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Ginsenoside-Rf

CAT: 0013-GTR19157108-01Size: 200 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19157108-01Size:200 mg
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Description
Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.
CAS Number
52286-58-5
Product Name Alternative
Panaxoside Rf
Purity
>98% (HPLC)
Solubility
Ethanol:5 mg/mL (62.42 mM)
Smiles
[H][C@@]1 (CC[C@]2 (C) [C@]1 ([H]) [C@H] (O) CC1[C@@]3 (C) CC[C@H] (O) C (C) (C) [C@]3 ([H]) [C@H] (C[C@@]21C) O[C@@H]1O[C@H] (CO) [C@@H] (O) [C@H] (O) [C@H]1O[C@@H]1O[C@H] (CO) [C@@H] (O) [C@H] (O) [C@H]1O) [C@@] (C) (O) CC\C=C (\C) C
Molecular Formula
C42H72O14
Molecular Weight
801.01
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.

Chemical Information

Ginsenoside Rf

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-(12)-beta-D-glucopyranoside, and in which a double bond has been introduced at the 24-25 position. It has a role as an antineoplastic agent, an apoptosis inducer and a plant metabolite. It is a 3beta-hydroxy-4,4-dimethylsteroid, a beta-D-glucoside, a tetracyclic triterpenoid, a 3beta-hydroxy steroid, a 12beta-hydroxy steroid, a 20-hydroxy steroid, a disaccharide derivative and a ginsenoside. It derives from a hydride of a dammarane.

CAS Number52286-58-5
PubChem CID441922
IUPAC Name(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
Molecular FormulaC42H72O14
Molecular Weight801.0
XLogP2.7
Topological Polar Surface Area239
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count14
Rotatable Bond Count10
Heavy Atom Count56
Formal Charge0
Complexity1410
SMILES
CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)O)C)O)C
InChI
InChI=1S/C42H72O14/c1-20(2)10-9-13-42(8,52)21-11-15-40(6)28(21)22(45)16-26-39(5)14-12-27(46)38(3,4)35(39)23(17-41(26,40)7)53-37-34(32(50)30(48)25(19-44)55-37)56-36-33(51)31(49)29(47)24(18-43)54-36/h10,21-37,43-52H,9,11-19H2,1-8H3/t21-,22+,23-,24+,25+,26+,27-,28-,29+,30+,31-,32-,33+,34+,35-,36-,37+,39+,40+,41+,42-/m0/s1
InChIKey
UZIOUZHBUYLDHW-XUBRWZAZSA-N
Chemical Structure
2D Structure
2D structure of Ginsenoside Rf
CAS: 52286-58-5
CID: 441922
Formula: C42H72O14
MW: 801.0
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight801.0
XLogP32.7
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count14
Rotatable Bond Count10
Exact Mass800.49220697
Monoisotopic Mass800.49220697
Topological Polar Surface Area239 Ų
Heavy Atom Count56
Formal Charge0
Complexity1410
Isotope Atom Count0
Defined Atom Stereocenter Count21
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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GTR19167809-01Ginsenoside Rk3
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GTR19162096-01Ginsenoside F1
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Alternative Products

CatalogName
T6S1500-01Ginsenoside Rf
MBS5758272Ginsenoside-Rf
A14583-100Ginsenoside Rf 100mg
A14583-10Ginsenoside Rf 10mg
A14583-5Ginsenoside Rf 5mg
A14583-1Ginsenoside Rf 1mg
A14583-50Ginsenoside Rf 50mg
A14583-25Ginsenoside Rf 25mg
HY-N0601RGinsenoside Rf (Standard)
HY-N890120-Gluco-ginsenoside-Rf

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