Home Other Building Blocks 13405-60-2
13405-60-2,MFCD11975493
Catalog No.:AA009BGR

13405-60-2 | 1-O-Galloyl-beta-d-glucose

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10mg
≥98%
in stock  
$106.00   $74.00
- +
50mg
≥98%
in stock  
$445.00   $311.00
- +
100mg
≥98%
in stock  
$783.00   $548.00
- +
250mg
≥98%
in stock  
$1,565.00   $1,095.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA009BGR
Chemical Name:
1-O-Galloyl-beta-d-glucose
CAS Number:
13405-60-2
Molecular Formula:
C13H16O10
Molecular Weight:
332.2601
MDL Number:
MFCD11975493
SMILES:
OC[C@H]1O[C@@H](OC(=O)c2cc(O)c(c(c2)O)O)[C@@H]([C@H]([C@@H]1O)O)O
Properties
Computed Properties
 
Complexity:
406  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Heavy Atom Count:
23  
Hydrogen Bond Acceptor Count:
10  
Hydrogen Bond Donor Count:
7  
Rotatable Bond Count:
4  
XLogP3:
-1.4  

Literature

Title: Aldose reductase inhibition alleviates hyperglycemic effects on human retinal pigment epithelial cells.

Journal: Chemico-biological interactions 20150605

Title: Beta-glucogallin reduces the expression of lipopolysaccharide-induced inflammatory markers by inhibition of aldose reductase in murine macrophages and ocular tissues.

Journal: Chemico-biological interactions 20130225

Title: The isolation and characterization of β-glucogallin as a novel aldose reductase inhibitor from Emblica officinalis.

Journal: PloS one 20120101

Title: Method development for β-glucogallin and gallic acid analysis: application to urinary pharmacokinetic studies.

Journal: Journal of pharmaceutical and biomedical analysis 20110325

Title: Galloyl glucoses from the seeds of Cornus officinalis with inhibitory activity against protein glycation, aldose reductase, and cataractogenesis ex vivo.

Journal: Biological & pharmaceutical bulletin 20110101

Title: Characterization of gallotannins from Astronium species by flow injection analysis- electrospray ionization-ion trap-tandem mass spectrometry and matrix-assisted laser desorption/ionization time-of- flight mass spectrometry.

Journal: European journal of mass spectrometry (Chichester, England) 20110101

Title: Diterpene esters and phenolic compounds from Sapium insigne (ROYLE) BENTH. ex HOOK. fil.

Journal: Chemical & pharmaceutical bulletin 20091101

Title: [Studies on chemical constituents of leaves of Psidium guajava].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20090301

Title: Identification of multiple constituents in the traditional Chinese medicine formula GuiZhiFuLing-Wan by HPLC-DAD-MS/MS.

Journal: Journal of pharmaceutical and biomedical analysis 20090220

Title: Chemical profiling of Radix Paeoniae evaluated by ultra-performance liquid chromatography/photo-diode-array/quadrupole time-of-flight mass spectrometry.

Journal: Journal of pharmaceutical and biomedical analysis 20090220

Title: High-speed separation and characterization of major constituents in Radix Paeoniae Rubra by fast high-performance liquid chromatography coupled with diode-array detection and time-of-flight mass spectrometry.

Journal: Rapid communications in mass spectrometry : RCM 20090101

Title: [Study on hydrolysable tannin constituents of seed of Juglans regia II].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20080701

Title: Comparative study of chemical constituents of rhubarb from different origins.

Journal: Chemical & pharmaceutical bulletin 20061101

Title: [The chemical constituents of Breynia rostrata].

Journal: Yao xue xue bao = Acta pharmaceutica Sinica 20060201

Title: Anti-babesial and anti-plasmodial compounds from Phyllanthus niruri.

Journal: Journal of natural products 20050401

Title: Novel lipid-peroxidation- and cyclooxygenase-inhibitory tannins from Picrorhiza kurroa seeds.

Journal: Chemistry & biodiversity 20040301

Title: [Studies on chemical constituents in fruits of Tibetan medicine Phyllanthus emblica].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20031001

Title: Gallotannin biosynthesis: two new galloyltransferases from Rhus typhina leaves preferentially acylating hexa- and heptagalloylglucoses.

Journal: Planta 20021101

Title: Gallic esters of sucrose as efficient radical scavengers in lipid peroxidation.

Journal: Journal of agricultural and food chemistry 20020605

Title: Inhibition of HIV-1 integrase by galloyl glucoses from Terminalia chebula and flavonol glycoside gallates from Euphorbia pekinensis.

Journal: Planta medica 20020501

Title: Ethyl m-digallate from red maple, Acer rubrum L., as the major resistance factor to forest tent caterpillar, Malacosoma disstria Hbn.

Journal: Journal of chemical ecology 20011201

Title: Gallotannin biosynthesis: beta-glucogallin: hexagalloyl 3-O-galloyltransferase from Rhus typhina leaves.

Journal: Phytochemistry 20011101

Title: A new galloylglucoside from Cleyera ochnacea DC.

Journal: Chemical & pharmaceutical bulletin 20011101

Title: Synthesis of gallotannins.

Journal: Carbohydrate research 20011015

Title: Ellagic acid formation from galloylglucoses by a crude enzyme of Cornus capitata adventitious roots.

Journal: Bioscience, biotechnology, and biochemistry 20010801

Title: Seasonal variation in the content of hydrolysable tannins in leaves of Betula pubescens.

Journal: Phytochemistry 20010501

Title: Inhibitory effects of ellagi- and gallotannins on rat intestinal alpha-glucosidase complexes.

Journal: Bioscience, biotechnology, and biochemistry 20010301

Title: Inhibitory effects of Egyptian folk medicines on human immunodeficiency virus (HIV) reverse transcriptase.

Journal: Chemical & pharmaceutical bulletin 19950401

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:13405-60-2 Molecular Formula|13405-60-2 MDL|13405-60-2 SMILES|13405-60-2 1-O-Galloyl-beta-d-glucose