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Astragaloside IV

CAS No.
84687-43-4
Chemical Name:
Astragaloside IV
Synonyms
ASTRAGALOSIDE;TA-65;Astragalus Polysaccharides;AS-IV;AST-IV;Astragalosid IV;Astragaloside IV;Astragaloside lV;AstraversianinXIV;Cyclosieversioside F
CBNumber:
CB8323949
Molecular Formula:
C41H68O14
Molecular Weight:
784.97
MDL Number:
MFCD16036240
MOL File:
84687-43-4.mol
Last updated:2024-03-22 09:48:13

Astragaloside IV Properties

Melting point 295-296°C
Boiling point 895.7±65.0 °C(Predicted)
Density 1.39
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility Methanol (Slightly, Sonicated), Pyridine (Slightly)
pka 12.91±0.70(Predicted)
color White to Off-White
Stability Hygroscopic
InChIKey QMNWISYXSJWHRY-BTUAQNSKSA-N
CAS DataBase Reference 84687-43-4(CAS DataBase Reference)
FDA UNII 1J6XA9YCFV

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
HS Code  29389090

Astragaloside IV price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHL89377 Astragaloside IV phyproof? Reference Substance 84687-43-4 10MG $574 2024-03-01 Buy
Sigma-Aldrich 74777 Astragaloside IV >98.0% 84687-43-4 1mg $369 2024-03-01 Buy
Sigma-Aldrich 1044108 Astragaloside IV United States Pharmacopeia (USP) Reference Standard 84687-43-4 100mg $383 2024-03-01 Buy
TCI Chemical A3305 Astragaloside IV 84687-43-4 250MG $110 2024-03-01 Buy
TCI Chemical A3305 Astragaloside IV 84687-43-4 1G $330 2024-03-01 Buy
Product number Packaging Price Buy
PHL89377 10MG $574 Buy
74777 1mg $369 Buy
1044108 100mg $383 Buy
A3305 250MG $110 Buy
A3305 1G $330 Buy

Astragaloside IV Chemical Properties,Uses,Production

Outline

Astragaloside IV is a cycloartane-type triterpene glycosides, it is one of the main active ingredients of traditional Chinese medicine Astragalus membranaceus, whose content is the main criteria for evaluation of the quality merits of Astragalus membranaceus. Astragaloside IV has effects in anti-tumor, anti-inflammatory, antioxidant, hypoglycemic, myocardial protection, anti-viral myocarditis, protecting brain tissue and anti-hepatitis B virus etc., and it has a wide range of pharmacological effects and very bright application.

Astragalus Extract

Astragalus extracts are the extraction of raw material products of dry roots of Astralgus membranceus (Fisch) Bge Var. Mongholicus (Bye).
[Crude Medicine Resources] There are about 1600 species under genus Astragalus in the world, and more than 200 species in China, among which about seven species used as medicines. Astragalus membranacus mainly distributes in Heilongjiang, Liaoning, Inner Mongolia, Hebei, Shandong, Shanxi, Shaanxi, Ningxia, Gansu, Qinghai, Xinjiang, Sichuan and Yunnan in China, and it also has distribution in Mongolia, North Korea and Russia. Radix Astragali mainly distributes in the Great Khingan, Nenjiang, Aihun, Sunwu, Morin Dawa banner in Inner Mongolia. Ninggu Astragali mainly distributes in Ning'an of Heilongjiang Province, Dongning, Linkou, Muling, Hailin. Zhenggu Astragali mainly distributes in Hebei, Zhangjiakou areas. Astragalus mongolicus mainly distributes in Jilin, Hebei, Shanxi and Inner Mongolia of China, and it also has distribution in Mongolia and Russia. The wild resources of Astragalus have been rare in China, with Astragalus membranacus and Astragalus mongolicus falling into the third-ranking national protection category. At present most Astragalus for medicinal use are cultivars, which are mainly produced in Hunyuan, Fanshi, Ying county, Dai county, Guangling of Shanxi, Guyang, Wuchuan, Zhuozi of Inner Mongolia, Heilongjiang and Jilin provinces.
[Main Components]Astragaloside IV, flavonoids, polysaccharides, amino acids, organic acids, trace elements, riboflavin, folic acid, vitamin P, sitosterol, lupeol, n-hexadecyl alcohol etc.
Astragalus membranaceus
Figure 1. Astragalus membranaceus
The above information is edited by the Chemicalbook of Cheng Jingmin.

