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Sigma-Aldrich

Neoeriocitrin

~95% (HPLC)

Synonym(s):

(S)-3′,4′,5,7-Tetrahydroxyflavanone-7-[2-O-(α-L-rhamnopyranosyl)-β-D-glucopyranoside], Eriodictyol 7-neohesperidoside

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About This Item

Empirical Formula (Hill Notation):
C27H32O15
CAS Number:
13241-32-2
Molecular Weight:
596.53
Beilstein/REAXYS Number:
1696764
EC Number:
236-215-3
MDL number:
MFCD00017474
UNSPSC Code:
85151701
PubChem Substance ID:
329763836
NACRES:
NA.47

assay

~95% (HPLC)

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

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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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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