Glycerin/kaolin/sodium fluoride

Dapagliflozin is a potent and selective SLC5A2 inhibitor with EC50 of 1.1 nM. It has good permeability across Caco-2 cell membranes and is a substrate for P-glycoprotein (P-gp). Dapagliflozin is not a significant P-gp inhibitor.A SGLT-2 inhibitor.

Dapagliflozin is a potent and selective SLC5A2 inhibitor with EC50 of 1.1 nM. It has good permeability across Caco-2 cell membranes and is a substrate for P-glycoprotein (P-gp). Dapagliflozin is not a significant P-gp inhibitor.A SGLT-2 inhibitor.

Dapagliflozin is a potent and selective SLC5A2 inhibitor with EC50 of 1.1 nM. It has good permeability across Caco-2 cell membranes and is a substrate for P-glycoprotein (P-gp). Dapagliflozin is not a significant P-gp inhibitor.A SGLT-2 inhibitor.

Dapagliflozin impurity is an enantiomer of Dapagliflozin which is a sodium-glucose transporter 2 inhibitor.Form:Solid.

Dapagliflozin impurity is an enantiomer of Dapagliflozin which is a sodium-glucose transporter 2 inhibitor.Form:Solid.

Dapagliflozin impurity is an enantiomer of Dapagliflozin which is a sodium-glucose transporter 2 inhibitor.Form:Solid.

Dapagliflozin impurity is an enantiomer of Dapagliflozin which is a sodium-glucose transporter 2 inhibitor.Form:Solid.

Dapagliflozin impurity is an enantiomer of Dapagliflozin which is a sodium-glucose transporter 2 inhibitor.Form:Solid.

General description &#948:-Undecalactone is a volatile flavor compound found in coconut meat , fresh peaches and tobacco. It is also a potent mosquito repellant.

A small molecule that binds to the farnesyl-binding pocket of PDE&delta (Kd = 41 nM) in cells thus inhibiting its interaction with KRAS and disrupting RAS signaling reduces proliferation and increases cell death of Panc-Tu-I tumor cells at 5 &muM

A small molecule that binds to the farnesyl-binding pocket of PDE&delta (Kd = 41 nM) in cells thus inhibiting its interaction with KRAS and disrupting RAS signaling reduces proliferation and increases cell death of Panc-Tu-I tumor cells at 5 &muM

A small molecule that binds to the farnesyl-binding pocket of PDE&delta (Kd = 41 nM) in cells thus inhibiting its interaction with KRAS and disrupting RAS signaling reduces proliferation and increases cell death of Panc-Tu-I tumor cells at 5 &muM