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G8503

Sigma-Aldrich

18α-Glycyrrhetinsäure

≥95%

Synonym(e):

18α-Glycyrrhetinsäure, 18-Isoglycyrrhetinsäure

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250 MG
€ 108,00
1 G
€ 400,00

€ 108,00


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250 MG
€ 108,00
1 G
€ 400,00

About This Item

Empirische Formel (Hill-System):
C30H46O4
CAS-Nummer:
Molekulargewicht:
470.68
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352115
PubChem Substanz-ID:
NACRES:
NA.22

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Qualitätsniveau

Assay

≥95%

SMILES String

[H][C@]12C[C@](C)(CC[C@]1(C)CC[C@]3(C)C2=CC(=O)C4[C@@]5(C)CC[C@H](O)C(C)(C)[C@]5([H])CC[C@@]34C)C(O)=O

InChI

1S/C30H46O4/c1-25(2)21-8-11-30(7)23(28(21,5)10-9-22(25)32)20(31)16-18-19-17-27(4,24(33)34)13-12-26(19,3)14-15-29(18,30)6/h16,19,21-23,32H,8-15,17H2,1-7H3,(H,33,34)/t19-,21+,22+,23-,26-,27+,28+,29-,30-/m1/s1

InChIKey

MPDGHEJMBKOTSU-PMTKVOBESA-N

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Allgemeine Beschreibung

18α-Glycyrrhetinic acid (18α-GA) is a bioactive triterpenoid found in licorice.[1] It shows selective inhibition of 11-HSD1 (11-hydroxysteroid dehydrogenase 1).[2] It also shows anti-proliferative and apoptotic effect on hepatic stellate cells (HSCs).[3]

Anwendung

18α-Glycyrrhetinic acid may be used to synthesize:[4]
  • 3-keto-18α-glycyrrhetinic acid
  • methyl esters of 18α-glycyrrhetinic acid
  • methyl esters of 3-keto-18α-glycyrrhetinic acid

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Analysenzertifikate (COA)

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Selective inhibition of 11?-hydroxysteroid dehydrogenase 1 by 18a-glycyrrhetinic acid but not 18?-glycyrrhetinic acid.
Classen-Houben D, et al.
The Journal of Steroid Biochemistry and Molecular Biology, 113(3), 248-252 (2009)
Sebastian M Goerke et al.
Tissue engineering. Part A, 18(23-24), 2395-2405 (2012-06-27)
Neovascularization represents an important issue in tissue-engineering applications, since survival of implanted cells strongly relies on sufficient oxygen and nutrient supply. We have recently observed that human bone marrow-derived mesenchymal stem cells (MSCs) support neovessel formation originating from coimplanted endothelial
Mohammad Shahidullah et al.
American journal of physiology. Cell physiology, 302(12), C1751-C1761 (2012-04-12)
In several tissues, transient receptor potential vanilloid 4 (TRPV4) channels are involved in the response to hyposmotic challenge. Here we report TRPV4 protein in porcine lens epithelium and show that TRPV4 activation is an important step in the response of
Manuel Viotti et al.
PLoS biology, 10(3), e1001276-e1001276 (2012-03-14)
Establishment of left-right (LR) asymmetry occurs after gastrulation commences and utilizes a conserved cascade of events. In the mouse, LR symmetry is broken at a midline structure, the node, and involves signal relay to the lateral plate, where it results
Simultaneous quantification of flavonoids and triterpenoids in licorice using HPLC.
Wang YC and Yang YS.
Journal of Chromatography. B, Biomedical Applications, 850(1), 392-399 (2007)

Questions

1–3 of 3 Questions  
  1. What is the stability of Product G8503, 18α-Glycyrrhetinic acid, once in solution?

    1 answer
    1. Unfortunately, we don't have any solution stability data available for this product.

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  2. What is the solubility of Product G8503, 18α-Glycyrrhetinic acid?

    1 answer
    1. It is soluble in chloroform:ethanol (2:3) at a concentration of 20 mg/mL.  It is expected to be soluble in dimethyl sulfoxide (DMSO) as well.

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  3. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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