🍃Croton nepetifolius

Composition

Molecules reported in Croton nepetifolius

• Methyleugenol 4 references Cinnamic acids and derivatives

  10.1002/(SICI)1099-1573(199805)12:3<172::AID-PTR212>3.0.CO;2-E 10.1021/NP50012A010

• Xanthoxylin 4 references Acyl phloroglucinols

  10.1002/(SICI)1099-1573(199805)12:3<172::AID-PTR212>3.0.CO;2-E 10.1021/NP50012A010

• α-Terpineol 4 references Menthane monoterpenoids $ Monocyclic monoterpenoids

  10.1002/(SICI)1099-1573(199805)12:3<172::AID-PTR212>3.0.CO;2-E 10.1021/NP50012A010

• β-Caryophyllene 4 references Caryophyllane sesquiterpenoids

  10.1002/(SICI)1099-1573(199805)12:3<172::AID-PTR212>3.0.CO;2-E 10.1021/NP50012A010

• Beta-Elemene 3 references Elemane sesquiterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• Elemene 3 references Elemane sesquiterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• Elemicin 3 references Cinnamic acids and derivatives

  10.1021/NP50012A010 10.1021/NP50017A019

• Humulene 3 references Humulane sesquiterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• Sabinene 3 references Thujane monoterpenoids

  10.1002/(SICI)1099-1573(199805)12:3<172::AID-PTR212>3.0.CO;2-E 10.1021/NP50012A010

• α-Humulene 3 references Humulane sesquiterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• α-Pinene 3 references Pinane monoterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• β-Pinene 3 references Pinane monoterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• 1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 2 references Elemane sesquiterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• 3-Propylcatechol 2 references Catechols with side chains

  10.1021/NP50012A010 10.1021/NP50017A019

• Gamma-elemene, (+)- 2 references Elemane sesquiterpenoids

  10.1021/NP50012A010 10.1021/NP50017A019

• α-Santalene 2 references Santalane sesquiterpenoids

  10.1021/NP50012A010 10.1055/S-1999-14025

• (1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 1 reference Aromadendrane sesquiterpenoids

  10.1055/S-1999-14025

• 1-Octacosanol 1 reference Fatty alcohols

  10.1021/NP50012A010

• (1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo(4.4.0.02,7)dec-3-ene 1 reference Copaane sesquiterpenoids

  10.1021/NP50012A010

• (1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 1 reference Bicyclogermacrane sesquiterpenoids $ Cyclogermacrane sesquiterpenoids

  10.1055/S-1999-14025

• (1Z,5Z,8S)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene 1 reference Germacrane sesquiterpenoids

  10.1055/S-1999-14025

• Alloaromadendren 1 reference Aromadendrane sesquiterpenoids

  10.1055/S-1999-14025

• alpha-Bergamotene 1 reference Bergamotane sesquiterpenoids

  10.1055/S-1999-14025

• alpha-Cubebene 1 reference Cubebane sesquiterpenoids

  10.1021/NP50012A010

• Ascaridole 1 reference Menthane monoterpenoids

  10.1021/NP50017A019

• Bicyclogermacrene 1 reference Bicyclogermacrane sesquiterpenoids $ Cyclogermacrane sesquiterpenoids

  10.1055/S-1999-14025

• Camphene 1 reference Camphane monoterpenoids $ Fenchane monoterpenoids

  10.1021/NP50012A010

• Camphor 1 reference Camphane monoterpenoids

  10.1021/NP50012A010

• Caryophyllene oxide 1 reference Caryophyllane sesquiterpenoids

  10.1055/S-1999-14025

• Estragole 1 reference Cinnamic acids and derivatives

  10.1021/NP50017A019

• Eugenol 1 reference Cinnamic acids and derivatives

  10.1021/NP50017A019

• (-)-Germacrene A 1 reference Germacrane sesquiterpenoids

  10.1055/S-1999-14025

• Germacrene B 1 reference Germacrane sesquiterpenoids

  10.1021/NP50017A019

• Germacrene C 1 reference Germacrane sesquiterpenoids

  10.1055/S-1999-14025

• Limonene 1 reference Menthane monoterpenoids $ Monocyclic monoterpenoids

  10.1055/S-1999-14025

• o-Propoxyphenol 1 reference

  10.1021/NP50017A019

• Spathulenol 1 reference Aromadendrane sesquiterpenoids

  10.1055/S-1999-14025

• Terpinolene 1 reference

  10.1021/NP50017A019

• δ-Cadinene 1 reference Cadinane sesquiterpenoids

  10.1021/NP50012A010

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.