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Ginsenoside Rf

Ginsenoside Rf structure

Ginsenoside Rf 

structure
  • CAS No:

    52286-58-5

  • Formula:

    C42H72O14

  • Chemical Name:

    Ginsenoside Rf

  • Synonyms:

    β-D-Glucopyranoside,(3β,6α,12β)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-β-D-glucopyranosyl-;Dammarane,β-D-glucopyranoside deriv.;(3β,6α,12β)-3,12,20-Trihydroxydammar-24-en-6-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside;Ginsenoside Rf;Panaxoside Rf;Rf ginsenoside;212055-75-9

  • Categories:

    Biochemical Engineering  >  Plant Extracts

Description

Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.


Ginsenoside Rf is a ginsenoside found in Panax ginseng and Panax japonicus var. major that is dammarane which is substituted by hydroxy groups at the 3beta, 6alpha, 12beta and 20 pro-S positions, in which the hydroxy group at position 6 has been converted to the corresponding beta-D-glucopyranosyl-(1->2)-beta-D-glucopyranoside, and in which a double bond has been introduced at the 24-25 position. It has a role as a plant metabolite, an apoptosis inducer and an antineoplastic agent. It is a 12beta-hydroxy steroid, a 3beta-hydroxy steroid, a beta-D-glucoside, a disaccharide derivative, a ginsenoside, a tetracyclic triterpenoid, a 20-hydroxy steroid and a 3beta-hydroxy-4,4-dimethylsteroid. It derives from a hydride of a dammarane.

Ginsenoside Rf Basic Attributes

801.01

801.01

JOS8BON5YW

29389090

Characteristics

239

2.7

1.3±0.1 g/cm3

197~198℃

505.5±34.3 °C

1.602

-20°C

Safety Information

NONH for all modes of transport

3

22

2-45-24/25

LY9536900

Xn

P264, P270, P301+P312, P330, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 41 companies from 2 notifications to the ECHA C&L Inventory.

Drug Information

ginsenoside Rf

Ginsenoside Rf Use and Manufacturing

Methods of Manufacturing

An activity assay of UGT109A1 was performed in a 100 muL reaction mixture containing 1 mMsubstrate (gensinosides Re, Rf, Rh1, or R1) dissolved in dimethyl sulfoxide (DMSO), 4 mM UDPG, 50mug purified UGT109A1, and 25 mM Tris-HCl buffer (pH 8.0). The reaction mixtures were incubatedat 37 C for 12 h and then terminated by adding 100 muL methanol. Subsequently, the reactants werecentrifuged at 10, 000× g for 20 min and filtered by a 0.22 mum filter prior to HPLC analysis.An activity assay of UGT109A1 was performed in a 100 muL reaction mixture containing 1 mMsubstrate (gensinosides Re, Rf, Rh1, or R1) dissolved in dimethyl sulfoxide (DMSO), 4 mM UDPG, 50mug purified UGT109A1, and 25 mM Tris-HCl buffer (pH 8.0). The reaction mixtures were incubatedat 37 C for 12 h and then terminated by adding 100 muL methanol. Subsequently, the reactants werecentrifuged at 10, 000× g for 20 min and filtered by a 0.22 mum filter prior to HPLC analysis.A solution of 20(S)-

Uses

Ginsenoside Rf is a new class of anti-tumor drugs isolated from ginseng, which is safe and efficient.

Computed Properties

Molecular Weight:801.0
XLogP3:2.7
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:10
Exact Mass:800.49220697
Monoisotopic Mass:800.49220697
Topological Polar Surface Area:239
Heavy Atom Count:56
Complexity:1410
Defined Atom Stereocenter Count:21
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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