Chemicals

A potent inhibitor of serotonin and norepinephrine reuptake (Kis = 4.6 and 15.6 nM, respectively, for rat synaptosomes) less effectively inhibits dopamine reuptake (Ki = 369 nM) effective in cells, tissues, and in vivo.

A potent inhibitor of serotonin and norepinephrine reuptake (Kis = 4.6 and 15.6 nM, respectively, for rat synaptosomes) less effectively inhibits dopamine reuptake (Ki = 369 nM) effective in cells, tissues, and in vivo.

CAS: 136434-34-9 MDL No: MFCD06407958 RTECS: XN0258000 Solid Molecular Formula: C₁₈H₁₉NOS&middotHCl MW: 333.88 Melting Point: 118-122&deg

CAS: 136434-34-9 MDL No: MFCD06407958 RTECS: XN0258000 Solid Molecular Formula: C₁₈H₁₉NOS&middotHCl MW: 333.88 Melting Point: 118-122&deg

The naturally occurring enantiomer of equol that demonstrates ER agonist activity similar to that of genistein (EC50 = 85 and 65 nM for human ER&alpha and ER&beta, respectively) preferentially binds ER&beta (Ki = 0.73 nM) with lower affinity for

The naturally occurring enantiomer of equol that demonstrates ER agonist activity similar to that of genistein (EC50 = 85 and 65 nM for human ER&alpha and ER&beta, respectively) preferentially binds ER&beta (Ki = 0.73 nM) with lower affinity for

The naturally occurring enantiomer of equol that demonstrates ER agonist activity similar to that of genistein (EC50 = 85 and 65 nM for human ER&alpha and ER&beta, respectively) preferentially binds ER&beta (Ki = 0.73 nM) with lower affinity for

The naturally occurring enantiomer of equol that demonstrates ER agonist activity similar to that of genistein (EC50 = 85 and 65 nM for human ER&alpha and ER&beta, respectively) preferentially binds ER&beta (Ki = 0.73 nM) with lower affinity for

Pure, optically active single isomer fo flurbiprofen.

Pure, optically active single isomer fo flurbiprofen.

Pure, optically active single isomer fo flurbiprofen.

Pure, optically active single isomer fo flurbiprofen.