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604-80-8,MFCD00017734
Catalog No.:AA00IKJF

604-80-8 | Narcissoside

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1mg
≥98%
in stock  
$46.00   $32.00
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5mg
≥98%
in stock  
$199.00   $139.00
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10mg
≥98%
in stock  
$348.00   $243.00
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25mg
≥98%
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$762.00   $533.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00IKJF
Chemical Name:
Narcissoside
CAS Number:
604-80-8
Molecular Formula:
C28H32O16
Molecular Weight:
624.5441
MDL Number:
MFCD00017734
SMILES:
COc1cc(ccc1O)c1oc2cc(O)cc(c2c(=O)c1O[C@@H]1O[C@H](CO[C@@H]2O[C@@H](C)[C@@H]([C@H]([C@H]2O)O)O)[C@H]([C@@H]([C@H]1O)O)O)O
Properties
Computed Properties
 
Complexity:
1040  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
10  
Heavy Atom Count:
44  
Hydrogen Bond Acceptor Count:
16  
Hydrogen Bond Donor Count:
9  
Rotatable Bond Count:
7  
XLogP3:
-1  

Downstream Synthesis Route
isorhamnetin3-O-2G-rhamnopyranosylrutinoside-7-O-α-L-rhamnopyranoside 
  6743-92-6   
isorhamnetin-3-O-α-L-rhamnopyranosyl-(1->2)-O-α-L-rhamnopyranosyl-(1->6)-O-β-D-glucopyranose 
  604-80-8 

[1]Phytochemistry,2000,vol.54,p.695-700

[1]ChemistryofNaturalCompounds,2001,vol.37,p.470-473

[1]ChemistryofNaturalCompounds,2001,vol.37,p.470-473

[1]ChemistryofNaturalCompounds,2002,vol.38,p.293-294

[2]ChemistryofNaturalCompounds,2007,vol.43,p.216-217

Literature

Title: The selected flavonol glycoside derived from Sophorae Flos improves glucose uptake and inhibits adipocyte differentiation via activation AMPK in 3T3-L1 cells.

Journal: Bioorganic & medicinal chemistry letters 20101015

Title: Vasorelaxing alkaloids and flavonoids from Cassytha filiformis.

Journal: Journal of natural products 20080201

Title: Anti-inflammatory, anti-tumor-promoting, and cytotoxic activities of constituents of marigold (Calendula officinalis) flowers.

Journal: Journal of natural products 20061201

Title: Alkaloids from Eschscholzia californica and their capacity to inhibit binding of [3H]8-Hydroxy-2-(di-N-propylamino)tetralin to 5-HT1A receptors in Vitro.

Journal: Journal of natural products 20060301

Title: [A new natural product from the roots of Hedysarum multijugum].

Journal: Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 20051018

Title: Antitubercular sterols from Thalia multiflora Horkel ex Koernicke.

Journal: Phytotherapy research : PTR 20051001

Title: Chemical constituents of the fruits of Morinda citrifolia (Noni) and their antioxidant activity.

Journal: Journal of natural products 20050401

Title: Antiprotozoal activity of the constituents of Conyza filaginoides.

Journal: Journal of natural products 20010501

Title: Inhibition of HIV infection by flavanoids.

Journal: Antiviral research 19931001

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SDS
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