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Kinsenoside

Product Name
Kinsenoside
CAS No.
151870-74-5
Chemical Name
Kinsenoside
Synonyms
Kinsenoside;(+)-Kinsenoside;(4R)-4-(beta-D-Glucopyranosyloxy)dihydro-2(3H)-furanone;2(3H)-Furanone, 4-(β-D-glucopyranosyloxy)dihydro-, (4R)-;(4R)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-one;(R)-4-(((2R,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)dihydrofuran-2(3H)-one;Keap1-Nrf2,Inhibitor,pulposus,disc,degeneration,Kinsenoside,inhibit,cells,nucleus,Nrf2,Apoptosis,intervertebral
CBNumber
CB22645474
Molecular Formula
C10H16O8
Formula Weight
264.23
MOL File
151870-74-5.mol
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Kinsenoside Property

Boiling point:
570.2±50.0 °C(Predicted)
Density 
1.59±0.1 g/cm3(Predicted)
storage temp. 
4°C, protect from light
solubility 
DMF:14.0(Max Conc. mg/mL);52.98(Max Conc. mM)
DMSO:33.0(Max Conc. mg/mL);124.89(Max Conc. mM)
PBS (pH 7.2):10.0(Max Conc. mg/mL);37.85(Max Conc. mM)
form 
A crystalline solid
pka
12.81±0.70(Predicted)
color 
White to light yellow
InChI
InChI=1/C10H16O8/c11-2-5-7(13)8(14)9(15)10(18-5)17-4-1-6(12)16-3-4/h4-5,7-11,13-15H,1-3H2/t4-,5-,7-,8+,9-,10-/s3
InChIKey
MQEPWBMWFIVRPS-MUOXDHKLNA-N
SMILES
O1C[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)CC1=O |&1:2,4,6,9,11,13,r|
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
25144
Product name
Kinsenoside
Purity
≥95%
Packaging
1mg
Price
$44
Updated
2024/03/01
Cayman Chemical
Product number
25144
Product name
Kinsenoside
Purity
≥95%
Packaging
5mg
Price
$193
Updated
2024/03/01
Cayman Chemical
Product number
25144
Product name
Kinsenoside
Purity
≥95%
Packaging
10mg
Price
$341
Updated
2024/03/01
TRC
Product number
K570200
Product name
Kinsenoside
Packaging
10mg
Price
$420
Updated
2021/12/16
Usbiological
Product number
300531
Product name
Kinsenoside
Packaging
25mg
Price
$907
Updated
2021/12/16
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Kinsenoside Chemical Properties,Usage,Production

Description

Kinsenoside is a glycoside originally isolated from A. formosanus that has diverse biological activities, including antihyperlipidemic, immunosuppressive, and anti-inflammatory properties. It increases lipolysis mediated by adipose triglyceride lipase and increases hydrolysis of triglycerides in C3H10T1/2 adipocytes. It also increases phosphorylation of peroxisome proliferator-activated receptor α (PPARα) and CREB as well as protein levels of SIRT1, PGC-1α, and carnitine palmitoyltransferase I. Kinsenoside downregulates the expression and phosphorylation of VEGF receptor 2 (VEGFR2) and inhibits crosstalk between the JAK2/STAT3 and PI3K/AKT signaling pathways in dendritic cells in vitro. It decreases the production of IFN-γ, IL-17, and TNF-α and increases the production of IL-10 in splenocytes isolated from mice with collagen-induced arthritis (CIA). Kinsenoside (300 mg/kg per day) decreases the expression of IL-1β, TNF-α, and matrix metalloproteinase-9 (MMP-9) and increases the expression of IL-10 in inflamed joints in a mouse model of collagen-induced arthritis and prevents paw edema and reduces the severity of arthritis.

Uses

Kinsenoside is an anti-hyperlipidemic agent isolated from the plant Anoect chilus.

Definition

ChEBI: (3R)-5-Oxotetrahydro-3-furanyl beta-D-glucopyranoside is a glycoside.

in vivo

Kinsenoside (10 mg/kg; ip; every 3 days for 4 weeks) promotes the expression of Nrf2 and ameliorates intervertebral disc degeneration (IDD) induced by Pentobarbital (50 mg/kg) in vivo in rat model[1].
Kinsenoside (100 mg/kg, 300 mg/kg; ip; 1 h before LPS induction) inhibits LPS (40 mg/kg; ip)-induced inflammatory model in mice[3].

References

[1] X M DU. Glycosidic constituents from in vitro Anoectochilus formosanus.[J]. Chemical & pharmaceutical bulletin, 2000, 48 11: 1803-1804. DOI: 10.1248/cpb.48.1803
[2] De Souza, F.I., Zumiotti, A.V., and Da Silva, C.F. Neuregulins 1-α and 1-β on the regeneration the peripheral nerves[J]. Acta Ortop Bras.
[3] HUNG-BO HSIAO. Kinsenoside inhibits the inflammatory mediator release in a type-II collagen induced arthritis mouse model by regulating the T cells responses[J]. BMC Complementary and Alternative Medicine, 2016, 16 1. DOI: 10.1186/s12906-016-1054-8
[4] MING XIANG. Effects of kinsenoside, a potential immunosuppressive drug for autoimmune hepatitis, on dendritic cells/CD8+T cells communication in mice[J]. Hepatology, 2016, 64 6: 2135-2150. DOI: 10.1002/hep.28825

Kinsenoside Preparation Products And Raw materials

Raw materials

Preparation Products

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Kinsenoside Suppliers

EMMX Biotechnology LLC
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888-539-0666
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888-539-0666
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info@emmx.com
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United States
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8447
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TargetMol Chemicals Inc.
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+1-781-999-5354; +17819995354
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marketing@targetmol.com
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United States
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Aladdin Scientific
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tp@aladdinsci.com
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United States
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52923
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TargetMol Chemicals Inc.
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+1-781-999-5354;
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support@targetmol.com
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United States
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FortopChem Technology Limited
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sales@fortopchem.com
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United States
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Cayman Chemical Company
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cayman@caymanchem.com
Country
United States
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6213
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81
United States Biological
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chemicals@usbio.net
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United States
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6214
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MedChemExpress
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sales@medchemexpress.com
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United States
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View Lastest Price from Kinsenoside manufacturers

Shanghai Standard Technology Co., Ltd.
Product
Kinsenoside 151870-74-5
Price
US $0.00/mg
Min. Order
20mg
Purity
≥98%(HPLC)
Supply Ability
10 g
Release date
2020-04-24

151870-74-5, KinsenosideRelated Search:


  • Kinsenoside
  • (4R)-4-(beta-D-Glucopyranosyloxy)dihydro-2(3H)-furanone
  • 2(3H)-Furanone, 4-(β-D-glucopyranosyloxy)dihydro-, (4R)-
  • (4R)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-one
  • (+)-Kinsenoside
  • Keap1-Nrf2,Inhibitor,pulposus,disc,degeneration,Kinsenoside,inhibit,cells,nucleus,Nrf2,Apoptosis,intervertebral
  • (R)-4-(((2R,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)dihydrofuran-2(3H)-one
  • 151870-74-5