ISORHAMNETIN-3-RUTINOSIDE CAS 604-80-8

Introduction：Basic information about ISORHAMNETIN-3-RUTINOSIDE CAS 604-80-8, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

ISORHAMNETIN-3-RUTINOSIDE Basic information

• Product Name: ISORHAMNETIN-3-RUTINOSIDE
• Synonyms: NARCISIN;NARCISSIN;ISORHAMNETIN-3-O-RUTINOSIDE;ISORHAMNETIN-3-RUTINOSIDE;Narcissoside, froM Hedyotis chrysotricha;3-[[6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-on;Narcissoside Narcissin;Isprhamnetin-3-rutinoside
• CAS: 604-80-8
• MF: C28H32O16
• MW: 624.55
• Product Categories: chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Flavanols
• Mol File: 604-80-8.mol

ISORHAMNETIN-3-RUTINOSIDE Chemical Properties

• Melting point: 182-184°C
• Boiling point: 953.1±65.0 °C(Predicted)
• density: 1.74
• storage temp.: 2-8°C
• solubility: DMSO (Slightly), Methanol (Slightly)
• pka: 6.17±0.40(Predicted)
• form: powder
• color: Yellow
• Major Application: metabolomics vitamins, nutraceuticals, and natural products
• InChIKey: UIDGLYUNOUKLBM-MCZPZOQCNA-N
• SMILES: O[C@@H]([C@H](CO[C@@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@@H](C)O1)O2)[C@@H](O)[C@H](O)[C@H]2OC3=C(C4=CC=C(O)C(OC)=C4)OC5=CC(O)=CC(O)=C5C3=O
• CAS DataBase Reference: 604-80-8

Safety Information

• Safety Statements: 24/25
• WGK Germany: WGK 3
• HS Code: 29389090
• Storage Class: 11 - Combustible Solids

ISORHAMNETIN-3-RUTINOSIDE Usage And Synthesis

Chemical Properties

Yellow powder

Uses

Narcissoside is a flavonoid from Nitraria tangutorum. Narcissoside may have antiproliferative activity in human colon cancer cell line (HT29).

Definition

ChEBI: Isorhamnetin-3-O-rutinoside is a disaccharide derivative, a glycosyloxyflavone, a monomethoxyflavone and a trihydroxyflavone.

in vivo

Narcissin (85 nmol, applied to the skin) inhibits TPA (1.7 nmol, applied to the skin)-induced tumor promotion in mice^[3].