Physical and Chemical Properties

White to pale yellow powders, melting point 295.0~296.0 ℃; Soluble in methanol, ethanol, acetone; Insoluble in chloroform, ethyl acetate and other weak polar organic solvents.

Pharmacological effects

1. Immunomodulatory effect: Astragaloside IV, mouse peritoneal macrophages and Mycobacterium tuberculosis were co-cultured to test the phagocytic ability to Mycobacterium tuberculosis of mouse peritoneal macrophages, and the content of γ-interferon (IFN-γ) and interleukin-1β (IL-1β) in the culture medium was detected as well. The results showed when the dose of astragaloside IV were 0.2,0.6,1.5,4.0 g L-1, the number of DNA copies (TB-DNA) of Mycobacterium tuberculosis that phagocyted by macrophages, and the IFN-γ and IL-1β levels in the supernatant were significantly higher than the control. Astragaloside IV can enhance macrophage’s phagocytic ability to Mycobacterium tuberculosis. Astragaloside IV could promote proliferation of T, B lymphocyte in vitro and in vivo and production of antibody in mice, and promote B cells proliferation in the thymus-independent area and promote the formation of a large number of plasma cells and synthesis of antibodies, but it had no significant effect on T cells in the thymus-dependent area.
2.Organ protection effect (1) Brain protection: astragaloside IV has a protective effect on brain injury in mice that induced by instant focal ischemia, which is related to its antioxidant effects, and astragaloside IV is expected to become the clinical drug in treatment of stroke. Astragaloside IV has a protective effect on blood-brain barrier after cerebral ischemia and reperfusion in rats.(2) Kidney protection: astragaloside IV has a protective effect on renal injury that induced by ischemia and reperfusion, and it can protect the kidney effectively when doing a kidney transplant, thus improve the success rate of transplant. Besides, astragaloside IV can down-regulate the content of monocyte chemoattractant protein-1 (MCP-1) in kidney tissues and the overexpression of mRNA.(3) Lung protection: astragaloside IV has a protective effect on lung injury that induced by ischemia and reperfusion, and it can reduce pulmonary bleeding and focal pulmonary hemorrhage in rats. Astragaloside IV can effectively inhibit ovalbumin-induced chronic asthma.(4) Myocardial protection: astragaloside IV can significantly improve myocardial ischemia and cardiac function in rats with myocardial infarction, and this effect is positively correlated with the dose and time. After the intraperitoneal injection of sterile Coxsackie virus (CVB3) to Balb/C mice, causing the myocarditis mice model, the mice were gavaged with 9% astragaloside IV for 7 days, the survival rate of mice with myocarditis increased, and the collagen synthesis and myocardium cell apoptosis reduced.(5) Liver protection: Astragaloside IV inhibits the collagen synthesis and proliferation of hepatic stellate cells, and has significant inhibition in fibrosis of liver cells.
3. Hypoglycemic effect: Taking rats with type-2 diabetes as research objects to study the regulation of astragaloside IV to hepatic glucose enzymes in rats with that streptomycin and high-fat diet induced diabetes, the results showed when the dose of astragaloside IV was 25, 50 mg/kg, the levels of blood glucose, and triglyceride (TG) and insulin in rats were significantly reduced, and related mRNA and protein expression were inhibited as well. In addition, astragaloside IV can inhibit TNF-α-induced 3T3-L1 adipocytes lipolysis, thereby reducing the level of free fatty acid (FFA), increasing insulin sensitivity, and having the hypoglycemic and hypolipidemic effect.
4. Anti-apoptotic effect: astragaloside IV can significantly reduce the apoptosis index of myocardial cells with CVB3 viral myocarditis. Astragaloside IV had a certain inhibition on Adriamycin-induced apoptosis of bone mesenchymal stem cells (BMSCs) in mice, but there was no significant dose-dependent manner.
5. Anti-inflammatory and antiviral effect: astragaloside IV significantly inhibited the xylene-induced ear edema in mice, with a strong anti-inflammatory effect. Astragaloside IV has the effect of anti-hepatitis B virus. After 10 days’ medical treatment, with the dose of 120,40 and 10 mg/kg astragaloside, its inhibition rate on HBV was 64.0%, 49.6% and 41.7%, respectively. It was also observed that the level of Hepatitis B Virus (DHBV) DNA decreased.
6. Anti-aging effect: the anti-aging effect of astragaloside IV is related to its functions in scavenging free radical and anti-lipid peroxidation, promoting protein turnover, eliminating nucleic acid metabolic disorders and promoting the proliferation and apoptosis of human skin fibroblasts. At lower concentrations (5~20 mg/L), astragaloside IV can promote proliferation of wrinkle and wrinkle-free skin fibroblasts and synthesis of type Ⅰ collagen in wrinkles, wrinkle-free and aged-skin fibroblasts, reducing the apoptosis rate of wrinkle and wrinkle-free skin fibroblasts.
7. Promoting cell proliferation: appropriate concentration of astragaloside IV can promote the rapid proliferation of chondrocytes and maintain the activity of chondrocytes, providing a new way for cartilage tissue engineering to get a lot of seed cells and maintain chondrocyte activity in a short term.
8. Other effects: astragaloside IV has a certain anti-cancer effect by inhibiting the gene expression of Vav3.1. By inhibiting the flow of calcium into the cells through NO-cGMP pathway and the release of intracellular calcium and the activity of phenylephrine and angiotensin Ⅱ, astragaloside IV has a relaxing effect on the aortic ring blood vessels and the isolated mesenteric artery of rats.

