72129

Neoeriocitrin

~95% (HPLC)

• Sinonimo/i: (S)-3′,4′,5,7-Tetrahydroxyflavanone-7-[2-O-(α-L-rhamnopyranosyl)-β-D-glucopyranoside], Eriodictyol 7-neohesperidoside
• Formula empirica (notazione di Hill): C₂₇H₃₂O₁₅
• Numero CAS: 13241-32-2
• Peso molecolare: 596.53
• Beilstein: 1696764
• Numero CE: 236-215-3
• Numero MDL: MFCD00017474
• Codice UNSPSC: 85151701
• ID PubChem: 329763836
• NACRES: NA.47

Proprietà

• Saggio: ~95% (HPLC)
• Livello qualitativo: 100
• Stato: powder
• Stringa SMILE: 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; OBKKEZLIABHSGY-DOYQYKRZSA-N

Descrizione

Azioni biochim/fisiol

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.

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable
• Dispositivi di protezione individuale: Eyeshields, Gloves, type N95 (US)