CAS 148356-01-8
:2,5-Dioxo-1-pyrrolidinyl 6-[[(3′,6′-dihydroxy-3-oxospiro[isobenzofuran-1(3H),9′-[9H]xanthen]-6-yl)carbonyl]amino]hexanoate
Description:
2,5-Dioxo-1-pyrrolidinyl 6-[[(3′,6′-dihydroxy-3-oxospiro[isobenzofuran-1(3H),9′-[9H]xanthen]-6-yl)carbonyl]amino]hexanoate, with CAS number 148356-01-8, is a complex organic compound characterized by its intricate molecular structure, which includes a pyrrolidine ring and a spiro-linked isobenzofuran and xanthen moiety. This compound features multiple functional groups, including carbonyls and hydroxyls, contributing to its potential reactivity and biological activity. The presence of the pyrrolidinyl group suggests possible applications in medicinal chemistry, particularly in drug design, due to its ability to interact with biological targets. The compound's solubility, stability, and reactivity can vary based on environmental conditions such as pH and temperature. Its unique structure may also impart specific optical properties, making it of interest in fields such as photochemistry and materials science. Overall, this compound exemplifies the complexity and diversity of organic molecules, with potential implications in various scientific and industrial applications.
Formula:C31H26N2O10
InChI:InChI=1S/C31H26N2O10/c34-18-6-9-21-24(15-18)41-25-16-19(35)7-10-22(25)31(21)23-14-17(5-8-20(23)30(40)42-31)29(39)32-13-3-1-2-4-28(38)43-33-26(36)11-12-27(33)37/h5-10,14-16,34-35H,1-4,11-13H2,(H,32,39)
InChI key:InChIKey=OEKZTXDDIMSZIG-UHFFFAOYSA-N
SMILES:O=C1OC2(C=3C1=CC=C(C(NCCCCCC(ON4C(=O)CCC4=O)=O)=O)C3)C=5C(OC=6C2=CC=C(O)C6)=CC(O)=CC5
Synonyms:- Hexanoic acid, 6-[[(3′,6′-dihydroxy-3-oxospiro[isobenzofuran-1(3H),9′-[9H]xanthen]-6-yl)carbonyl]amino]-, 2,5-dioxo-1-pyrrolidinyl ester
- 2,5-Dioxo-1-pyrrolidinyl 6-[[(3′,6′-dihydroxy-3-oxospiro[isobenzofuran-1(3H),9′-[9H]xanthen]-6-yl)carbonyl]amino]hexanoate
- Spiro[isobenzofuran-1(3H),9′-[9H]xanthene]-6-carboxamide, N-[6-[(2,5-dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]-3′,6′-dihydroxy-3-oxo-
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Found 2 products.
6-SFX
CAS:6-SFX is a small molecule inhibitor of the protein interactions. It can be used as a research tool for studying protein interactions, and it has been shown to have an inhibitory effect on receptor activation. 6-SFX binds to the ligand binding site of the receptor and prevents the interaction between the ligand and receptor. This inhibits ion channel activity, which leads to decreased production of neurotransmitters such as dopamine, serotonin, and glutamate. 6-SFX also inhibits phosphorylation by inhibiting protein kinase C (PKC) signaling pathways in cells. 6-SFX has been shown to have high purity that is suitable for use in life sciences research.
Formula:C31H26N2O10Purity:Min. 95%Molecular weight:586.5 g/mol
