Activin and Inhibin

Fludarabine triphosphate (F-ara-ATP) trisodium, the active metabolite of Fludarabine ( HY-B0069 ), is a potent, noncompetitive and specific inhibitor of DNA primase , with an IC 50 of 2.3 μM and a K i of 6.1 μM. Fludarabine triphosphate trisodium

Fludarabine triphosphate (F-ara-ATP) trisodium, the active metabolite of Fludarabine ( HY-B0069 ), is a potent, noncompetitive and specific inhibitor of DNA primase , with an IC 50 of 2.3 μM and a K i of 6.1 μM. Fludarabine triphosphate trisodium

Fludarabine triphosphate (F-ara-ATP) trisodium, the active metabolite of Fludarabine ( HY-B0069 ), is a potent, noncompetitive and specific inhibitor of DNA primase , with an IC 50 of 2.3 μM and a K i of 6.1 μM. Fludarabine triphosphate trisodium

Flumazenil acid is a metabolite of Flumazenil. Flumazenil is a GABAA receptor antagonist .Form:Solid.

Flumazenil acid is a metabolite of Flumazenil. Flumazenil is a GABAA receptor antagonist .Form:Solid.

Flumazenil acid is a metabolite of Flumazenil. Flumazenil is a GABAA receptor antagonist .Form:Solid.

Flumazenil acid is a metabolite of Flumazenil. Flumazenil is a GABAA receptor antagonist .Form:Solid.

Flumazenil acid is a metabolite of Flumazenil. Flumazenil is a GABAA receptor antagonist .Form:Solid.

Flumexadol is a selective and affinity 5-HT 2C receptor agonist with a K i of 25 nM for the (+)-enantiomer of Flumexadol, and is 40-fold selective over the 5-HT 2A receptor. Flumexadol is an orally active non-narcotic analgesicIn VivoIn rats and

Flumexadol is a selective and affinity 5-HT 2C receptor agonist with a K i of 25 nM for the (+)-enantiomer of Flumexadol, and is 40-fold selective over the 5-HT 2A receptor. Flumexadol is an orally active non-narcotic analgesicIn VivoIn rats and

Flumexadol is a selective and affinity 5-HT 2C receptor agonist with a K i of 25 nM for the (+)-enantiomer of Flumexadol, and is 40-fold selective over the 5-HT 2A receptor. Flumexadol is an orally active non-narcotic analgesicIn VivoIn rats and

Fluoflavine (ML-090) is a selective NOX1 inhibitor with an IC 50 of 90 nM. Fluoflavine has &gt:100 selectivity for NOX1 over NOX2 , NOX3, NOX4 (all IC 50 &gt:10 μM). ML-090 has an IC 50 of 360 nM in HEK293 cells.Form:Solid.