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L651647-5mgLY3154207 is a potent, subtype selective, and orally available human dopamine D1 receptor positive allosteric modulator (PAM) with minimal allosteric agonist activity ( EC 50 =3 nM)In VitroIn HEK293 cells transiently expressing human, dog, rhesus
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L656763-1mlLY3154207 is a potent, subtype selective, and orally available human dopamine D1 receptor positive allosteric modulator (PAM) with minimal allosteric agonist activity ( EC 50 =3 nM)In VitroIn HEK293 cells transiently expressing human, dog, rhesus
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L648774-100mgLY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC 50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducerIn VitroLY3177833 (10 μM: 4 days) increases SA-β-gal content in Hep3B cells. MCE has not
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L648774-10mgLY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC 50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducerIn VitroLY3177833 (10 μM: 4 days) increases SA-β-gal content in Hep3B cells. MCE has not
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L648774-1mgLY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC 50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducerIn VitroLY3177833 (10 μM: 4 days) increases SA-β-gal content in Hep3B cells. MCE has not
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L648774-50mgLY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC 50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducerIn VitroLY3177833 (10 μM: 4 days) increases SA-β-gal content in Hep3B cells. MCE has not
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L648774-5mgLY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC 50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducerIn VitroLY3177833 (10 μM: 4 days) increases SA-β-gal content in Hep3B cells. MCE has not
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L655564-1mlLY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC 50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducerIn VitroLY3177833 (10 μM: 4 days) increases SA-β-gal content in Hep3B cells. MCE has not
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L647109-10mgLY3372689 (Formulaic Ia) is an orally active O-GlcNAcase (OGA) enzyme inhibitor. LY3372689 can be used for tauopathies research, including Alzheimer’s disease.In VivoLY3372689 shows a dose-dependent change in OGA enzyme occu-pancy (EO) following a
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L647109-25mgLY3372689 (Formulaic Ia) is an orally active O-GlcNAcase (OGA) enzyme inhibitor. LY3372689 can be used for tauopathies research, including Alzheimer’s disease.In VivoLY3372689 shows a dose-dependent change in OGA enzyme occu-pancy (EO) following a
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L647109-5mgLY3372689 (Formulaic Ia) is an orally active O-GlcNAcase (OGA) enzyme inhibitor. LY3372689 can be used for tauopathies research, including Alzheimer’s disease.In VivoLY3372689 shows a dose-dependent change in OGA enzyme occu-pancy (EO) following a
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L654874-1mlLY3372689 (Formulaic Ia) is an orally active O-GlcNAcase (OGA) enzyme inhibitor. LY3372689 can be used for tauopathies research, including Alzheimer’s disease.In VivoLY3372689 shows a dose-dependent change in OGA enzyme occu-pancy (EO) following a