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Compound E

Compound E is a γ-secretase and notch patchway inhibitor which induces neuronal differentiation. Compound E enhances growth inhibition, differentiation, and migration of neuroblastoma cells.

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SML02B 10 mg $900.00
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SKUSML02B
Size10 mg
Molecular NameCompound E
FormPowder
Alternative NamesXXI, Compound E (secretase inhibitor), DuPont E, C-E, γ-secretase inhibitor XXI, Gammasecretase inhibitor XXI, gamma inhibitor
Chemical NameBenzeneacetamide, N-[(1S)-2-[[(3S)-2,3-dihydro-1-methyl-2-oxo-5-phenyl-1H-1,4- benzodiazepin-3-yl]amino]-1-methyl-2-oxoethyl]-3,5-difluoro-
Chemical FormulaC27H24F2N4O3
Molecular Weight490.50
CAS Number209986-17-4
PurityGreater than 95% by LCMS
Physical AppearanceWhite to off-white (Solid)
Targetγ-secretase
Shelf-Life≥ 2 years
StorageStore at -20°C
Small Molecules for Stem Cell Research

Compound E is a potent γ-secretase inhibitor that specifically blocks β-amyloid-40 (IC50 of 0.24), β-amyloid-42 (IC50 of 0.37), and cleavage of the Notch domain (IC50 of 0.32). Compound E has been shown to promote the differentiation of embryonic stem cells (ESCs) to primitive neural precursors in addition to generating a self-renewing progenitor neuroepithelia stem cell population (Li, et al.) when combined with CHIR99021, SB431542, and hLIF. Forebrain GABA interneurons have also been derived from human pluripotent stem cells (PSCs) through the utilization of Compound E (Liu, et al.); additionally, it has shown promising effects in Alzheimer’s disease models using iPSC-derived neurons (Yagi, et al.).

Alternative names: XXI, Compound E (secretase inhibitor), DuPont E, C-E, γ-secretase inhibitor XXI, Gammasecretase inhibitor XXI, gamma inhibitor
Applications:enhances growth inhibition, differentiation of hPSCs
Cell types: neural, hPSCs, hESCs

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References and Publications
  1. Li, et al. 2011. Rapid induction and long-term self-renewal of primitive neural precursors from human embryonic stem cells by small molecule inhibitors. PNAS. 108(20): 8299-304.
  2. Liu, et al. 2013. Directed differentiation of forebrain GABA interneurons from human pluripotent stem cells. Nature Protocols. 8: 1670-1679.
  3. Yagi, et al. 2011. Modeling familial Alzheimer’s disease with induced pluripotent stem cells. Human Molecular Genetics. 20(23): 4530-4539.
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