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  • DC Chemicals Limited
  • China
  • Product Name: GNE-495
  • Price: $800.0/100mg $1600.0/250mg $3040.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

1449277-10-4

1449277-10-4 structure
1449277-10-4 structure
  • Name: GNE-495
  • Chemical Name: GNE-495
  • CAS Number: 1449277-10-4
  • Molecular Formula: C22H20FN5O2
  • Molecular Weight: 405.425
  • Catalog: Signaling Pathways MAPK/ERK Pathway MAP4K
  • Create Date: 2018-03-14 05:20:08
  • Modify Date: 2024-01-30 19:32:37
  • GNE-495 is a potent and selective MAP4K4 inhibitor with an IC50 of 3.7 nM.

Name GNE-495
Synonyms 1,7-Naphthyridine-5-carboxamide, 8-amino-N-[1-(cyclopropylcarbonyl)-3-azetidinyl]-2-(3-fluorophenyl)-
8-Amino-N-[1-(cyclopropylcarbonyl)-3-azetidinyl]-2-(3-fluorophenyl)-1,7-naphthyridine-5-carboxamide
Description GNE-495 is a potent and selective MAP4K4 inhibitor with an IC50 of 3.7 nM.
Related Catalog
Target

MAP4K4:3.7 nM (IC50)

In Vitro GNE-495 is a potent and selective MAP4K4 inhibitor with efficacy in retinal angiogenesis. GNE-495 shows the best balance of MAP4K4 inhibition, permeability, microsomal stability, and cellular potency[1].
In Vivo GNE-495 is administered intraperitoneally to neonatal mouse pups at high doses: 25 and 50 mg/kg. GNE-495 shows good in vivo profile in all species tested, with low clearances, moderate terminal half-lives, and reasonable oral exposure levels (F=37-47%)[1].
Animal Admin Rats, Mice and Pups [1] For the brain cassette study, three male Sprague-Dawley (SD) rats are dosed with intravenous (IV) bolus of six test compounds (e.g., GNE-495; 0.5 mg/kg). For the mouse PK study, female CD-1 mice are administered IV bolus doses of GNE-495 (1 mg/kg). In addition, female CD-1 mice are administered GNE-495 (5 mg/kg) via oral (PO) gavage. A dosing volume of 2 mL/kg is used for the rat brain cassette PK and 5 mL/kg is used for all other dosing. Animals are not fasted prior to dose administration, and water and food are available ad libitum. Following administration of the compound of interest, three blood samples (~60 μL) are collected at each time point from individual mice up to either 9 or 24 hours post-dose using a serial sampling approach. Immediately upon collection, the blood is mixed with K2EDTA and stored on ice or in a chilled Kryorack prior to centrifugation to obtain plasma. Within 1 hr of collection, blood samples are centrifuged at approximately 1000-2000× g for 10-15 min at 4°C, and plasma is harvested. The plasma samples are stored at -70 to -80°C until analysis. For neonate PK, 3-day old CD1 pups are injected with 25 mg/kg and 50 mg/kg GNE-495 intraperitoneally, blood samples are collected at the time points indicated, retinas are collected one hour post-dose and snap frozen in liquid nitrogen and stored at -80°C until analysis. Plasma and retinal lysate concentrations are determined by LC/MS/MS.
References

[1]. Ndubaku CO et al. Structure-Based Design of GNE-495, a Potent and Selective MAP4K4 Inhibitor with Efficacy in Retinal Angiogenesis. ACS Med Chem Lett. 2015 Jun 29;6(8):913-8.

Density 1.5±0.1 g/cm3
Boiling Point 734.5±60.0 °C at 760 mmHg
Molecular Formula C22H20FN5O2
Molecular Weight 405.425
Flash Point 398.0±32.9 °C
Exact Mass 405.160095
LogP 2.54
Vapour Pressure 0.0±2.4 mmHg at 25°C
Index of Refraction 1.712
Storage condition 2-8℃