Apexbio B6707 Sphingosin E

E-4031

B6077-10 10 mg
EUR 177
Description: IC50: 7.7 nM for hERGE-4031 is an antiarrhythmic agent blocking the ATP-sensitive potassium channel.ATP-sensitive potassium channels are distributed in tissues widely including muscle, pancreatic beta cells and brain.

Apexbio Reagents Laboratories manufactures the apexbio b6707 sphingosin e reagents distributed by Genprice. The Apexbio B6707 Sphingosin E reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Apexbio Reagents. Other Apexbio products are available in stock. Specificity: Apexbio Category: B6707 Group: Sphingosin E

E-3810

5 mg
EUR 367
Description: E-3810 is a small-molecule dual inhibitor of VEGF and FGF receptors with IC 50 values of 7, 25, 10, 17.5, 82.5 and 237.5 nM for VEGFR-1, 2, 3, FGFR-1, 2 and 3, respectively [1].

E-3810

10 mM (in 1mL DMSO)
EUR 384
Description: E-3810 is a small-molecule dual inhibitor of VEGF and FGF receptors with IC 50 values of 7, 25, 10, 17.5, 82.5 and 237.5 nM for VEGFR-1, 2, 3, FGFR-1, 2 and 3, respectively [1].

E-3810

50 mg
EUR 1520
Description: E-3810 is a small-molecule dual inhibitor of VEGF and FGF receptors with IC 50 values of 7, 25, 10, 17.5, 82.5 and 237.5 nM for VEGFR-1, 2, 3, FGFR-1, 2 and 3, respectively [1].

E 64d

1 mg
EUR 108
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.

E 64d

100 mg
EUR 1500
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.

E 64d

25 mg
EUR 537
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.

E 64d

5 mg
EUR 177
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.

Sphingosin E information

Paraherquamide E

P070-2.5MG 2.5 mg
EUR 1325

Phenelfamycin E

P078-1MG 1 mg
EUR 318

Phenelfamycin E

P078-5MG 5 mg
EUR 1040

Roquefortine E

R035-1MG 1 mg
EUR 224

Roquefortine E

R035-5MG 5 mg
EUR 708

E-4031

B6077-10 10 mg
EUR 177
Description: IC50: 7.7 nM for hERGE-4031 is an antiarrhythmic agent blocking the ATP-sensitive potassium channel.ATP-sensitive potassium channels are distributed in tissues widely including muscle, pancreatic beta cells and brain.

E-4031

B6077-5 5 mg
EUR 125
Description: IC50: 7.7 nM for hERGE-4031 is an antiarrhythmic agent blocking the ATP-sensitive potassium channel.ATP-sensitive potassium channels are distributed in tissues widely including muscle, pancreatic beta cells and brain.

Vitamin E

B6145-100 100 mg
EUR 196

Vitamin E

B6145-500 500 mg
EUR 463

E-3810

A3378-10 10 mg
EUR 567
Description: E-3810 is a small-molecule dual inhibitor of VEGF and FGF receptors with IC 50 values of 7, 25, 10, 17.5, 82.5 and 237.5 nM for VEGFR-1, 2, 3, FGFR-1, 2 and 3, respectively [1].

E-3810

A3378-5 5 mg
EUR 367
Description: E-3810 is a small-molecule dual inhibitor of VEGF and FGF receptors with IC 50 values of 7, 25, 10, 17.5, 82.5 and 237.5 nM for VEGFR-1, 2, 3, FGFR-1, 2 and 3, respectively [1].

E-3810

A3378-5.1 10 mM (in 1mL DMSO)
EUR 384
Description: E-3810 is a small-molecule dual inhibitor of VEGF and FGF receptors with IC 50 values of 7, 25, 10, 17.5, 82.5 and 237.5 nM for VEGFR-1, 2, 3, FGFR-1, 2 and 3, respectively [1].

E-3810

A3378-50 50 mg
EUR 1520
Description: E-3810 is a small-molecule dual inhibitor of VEGF and FGF receptors with IC 50 values of 7, 25, 10, 17.5, 82.5 and 237.5 nM for VEGFR-1, 2, 3, FGFR-1, 2 and 3, respectively [1].

E 64d

A1903-1 1 mg
EUR 108
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.

E 64d

A1903-100 100 mg
EUR 1500
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.

E 64d

A1903-25 25 mg
EUR 537
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.

E 64d

A1903-5 5 mg
EUR 177
Description: E-64d, a membrane permeant derivative of E-64c, a thiol protease inhibitor1, was tested for ability to inhibit calpain activity in intact platelets.E-64c or E-64d also inhibited (lanes 3-8), demonstrating their effect on calpain.