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Catalog Number | ACM1021950797 |
CAS Number | 1021950-79-7 |
Synonyms | Oleracein E |
Molecular Weight | 219.24 |
InChI | InChI=1S/C12H13NO3/c14-10-5-7-3-4-13-9(1-2-12(13)16)8(7)6-11(10)15/h5-6,9,14-15H,1-4H2 |
InChI Key | LJIDRFNRDLYHNC-UHFFFAOYSA-N |
Purity | 95%+ |
Complexity | 307 |
Covalently-Bonded Unit Count | 1 |
Defined Atom Stereocenter Count | 0 |
Exact Mass | 219.08954328 |
Heavy Atom Count | 16 |
Hydrogen Bond Acceptor Count | 3 |
Hydrogen Bond Donor Count | 2 |
Monoisotopic Mass | 219.08954328 |
PhysicalState | Powder |
Rotatable Bond Count | 0 |
Topological Polar Surface Area | 60.8 Ų |
What is the chemical name of the compound with the CAS number 1021950-79-7?
The chemical name of the compound is 8,9-Dihydroxy-1,5,6,10B-tetrahydropyrrolo[2,1-A]isoquinolin-3(2H)-one.
What are some synonyms for 8,9-Dihydroxy-1,5,6,10B-tetrahydropyrrolo[2,1-A]isoquinolin-3(2H)-one?
Some synonyms mentioned are Trolline, Oleracein E, and Pyrrolo[2,1-a]isoquinolin-3(2H)-one.
What is the molecular formula of 8,9-Dihydroxy-1,5,6,10B-tetrahydropyrrolo[2,1-A]isoquinolin-3(2H)-one?
The molecular formula is C12H13NO3.
What is the molecular weight of 8,9-Dihydroxy-1,5,6,10B-tetrahydropyrrolo[2,1-A]isoquinolin-3(2H)-one?
The molecular weight is 219.24 g/mol.
What is the main usage of Oleracein E?
Oleracein E is mentioned to possess potent antioxidant activity.
How did pretreatment with OE affect rotenone-treated SH-SY5Y human neuroblastoma cells?
Pretreatment with OE decreased lactic acid dehydrogenase (LDH) release and the apoptosis rate in the cells.
What effect did OE have on reactive oxygen species (ROS) levels in the cells?
OE reduced ROS levels in the cells.
What signaling pathway did OE inhibit in the mechanistic study?
OE inhibited extracellular signal-regulated kinase (ERK) 1/2 phosphorylation.
How did OE prevent cytochrome C release in the cells?
OE prevented cytochrome C release by reducing the up-regulation of the proapoptotic protein Bax.
What is the role of OE in caspase-3 activation according to the reference?
OE prevented caspase-3 activation in the cells.
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