Cas no 625096-18-6 (Viniferol D)

Viniferol D is a stilbenoid compound derived from natural sources, primarily known for its role as a phytoalexin with notable biological activity. It exhibits strong antioxidant properties, making it valuable in research applications focused on oxidative stress mitigation. Viniferol D also demonstrates potential anti-inflammatory and antimicrobial effects, contributing to its relevance in pharmaceutical and agrochemical studies. Its structural similarity to resveratrol allows for comparative investigations into enhanced stability and efficacy. The compound is typically isolated from grapevines (Vitis vinifera) and is of interest for its role in plant defense mechanisms. Analytical methods for Viniferol D include HPLC and LC-MS, ensuring high purity for experimental use.
Viniferol D structure
Viniferol D structure
Product Name:Viniferol D
CAS No:625096-18-6
MF:C42H32O9
MW:680.698092460632
CID:837144
PubChem ID:71307315
Update Time:2025-05-19

Viniferol D Chemical and Physical Properties

Names and Identifiers

    • Viniferol D
    • (3S,4S,4aR,5R,9bR,10S)-4-(3,5-Dihydroxyphenyl)-3,5,10-tris(4-hydr oxyphenyl)-3,4,4a,5,9b,10-hexahydro-11-oxabenzo[5,6]cyclohepta[1, 2,3,4-jkl]-as-indacene-2,6,8-triol
    • (3S,4S,4AR,5R,9bR,10S)-4-(3,5-dihydroxyphenyl)-3,5,10-tris(4-hydroxyphenyl)-3,4,4a,5,9b,10-hexahydrobenzo[5,6]azuleno[7,8,1-cde]benzofuran-2,6,8-triol
    • AKOS032961604
    • (1R,2S,3S,9S,10R,17R)-2-(3,5-dihydroxyphenyl)-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol
    • FS-8900
    • Benz[5,6]azuleno[7,8,1-cde]benzofuran-2,6,8-triol,4-(3,5-dihydroxyphenyl)-3,4,4a,5,9b,10-hexahydro-3,5,10-tris(4-hydroxyphenyl)-, (3R,4R,4aS,5S,9bS,10R)-rel-(+)-
    • 625096-18-6
    • (+)-Viniferol D
    • [ "" ]
    • Inchi: 1S/C42H32O9/c43-23-7-1-19(2-8-23)33-35(22-13-26(46)15-27(47)14-22)40-34(20-3-9-24(44)10-4-20)36-29(16-28(48)17-30(36)49)37-39-32(18-31(50)38(33)41(39)40)51-42(37)21-5-11-25(45)12-6-21/h1-18,33-35,37,40,42-50H/t33-,34-,35-,37-,40+,42-/m1/s1
    • InChI Key: QDEHKEFWCRAFDN-MOTQTELBSA-N
    • SMILES: O1C2=CC(=C3[C@H](C4C=CC(=CC=4)O)[C@@H](C4C=C(C=C(C=4)O)O)[C@@H]4[C@H](C5C=CC(=CC=5)O)C5C(=CC(=CC=5[C@@H]([C@H]1C1C=CC(=CC=1)O)C2=C43)O)O)O

Computed Properties

  • Exact Mass: 680.20463259g/mol
  • Monoisotopic Mass: 680.20463259g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 8
  • Hydrogen Bond Acceptor Count: 9
  • Heavy Atom Count: 51
  • Rotatable Bond Count: 4
  • Complexity: 1180
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 6
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 6.8
  • Topological Polar Surface Area: 171?2

