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209984-68-9

209984-68-9 structure
209984-68-9 structure
  • Name: LY900009
  • Chemical Name: (2S)-2-Hydroxy-3-methyl-N-[(2S)-1-{[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]amino}-1-oxo-2-propanyl]butanamide
  • CAS Number: 209984-68-9
  • Molecular Formula: C23H27N3O4
  • Molecular Weight: 409.48
  • Create Date: 2018-06-21 18:02:55
  • Modify Date: 2025-08-25 18:11:22
  • LY900009 is a potent and orally active, First-in-class inhibitor of Notch signaling via selective inhibition of the γ-secretase protein (GSI). LY900009 inhibited Notch signalling in tumor cell lines and endothelial cells (IC50 range: 0.005-20 nM). LY900009 can be used for advanced cancer research[1].

Name (2S)-2-Hydroxy-3-methyl-N-[(2S)-1-{[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]amino}-1-oxo-2-propanyl]butanamide
Synonyms Butanamide, N-[(1S)-2-[[(7S)-6,7-dihydro-5-methyl-6-oxo-5H-dibenz[b,d]azepin-7-yl]amino]-1-methyl-2-oxoethyl]-2-hydroxy-3-methyl-, (2S)-
(2S)-2-Hydroxy-3-methyl-N-[(2S)-1-{[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]amino}-1-oxo-2-propanyl]butanamide
LY900009
Description LY900009 is a potent and orally active, First-in-class inhibitor of Notch signaling via selective inhibition of the γ-secretase protein (GSI). LY900009 inhibited Notch signalling in tumor cell lines and endothelial cells (IC50 range: 0.005-20 nM). LY900009 can be used for advanced cancer research[1].
Related Catalog
In Vivo 在大鼠模型中,LY900009 (口服灌胃;3 mg/kg;单剂量) 通过形成渗漏脉管系统抑制血管生成,并在 Notch 依赖性肿瘤模型中导致肿瘤消退[1]。
References

[1]. Shubham Pant, et al. A first-in-human phase I study of the oral Notch inhibitor, LY900009, in patients with advanced cancer. Eur J Cancer. 2016 Mar;56:1-9.  

Density 1.3±0.1 g/cm3
Boiling Point 781.5±60.0 °C at 760 mmHg
Molecular Formula C23H27N3O4
Molecular Weight 409.48
Flash Point 426.5±32.9 °C
Exact Mass 409.200165
LogP 3.97
Vapour Pressure 0.0±2.8 mmHg at 25°C
Index of Refraction 1.622
Storage condition -20℃
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