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Ginsenoside Rg2

Ginsenoside Rg2 Struktur
52286-74-5
CAS-Nr.
52286-74-5
Englisch Name:
Ginsenoside Rg2
Synonyma:
CHIKUSETSUSAPONIN I;anaxatriol;GinsesideRg2;Panaxoside Rg2;product/154570;PROSAPOGENIN C2;GINSENOSIDE RG2;Ginsenosdie Rg2;mannopyranosyl)-;iGInsenoside Rg2
CBNumber:
CB1483174
Summenformel:
C42H72O13
Molgewicht:
785.03
MOL-Datei:
52286-74-5.mol

Ginsenoside Rg2 Eigenschaften

Schmelzpunkt:
187~189℃
Siedepunkt:
881.0±65.0 °C(Predicted)
Dichte
1.30±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
L?slichkeit
Methanol (Slightly, Heated, Sonicated), Pyridine (Slightly, Sonicated)
pka
12.85±0.70(Predicted)
Aggregatzustand
Solid
Farbe
White to Off-White
Stabilit?t:
Hygroscopic
Major Application
food and beverages
Kosmetik-Inhaltsstoffe Funktionen
SKIN CONDITIONING - HUMECTANT
HAIR CONDITIONING
InChIKey
AGBCLJAHARWNLA-DJZXLMSJSA-N
LogP
6.830 (est)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn
R-S?tze: 22
S-S?tze: 24/25
WGK Germany  3
RTECS-Nr. LZ6430000
HS Code  29389090
Speicherklasse 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Toxizit?t mouse,LD50,intraperitoneal,1340mg/kg (1340mg/kg),Arzneimittel-Forschung. Drug Research. Vol. 25, Pg. 343, 1975.
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
Sicherheit

Ginsenoside Rg2 Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Ginsenosides are pharmacologically active natural compounds from ginseng and other plants of the genus Panax. Structurally, they are steroid glycosides derived from the triterpene squalene. Ginsenoside Rg2 is a protopanaxatriol that is more abundant in some Panax species (e.g., white and red P. ginseng) than others. This ginsenoside and its metabolites have diverse in vitro and in vivo effects, including neuroprotective, anti-inflammatory, and anti-diabetic actions. It also protects against DNA damage and apoptosis induced by ultraviolet light. Notably, this ginsenoside is increased by the metabolism of other bioactive ginsenosides during the steaming or heating of plant materials, particularly in P. quinquefolium.

Chemische Eigenschaften

White solid

Verwenden

20(S)-Ginsenoside Rg2 is used as an aldose reductase inhibitor and my exert anti-inflammatory and immunomodulatory activity. It exists as a bioactive metabolite of the ginsenoside component of Panax ginseng.

Ginsenoside Rg2 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Ginsenoside Rg2 Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 300)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Shanghai Zheyan Biotech Co., Ltd.
18017610038
zheyansh@163.com CHINA 3619 58
career henan chemical co
+86-0371-86658258 +8613203830695
sales@coreychem.com China 29815 58
Chengdu Biopurify Phytochemicals Ltd.
+86-28-82633860; +8618080483897
sales@biopurify.com China 4616 58
Nanjing Dolon Biotechnology Co.,Ltd.
18905173768
52513593@qq.com CHINA 2972 58
NanJing Spring & Autumn Biological Engineering CO., LTD.
+8613815430202
sale02@cqherb.com CHINA 376 58
BOC Sciences
+1-631-485-4226
inquiry@bocsci.com United States 19936 58
Shanghai Standard Technology Co., Ltd.
18502101150
ft-sales@nature-standard.com CHINA 1923 58
Wuhan ChemNorm Biotech Co.,Ltd.
+86-27-8439 4403 18971486879
sales@chemnorm.com CHINA 2935 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354
marketing@targetmol.com United States 32466 58
Hubei Ipure Biology Co., Ltd
+8613367258412
ada@ipurechemical.com China 10236 58

52286-74-5()Verwandte Suche:


  • anaxatriol
  • beta-d-glucopyranoside,(3-beta,6-alpha,12-beta)-3,12,20-trihydroxydammar-24-en
  • mannopyranosyl)-
  • trihydroxydammar-24-en-6-yl2-O-(6-deoxy-α-L-
  • β-D-Glucopyranoside,(3β,6α,12β)-3,12,20-
  • Ginsenoside 20(s)-Rg2
  • (20S)-Ginsenoside Rg2
  • [3β,12β,20-Trihydroxy-5α-dammar-24-en-6α-yl]2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
  • [3β,12β,20-Trihydroxydammar-24-en-6α-yl]2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
  • 6α-(2-O-α-L-Rhamnopyranosyl-β-D-glucopyranosyloxy)-dammara-24-ene-3β,12β,20-triol
  • GINSENOSIDE Rg2(SH)
  • Ginsenoside Rg2 ,98%
  • GinsesideRg2
  • iGInsenoside Rg2
  • PROSAPOGENIN C2
  • GINSENOSIDE RG2
  • CHIKUSETSUSAPONIN I, PROSAPOGENIN C2
  • (6)-(alpha-l-rhamnopyranosyl(1-rham-2-glu)-beta-d-glucopyranosyl)-20s-protop
  • -6-yl-2-o-(6-deoxy-alpha-l-mannopyranosyl)-
  • (3β,6α,12β)-3,12,20-Trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
  • b-D-Glucopyranoside, (3b,6a,12b)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-a-L-mannopyranosyl)-
  • Ginsenosdie Rg2
  • Ginsenoside Rg2 (Chikusetsusaponin I
  • Panaxoside Rg2
  • product/154570
  • β-D-Glucopyranoside, (3β,6α,12β)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-
  • (2S,3R,4R,5R,6S)-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-methyloxane-3,4,5-triol
  • CHIKUSETSUSAPONIN I
  • (2S,3R,4R,5R,6S)-2-(((2R,3R,4S,5S,6R)-2-(((3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-Dihydroxy-17-((S)-2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethylhexadecahydro-1H-cyclopenta[a]phenanthren-6-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triol
  • GINSENOSIDE Rg2 (S-FORM)
  • Ginsenoside Rg2-RM
  • Ginsenoside Rg2(P)
  • Ginsenoside Rg2, 10 mM in DMSO
  • Ginsenoside Rg2 (Standard)
  • 52286-74-5
  • 55086-74-5
  • 55286-74-5
  • C42H72O13
  • C40H68O14
  • Inhibitors
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Saponins
  • chemical reagent
  • Ginsenoside series
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