ORGANISM

🥬Dame's-violet

Hesperis matronalis

39 molecules reported in this organism, across 46 literature references.

Taxonomy

Classification

Kingdom: Archaeplastida
Order: Brassicales
Family: Brassicaceae
Genus: Hesperis

Provenance

Contributing sources

LOTUS
Taxonomy: LOTUS (GBIF / NCBI / OTT)

Composition

Molecules reported in Hesperis matronalis

2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, trans- 2 references Acyclic monoterpenoids

10.1016/0031-9422(94)00332-N 10.1016/J.PHYTOCHEM.2006.12.009
2-Phenylethanol 2 references Phenylethanoids

10.1016/0031-9422(94)00332-N 10.1016/J.PHYTOCHEM.2006.12.009
Benzyl Alcohol 2 references

10.1016/0031-9422(94)00332-N 10.1016/J.PHYTOCHEM.2006.12.009
(E)-β-Ocimene 2 references Acyclic monoterpenoids

10.1016/0031-9422(94)00332-N 10.1016/J.PHYTOCHEM.2006.12.009
Myrcene 2 references Acyclic monoterpenoids

10.1016/0031-9422(94)00332-N 10.1016/J.PHYTOCHEM.2006.12.009
(Z)-β-Ocimene 2 references Acyclic monoterpenoids

10.1016/0031-9422(94)00332-N 10.1016/J.PHYTOCHEM.2006.12.009
β-Myrcene 2 references Acyclic monoterpenoids

10.1016/0031-9422(94)00332-N 10.1016/J.PHYTOCHEM.2006.12.009
1,8-Cineole 1 reference Menthane monoterpenoids $ Monocyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
1-isothiocyanato-6-[(S)-methylsulfinyl]hexane 1 reference

10.3891/ACTA.CHEM.SCAND.17-0846
2-Phenylethyl Acetate 1 reference

10.1016/0031-9422(94)00332-N
(3S)-2,2-dimethyl-3-[(2E)-3-methylpenta-2,4-dienyl]oxirane 1 reference Acyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
4,8,12-Trimethyl-1,3,7,11-tridecatetraene 1 reference Hydrocarbons

10.1016/J.PHYTOCHEM.2006.12.009
6-Methyl-5-hepten-2-one 1 reference Acyclic monoterpenoids $ Apocarotenoids (Ψ-) $ Oxygenated hydrocarbons

10.1016/J.PHYTOCHEM.2006.12.009
(-)-alpha-Pinene 1 reference Pinane monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
Benzaldehyde 1 reference

10.1016/J.PHYTOCHEM.2006.12.009
Benzenepropanoic acid 1 reference

10.1016/0031-9422(94)00332-N
Benzyl acetate 1 reference Cinnamic acids and derivatives

10.1016/0031-9422(94)00332-N
Benzyl Benzoate 1 reference Simple phenolic acids

10.1016/J.PHYTOCHEM.2006.12.009
Benzyl propionate 1 reference Wax monoesters

10.1016/J.PHYTOCHEM.2006.12.009
beta-Ocimene 1 reference Acyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
(-)-beta-Pinene 1 reference Pinane monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
(E,E)-4,8,12-Trimethyl-1,3,7,11-tridecatetraene 1 reference Hydrocarbons

10.1016/J.PHYTOCHEM.2006.12.009
Eugenol 1 reference Cinnamic acids and derivatives

10.1016/J.PHYTOCHEM.2006.12.009
(L)-alpha-terpineol 1 reference Menthane monoterpenoids $ Monocyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
Limonene 1 reference Menthane monoterpenoids $ Monocyclic monoterpenoids

10.1016/0031-9422(94)00332-N
Linalool 1 reference Acyclic monoterpenoids

10.1016/0031-9422(94)00332-N
(-)-Linalool 1 reference Acyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
Linalool oxide, cis- 1 reference Acyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
Linalool oxide III 1 reference Acyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
Methyl Anthranilate 1 reference Aminoacids $ Anthranillic acid derivatives

10.1016/J.PHYTOCHEM.2006.12.009
Methyl Salicylate 1 reference Simple phenolic acids

10.1016/J.PHYTOCHEM.2006.12.009
Phenylacetaldehyde 1 reference Cinnamic acids and derivatives

10.1016/0031-9422(94)00332-N
Phenylacetonitrile 1 reference

10.1016/J.PHYTOCHEM.2006.12.009
Sabinene 1 reference Thujane monoterpenoids

10.1016/0031-9422(94)00332-N
(+)-Sabinene 1 reference Thujane monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009
α-Pinene 1 reference Pinane monoterpenoids

10.1016/0031-9422(94)00332-N
α-Terpineol 1 reference Menthane monoterpenoids $ Monocyclic monoterpenoids

10.1016/0031-9422(94)00332-N
β-Pinene 1 reference Pinane monoterpenoids

10.1016/0031-9422(94)00332-N
1 reference Menthane monoterpenoids $ Monocyclic monoterpenoids

10.1016/J.PHYTOCHEM.2006.12.009

Occurrence records from LOTUS. A molecule being reported in an organism means it was detected there in the cited work; it does not mean the organism is a commercial source of it.