Compound E, gamma;-secretase inhibitor - ≥99%, high purity , CAS No.209986-17-4

  • ≥99%
Item Number
C275008
Grouped product items
SKUSizeAvailabilityPrice Qty
C275008-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$157.90
C275008-250μg
250μg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$47.90

Cell-permeable, selective, non-competitive, potent γ-secretase inhibitor

Basic Description

SynonymsE98743 | BS-15830 | 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-difluorobenzeneacetamide | EX-A3838 | CHEBI:131161 | C27H24F2N4O3 | GSI-XXI | Compound E | gamma-Secretase Inhibitor XXI | H
Specifications & Purity≥99%
Biochemical and Physiological MechanismsCell-permeable, selective, non-competitive, potent γ-secretase inhibitor (IC 50 = 0.3 nM). Active in vitro and in vivo .
Storage TempStore at -20°C,Desiccated
Shipped InIce chest + Ice pads
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.

Associated Targets(Human)

APH1A Tbio Gamma-secretase (4915 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name (2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]-N-[(3S)-1-methyl-2-oxo-5-phenyl-3H-1,4-benzodiazepin-3-yl]propanamide
INCHI InChI=1S/C27H24F2N4O3/c1-16(30-23(34)14-17-12-19(28)15-20(29)13-17)26(35)32-25-27(36)33(2)22-11-7-6-10-21(22)24(31-25)18-8-4-3-5-9-18/h3-13,15-16,25H,14H2,1-2H3,(H,30,34)(H,32,35)/t16-,25+/m0/s1
InChi Key JNGZXGGOCLZBFB-IVCQMTBJSA-N
Canonical SMILES CC(C(=O)NC1C(=O)N(C2=CC=CC=C2C(=N1)C3=CC=CC=C3)C)NC(=O)CC4=CC(=CC(=C4)F)F
Isomeric SMILES C[C@@H](C(=O)N[C@@H]1C(=O)N(C2=CC=CC=C2C(=N1)C3=CC=CC=C3)C)NC(=O)CC4=CC(=CC(=C4)F)F
PubChem CID 11306390
Molecular Weight 490.5

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in DMSO to 100 mM

Related Documents

References

1. Naylor RW et al..  (2018)  A novel mechanism of gland formation in zebrafish involving transdifferentiation of renal epithelial cells and live cell extrusion..  Elife,    [PMID:30394875]
2. Liu X et al..  (2018)  BMP9 overexpressing adipose-derived mesenchymal stem cells promote cartilage repair in osteoarthritis-affected knee joint via the Notch1/Jagged1 signaling pathway..  Exp Ther Med,  16  (6): (4623-4631).  [PMID:30542413]
3. Kang Y et al..  (2018)  Improving Cell Survival in Injected Embryos Allows Primed Pluripotent Stem Cells to Generate Chimeric Cynomolgus Monkeys..  Cell Rep,  25  (9): (2563-2576.e9).  [PMID:30485820]
4. Zhang YF et al..  (2022)  MicroRNA-582-5p Contributes to the Maintenance of Neural Stem Cells Through Inhibiting Secretory Protein FAM19A1..  Front Cell Neurosci,  16  (866020).  [PMID:35685988]
5. Alhashem Z et al..  (2022)  Notch controls the cell cycle to define leader versus follower identities during collective cell migration..  Elife,  11    [PMID:35438077]
6. Slaninova V et al..  (2016)  Notch stimulates growth by direct regulation of genes involved in the control of glycolysis and the tricarboxylic acid cycle..  Open Biol,  (2): (150155).  [PMID:26887408]

Solution Calculators