Cas no 1187303-40-7 (Cuniloside B)

Cuniloside B structure
Cuniloside B structure
Product Name:Cuniloside B
CAS No:1187303-40-7
MF:C26H40O10
MW:512.589809417725
MDL:MFCD20274754
CID:837646
PubChem ID:91895372
Update Time:2025-07-15

Cuniloside B Chemical and Physical Properties

Names and Identifiers

    • Cuniloside B
    • 1,6-Bis-O-{[(4R)-4-(2-hydroxy-2-propanyl)-1-cyclohexen-1-yl]carbo nyl}-β-D-glucopyranose
    • 1,6-Dinitrophenazin
    • 1,6-dinitro-phenazine
    • BZGCNHUWISZVPK-UHFFFAOYSA
    • eucalmaidin E
    • Phenazine,1,6-dinitro
    • [ "Eucalmaidin E" ]
    • [(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carbonyl]oxyoxan-2-yl]methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate
    • HY-N3649
    • FS-10198
    • AKOS032962402
    • CS-0023996
    • beta-D-Glucopyranose, 1,6-bis((4R)-4-(1-hydroxy-1-methylethyl)-1-cyclohexene-1-carboxylate)
    • starbld0000836
    • 1187303-40-7
    • DA-52164
    • ((2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-((4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carbonyl)oxyoxan-2-yl)methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate
    • MDL: MFCD20274754
    • Inchi: 1S/C26H40O10/c1-25(2,32)16-9-5-14(6-10-16)22(30)34-13-18-19(27)20(28)21(29)24(35-18)36-23(31)15-7-11-17(12-8-15)26(3,4)33/h5,7,16-21,24,27-29,32-33H,6,8-13H2,1-4H3/t16-,17-,18+,19+,20-,21+,24-/m0/s1
    • InChI Key: JOLLIDAUJSAZHE-SKNUFNKISA-N
    • SMILES: O1[C@H]([C@@H]([C@H]([C@@H]([C@H]1COC(C1=CC[C@@H](CC1)C(C)(C)O)=O)O)O)O)OC(C1=CC[C@@H](CC1)C(C)(C)O)=O

Computed Properties

  • Exact Mass: 512.26200
  • Monoisotopic Mass: 512.26214747g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 10
  • Heavy Atom Count: 36
  • Rotatable Bond Count: 9
  • Complexity: 876
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 7
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.8
  • Topological Polar Surface Area: 163?2

Experimental Properties

  • Color/Form: Powder
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 680.4±55.0 °C at 760 mmHg
  • Flash Point: 221.3±25.0 °C
  • PSA: 162.98000
  • LogP: 0.87520
  • Vapor Pressure: 0.0±4.8 mmHg at 25°C

Cuniloside B Security Information

Cuniloside B Pricemore >>

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Cuniloside B Production Method

Additional information on Cuniloside B

Introduction to Cuniloside B (CAS No: 1187303-40-7)

Cuniloside B, a naturally occurring compound with the chemical formula CAS No: 1187303-40-7, has garnered significant attention in the field of pharmaceutical research due to its unique structural properties and potential biological activities. This compound, which belongs to the flavonoid family, has been extensively studied for its therapeutic implications in various diseases, particularly in oncology and neurodegenerative disorders. The structural elucidation and pharmacological profiling of Cuniloside B have opened new avenues for drug development, making it a subject of intense interest among researchers.

The molecular structure of Cuniloside B features a glycosidic linkage between a flavonoid aglycone and a sugar moiety, which contributes to its solubility and bioavailability. This structural characteristic is crucial for its absorption and distribution within the body, making it an attractive candidate for therapeutic applications. Recent studies have highlighted the anti-inflammatory and antioxidant properties of Cuniloside B, which are attributed to its ability to scavenge free radicals and modulate inflammatory pathways.

One of the most compelling aspects of Cuniloside B is its potential role in cancer therapy. Preclinical studies have demonstrated that Cuniloside B can induce apoptosis in various cancer cell lines by inhibiting key signaling pathways such as PI3K/Akt and MAPK. These pathways are often dysregulated in cancer cells, leading to uncontrolled cell growth and survival. The ability of Cuniloside B to disrupt these pathways suggests its potential as a chemotherapeutic agent. Additionally, its selective toxicity towards cancer cells without significant toxicity to normal cells makes it an appealing candidate for further clinical development.

Another area where Cuniloside B has shown promise is in the treatment of neurodegenerative diseases. Research indicates that Cuniloside B can protect against neurotoxicity induced by oxidative stress and inflammation, which are hallmark features of conditions such as Alzheimer's disease and Parkinson's disease. Studies have shown that Cuniloside B can cross the blood-brain barrier, allowing it to exert its effects directly within the central nervous system. This property is critical for developing effective treatments for neurodegenerative disorders, where targeted delivery is essential.

The pharmacokinetic profile of Cuniloside B has also been a focus of recent research. Studies have shown that Cuniloside B exhibits moderate oral bioavailability, with a half-life that allows for repeated dosing regimens. This makes it feasible for clinical translation, provided that issues related to metabolism and excretion can be addressed. Efforts are underway to optimize the pharmacokinetic properties of Cuniloside B through structural modifications, which could enhance its therapeutic efficacy.

In conclusion, Cuniloside B (CAS No: 1187303-40-7) is a promising natural product with a wide range of potential applications in medicine. Its unique structural features and biological activities make it an attractive candidate for further research and development. As our understanding of its mechanisms of action continues to grow, so too does the potential for novel therapeutic interventions based on this compound. The ongoing studies into Cuniloside B highlight the importance of natural products in the discovery of new drugs and their potential to address some of the most challenging diseases faced by humanity.

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