Experimental Properties

  • Color/Form: Powder
  • Density: 1.5±0.1 g/cm3

Viniferol D Security Information

Viniferol D Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd.
V12350-5mg
(3S,4S,4aR,5R,9bR,10S)-4-(3,5-Dihydroxyphenyl)-3,5,10-tris(4-hydr oxyphenyl)-3,4,4a,5,9b,10-hexahydro-11-oxabenzo[5,6]cyclohepta[1, 2,3,4-jkl]-as-indacene-2,6,8-triol
625096-18-6 ,HPLC≥98%
5mg
¥6400.0 2023-09-06
SHANG HAI TAO SHU Biotechnology Co., Ltd.
TMA1203-1 mg
Viniferol D
625096-18-6
1mg
¥3235.00 2022-04-26
TRC
V213540-1mg
Viniferol D
625096-18-6
1mg
820.00 2021-07-15
TRC
V213540-2.5mg
Viniferol D
625096-18-6
2.5mg
1335.00 2021-07-15
TRC
V213540-5mg
Viniferol D
625096-18-6
5mg
2720.00 2021-07-15
A2B Chem LLC
AB53790-5mg
Benz[5,6]azuleno[7,8,1-cde]benzofuran-2,6,8-triol,4-(3,5-dihydroxyphenyl)-3,4,4a,5,9b,10-hexahydro-3,5,10-tris(4-hydroxyphenyl)-, (3R,4R,4aS,5S,9bS,10R)-rel-(+)-
625096-18-6 97.5%
5mg
$869.00 2024-04-19
TargetMol Chemicals
TMA1203-1 ml * 10 mm
Viniferol D
625096-18-6
1 ml * 10 mm
¥ 6860 2024-07-19
A2B Chem LLC
AB53790-1mg
Benz[5,6]azuleno[7,8,1-cde]benzofuran-2,6,8-triol,4-(3,5-dihydroxyphenyl)-3,4,4a,5,9b,10-hexahydro-3,5,10-tris(4-hydroxyphenyl)-, (3R,4R,4aS,5S,9bS,10R)-rel-(+)-
625096-18-6 97
1mg
$699.00 2024-04-19
TargetMol Chemicals
TMA1203-5 mg
Viniferol D
625096-18-6 98%
5mg
¥ 4,510 2023-07-10
TargetMol Chemicals
TMA1203-1 mL * 10 mM (in DMSO)
Viniferol D
625096-18-6 98%
1 mL * 10 mM (in DMSO)
¥ 6860 2023-09-15

Additional information on Viniferol D

Exploring the Potential of Viniferol D: A Comprehensive Overview

Viniferol D, identified by the CAS registry number 625096-18-6, is a compound that has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields. This compound, belonging to the class of polyphenols, has been extensively studied for its role in biological systems and its potential benefits in health and wellness. In this article, we delve into the latest research findings, structural characteristics, and promising applications of Viniferol D.

The structural elucidation of Viniferol D has been a focal point of recent studies. Researchers have employed advanced spectroscopic techniques such as NMR and mass spectrometry to determine its molecular structure. The compound is characterized by a complex arrangement of aromatic rings and hydroxyl groups, which contribute to its antioxidant properties. These structural features make Viniferol D a compelling candidate for use in antioxidant-rich products, including dietary supplements and skincare formulations.

One of the most exciting developments in the study of Viniferol D is its demonstrated ability to combat oxidative stress. Oxidative stress is a major contributor to aging and various chronic diseases, including cardiovascular conditions and neurodegenerative disorders. Recent in vitro studies have shown that Viniferol D exhibits potent free radical scavenging activity, which could be harnessed to develop innovative therapeutic agents. Furthermore, preclinical trials have indicated that this compound may enhance cellular resilience against oxidative damage, paving the way for future clinical applications.

The bioavailability and metabolic profile of Viniferol D are critical factors influencing its potential as a bioactive agent. Recent research has focused on understanding how this compound is absorbed, distributed, metabolized, and excreted within the human body. Studies suggest that Viniferol D undergoes extensive metabolism in the liver, where it is converted into various metabolites that retain some of its original biological activity. This insight is crucial for optimizing dosage forms and delivery systems to maximize its efficacy.

In terms of applications, Viniferol D holds promise across multiple industries. In the food industry, it is being explored as a natural preservative due to its antimicrobial properties. In cosmetics, its antioxidant properties make it an ideal ingredient for anti-aging products aimed at protecting the skin from environmental stressors. Additionally, preliminary studies suggest that Viniferol D could be utilized in functional foods designed to promote overall health and well-being.

The synthesis and production of Viniferol D present both challenges and opportunities. Traditional extraction methods from plant sources are labor-intensive and yield limited quantities of the compound. To address this, researchers are developing novel synthetic routes using biotechnological approaches such as microbial fermentation. These methods not only enhance scalability but also offer greater control over product purity and consistency.

In conclusion, Viniferol D, with its unique chemical structure and diverse biological activities, represents a valuable asset in the quest for innovative solutions in health, beauty, and nutrition. As research continues to uncover new dimensions of this compound's potential, it is poised to make significant contributions across various sectors. Stay tuned for further updates on this intriguing molecule!

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