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-411575 |
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| A4019-10 | ApexBio | 10 mg | EUR 240 |
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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. |
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LY-411575 |
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| A4019-100 | ApexBio | 100 mg | EUR 853.2 |
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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. |
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LY-411575 |
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| A4019-5 | ApexBio | 5 mg | EUR 160.8 |
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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. |
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LY-411575 |
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| A4019-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 240 |
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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. |
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LY-411575 |
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| A4019-50 | ApexBio | 50 mg | EUR 602.4 |
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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. |
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LY 294002 |
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| 20-abx076741 | Abbexa |
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LY 294002 |
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| A8250-10 | ApexBio | 10 mg | EUR 184.8 |
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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. |
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LY 294002 |
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| A8250-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 135.6 |
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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. |
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LY 294002 |
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| A8250-50 | ApexBio | 50 mg | EUR 351.6 |
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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. |
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LY 294002 |
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| A8250-S | ApexBio | Evaluation Sample | EUR 97.2 |
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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. |
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LY 303511 |
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| A3568-10 | ApexBio | 10 mg | EUR 385.2 |
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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. |
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LY 303511 |
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| A3568-5 | ApexBio | 5 mg | EUR 277.2 |
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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. |
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LY 303511 |
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| A3568-50 | ApexBio | 50 mg | EUR 1514.4 |
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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. |
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LY 344864 |
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| A3569-10 | ApexBio | 10 mg | EUR 297.6 |
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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]. |
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LY 344864 |
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| A3569-5 | ApexBio | 5 mg | EUR 211.2 |
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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]. |
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LY 344864 |
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| A3569-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 226.8 |
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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]. |
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LY 344864 |
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| A3569-50 | ApexBio | 50 mg | EUR 884.4 |
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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]. |
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