R) isomers of willardiine and 5 bromowillardiine were potent agonists, producing rapidly but incompletely desensitizing responses . At a concentration of 1. 8 mM, Ca2+ inhibited the currents induced by 100 microM willardiine by approximately 50% . in vivo: In newborn mice (P5,