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Home Other Building Blocks Mulberroside A

Mulberroside A

CAS No.:
102841-42-9
Catalog Number:
AG008TMN
Molecular Formula:
C26H32O14
Molecular Weight:
568.5239
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5mg
99%
1 week
United States
$215
- +
10mg
99%
1 week
United States
$307
- +
50mg
99%
1 week
United States
$807
- +
Product Description
Catalog Number:
AG008TMN
Chemical Name:
Mulberroside A
CAS Number:
102841-42-9
Molecular Formula:
C26H32O14
Molecular Weight:
568.5239
MDL Number:
MFCD16294844
IUPAC Name:
(2S,3R,4S,5S,6R)-2-[3-hydroxy-4-[(E)-2-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
InChI:
InChI=1S/C26H32O14/c27-9-17-19(31)21(33)23(35)25(39-17)37-14-4-3-12(16(30)8-14)2-1-11-5-13(29)7-15(6-11)38-26-24(36)22(34)20(32)18(10-28)40-26/h1-8,17-36H,9-10H2/b2-1+/t17-,18-,19-,20-,21+,22+,23-,24-,25-,26-/m1/s1
InChI Key:
HPSWAEGGWLOOKT-VUNDNAJOSA-N
SMILES:
OC[C@H]1O[C@@H](Oc2ccc(c(c2)O)/C=C/c2cc(O)cc(c2)O[C@@H]2O[C@H](CO)[C@H]([C@@H]([C@H]2O)O)O)[C@@H]([C@H]([C@@H]1O)O)O
Properties
Complexity:
816  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
10  
Defined Bond Stereocenter Count:
1  
Exact Mass:
568.179g/mol
Formal Charge:
0
Heavy Atom Count:
40  
Hydrogen Bond Acceptor Count:
14  
Hydrogen Bond Donor Count:
10  
Isotope Atom Count:
0
Molecular Weight:
568.528g/mol
Monoisotopic Mass:
568.179g/mol
Rotatable Bond Count:
8  
Topological Polar Surface Area:
239A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.8  
Literature
Title Journal
Mulberroside A suppresses PXR-mediated transactivation and gene expression of P-gp in LS174T cells. Journal of biochemical and molecular toxicology 20170501
Down-regulation of P-gp expression and function after Mulberroside A treatment: potential role of protein kinase C and NF-kappa B. Chemico-biological interactions 20140425
Antihyperuricemic and nephroprotective effects of resveratrol and its analogues in hyperuricemic mice. Molecular nutrition & food research 20120901
Evaluation of the inhibition of mushroom tyrosinase and cellular tyrosinase activities of oxyresveratrol: comparison with mulberroside A. Journal of enzyme inhibition and medicinal chemistry 20120801
In vitro pharmacokinetic characterization of mulberroside A, the main polyhydroxylated stilbene in mulberry (Morus alba L.), and its bacterial metabolite oxyresveratrol in traditional oral use. Journal of agricultural and food chemistry 20120307
Enhancement of the tyrosinase inhibitory activity of Mori Cortex Radicis extract by biotransformation using Leuconostoc paramesenteroides PR. Bioscience, biotechnology, and biochemistry 20120101
Inhibitory effect of mulberroside A and its derivatives on melanogenesis induced by ultraviolet B irradiation. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20111201
Mulberroside a possesses potent uricosuric and nephroprotective effects in hyperuricemic mice. Planta medica 20110501
Biotransformation of mulberroside A from Morus alba results in enhancement of tyrosinase inhibition. Journal of industrial microbiology & biotechnology 20100601
Anti-inflammatory and analgesic properties of cis-mulberroside A from Ramulus mori. Fitoterapia 20100401
Three major metabolites of mulberroside A in rat intestinal contents and feces. Planta medica 20100301
Oxyresveratrol as an antibrowning agent for cloudy apple juices and fresh-cut apples. Journal of agricultural and food chemistry 20070404
In-vitro and in-vivo anti-inflammatory effect of oxyresveratrol from Morus alba L. The Journal of pharmacy and pharmacology 20031201
Properties