Cas no 163047-23-2 (Anemarrhenasaponin III)
Anemarrhenasaponin III Chemical and Physical Properties
Names and Identifiers
-
- b-D-Galactopyranoside, (3b,5b,15a,25S)-15-hydroxyspirostan-3-yl 2-O-b-D-glucopyranosyl- (9CI)
- AnemarrhenasaponinIII
- Anemarrhenasaponin III
- B0005-479886
- 163047-23-2
- AKOS040760267
- 2-[4,5-dihydroxy-6-(hydroxymethyl)-2-(3-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
- FS-7263
- (2S,3R,4S,5S,6R)-2-(((2R,3R,4S,5R,6R)-4,5-Dihydroxy-2-(((2aR,4S,5'S,6aS,6bS,8aS,8bR,9S,10R,11aR,12R,12aS,12bR)-12-hydroxy-5',6a,8a,9-tetramethyldocosahydrospiro[naphtho[2',1':4,5]indeno[2,1-b]furan-10,2'-pyran]-4-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyr
-
- Inchi: 1S/C39H64O14/c1-17-7-12-39(48-16-17)18(2)25-33(53-39)29(44)26-21-6-5-19-13-20(8-10-37(19,3)22(21)9-11-38(25,26)4)49-36-34(31(46)28(43)24(15-41)51-36)52-35-32(47)30(45)27(42)23(14-40)50-35/h17-36,40-47H,5-16H2,1-4H3
- InChI Key: FZEHHXRFTMAICH-UHFFFAOYSA-N
- SMILES: O1C2(CCC(C)CO2)C(C)C2C1C(C1C3CCC4CC(CCC4(C)C3CCC12C)OC1C(C(C(C(CO)O1)O)O)OC1C(C(C(C(CO)O1)O)O)O)O
Computed Properties
- Exact Mass: 756.429607g/mol
- Monoisotopic Mass: 756.429607g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 8
- Hydrogen Bond Acceptor Count: 14
- Heavy Atom Count: 53
- Rotatable Bond Count: 6
- Complexity: 1310
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 23
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.3
- Topological Polar Surface Area: 217
- Molecular Weight: 756.9g/mol
Anemarrhenasaponin III Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | BZP1593-10mg |
Anemarrhenasaponin III |
163047-23-2 | HPLC≥98% | 10mg |
¥1800元 | 2023-09-15 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | A46940-10mg |
b-D-Galactopyranoside, (3b,5b,15a,25S)-15-hydroxyspirostan-3-yl 2-O-b-D-glucopyranosyl- (9CI) |
163047-23-2 | ,HPLC≥98% | 10mg |
¥2252.0 | 2023-09-08 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TN1382-5 mg |
Anemarrhenasaponin III |
163047-23-2 | 5mg |
¥4861.00 | 2022-04-26 | ||
| TargetMol Chemicals | TN1382-10 mg |
Anemarrhenasaponin III |
163047-23-2 | 98% | 10mg |
¥ 2,380 | 2023-07-11 | |
| TargetMol Chemicals | TN1382-1 mL * 10 mM (in DMSO) |
Anemarrhenasaponin III |
163047-23-2 | 98% | 1 mL * 10 mM (in DMSO) |
¥ 2480 | 2023-09-15 | |
| TargetMol Chemicals | TN1382-10mg |
Anemarrhenasaponin III |
163047-23-2 | 10mg |
¥ 2380 | 2024-07-20 | ||
| TargetMol Chemicals | TN1382-1 ml * 10 mm |
Anemarrhenasaponin III |
163047-23-2 | 1 ml * 10 mm |
¥ 2480 | 2024-07-20 |
Anemarrhenasaponin III Related Literature
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Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
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Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
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José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
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Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
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Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
Additional information on Anemarrhenasaponin III
Recent Advances in the Study of Anemarrhenasaponin III (CAS: 163047-23-2): A Comprehensive Research Brief
Anemarrhenasaponin III (CAS: 163047-23-2) is a bioactive saponin derived from the rhizome of Anemarrhena asphodeloides, a traditional Chinese medicinal herb. Recent studies have highlighted its potential therapeutic applications, particularly in anti-inflammatory, neuroprotective, and anticancer activities. This research brief synthesizes the latest findings on Anemarrhenasaponin III, focusing on its molecular mechanisms, pharmacological effects, and clinical relevance.
A 2023 study published in the Journal of Ethnopharmacology investigated the anti-inflammatory properties of Anemarrhenasaponin III. The research demonstrated that the compound significantly inhibits the NF-κB signaling pathway, reducing the production of pro-inflammatory cytokines such as TNF-α and IL-6. These findings suggest its potential as a novel therapeutic agent for chronic inflammatory diseases, including rheumatoid arthritis and inflammatory bowel disease.
In the field of neuroprotection, a recent Frontiers in Pharmacology article (2024) explored the effects of Anemarrhenasaponin III on Alzheimer's disease models. The study revealed that the saponin attenuates oxidative stress and amyloid-beta aggregation, improving cognitive function in transgenic mice. These results underscore its promise as a candidate for neurodegenerative disorder treatment.
Oncology research has also made strides in understanding Anemarrhenasaponin III's anticancer potential. A 2024 Cancer Letters publication reported that the compound induces apoptosis in hepatocellular carcinoma cells via the PI3K/AKT/mTOR pathway inhibition. Notably, it exhibited synergistic effects with conventional chemotherapeutic agents, suggesting its utility in combination therapies.
Pharmacokinetic studies have advanced significantly, with a 2023 Phytomedicine paper characterizing the absorption, distribution, metabolism, and excretion (ADME) profile of Anemarrhenasaponin III. The research identified key metabolites and proposed optimal dosing strategies for future clinical trials.
Despite these promising developments, challenges remain in the clinical translation of Anemarrhenasaponin III. Current research gaps include limited human trial data and the need for improved formulation strategies to enhance bioavailability. Ongoing studies are addressing these issues through nanotechnology-based delivery systems and structural modifications.
In conclusion, Anemarrhenasaponin III (163047-23-2) represents a multifaceted bioactive compound with significant therapeutic potential across multiple disease areas. Continued research efforts are expected to further elucidate its mechanisms of action and accelerate its development into clinically viable treatments.
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