Chemodex

Ginkgolide A

CHF 122.00
In stock
CDX-G0221-M02525 mgCHF 122.00
More Information
Product Details
Synonyms BN-52020
Product Type Chemical
Properties
Formula

C20H24O9

MW 408.4
CAS 15291-75-5
RTECS KC9943000
Source/Host Chemicals Plant
Purity Chemicals ≥98% (HPLC)
Appearance White powder.
Solubility Soluble in DMSO (20mg/ml), DMF (20mg/ml) or ethanol (3mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key FPUXKXIZEIDQKW-VKMVSBOZSA-N
Smiles O=C1[C@@H](C)[C@]([C@](O1)([H])C2)(O)[C@]([C@]32[C@H]4C[C@@H](C(C)(C)C)[C@]53[C@H]6O)(C(O4)=O)O[C@]5([H])OC6=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

Ginkgolide A is a terpenoid lactone originally isolated from G. biloba leaves. It shows diverse biological activities, including antioxidant, neuroprotective, anti-inflammatory and antiproliferative effects. Ginkgolide A inhibits platelet activating factor (PAF)-dependent aggregation of human platelets. It inhibits nitric oxide (NO) production. It also shows anxiolytic-like activity. It Inhibits NF-κ activity by NF-κ-specific suppressor IκBα. Ginkgolide A is a ligand of pregnane X receptor (PXR). It showed hepatoprotective efficacy by inducing cellular lipoapoptosis and by inhibiting cellular inflammation in NAFLD. Ginkgolide A reduced the proliferation rate of OVCA429 ovarian cancer cells by 40%.

Product References

(1) H.W. Zhao & X.Y. Li; Int. Immunopharmacol. 2, 1551 (2002) | (2) H. Kuribara, et al.; J. Nat. Prod. 66, 1333 (2003) | (3) E. Koch; Phytomedicine 12, 10 (2005) | (4) B. Ye, et al.; Cancer Lett. 251, 43 (2007) | (5) Q. Zhao, et al.; Int. Immunopharmacol. 25, 242 (2015) | (6) N. Ye, et al.; Biomol. Ther. 24, 40 (2016) | (7) J. Zhaocheng, et al.; Pharmazie 71, 588 (2016) | (8) H.S. Jeong, et al.; Biomed. Pharmacother. 88, 625 (2017) | (9) Y. Li, et al.; Int. J. Mol. Sci. 18, E794 (2017) | (10) L.C. Kuo, et al.; J. Agric. Food Chem. 67, 81 (2019) | (11) S. Mohandas & B. Vairappan; Chem. Biol. Interact. 315, 108891 (2019) | (12) W. You, et al.; Pharmazie 74, 698 (2019)

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