Pseudoginsenoside F11

Modify Date: 2024-01-02 12:35:29

Pseudoginsenoside F11 Structure
Pseudoginsenoside F11 structure
Common Name Pseudoginsenoside F11
CAS Number 69884-00-0 Molecular Weight 801.013
Density 1.3±0.1 g/cm3 Boiling Point 885.3±65.0 °C at 760 mmHg
Molecular Formula C42H72O14 Melting Point N/A
MSDS Chinese USA Flash Point 489.2±34.3 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of Pseudoginsenoside F11


Pseudoginsenoside-F11 (PF11), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice. IC50 value: Inhibition of diprenorphine binding with an IC50 of 6.1 μM Target:In vitro: Biochemical experiments revealed that PF11 could inhibit diprenorphine (DIP) binding with an IC50 of 6.1 μM and reduced the binding potency of morphine in Chinese hamster ovary (CHO)-μ cells [2].In vivo: One in vivo model of cisplatin-induced acute renal failure was performed. The results showed that pretreatment with Pseudoginsenoside F11 reduced cisplatin-elevated blood urea nitrogen and creatinine levels, as well as ameliorated the histophathological damage [1]. We tested the effects of Pseudoginsenoside F11 on morphine-induced development of behavioral sensitization and alterations in glutamate levels in the medial prefrontal cortex (mPFC) in freely moving mice by using in vivo microdialysis. As the results shown, Pseudoginsenoside F11 antagonized the development of behavioral sensitization and decrease of glutamate in the mPFC induced by morphine [3].

 Names

Name (3b,6a,12b,24R)-20,24-Epoxy-3,12,25-trihydroxydammaran-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
Synonym More Synonyms

 Pseudoginsenoside F11 Biological Activity

Description Pseudoginsenoside-F11 (PF11), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice. IC50 value: Inhibition of diprenorphine binding with an IC50 of 6.1 μM Target:In vitro: Biochemical experiments revealed that PF11 could inhibit diprenorphine (DIP) binding with an IC50 of 6.1 μM and reduced the binding potency of morphine in Chinese hamster ovary (CHO)-μ cells [2].In vivo: One in vivo model of cisplatin-induced acute renal failure was performed. The results showed that pretreatment with Pseudoginsenoside F11 reduced cisplatin-elevated blood urea nitrogen and creatinine levels, as well as ameliorated the histophathological damage [1]. We tested the effects of Pseudoginsenoside F11 on morphine-induced development of behavioral sensitization and alterations in glutamate levels in the medial prefrontal cortex (mPFC) in freely moving mice by using in vivo microdialysis. As the results shown, Pseudoginsenoside F11 antagonized the development of behavioral sensitization and decrease of glutamate in the mPFC induced by morphine [3].
Related Catalog
References

[1]. Wang H, et al. The pseudoginsenoside F11 ameliorates cisplatin-induced nephrotoxicity without compromising its anti-tumor activity in vivo. Scientific Reports [2014, 4:4986]

[2]. Li Zhu, et al. Pseudoginsenoside-F11 attenuates morphine-induced signalling in Chinese hamster ovary-μ cells. Neuroreport, 25 May 2001 - Volume 12 - Issue 7 - pp 1453-1456

[3]. Yue Hao, et al. Pseudoginsenoside-F11 decreases morphine-induced behavioral sensitization and extracellular glutamate levels in the medial prefrontal cortex in mice. Pharmacology Biochemistry and Behavior Volume 86, Issue 4, April 2007, Pages 660–666

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 885.3±65.0 °C at 760 mmHg
Molecular Formula C42H72O14
Molecular Weight 801.013
Flash Point 489.2±34.3 °C
Exact Mass 800.492188
PSA 228.22000
LogP 5.27
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.599
Storage condition 2-8°C

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Hazard Codes Xn
Risk Phrases 22
Safety Phrases 24/25
RIDADR NONH for all modes of transport
HS Code 29389090

 Synonyms

(3β,6α,12β,24R)-3,12,25-Trihydroxy-20,24-epoxydammaran-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-mannopyranoside
pseudo-ginsenoside-Fll
GINSENOSIDE A1
β-D-Mannopyranoside, (3β,6α,12β,24R)-20,24-epoxy-3,12,25-trihydroxydammaran-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-
(3b,6a,12b,24R)-20,24-Epoxy-3,12,25
MFCD00803938
PSEUDOGINSENOSIDE
Pseuginsenoside F11
(24R)-Pseudoginsenoside F11
24(S)-pseudo-ginsenoside-F11
Pseudoginsenoside FII
Pseudoginsenoside-F11
Pseuginsensoside F11
Pseudoginsenoside F11
Top Suppliers:I want be here




Get all suppliers and price by the below link:

Pseudoginsenoside F11 suppliers


Price: $93/10mM*1mLinDMSO

Reference only. check more Pseudoginsenoside F11 price