Ginsenoside-Rf
CAS No. 52286-58-5
Ginsenoside-Rf( Panaxoside Rf )
Catalog No. M21460 CAS No. 52286-58-5
Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 86 | In Stock |
|
| 10MG | 150 | In Stock |
|
| 25MG | 305 | In Stock |
|
| 50MG | 492 | In Stock |
|
| 100MG | 701 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameGinsenoside-Rf
-
NoteResearch use only, not for human use.
-
Brief DescriptionGinsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.
-
DescriptionGinsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.
-
In VitroGinsenoside Rf is a saponin, which is present in only trace amounts within ginseng. At saturating concentrations, Ginsenoside Rf rapidly and reversibly inhibits N-type, and other high-threshold, Ca2+ channels in rat sensory neurons to the same degree as a maximal dose of opioids. The effect is dose-dependent (half-maximal inhibition: 40 μM) and it is virtually eliminated by pretreatment of the neurons with pertussis toxin, an inhibitor of G(o) and Gi GTP-binding proteins. Ginsenoside Rf also inhibits Ca2+ channels in the hybrid F-11 cell line.
-
In VivoSince inhibition of Ca2+ channels in sensory neurons contributes to antinociception by opioids, analgesic actions of Ginsenoside Rf are tested. Dose-dependent antinociception is found by systemic administration of Ginsenoside Rf in mice using two separate assays of tonic pain: in the acetic acid abdominal constriction test, the ED50 is 56±9 mg/kg, a concentration similar to those reported for aspirin and acetaminophen in the same assay; in the tonic phase of the biphasic formalin test, the ED50 is 129±32 mg/kg.
-
SynonymsPanaxoside Rf
-
PathwayGPCR/G Protein
-
TargetCalcium Channel
-
RecptorN-type Ca2+ channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number52286-58-5
-
Formula Weight801.01
-
Molecular FormulaC42H72O14
-
Purity>98% (HPLC)
-
SolubilityEthanol: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
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Nah SY et al. A trace component of ginseng that inhibits Ca
molnova catalog
related products
-
Fluspirilene
Fluspirilene (R 6218) is a non-competitive L-type calcium channel antagonist (IC50: 0.03 μM).Fluspirilene is a long-acting antipsychotic compound used in the treatment of schizophrenia.
-
Tetrandrine
Tetrandrine (NSC 77037;Fanchinine) is a bis-benzylisoquinoline alkaloid that acts a calcium channel blocker.
-
Etripamil
Etripamil displays atrioventricular nodal conduction and prolongs atrioventricular nodal refractory periods by inhibiting calcium ion influx through the calcium slow channels in the atrioventricular node cells. Etripamil is an antagonist of short-acting L-type calcium-channel.
Cart
sales@molnova.com