Cas no 83207-58-3 (Astragaloside A)
Astragaloside A Chemical and Physical Properties
Names and Identifiers
-
- Astragaloside A
- Astragaloside IV
- Arsenobetaine in water
- Astragaloside
- Astragaloside A?
- Astragalin A
- ASTRAGALOSIDE IV(RG)
- Astragalus Polysaccharides
- Astramembrannin I
- Astrasieversianin XIV
- cyclosieversioside F
- cyclosiversioside F
- astragaloside iv(p)
- astragaloside iv(a)
- astragaloside iv ,98%
- astragaloside a(astragaloside iv)
- (3β,6α,16β,24R)-20,24-Epoxy-16,25-dihydroxy-3-(β-D-xylopyranosyloxy)-9,19-cyclolanostan-6-yl β-D-glucopyranoside (ACI)
- 1H,19H-Cyclopropa[9,10]cyclopenta[a]phenanthrene, β-D-glucopyranoside deriv. (ZCI)
- 9,19-Cyclolanostane, β-D-glucopyranoside deriv. (ZCI)
- UNII-3A592W8XKE
- (+)-ASTRAGALOSIDE A
- Q27256953
- Astragaloside-A
- BRD-K08188887-001-02-4
- DTXSID301347884
- (2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
- HMS3884H17
- CS-3710
- s2415
- (2R,3R,4S,5S,6R)-2-(((2aR,3R,4S,5aS,5bS,7S,7aR,9S,11aR,12aS)-4-Hydroxy-3-((2S,5R)-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)hexadecahydrocyclopenta[a]cyclopropa[e]phenanthren-7-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
- 3A592W8XKE
- HY-N0099
- AKOS022168196
- 83207-58-3
- beta-D-Glucopyranoside, (3beta,6alpha,16beta,24R)-20,24-epoxy-16,25-dihydroxy-3-(beta-D-xylopyranosyloxy)-9,19-cyclolanostan-6-yl
- .BETA.-D-GLUCOPYRANOSIDE, (3.BETA.,6.ALPHA.,16.BETA.,24R)-20,24-EPOXY-16,25-DIHYDROXY-3-(.BETA.-D-XYLOPYRANOSYLOXY)-9,19-CYCLOLANOSTAN-6-YL-
- CCG-270471
- Benzene, 2-ethynyl-1-fluoro-4-methyl-
- (2R,4S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-Hydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
- PD118008
- BETA-D-GLUCOPYRANOSIDE, (3BETA,6ALPHA,16BETA,24R)-20,24-EPOXY-16,25-DIHYDROXY-3-(BETA-D-XYLOPYRANOSYLOXY)-9,19-CYCLOLANOSTAN-6-YL-
- Astragaloside A?
- astragaloside IV OF astragaloside a
- 3beta,6alpha,16beta,20R,24S
- G79087
- (2R,3R,4S,5S,6R)-2-(((1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-((2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl)-7,7,12,16-tetramethyl-6-((2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl)oxy-9-pentacyclo(9.7.0.01,3.03,8.012,16)octadecanyl)oxy)-6-(hydroxymethyl)oxane-3,4,5-triol
-
- MDL: MFCD16036240
- Inchi: 1S/C41H68O14/c1-35(2)24(54-33-29(48)26(45)20(44)17-51-33)9-11-41-18-40(41)13-12-37(5)31(39(7)10-8-25(55-39)36(3,4)50)19(43)15-38(37,6)23(40)14-21(32(35)41)52-34-30(49)28(47)27(46)22(16-42)53-34/h19-34,42-50H,8-18H2,1-7H3/t19-,20+,21-,22+,23-,24-,25+,26-,27+,28-,29+,30+,31-,32-,33-,34+,37+,38-,39-,40-,41+/m0/s1
- InChI Key: QMNWISYXSJWHRY-AUJDEUPOSA-N
- SMILES: C[C@@]12C[C@H](O)[C@H]([C@@]3(CC[C@H](C(O)(C)C)O3)C)[C@@]1(C)CC[C@@]13C[C@]41CC[C@H](O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O)C(C)(C)[C@@H]4[C@H](C[C@@H]23)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1
Computed Properties
- Exact Mass: 784.46100
- Monoisotopic Mass: 784.46090684 g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 9
- Hydrogen Bond Acceptor Count: 14
- Heavy Atom Count: 55
- Rotatable Bond Count: 7
- Complexity: 1460
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 21
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 228
- Molecular Weight: 785.0
- XLogP3: 1.3
Experimental Properties
- Color/Form: No data available
- Density: 1.39
- Melting Point: No data available
- Boiling Point: 895.7°C at 760 mmHg
- Flash Point: 495.5±34.3 °C
- Refractive Index: 1.62
- PSA: 228.22000
- LogP: 0.72410
Astragaloside A Security Information
- Signal Word:Warning
- Hazard Statement: H302-H315-H319-H335
- Warning Statement: P261-P305+P351+P338
- Safety Instruction: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Storage Condition:Powder -20°C 3 years ? 4°C 2 years In solvent -80°C 6 months ? -20°C 1 month
Astragaloside A Customs Data
- HS CODE:2932999099
- Customs Data:
China Customs Code:
2932999099Overview:
2932999099. Other heterocyclic compounds containing only oxygen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Astragaloside A Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-PQ787-10mg |
Astragaloside A |
83207-58-3 | 98+% | 10mg |
1042CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-PQ787-5mg |
Astragaloside A |
83207-58-3 | 98+% | 5mg |
811CNY | 2021-05-07 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A274907-5mg |
Astragaloside A (Astragaloside IV) |
83207-58-3 | ≥98% | 5mg |
¥2,070.00 | 2021-05-28 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A274907-10mg |
Astragaloside A (Astragaloside IV) |
83207-58-3 | ≥98% | 10mg |
¥3,630.00 | 2021-05-28 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X12955-10mg |
Astragaloside A |
83207-58-3 | 98% | 10mg |
¥75.0 | 2024-07-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X12955-1g |
Astragaloside A |
83207-58-3 | 1g |
¥488.0 | 2021-09-03 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X12955-5g |
Astragaloside A |
83207-58-3 | 5g |
¥1858.0 | 2021-09-03 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X12955-250mg |
Astragaloside A |
83207-58-3 | 250mg |
¥198.0 | 2021-09-03 | ||
| DC Chemicals | DC8641-100 mg |
Astragaloside A |
83207-58-3 | >98% | 100mg |
$250.0 | 2022-03-01 | |
| DC Chemicals | DC8641-250 mg |
Astragaloside A |
83207-58-3 | >98% | 250mg |
$500.0 | 2022-03-01 |
Astragaloside A Suppliers
Astragaloside A Related Literature
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
-
Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
-
Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
Additional information on Astragaloside A
