General Information of Natural Product (ID: NP1200)
  Natural Product Name
Peruviol
  Synonyms
d-Nerolidol; 142-50-7; (+)-Nerolidol; (S)-cis-Nerolidol; Peruviol; (s)-nerolidol; UNII-89V5Z0JC8J; (3S,6Z)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol; (Z)-Nerolidol; 89V5Z0JC8J; NSC60598; NSC406963; NSC 60598; Nerolidol (VAN); 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (3S,6Z)-; Nerolidol, cis-(+)-; 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-; 1,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, [S-(Z)]-; Nerolidiol; 1,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (Z)-(S)-(+)-; MFCD00085350; EINECS 205-540-2; (+)-cis-Nerolidol; NSC 406963; (3S,6Z)-nerolidol; (6Z)-(+)-nerolidol; (6Z)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol; Nerolidol, (6Z)-(+)-; CHEMBL561014; SCHEMBL6514677; DTXSID4047048; CHEBI:176337; NSC-60598; ZINC13319968; NSC-406963; Q27270067; (3S,6Z)-3,7,11-trimethyl-1,6,10-dodecatrien-3-ol; UNII-81K23DEF7B component FQTLCLSUCSAZDY-QKXCFHHRSA-N; UNII-C65VP6N2VX component FQTLCLSUCSAZDY-QKXCFHHRSA-N; UNII-QR6IP857S6 component FQTLCLSUCSAZDY-QKXCFHHRSA-N; (Z)-(S)-(+)-3,7,11-trimethyl-1,6,10-Dodecatrien-3-ol; 3,7,11-Trimethyl-(3S,6Z)-(+)-1,6,10-Dodecatrien-3-ol; 3,7,11-Trimethyl-(Z)-(S)-(+)-1,6,10-Dodecatrien-3-ol; 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (3S,6Z)-(+)-
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  Formula C15H26O
  Weight 222.37
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C15H26O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6,9,11,16H,1,7-8,10,12H2,2-5H3/b14-11-/t15-/m1/s1
  InChI Key FQTLCLSUCSAZDY-QKXCFHHRSA-N
  Isomeric SMILES CC(=CCC/C(=C\\CC[C@@](C)(C=C)O)/C)C
  Canonical SMILES CC(=CCCC(=CCCC(C)(C=C)O)C)C
  External Links PubChem ID 5356544
CAS ID 142-50-7
NPASS ID NPC194586
CHEMBL ID CHEMBL561014
  NP Activity Charts   Click to show/hide

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Cannabis sativa
  Factor Name: Developmental Stage Variation; Harvest Time Variation [1]
              Species Info Factor Info
               Experiment Detail
Hemp plants (cultivar USO-31) were cultivated for the production of hemp herb under non-standard agro-climatic conditions on clay-stony soil in the southern part of central Slovakia. The size of the managed soil was 0.42 hectares. No pre-crop was applied before sowing. In the autumn, classic manure was used as fertilizer, which was subsequently ploughed. In the spring, shallow ploughing was carried out. The seeds were sown by hand on 20 April 2019. Subsequently, the growing season began, which lasted until 12 September 2019, when it ended with the mowing of the stand using a drum rotary mower pulled by a tractor. During the growing season, the samples were taken three times, focusing on inflorescences and leaves. The first samples were harvested on 30 June 2019, before the flowering of the plant. The plants were short and reached a height of about 30 cm. The second samples were harvested on 3 August 2019 (the plants were already in the flowering phase). The inflorescences in the upper parts of the plant reached lengths of 2 to 30 cm. In this phase, there were also male inflorescences in the stand, which were already in a more advanced stage of flowering. The height of the plants ranged from 20-150 cm. The third sample was harvested on 1 September 2019, after flowering. The samples of hemp (the same genus) after flowering harvested in 2018 were analyzed too. Hemp plants from the year 2018 season were much more developed, reaching a height of 2 m, and were more densely inseminated.
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               Factor Function
The highest content of polyphenolic compounds was analyzed in the sample harvested before flowering (17.217 mg/g). According to this study, the harvest in June (before flowering) is the most convenient for the achievement of the highest antioxidant activity and polyphenolic content. Among the secondary metabolites in hemp, terpenes and cannabinoids are the most attractive for research and further processing. The highest amounts were found in the sample collected during flowering. The concentrations of major terpenes beta-caryophyllene and alpha-humulene were maximal during flowering, at 72.10 and 36.75 mg/g respectively. The accumulation of cannabinoids was also highest at this stage. The concentration of cannabidiol was 3.81 mg/g. The harvest of female plants is essential in July due to the CBD concentration maximum.
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               Factor Part Location NP Content
 
Harvesting time: after flowering; 2018
Green plant parts Slovakia
NP Content: 93.58 ± 3.63 µg/g dry weight
References
1 Influence of Technological Maturity on the Secondary Metabolites of Hemp Concentrate ( Cannabis sativa L.)