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62025-49-4,MFCD06410948
Catalog No.:AA00EBEE

62025-49-4 | Ginsenoside f2

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1mg
≥95%
in stock  
$46.00   $32.00
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5mg
≥95%
in stock  
$166.00   $116.00
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10mg
≥95%
in stock  
$285.00   $199.00
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25mg
≥95%
in stock  
$652.00   $456.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00EBEE
Chemical Name:
Ginsenoside f2
CAS Number:
62025-49-4
Molecular Formula:
C42H72O13
Molecular Weight:
785.0133
MDL Number:
MFCD06410948
SMILES:
OCC1OC(OC2CCC3(C(C2(C)C)CCC2(C3CC(O)C3C2(C)CCC3C(OC2OC(CO)C(C(C2O)O)O)(CCC=C(C)C)C)C)C)C(C(C1O)O)O
Properties
Computed Properties
 
Complexity:
1370  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
20  
Heavy Atom Count:
55  
Hydrogen Bond Acceptor Count:
13  
Hydrogen Bond Donor Count:
9  
Rotatable Bond Count:
10  
XLogP3:
4  

Literature

Title: Inhibitory effects of herbal constituents on P-glycoprotein in vitro and in vivo: herb-drug interactions mediated via P-gp.

Journal: Toxicology and applied pharmacology 20140301

Title: Ginsenoside F2 induces apoptosis accompanied by protective autophagy in breast cancer stem cells.

Journal: Cancer letters 20120828

Title: Inhibition of P-glycoprotein leads to improved oral bioavailability of compound K, an anticancer metabolite of red ginseng extract produced by gut microflora.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20120801

Title: Ginsenosidases and the pathogenicity of Pythium irregulare.

Journal: Phytochemistry 20120601

Title: Cytotoxicity and inhibition of DNA topoisomerase I of polyhydroxylated triterpenoids and triterpenoid glycosides.

Journal: Bioorganic & medicinal chemistry letters 20100501

Title: Partial purification and characterization of three ginsenoside-metabolizing beta-glucosidases from Pythium irregulare.

Journal: Phytochemistry 20091201

Title: Development and validation of a reversed-phase HPLC method for quantitative determination of ginsenosides Rb1, Rd, F2, and compound K during the process of biotransformation of ginsenoside Rb1.

Journal: Journal of separation science 20080401

Title: Microbial conversion of ginsenoside Rb1 to minor ginsenoside F2 and gypenoside XVII by Intrasporangium sp. GS603 isolated from soil.

Journal: Journal of microbiology and biotechnology 20071201

Title: Marked production of ginsenosides Rd, F2, Rg3, and compound K by enzymatic method.

Journal: Chemical & pharmaceutical bulletin 20071001

Title: Mai TT, et al. Ginsenoside F2 induces apoptosis accompanied by protective autophagy in breast cancer stem cells. Cancer Lett. 2012 Aug 28;321(2):144-53.

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Tags:62025-49-4 Molecular Formula|62025-49-4 MDL|62025-49-4 SMILES|62025-49-4 Ginsenoside f2