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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
lyratol C [CHEBI:66607] (1)
05. Industrial Uses
05. Industrial Uses
lyratol C [CHEBI:66607] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Solanum lyratum (3)
07. Part of Biological Source of Chemical
07. Part of Biological Source of Chemical
whole plant [PO:0000003] (150)
08. Chemical Category
08. Chemical Category
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
lyratol C [CHEBI:66607] (1)
ChEBI Compound Accession Identifier :
[CHEBI:66607]
ChEBI Compound Description :
An sesquiterpenoid that is decahydronaphthalene substituted by hydroxy groups at positions 1 and 2, a methyl group at position 8a, a methylidene group at position 4 and a 1,2-dihydroxypropan-2-yl at position 6 (the 1R,2R,4aR,6S,8aS stereoisomer) . Isolated from Solanum lyratum, it exhibits cytotoxicity against human cancer cell lines.
ChEBI Compound Identification Number :
66607
ChEBI InChI Value :
InChI=1S/C15H26O4/c1-9-6-12(17)13(18)14(2)5-4-10(7-11(9)14)15(3,19)8-16/h10-13,16-19H,1,4-8H2,2-3H3/t10-,11+,12+,13-,14-,15?/m0/s1
ChEBI InChIKey Value :
QLYUSONKBWKHRY-MKGDQNAVSA-N
ChEBI Compound Name :
lyratol C
ChEBI SMILES Value :
[H][C@@]1(CC[C@]2(C)[C@@H](O)[C@H](O)CC(=C)[C@@]2([H])C1)C(C)(O)CO
ChEBI Substance ID :
160710809
ChEBI URL :
ChEBI:66607
ChemSpider ID :
28639005
Ontomatica Chemical Accession Key (OnChAKey) :
QLYUSONKBWKHRY_MKGDQNAVSA_N_000_000000
PubChem Compound ID :
42604342