Cas no 1181216-83-0 (Schisanwilsonin H)

Schisanwilsonin H is a bioactive lignan compound isolated from the Schisandra genus, known for its complex tricyclic structure and potential pharmacological properties. This compound exhibits notable antioxidant and anti-inflammatory effects, making it a subject of interest in medicinal chemistry research. Its unique molecular framework, characterized by a dibenzocyclooctadiene skeleton, contributes to its ability to modulate cellular signaling pathways. Schisanwilsonin H has demonstrated promising activity in preclinical studies, particularly in neuroprotection and hepatoprotection. Its high purity and stability under standard conditions ensure reliability for experimental applications. Researchers value this compound for its structural specificity and potential as a lead molecule in drug discovery.
Schisanwilsonin H structure
Schisanwilsonin H structure
Product Name:Schisanwilsonin H
CAS No:1181216-83-0
MF:C30H32O9
MW:536.569689750671
CID:2087232
PubChem ID:21672542
Update Time:2025-06-14

Schisanwilsonin H Chemical and Physical Properties

Names and Identifiers

    • Schisanwilsonin H
    • Schisanwilsonin C
    • Arisanschinin K
    • Schisantherrin A
    • SCHEMBL3711074
    • FS-7691
    • CS-0023643
    • [(8S,9R,10S)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] benzoate
    • SchisanwilsoninH
    • 1181216-83-0
    • HY-N2988
    • Gomisin C
    • Wuweizi ester A
    • Schizantherin A
    • Schisantherin
    • Schisantherin A
    • (8S,9R,10S)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0(2),?.0(1)?,(1)?]nonadeca-1(12),2(7),3,5,13,18-hexaen-8-yl benzoate
    • DA-67485
    • FS74438
    • Inchi: 1S/C30H32O9/c1-16-12-18-13-21-25(38-15-37-21)26(35-5)22(18)23-19(14-20(33-3)24(34-4)27(23)36-6)28(30(16,2)32)39-29(31)17-10-8-7-9-11-17/h7-11,13-14,16,28,32H,12,15H2,1-6H3/t16-,28-,30+/m0/s1
    • InChI Key: UFCGDBKFOKKVAC-VLPWJMHXSA-N
    • SMILES: O[C@@]1(C)[C@H](C2C=C(C(=C(C=2C2C(=C3C(=CC=2C[C@@H]1C)OCO3)OC)OC)OC)OC)OC(C1C=CC=CC=1)=O

Computed Properties

  • Exact Mass: 536.20500
  • Monoisotopic Mass: 536.20463259g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 9
  • Heavy Atom Count: 39
  • Rotatable Bond Count: 7
  • Complexity: 833
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 3
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.735
  • Topological Polar Surface Area: 102?2

Experimental Properties

  • Color/Form: Cryst.
  • Density: 1.33±0.1 g/cm3 (20 oC 760 Torr),
  • Solubility: Insuluble (7.0E-4 g/L) (25 oC),
  • PSA: 101.91000
  • LogP: 4.95800

Schisanwilsonin H Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI TAO SHU Biotechnology Co., Ltd.
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TargetMol Chemicals
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A2B Chem LLC
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Additional information on Schisanwilsonin H

Exploring Schisanwilsonin H (CAS No. 1181216-83-0): A Comprehensive Overview of Its Properties and Applications

In the realm of natural products and bioactive compounds, Schisanwilsonin H (CAS No. 1181216-83-0) has garnered significant attention for its unique structural features and potential therapeutic benefits. This compound, classified as a triterpenoid, is derived from the Schisandra genus, a group of plants renowned for their medicinal properties in traditional Chinese medicine. Researchers and pharmaceutical developers are increasingly interested in Schisanwilsonin H due to its promising bioactivities, including anti-inflammatory, antioxidant, and neuroprotective effects.

The growing interest in Schisanwilsonin H aligns with the current trend of exploring natural compounds for drug discovery and health supplements. With the rise of holistic health and plant-based medicine, consumers and scientists alike are searching for compounds like Schisanwilsonin H that offer minimal side effects and high efficacy. Online searches frequently include queries such as "Schisanwilsonin H benefits", "CAS 1181216-83-0 uses", and "natural triterpenoids for health", reflecting the public's curiosity about this compound.

From a chemical perspective, Schisanwilsonin H (CAS No. 1181216-83-0) exhibits a complex molecular structure characterized by multiple rings and functional groups, which contribute to its biological activity. Studies suggest that it may interact with cellular pathways involved in oxidative stress and inflammation, making it a candidate for treating conditions like neurodegenerative diseases and metabolic disorders. Its mechanism of action is often compared to other well-known triterpenoids, such as ursolic acid and oleanolic acid, which are widely studied for their health benefits.

The extraction and synthesis of Schisanwilsonin H are areas of active research. While it can be isolated from Schisandra chinensis and related species, efforts are underway to develop synthetic analogs to improve yield and bioavailability. This is particularly relevant given the increasing demand for sustainable sourcing of bioactive compounds. Researchers are also investigating Schisanwilsonin H derivatives to enhance its pharmacological properties, addressing common search terms like "how to synthesize Schisanwilsonin H" and "bioavailability of triterpenoids".

In addition to its potential therapeutic applications, Schisanwilsonin H is being explored in the cosmeceutical industry. Its antioxidant properties make it a promising ingredient for anti-aging skincare products, a topic frequently searched by consumers interested in natural skincare solutions. The compound's ability to neutralize free radicals and protect skin cells from environmental damage aligns with the growing preference for clean beauty and science-backed formulations.

Despite its potential, challenges remain in the widespread adoption of Schisanwilsonin H. Issues such as low solubility and limited clinical trials need to be addressed to fully unlock its benefits. However, the compound's versatility and alignment with current health trends ensure its continued relevance in scientific and consumer discussions. As research progresses, Schisanwilsonin H (CAS No. 1181216-83-0) may well become a cornerstone in the development of next-generation natural therapeutics and cosmeceuticals.

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