Cas no 136040-43-2 (Schisanlactone E)

Schisanlactone E is a bioactive triterpenoid compound derived from Schisandra chinensis, a plant known for its medicinal properties. This compound exhibits notable anti-inflammatory and hepatoprotective effects, making it valuable for pharmacological research. Its unique structural features, including a lactone ring and oxygenated functional groups, contribute to its biological activity. Schisanlactone E has demonstrated potential in modulating oxidative stress and inhibiting pro-inflammatory cytokines, suggesting applications in studying liver disorders and inflammatory conditions. Its high purity and stability under standard conditions ensure reliability for experimental use. Researchers favor Schisanlactone E for its well-characterized properties and reproducible results in preclinical studies.
Schisanlactone E structure
Schisanlactone E structure
Product Name:Schisanlactone E
CAS No:136040-43-2
MF:C30H44O4
MW:468.667969703674
CID:191382
PubChem ID:14844611
Update Time:2025-10-29

Schisanlactone E Chemical and Physical Properties

Names and Identifiers

    • 1H-Cyclopenta[a]cyclopropa[e]naphthalene-3a(4H)-propanoicacid,7-[(1S)-1-[(2R)-3,6-dihydro-5-methyl-6-oxo-2H-pyran-2-yl]ethyl]decahydro-6a,9a-dimethyl-3-(1-methylethenyl)-,(3S,3aR,4aS,6aR,7R,9aS,9bS)-
    • 1H-Cyclopenta[a]cyclopropa[e]naphthalene-3a(4H)-propanoicacid,7-[(1S)-1-[(2R)-3,6-dihydro-5-me...
    • 1H-Cyclopenta[a]cyclopropa[e]naphthalene-3a(4H)-propanoicacid,7-[(1S)-1-[(2R)-3,6-dihydro-5-methyl-6-oxo-2H-pyran-2-yl]ethyl]
    • SCHISANLACTONE E
    • Kadsulactone acid
    • (3S,3aR,4aS,6aR,7R,9aS,9bS)-7-[(1S)-1-[(2R)-3,6-Dihydro-5-methyl-6-oxo-2H-pyran-2-yl]ethyl]decahydro-6a,9a-dimethyl-3-(1-methylethenyl)-1H-cyclopenta[a]cyclopropa[e]naphthalene-3a(4H)-propanoic acid
    • X1227
    • HY-N9505
    • 136040-43-2
    • AKOS040760694
    • CS-0182025
    • 3-[(1S,4R,5R,8S,9S,12S,13R)-4,8-Dimethyl-5-[(1S)-1-[(2R)-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-12-prop-1-en-2-yl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid
    • FS-7027
    • 3-[(1S,4R,5R,8S,9S,12S,13R)-4,8-DIMETHYL-5-[(1S)-1-[(2R)-5-METHYL-6-OXO-2,3-DIHYDROPYRAN-2-YL]ETHYL]-12-(PROP-1-EN-2-YL)TETRACYCLO[7.5.0.0(1),(1)(3).0?,?]TETRADECAN-13-YL]PROPANOIC ACID
    • DA-54584
    • Schisanlactone E
    • Inchi: 1S/C30H44O4/c1-18(2)21-8-10-24-28(6)13-11-22(20(4)23-9-7-19(3)26(33)34-23)27(28,5)15-16-30(24)17-29(21,30)14-12-25(31)32/h7,20-24H,1,8-17H2,2-6H3,(H,31,32)/t20-,21-,22+,23+,24-,27+,28-,29+,30-/m0/s1
    • InChI Key: RRSQKAFYPICCAZ-PTWMZBRVSA-N
    • SMILES: O1C(C(C)=CC[C@@H]1[C@@H](C)[C@H]1CC[C@]2(C)[C@]1(C)CC[C@@]13C[C@]1(CCC(=O)O)[C@H](C(=C)C)CC[C@H]32)=O

Computed Properties

  • Exact Mass: 468.32400
  • Monoisotopic Mass: 468.32395988g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 34
  • Rotatable Bond Count: 6
  • Complexity: 950
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 9
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 8.2
  • Topological Polar Surface Area: 63.6

Experimental Properties

  • Color/Form: Cryst.
  • Density: 1.12
  • Melting Point: 120-122 oC
  • PSA: 63.60000
  • LogP: 6.94430

Schisanlactone E Pricemore >>

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