Methods of Determination

Determination of Astragaloside IV by HPLC
Chromatographic conditions: Column: C18 5u 4.6mm × 250mm; mobile phase: acetonitrile-water (1: 2); flow rate: 0.8ml/min; column temperature: 25℃; detection wavelength: 200nm.
Preparation of the test solution: Accurately weigh 0.1g of the extract powder, and add appropriate amount of water to do ultrasound dissolution, and then shake and extract it in 15ml × 4 n-butanol (water-saturated) to get a butanol layer until it is evaporated to dryness, and melt the residue with methanol and set the volume to 10ml, after mixing evenly, flit it through 0.45μm micro porous membrane.
Preparation of the standard solution: Accurately weigh an appropriate amount of standard astragaloside IV and dissolve it in methanol, and prepare the solution with the concentration of 0.1mg/ml.
Determination: draw the test solution and standard solution 20μl respectively by using the micro-injectors, and inject it to the liquid chromatograph, and record the peak area and calculate the content by external standard method.

Extraction Process

Astragaloside IV has a very low content in Astragalus. Currently, the traditional boiling water extraction and reflux boiling ethanol extraction used in astragaloside IV extraction have the shortcomings like high extraction temperature, low extraction rate and time consuming. The latest extraction techniques include high-speed centrifugal extraction, microwave assisted extraction, ultrasonic extraction, ultrafiltration, supercritical fluid extraction, high pressure extraction, high-speed countercurrent extraction. New extraction technology plays an important role in improving astragaloside IV extraction rate, shortening the extraction time and preventing damage of the active ingredient.
The process of astragaloside IV extraction by Supercritical CO2 Extraction: Weigh 15g of Astragalus IV and crush it to 40 meshes, put it into the extraction kettle and pour into quantitative entrainment agent (volume fraction 75% ethanol). Put the extraction kettle into the supercritical device. Adjust the temperature and pressure of the supercritical carbon dioxide fluid, and pump the supercritical carbon dioxide fluid into the kettle with a constant flow rate. Separate and collect the extracts by cyclone separation, and centrifuge, concentrate and dry the extracts.
The optimal conditions of astragaloside IV extraction by Supercritical CO2 Extraction: extraction pressure 40Mpa, temperature 45 ℃, extraction time 2 hours, entrainer 95% ethanol, entrainer amount 4ml (95% ethanol)/g (dry Astragalus powder), CO2 flow rate10kg/kg.h.

