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Merck

89556

Supelco

Ginkgolid J

analytical standard

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About This Item

Empirische Formel (Hill-System):
C20H24O10
CAS-Nummer:
Molekulargewicht:
424.40
UNSPSC-Code:
85151701
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Assay

≥90% (HPLC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

food and beverages

Format

neat

Lagertemp.

2-8°C

SMILES String

[H]C1[C@]2([H])OC(=O)[C@@H](C)[C@]2(O)[C@@]34OC5OC(=O)[C@H](O)C56[C@@H]([C@H](O)[C@@H](OC3=O)[C@@]146)C(C)(C)C

InChI

1S/C20H24O10/c1-6-12(23)27-7-5-17-11-8(21)9(16(2,3)4)18(17)10(22)13(24)29-15(18)30-20(17,14(25)28-11)19(6,7)26/h6-11,15,21-22,26H,5H2,1-4H3/t6-,7+,8-,9+,10+,11-,15+,17?,18+,19-,20-/m1/s1

InChIKey

LMEHVEUFNRJAAV-XNSMQBOTSA-N

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Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Sonstige Hinweise

This compound is commonly found in plants of the genus: ginkgo

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Ottavio Vitolo et al.
Neurobiology of aging, 30(2), 257-265 (2007-07-21)
A new Ginkgo biloba extract P8A (TTL), 70% enriched with terpene trilactones, prevents A beta(1-42) induced inhibition of long-term potentiation in the CA1 region of mouse hippocampal slices. This neuroprotective effect is attributed in large part to ginkgolide J that
Stanislav Jaracz et al.
The Journal of organic chemistry, 67(13), 4623-4626 (2002-06-22)
Protocols for selective acetylation of the hydroxyl groups of ginkgolide C have been developed. These acetylations have given rise to various ginkgolide C acetates and iso-ginkgolide C acetates, the latter having a rearranged skeleton resulting from translactonization. These acetyl derivatives
Edward Croom et al.
Journal of AOAC International, 90(3), 647-658 (2007-06-22)
A single-laboratory validation was completed for a method to determine total terpene lactones in Ginkgo biloba products. The method determines terpene lactones on the basis of the main terpene lactones (Bilobalide, Ginkgolide A, Ginkgolide B, Ginkgolide C, and Ginkgolide J)
Chen Ding et al.
Analytical chemistry, 76(15), 4332-4336 (2004-07-31)
A method was developed for the extraction and quantification of pharmacologically active terpene trilactones (ginkgolides, bilobalide) from the tissues of Ginkgo biloba L. and pharmaceutical ginkgo products by RP-HPLC, based on the theory of terpene trilactones ionization. Four ginkgolides (GA
M G Ferreira et al.
Lipids, 26(12), 1329-1332 (1991-12-01)
Renal vascular escape is a physiological phenomenon of adaptation that occurs in vascular smooth muscle. It has been described in many preparations subjected to electrical stimulation or treated with vasoactive agents, such as noreprinephrine, angiotensin and vasopressin. We have recently

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