General Information of Natural Product (ID: NP0412)
  Natural Product Name
Lilac Aldehyde
  Synonyms
Lilac aldehyde; Lilac aldehyde B; 2-(5-ethenyl-5-methyloxolan-2-yl)propanal; Lilac aldehyde A; 67920-63-2; 2-(5-Methyl-5-vinyltetrahydro-2-furanyl)propanal; 2-(5-methyl-5-vinyltetrahydrofuran-2-yl)propanal; 2-(5-ethenyl-5-methyltetrahydrofuran-2-yl)propanal; Lilac aldehyde C; Lilac aldehyde D; (+/-)-lilac aldehyde; Lilac aldehyde (isomer II); SCHEMBL3505874; CHEBI:25038; 2-Furanacetaldehyde, 5-ethenyltetrahydro-alpha,5-dimethyl-; DTXSID90867402; (+/-)-2-(5-Methyl-5-vinyltetrahydrofuran-2-yl)propionaldehyde; 2-(5-Methyl-5-vinyltetrahydro-2-furanyl)propanal #; Q27109862; 5-Ethenyltetrahydro-alpha,5-dimethyl-2-Furanacetaldehyde; 2-Furanacetaldehyde, 5-ethenyltetrahydro-.alpha.,5-dimethyl-, (.alpha.S,2S,5S)-
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  Formula C10H16O2
  Weight 168.23
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C10H16O2/c1-4-10(3)6-5-9(12-10)8(2)7-11/h4,7-9H,1,5-6H2,2-3H3
  InChI Key YPZQHCLBLRWNMJ-UHFFFAOYSA-N
  Isomeric SMILES CC(C=O)C1CCC(O1)(C)C=C
  Canonical SMILES CC(C=O)C1CCC(O1)(C)C=C
  External Links PubChem ID 155007
CAS ID 67920-63-2

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Arabidopsis thaliana
  Factor Name: T-DNA Knock-Out Treatment [1]
              Species Info Factor Info
               Experiment Detail
In vitro cultivation of Arabidopsis wildtype and mutant plants: Seeds were sterilized according to standard lab routines (EtOH, NaOCl/NaOH) prior to aseptical (in vitro) cultivation in 500 ml screw cap jars on MS medium (4.3 g/l; 50 ml/jar) containing Bacto- and Phytoagar (1:2; 6 g/l) and 30 g/l sucrose. Ten seeds were pipetted into each jar and plants grown for 6 weeks until flowering at a temperature of 20 ℃ under a 16/8 h day/ night regime using fluorescent tubes (Osram Lumilux Plus Eco 36 W). Both Arabidopsis thaliana wildtype plants of ecotype Columbia-0 (Col) and 4 Col-derived T-DNA knock-out mutants (homozygous lines) showing deficiencies in the GLS biosynthesis pathway were used in this study (five parallels for wildtype and mutants): TGG1 (Atg526000; Salk_130469), TGG2 (At5g25980; Salk_038730), Cyp83A1 (At4g13770) and Cyp83B1 (At4g31500; Salk_028573). Greenhouse-cultivation of Arabidopsis ecotypes: The following Arabidopsis ecotypes were used in the study: Columbia (Col), Cape Verde Islands (Cvi), Landsberg erecta (Ler) and Wassilewskija (Ws). Single plants were greenhouse-cultivated on fertilized soil (P-Jord; Emmaljunga Torvmull AB) in plug trays (9 × 6 cells) at a temperature of 20 ℃ (three parallels for each ecotype). Due to the 6-weeks growth period (November/December 2003), the plants were cultivated under a 16/8 h day/night regime using metal halide lamps (Osram HQI-T 400 W) placed 130 cm above the trays. Depending on the ecotypical plant development, whole plants were sampled after 3-4 weeks right before bolting for in vivo studies, while investigations of single plant organs (leaf, stem, inflorescence) were carried out after 5-6 weeks of cultivation.
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               Factor Function
Metabolites from methionine, leucine and phenylalanine-derived glucosinolates were most abundant (4-methylthiobutyl, 4-methylpentyl, 2-phenylethyl). In addition, 24 monoterpenes, 26 sesquiterpenes and 12 aromatic structures, predominantly observed in inflorescenses, are described. Excluding the vast group of straight chain aliphatic structures, a total of 102 volatile compounds were detected, of which 59 are reported in Arabidopsis thaliana for the first time, thus emphasizing the sensitivity and applicability of solid-phase microextraction for volatile profiling of plant secondary metabolites.
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               Factor Part Location NP Content
 
Inflorescences: A. thaliana wildtype detected in vivo
Flowers Norway
NP Content: 0.24 %
 
Inflorescences: A. thaliana wildtype detected in vivo
Flowers Norway
NP Content: 0.17 %
References
1 Volatile profiling of Arabidopsis thaliana - Putative olfactory compounds in plant communication