ChemicalBook > CAS DataBase List > GLUCOCEREBROSIDES

GLUCOCEREBROSIDES

Product Name
GLUCOCEREBROSIDES
CAS No.
497155-61-0
Chemical Name
GLUCOCEREBROSIDES
Synonyms
GLUCOSYLCERAMIDE;GLUCOCEREBROSIDES;Glucosylceramide (Soy);Glucocerebrosides (soy);Glucosylceramides (soy);Glycosphingolipids, soya;Glucosylceramide (plant);GLC-CER, GAUCHER'S SPLEEN;CERAMIDE BETA-D-GLUCOSIDE;Glucocerebrosides (Soy, 98%)
CBNumber
CB9478147
Molecular Formula
C9H18N2O7
Formula Weight
266.24842
MOL File
497155-61-0.mol
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GLUCOCEREBROSIDES Property

storage temp. 
−20°C
solubility 
chloroform/methanol (9:1): 20 mg/mL, clear, slightly yellow
form 
lyophilized powder
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Safety

Hazard Codes 
B
Safety Statements 
22-24/25
WGK Germany 
3
10
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
25850
Product name
Glucocerebrosides (soy)
Purity
≥98%
Packaging
5mg
Price
$111
Updated
2024/03/01
Cayman Chemical
Product number
25850
Product name
Glucosylceramides (soy)
Purity
≥98%
Packaging
10mg
Price
$177
Updated
2024/03/01
Cayman Chemical
Product number
25850
Product name
Glucosylceramides (soy)
Purity
≥98%
Packaging
50mg
Price
$820
Updated
2024/03/01
Cayman Chemical
Product number
25850
Product name
Glucosylceramides (soy)
Purity
≥98%
Packaging
100mg
Price
$1517
Updated
2024/03/01
Cayman Chemical
Product number
25850
Product name
Glucocerebrosides (soy)
Purity
≥98%
Packaging
1mg
Price
$30
Updated
2021/12/16
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GLUCOCEREBROSIDES Chemical Properties,Usage,Production

Uses

Glucosylceramide (Soy) is a major sphingolipid of plant tissue and, thus, abundant in nature and in dietary food sources.

Biological Activity

The lipid backbones of mammalian GluCer (sphingosine, d18:1(delta4), and ceramide) induce cell death (apoptosis) and inhibit colon carcinogenesis, it is critical to know the structures of GluCer present in plants as a first step toward understanding this potential link between diet and cancer. Previously unexplained fragmentations th at were diagnostic for the type of sphingoid base backbone (i.e. by homolytic cleavage of the doubly allylic C-6-C-7 bond to yield a stable distonic allylic radical cation and an allylic radical neutral) were also identified. Hence this method should be useful in the identification of double bonds in sphingolipids, and structure-function relationships between sphingolipids and colon carcinogenesis.?

GLUCOCEREBROSIDES Preparation Products And Raw materials

Raw materials

Preparation Products

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GLUCOCEREBROSIDES Suppliers

Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 13167063860
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Yichang Zhongyitai Trading Co., Ltd.
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Codow Chemical Co.,Ltd.
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Career Henan Chemica Co
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Aikon International Limited
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SHANGHAI ZZBIO CO., LTD.
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Cayman Chemical Company
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Enzo Biochem Inc
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Merck KGaA
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Guangzhou Lucheng Biotechnology Co., Ltd.
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Guangzhou Yaco Biotechnology Co., Ltd.
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Xiamen Research Biotechnology Co., Ltd.
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497155-61-0, GLUCOCEREBROSIDESRelated Search:


  • Glucocerebrosides (Soy, 98%)
  • Glycosphingolipids, soya
  • GLUCOCEREBROSIDES (SOY, 98%);GLUCOSYLCERAMIDE (SOY)
  • Glucosylceramide (Soy)
  • GLC-CER, GAUCHER'S SPLEEN
  • GLUCOSYLCERAMIDE
  • GLUCOCEREBROSIDES
  • GLUCOCEREBROSIDES, GAUCHER'S SPLEEN
  • CERAMIDE BETA-D-GLUCOSIDE
  • Glucocerebrosides from human kidney
  • Glucocerebrosides (soy)
  • Glycosylceramide - from plant origin
  • Glucosylceramides (soy)
  • Glucosylceramide (plant)
  • 497155-61-0
  • Glycan Component Classes
  • Neutral glycosphingolipids
  • Neutral GlycosphingolipidsLipids
  • Glycosphingolipids
  • Sphingolipids