72129

Neoeriocitrin

~95% (HPLC)

• Synonym(s): (S)-3′,4′,5,7-Tetrahydroxyflavanone-7-[2-O-(α-L-rhamnopyranosyl)-β-D-glucopyranoside], Eriodictyol 7-neohesperidoside
• Empirical Formula (Hill Notation): C₂₇H₃₂O₁₅
• CAS Number: 13241-32-2
• Molecular Weight: 596.53
• Beilstein: 1696764
• EC Number: 236-215-3
• MDL number: MFCD00017474
• UNSPSC Code: 85151701
• PubChem Substance ID: 329763836
• NACRES: NA.47

Properties

• Assay: ~95% (HPLC)
• Quality Level: 100
• form: powder
• SMILES string: C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2Oc3cc(O)c4C(=O)C[C@H](Oc4c3)c5ccc(O)c(O)c5)[C@H](O)[C@H](O)[C@H]1O
• InChI: 1S/C27H32O15/c1-9-20(33)22(35)24(37)26(38-9)42-25-23(36)21(34)18(8-28)41-27(25)39-11-5-14(31)19-15(32)7-16(40-17(19)6-11)10-2-3-12(29)13(30)4-10/h2-6,9,16,18,20-31,33-37H,7-8H2,1H3/t9-,16-,18+,20-,21+,22+,23-,24+,25+,26-,27+/m0/s1
• InChI key: OBKKEZLIABHSGY-DOYQYKRZSA-N

Description

Biochem/physiol Actions

Neoeriocitrin was one of several flavonoids that completely blocked the okadaic acid-induced inhibition of autophagy in cultured mouse hepatocytes. It is suggested as tool in the study of intracellular protein phosphorylation and as a potential protectant against pathological hyperphosphorylations.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves