Medchemexpress Hy-101943 Ly 345899

Lab Reagents

Human IgG antibody Laboratories manufactures the medchemexpress hy-101943 ly 345899 reagents distributed by Genprice. The Medchemexpress Hy-101943 Ly 345899 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 MedChemExpress Inc.. Other Medchemexpress products are available in stock. Specificity: Medchemexpress Category: Hy-101943 Group: Ly 345899

Ly 345899 information

LY-411575

A4019-10 10 mg
EUR 240
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-100 100 mg
EUR 853.2
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-5 5 mg
EUR 160.8
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-5.1 10 mM (in 1mL DMSO)
EUR 240
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-50 50 mg
EUR 602.4
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY 294002

20-abx076741
  • EUR 811.20
  • EUR 343.20
  • 25 mg
  • 5 mg

LY 294002

A8250-10 10 mg
EUR 184.8
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 294002

A8250-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 294002

A8250-50 50 mg
EUR 351.6
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 294002

A8250-S Evaluation Sample
EUR 97.2
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 303511

A3568-10 10 mg
EUR 385.2
Description: Description:IC50 Value:N/ALY303511, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhibit PI3-K.in vitro: 100 ?M LY303511 significantly reduced the fraction of cells in S phase.

LY 303511

A3568-5 5 mg
EUR 277.2
Description: Description:IC50 Value:N/ALY303511, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhibit PI3-K.in vitro: 100 ?M LY303511 significantly reduced the fraction of cells in S phase.

LY 303511

A3568-50 50 mg
EUR 1514.4
Description: Description:IC50 Value:N/ALY303511, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhibit PI3-K.in vitro: 100 ?M LY303511 significantly reduced the fraction of cells in S phase.

LY 344864

A3569-10 10 mg
EUR 297.6
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].

LY 344864

A3569-5 5 mg
EUR 211.2
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].

LY 344864

A3569-5.1 10 mM (in 1mL DMSO)
EUR 226.8
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].

LY 344864

A3569-50 50 mg
EUR 884.4
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].