Toxicological analysis

The results of astragaloside IV ’s effects on embryonic and fetal development of SD rats and New Zealand rabbits showed: when the dose was higher than 1 mg/kg, astragaloside IV showed maternal toxicity; when the dose was higher than 0.5 mg/kg, it showed fetal toxicity. Therefore, it is recommended that pregnant women should use astragaloside IV with caution. Further research showed astragaloside IV can significantly delay the development of rat hair, eye opening and Parry reflection. But astragaloside IV had no significant effect on memory and learning ability.

Uses

vasodilator, antihypertensive, antiaging

Uses

Astragaloside IV has cardiovascular protective effects, protecting the vascular endothelial cells. In addition it is attributed to have anti0inflammatory and anti-virus effects as well. This is due to its scavenging ability of oxygen free radicals, regulation of mineral homeostasis and antioxidative effects.

Definition

ChEBI: Astragaloside IV is a pentacyclic triterpenoid that is cycloastragenol having beta-D-xylopyranosyl and beta-D-glucopyranosyl residues attached at positions O-3 and O-6 respectively. It is isolated from Astragalus membranaceus var mongholicus. It has a role as an EC 4.2.1.1 (carbonic anhydrase) inhibitor, an anti-inflammatory agent, a neuroprotective agent, an antioxidant, a pro-angiogenic agent and a plant metabolite. It is a triterpenoid saponin and a pentacyclic triterpenoid. It is functionally related to a cycloastragenol.

Astragaloside IV Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 423)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Haibo Biotechnology Co., Ltd
+undefined18602966907 qinhe02@xaltbio.com China 1000 58
Chongqing Zhihe Biopharmaceutical Co., Ltd.
+86-18580541567 +86-17782035140 sales@zhswyy.com China 338 58
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886 info@dakenam.com China 15371 58
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9352 55
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Chengdu Biopurify Phytochemicals Ltd.
+8618080483897 sales@biopurify.com China 3424 58
Nanjing Dolon Biotechnology Co.,Ltd.
18905173768 sales@dolonchem.com CHINA 2972 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Casorganics US Corp
+17326109938 sales@casorganics.com CHINA 174 58

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View Lastest Price from Astragaloside IV manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Astragaloside IV  pictures 2024-04-19 Astragaloside IV
84687-43-4
US $3100.00-3000.00 / Kilograms 1Kilograms 98% 100tons Hebei Dangtong Import and export Co LTD
Astragaloside IV pictures 2024-04-12 Astragaloside IV
84687-43-4
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
Astragaloside IV pictures 2024-04-12 Astragaloside IV
84687-43-4
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
  • Astragaloside IV  pictures
  • Astragaloside IV
    84687-43-4
  • US $3100.00-3000.00 / Kilograms
  • 98%
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Astragaloside IV Spectrum

