151870-74-5,MFCD11100290
Catalog No.:AA00AKLV

151870-74-5 | Kinsenoside

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥95%
in stock  
$63.00   $44.00
- +
5mg
≥95%
in stock  
$276.00   $193.00
- +
10mg
≥95%
in stock  
$488.00   $341.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00AKLV
Chemical Name:
Kinsenoside
CAS Number:
151870-74-5
Molecular Formula:
C10H16O8
Molecular Weight:
264.2292
MDL Number:
MFCD11100290
SMILES:
OC[C@H]1O[C@@H](O[C@H]2COC(=O)C2)[C@@H]([C@H]([C@@H]1O)O)O
Properties
Computed Properties
 
Complexity:
308  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
6  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-2.4  

Literature

Title: Kinsenoside, a high yielding constituent from Anoectochilus formosanus, inhibits carbon tetrachloride induced Kupffer cells mediated liver damage.

Journal: Journal of ethnopharmacology 20110517

Title: Kinsenoside isolated from Anoectochilus formosanus suppresses LPS-stimulated inflammatory reactions in macrophages and endotoxin shock in mice.

Journal: Shock (Augusta, Ga.) 20110201

Title: Pharmacologically active compounds in the Anoectochilus and Goodyera species.

Journal: Journal of natural medicines 20080401

Title: Antihyperglycemic activity of kinsenoside, a high yielding constituent from Anoectochilus roxburghii in streptozotocin diabetic rats.

Journal: Journal of ethnopharmacology 20071101

Title: The hepatoprotective activity of kinsenoside from Anoectochilus formosanus.

Journal: Phytotherapy research : PTR 20070101

Title: A novel total synthesis of kinsenoside and goodyeroside A relying on the efficient reaction of the chiral 2(5H)-furanones.

Journal: Journal of Asian natural products research 20051001

Title: Higher yielding isolation of kinsenoside in Anoectochilus and its antihyperliposis effect.

Journal: Biological & pharmaceutical bulletin 20010101

Title: Qi CX, et al. Kinsenoside: A Promising Bioactive Compound from Anoectochilus Species. Curr Med Sci. 2018 Feb;38(1):11-18.

Title: Wang Y, et al. Kinsenoside ameliorates intervertebral disc degeneration through the activation of AKT-ERK1/2-Nrf2 signaling pathway. Aging (Albany NY). 2019 Sep 23;11(18):7961-7977.

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SDS
Tags:151870-74-5 Molecular Formula|151870-74-5 MDL|151870-74-5 SMILES|151870-74-5 Kinsenoside
Catalog No.: AA00AKLV
151870-74-5,MFCD11100290
151870-74-5 | Kinsenoside
Pack Size: 1mg
Purity: ≥95%
in stock
$63.00 $44.00
Pack Size: 5mg
Purity: ≥95%
in stock
$276.00 $193.00
Pack Size: 10mg
Purity: ≥95%
in stock
$488.00 $341.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA00AKLV
Chemical Name: Kinsenoside
CAS Number: 151870-74-5
Molecular Formula: C10H16O8
Molecular Weight: 264.2292
MDL Number: MFCD11100290
SMILES: OC[C@H]1O[C@@H](O[C@H]2COC(=O)C2)[C@@H]([C@H]([C@@H]1O)O)O
Properties
Complexity: 308  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 6  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 8  
Hydrogen Bond Donor Count: 4  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -2.4  
Literature fold

Title: Kinsenoside, a high yielding constituent from Anoectochilus formosanus, inhibits carbon tetrachloride induced Kupffer cells mediated liver damage.

Journal: Journal of ethnopharmacology20110517

Title: Kinsenoside isolated from Anoectochilus formosanus suppresses LPS-stimulated inflammatory reactions in macrophages and endotoxin shock in mice.

Journal: Shock (Augusta, Ga.)20110201

Title: Pharmacologically active compounds in the Anoectochilus and Goodyera species.

Journal: Journal of natural medicines20080401

Title: Antihyperglycemic activity of kinsenoside, a high yielding constituent from Anoectochilus roxburghii in streptozotocin diabetic rats.

Journal: Journal of ethnopharmacology20071101

Title: The hepatoprotective activity of kinsenoside from Anoectochilus formosanus.

Journal: Phytotherapy research : PTR20070101

Title: A novel total synthesis of kinsenoside and goodyeroside A relying on the efficient reaction of the chiral 2(5H)-furanones.

Journal: Journal of Asian natural products research20051001

Title: Higher yielding isolation of kinsenoside in Anoectochilus and its antihyperliposis effect.

Journal: Biological & pharmaceutical bulletin20010101

Title: Qi CX, et al. Kinsenoside: A Promising Bioactive Compound from Anoectochilus Species. Curr Med Sci. 2018 Feb;38(1):11-18.

Title: Wang Y, et al. Kinsenoside ameliorates intervertebral disc degeneration through the activation of AKT-ERK1/2-Nrf2 signaling pathway. Aging (Albany NY). 2019 Sep 23;11(18):7961-7977.

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