Chemodex

Astragaloside IV

CHF 237.00
In stock
CDX-A0577-M05050 mgCHF 237.00
CDX-A0577-M100100 mgCHF 393.00
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Product Details
Synonyms AS-IV; AST-IV; Astrasieversianin XIV; Cyclosieversioside F; Cyclosiversioside F; Astramembrannin I; Astragaloside A
Product Type Chemical
Properties
Formula

C41H68O14

MW 784.98
CAS 84687-43-4
Source/Host Chemicals Plant
Purity Chemicals ≥98% (HPLC)
Appearance White to off-white powder.
Solubility Soluble in DMSO (30mg/ml) or DMF (20mg/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 QMNWISYXSJWHRY-RXMVGYINSA-N
Smiles O[C@H]1C[C@@]2(C)[C@]3([H])C[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@]5([H])C(C)(C)[C@@H](O[C@H]6OC[C@@H](O)[C@H](O)[C@H]6O)CC[C@]57[C@]3(C7)CC[C@]2(C)[C@H]1[C@]8(C)O[C@H](C(C)(O)C)CC8
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

Astragaloside IV (AS-IV) is a bioactive saponin and constituent of the traditional chinese medicine plant Astragali radix. AS-IV has multiple pharmacologic effects, including anti-inflammatory, antioxidative, anti-asthma, antidiabetes, anticancer, immunoregulation, neuroprotective and cardioprotective properties via numerous signaling pathways. This includes inhibition of NF-κB, inducing hypoxia-inducible factor-1α accumulation via PI3K/Akt pathway, reducing Aβ production in Alzheimer's disease through inhibition of BACE1, working as a natural PPARγ agonist, improving lipid metabolism in obese mice, enhancing chemosensitivity through CD276 (B7-H3)-pathway inhibition, and suppressing glucose-induced NLRP3 inflammasome activation.

Product References

(1) Y.P. Wang, et al.; Acta Pharmacol. Sin. 23, 263 (2002) | (2) W.J. Zhang, et al.; Thromb. Haemost. 90, 904 (2003) | (3) M.E. Xu, et al.; Acta Pharmacol. Sin. 27, 229 (2006) | (4) W.S. Chan, et al.; Neurochem. Int. 55, 414 (2009) | (5) L. Zhang, et al.; J. Pharmacol. Exp. Ther. 338, 485 (2011) | (6) X. Chen, et al.; J. Ethnopharmacol. 139, 721 (2012) | (7) D. Gui, et al.; PLoS One 7, e39824 (2012) | (8) S. Ren, et al.; J. Tradit. Chin. Med. 33, 413 (2013) (Review) | (9) H. Wu, et al.; Sci. Rep. 6, 30190 (2016) | (10) C.S. He, et al.; Cell Physiol. Biochem. 40, 1221 (2016) | (11) X. Wang, et al.; Mol. Neurobiol. 54, 2939 (2017) | (12) L. Li, et al.; Fundam. Clin. Pharmacol. 31, 17 (2017) (Review) | (13) L. Xia, et al.; Exp. Ther. Med. 14, 5569 (2017) | (14) P. Sun, et al.; Front. Biosci. 24, 597 (2019) | (15) B. Leng, et al.; Mediators Inflamm. 2019, 1082497 (2019) | (16) Z. Zhang, et al.; Mol. Med. Rep. 20, 4612 (2019)

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