AstragalosideIV/CH83947 AstragalosideIV/CH90651 Astrasieversianin XIV Astragaloside IV 20,24-epoxy-16,25-dihydroxy-3-(β-D- xylopyranosyloxy)-9,19-cyclolanostan-6-yl β-D-Glucopyranoside, (3β,6α,16β,20R,24S)- beta-D-Glucopyranoside, (3beta,6alpha,16beta,20R,24S)-20,24-epoxy-16,25-dihydroxy-3-(beta-D-xylopyranosyloxy)-9,19-cyclolanostan-6-yl ASTRAGALOSIDE IV(RG) Astragalosid IV Cyclosieversioside F AstraversianinXIV 9,19-CYCLOLANOSTANE-BETA-D-GLUCOPYRANOSIDE AST-IV Astragaloside, 98%, from Astragalus membranaceus (Fisch.) Bunge. (S)-Amlodipine Besylate (103129-82-4(free base)) A-674563 HCl (552325-73-2(free base)) Arg-Gly-Asp TFA (99896-85-2(free base)) BPR1J-097 hydrochloride (1327167-19-0(free base)) DAMGO TFA (78123-71-4(Free base)) EPZ020411 2HCl (1700663-41-7(free base)) GSK2879552 2HCl (1401966-69-5(free base)) LDC-4297 HCl (1453834-21-3(free base)) LMPTP INHIBITOR 1 hydrochloride (1908414-82-3(free base)) MS049 2HCl (1502816-23-0(free base)) NVP-BSK805 2HCl (1092499-93-8(free base)) PQ401 hydrochloride (196868-63-0(free base)) Pyridostatin Trihydrochloride(free base 1085412-37-8 ) SAG hydrochloride (912545-86-9(free base)) SB1317 hydrochloride (937270-47-8(free base)) SSD114 hydrochloride T.cruzi Inhibitor (1350920-22-7(free base)) TAPI-1 trifluoroacetate (171235-71-5(free base)) UNC2025 2HCl (1429881-91-3(free base)) Astragaloside IV Pure Plant Extracts 84687-43-4 Astragalus Extract Colorless Crystal Astragaloside lV good price Astragaloside IV 84687-43-4 β-D-Glucopyranoside, (3β,6α,16β,20R,24S)-20,24-epoxy-16,25-dihydroxy-3-(β-D-xylopyranosyloxy)-9,19-cyclolanostan-6-yl Astragaloside IV USP/EP/BP Astragalus extract USP/EP/BP Astragaloside IV, >1% Astragalus Polysaccharides TA-65 ASTRAGALOSIDE AS-IV BPR1J 097 hydrochloride (1327167 19 0(free base)),BPR-1J-097 hydrochloride (1327167-19-0(free base)),BPR1J097 hydrochloride (1327167190(free base)) SAG hydrochloride (912545 86 9(free base)),SAG hydrochloride (912545869(free base)) PQ-401 hydrochloride (196868-63-0(free base)),PQ401 hydrochloride (196868 63 0(free base)),PQ401 hydrochloride (196868630(free base)) DAMGO TFA (78123714(Free base)),DAMGO TFA (78123 71 4(Free base)) A 674563 HCl (552325 73 2(free base)),A674563 HCl (552325732(free base)) ArgGlyAsp TFA (99896852(free base)),Arg Gly Asp TFA (99896 85 2(free base)) NVP BSK805 2HCl (1092499 93 8(free base)),NVPBSK805 2HCl (1092499938(free base)),NVP-BSK-805 2HCl (1092499-93-8(free base)) GSK2879552 2HCl (1401966 69 5(free base)),GSK2879552 2HCl (1401966695(free base)),GSK-2879552 2HCl (1401966-69-5(free base)) LDC4297 HCl (1453834213(free base)),LDC 4297 HCl (1453834 21 3(free base)) UNC-2025 2HCl (1429881-91-3(free base)),UNC2025 2HCl (1429881913(free base)),UNC2025 2HCl (1429881 91 3(free base)) (2R,3R,4S,5S,6R)-2-(((2aR,3R,4S,5aS,5bS,7S,7aR,9S,11aR,12aS)-4-Hydroxy-3-((2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyltetrahydrofuran-2-yl)-2a,5a,8,8-tetramethyl-9-(((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)tetradecahydro-1H,12H-cyclopenta[a]cyclopropa[e]phenanthren-7-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 84687-43-4 84678-43-4