72129
Neoeriocitrin
~95% (HPLC)
别名:
(S)-3′,4′,5,7-Tetrahydroxyflavanone-7-[2-O-(α-L-rhamnopyranosyl)-β-D-glucopyranoside], Eriodictyol 7-neohesperidoside
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关于此项目
经验公式（希尔记法）:
C27H32O15
化学文摘社编号:
分子量:
596.53
UNSPSC Code:
85151701
NACRES:
NA.47
PubChem Substance ID:
EC Number:
236-215-3
Beilstein/REAXYS Number:
1696764
MDL number:
Assay:
~95% (HPLC)
Form:
powder
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
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.
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)