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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Nardostachys chinensis (2)
07. Part of Biological Source of Chemical
07. Part of Biological Source of Chemical
root [PO:0009005] (486)
08. Chemical Category
08. Chemical Category
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
nardoperoxide [CHEBI:66611] (1)
ChEBI Compound Accession Identifier :
[CHEBI:66611]
ChEBI Compound Description :
A sesquiterpenoid that is 1,4,5,6,7,8-hexahydro-4,7-epidioxyazulen-3(2H)-one substituted by a hydroxy group at position 8, methyl groups at positions 1 and 4 and an isopropyl group at position 7 (the (1R,4R,7R,8R stereoisomer). Isolated from Nardostachys chinensis, it exhibits antimalarial activity.
ChEBI Compound Identification Number :
66611
ChEBI InChI Value :
InChI=1S/C15H22O4/c1-8(2)15-6-5-14(4,18-19-15)12-10(16)7-9(3)11(12)13(15)17/h8-9,13,17H,5-7H2,1-4H3/t9-,13-,14-,15-/m1/s1
ChEBI InChIKey Value :
BDBRZURCDWHOCK-SEWBAHNZSA-N
ChEBI Compound Name :
nardoperoxide
ChEBI SMILES Value :
CC(C)[C@@]12CC[C@@](C)(OO1)C1=C([C@H](C)CC1=O)[C@H]2O
ChEBI Substance ID :
160710362
ChEBI URL :
ChEBI:66611
ChemSpider ID :
8643538
Ontomatica Chemical Accession Key (OnChAKey) :
BDBRZURCDWHOCK_SEWBAHNZSA_N_000_000000
PubChem Compound ID :
10468127