EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

narcissin flavonol
isorhamnetin 3-O-rutinoside

Supplier Sponsors

CAS Number: 604-80-8Picture of molecule3D/inchi
FDA UNII: N4AX11L1TF
Nikkaji Web:J16.152G
XlogP3-AA:-1.00 (est)
Molecular Weight:624.55024000
Formula:C28 H32 O16
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:pharmaceuticals / chemical synthisis
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Flash Point: 32.00 °F. TCC ( 0.00 °C. ) (est)
Soluble in:
 water, 2048 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
Narcissin 98%
BOC Sciences
For experimental / research use only.
isorhamnetin-3-O-rutinoside
ExtraSynthese
For experimental / research use only.
isoRhamnetin-3-O-rutinoside (HPLC) ≥99%
Santa Cruz Biotechnology
For experimental / research use only.
Narcissoside
Sigma-Aldrich: Sigma
For experimental / research use only.
Narcissoside ≥95% (HPLC)
sds
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-mouse LD > 4 gm/kg
Dokl Akad Nauk resp. Uzb.Vol. (2), Pg. 41, 1992.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
pharmaceuticals / chemical synthisis
Recommendation for narcissin flavonol usage levels up to:
 not for fragrance use.
 
Recommendation for narcissin flavonol flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :5481663
National Institute of Allergy and Infectious Diseases:Data
Chemidplus:0000604808
 
References:
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5481663
Pubchem (sid):135077206
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEMBL:View
HMDB (The Human Metabolome Database):Search
FooDB:FDB000609
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 bean black bean shoot
Search Trop Picture
 buckthorn sea buckthorn
Search Trop Picture
 ginkgo biloba leaf
Search Trop Picture
 rape
Search Trop Picture
 
Synonyms:
 narcissin (6CI,7CI,8CI)
 narcissoside
isorhamnetin 3-O-rutinoside
isorhamnetin 3-rhamnoglucoside
isorhamnetin 3-rutinoside
isorhamnetin-3-O-rutinoside
 

Articles:

PubMed:Antioxidant, 5-Lipoxygenase Inhibitory and Cytotoxic Activities of Compounds Isolated from the Ferula lutea Flowers.
PubMed:α-Glucosidase inhibition, 15-lipoxygenase inhibition, and brine shrimp toxicity of extracts and isolated compounds from Terminalia macroptera leaves.
PubMed:Extraction and isolation of flavonoid glycosides from Flos Sophorae Immaturus using ultrasonic-assisted extraction followed by high-speed countercurrent chromatography.
PubMed:Bioassay-guided isolation of antioxidants from Astragalus altaicus by combination of chromatographic techniques.
PubMed:DPPH radical scavenging and xanthine oxidase inhibitory activity of Terminalia macroptera leaves.
PubMed:Efficacy of marigold extract-loaded formulations against UV-induced oxidative stress.
PubMed:Protective effect of Calendula officinalis extract against UVB-induced oxidative stress in skin: evaluation of reduced glutathione levels and matrix metalloproteinase secretion.
PubMed:Flavonoids and isoflavonoids from Sophorae Flos improve glucose uptake in vitro.
PubMed:[HPLC investigation of antioxidant components in Solidago herba].
PubMed:[A new natural product from the roots of Hedysarum multijugum].
PubMed:Effect of bioactive compounds from Sainfoin ( Onobrychis viciifolia Scop.) on the in vitro larval migration of Haemonchus contortus: role of tannins and flavonol glycosides.
PubMed:The influence of Calendulae officinalis flos extracts on cell cultures, and the chromatographic analysis of extracts.
PubMed:Phytochemical analysis of ethyl acetate extract from Astragalus corniculatus Bieb. and brain antihypoxic activity.
PubMed:Constituents of the stems and fruits of Opuntia ficus-indica var. saboten.
PubMed:Antiprotozoal activity of the constituents of Teloxys graveolens.
PubMed:Antiprotozoal activity of the constituents of Conyza filaginoides.
PubMed:Anti-tumor promoting activity of polyphenols from Cowania mexicana and Coleogyne ramosissima.
PubMed:[Glycosides of phenolic acid and flavonoids from the leaves of Glycyrrhiza uralensis Ficsh].
PubMed:Minor components in food plants--Note I. Flavonol glycosides from Ullucus tuberosus.
PubMed:[Chemical constituents of Bupleurum Longicaule Wall. ex DC. var. giraldii Wolff].
PubMed:[Constituents of Berchemia racemosa Sieb. et Zucc].
PubMed:[Comparison of effects of narcissin and ligustrazin on cardiac hemodynamics].
PubMed:Biological and phytochemical investigation of plants XVI: Strumpfia maritima (Rubiaceae).
PubMed:Isolation of isorhamnetin-3-rutinoside (Narcissin) and quercetin-3-glucoside from the leaves and stems of Leontice leontopetalum.
PubMed:The flavonol glycosides in the fruit of Pyrus communis L. cultivar Bon Chrétien.
 
Notes:
None found
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