Introduction to Astragaloside A (CAS No. 83207-58-3)
Astragaloside A, a bioactive compound with the chemical name Astragaloside A, is a prominent flavonoid glycoside derived from the genus *Astragalus*, particularly from *Astragalus membranaceus* and *Astragalus mongholicus*. This compound has garnered significant attention in the field of pharmaceutical research due to its diverse biological activities and potential therapeutic applications. With a CAS number of 83207-58-3, Astragaloside A is widely recognized for its role in traditional Chinese medicine and has been the subject of numerous studies exploring its pharmacological mechanisms and clinical efficacy.
The structural composition of Astragaloside A contributes to its unique pharmacological properties. It is characterized by a flavone backbone linked to a rhamnose sugar, forming a glycosidic structure that enhances its solubility and bioavailability. This structural feature is crucial for its absorption and distribution within the body, making it an attractive candidate for drug development. The presence of multiple hydroxyl groups in its molecular structure also facilitates various interactions with biological targets, contributing to its multifaceted biological activities.
Recent research has highlighted the anti-inflammatory properties of Astragaloside A, which are attributed to its ability to modulate inflammatory signaling pathways. Studies have demonstrated that this compound can inhibit the production of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6). These findings are particularly relevant in the context of chronic inflammatory diseases, where Astragaloside A has shown promise in reducing inflammation and alleviating symptoms associated with conditions like rheumatoid arthritis and inflammatory bowel disease.
Beyond its anti-inflammatory effects, Astragaloside A has been extensively studied for its antioxidant properties. Oxidative stress plays a critical role in the pathogenesis of various diseases, including neurodegenerative disorders, cardiovascular diseases, and cancer. By scavenging reactive oxygen species (ROS) and enhancing the activity of endogenous antioxidant enzymes, Astragaloside A helps mitigate oxidative damage and protect cells from oxidative stress-induced damage. This has led to investigations into its potential use as a therapeutic agent for conditions where oxidative stress is a prominent feature.
In addition to its anti-inflammatory and antioxidant activities, Astragaloside A has demonstrated potential in enhancing immune function. Research indicates that this compound can stimulate the proliferation of immune cells such as lymphocytes and macrophages, thereby bolstering the body's defense mechanisms. Furthermore, studies have shown that Astragaloside A can modulate the balance between Th1 and Th2 immune responses, which is crucial for maintaining immune homeostasis. These findings suggest that Astragaloside A may be beneficial in treating immunodeficiency disorders and enhancing vaccine efficacy.
The cardioprotective effects of Astragaloside A have also been a focus of recent research. Studies have shown that this compound can protect against ischemia-reperfusion injury in the heart by reducing oxidative stress, inhibiting apoptosis, and improving myocardial contractility. Additionally, Astragaloside A has been found to have vasodilatory effects, which can help lower blood pressure and improve blood flow. These properties make it a promising candidate for the development of cardiovascular therapeutics.
Another area of interest is the potential anticancer activity of Astragaloside A. Preclinical studies have demonstrated that this compound can induce apoptosis in various cancer cell lines by inhibiting key signaling pathways such as Akt/mTOR and NF-κB. Furthermore, Astragaloside A has been shown to suppress tumor growth and metastasis in animal models. These findings have prompted further investigation into its mechanisms of action and potential applications in cancer treatment.
The neuroprotective effects of Astragaloside A have also been explored in recent years. Research suggests that this compound can protect against neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease by reducing oxidative stress, inhibiting neuroinflammation, and promoting neuronal survival. These findings are particularly encouraging given the increasing prevalence of neurodegenerative disorders worldwide.
The pharmacokinetic profile of Astragaloside A is another critical aspect that has been studied extensively. Research indicates that this compound exhibits good oral bioavailability but undergoes rapid metabolism upon absorption. However, recent advancements in drug delivery systems have helped overcome these limitations by formulating sustained-release formulations that enhance retention time within the body. These developments are crucial for optimizing therapeutic efficacy while minimizing side effects.
In conclusion, Astragaloside A (CAS No. 83207-58-3) is a multifaceted bioactive compound with significant therapeutic potential across various medical conditions. Its diverse biological activities, including anti-inflammatory, antioxidant, immunomodulatory, cardioprotective, anticancer, and neuroprotective effects, make it an attractive candidate for further clinical development. Ongoing research continues to uncover new insights into its mechanisms of action and potential applications, paving the way for innovative treatments in medicine.
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