NCBI Taxonomy: 95182

Amphipyrinae (ncbi_taxid: 95182)

found 15 associated metabolites at subfamily taxonomy rank level.

Ancestor: Noctuidae

Child Taxonomies: Nedra, Stiria, Condica, Feralia, Elaphria, Psaphida, Fota, Fala, Data, Amphipyra, Basilodes, Aucha, Acopa, Spodoptera, Bagada, Nacopa, Nocloa, Ancara, Provia, Azenia, Axenus, Magusa, Cropia, Amolita, Eccleta, Oslaria, Dyrzela, Mudaria, Callyna, Airamia, Valeria, Galgula, Crimona, Sesamia, Sasunaga, Atrephes, Ruacodes, Tristyla, Oxythres, Barybela, Cosmodes, Eremaula, Eutamsia, Pansemna, Syntheta, Aleptina, Euamiana, Chasmina, Unciella, Busseola, Grotella, Plagiomimicus, Paramiana, Lophomyra, Chalconyx, Oxycnemis, Musothyma, Bryonycta, Emarginea, Allophyes, Anycteola, Lythrodes, Viridemas, Xylocampa, Homolagoa, Annaphila, Apsaphida, Proteuxoa, Phosphila, Prospalta, Triocnemis, Pleromella, Eremochroa, Neumichtis, Satrapodes, Orthogonia, Pachythrix, Paromphale, StauropusX, Speocropia, Miracavira, Prothrinax, Walterella, Chrysoecia, Eulithosia, Heminocloa, Anorthodes, Leucosigma, Chamaeclea, Polionycta, Helioscota, Prometopus, Nephelistis, Paratrachea, Lophocalama, Leucocnemis, Neumoegenia, Amphipyrine, Copivaleria, Hypoperigea, Diplonephra, Meganephria, Redingtonia, Dipterygina, Neogrotella, Hemioslaria, Chalcopasta, Thoracolopha, Calophasidia, Platyprosopa, Asteroscopus, Policocnemis, Aleptinoides, Cirrhophanus, Brachionycha, Copibryophila, Supralathosea, Grotellaforma, Thurberiphaga, Argentostiria, Hemictenophora, Metaponpneumata, Lineostriastiria, Pseudocopivaleria, unclassified Amphipyrinae

Perillic acid

4-(1-Methylethenyl)-1-cyclohexene-1-carboxylic acid

C10H14O2 (166.0994)


Perillic acid, also known as perillate, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Perillic acid is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Perillic acid is an intermediate in the Limonene and pinene degradation pathway. (KEGG); Its measurement in urine is used to monitor cancer patients receiving oral Limonene (a farnesyl transferase inhibitor that has shown antitumor properties)(PubMed ID 8723738 ). Perillic acid is found in cardamom. C471 - Enzyme Inhibitor > C2020 - Farnesyl Transferase Inhibitor

   

Perillic acid

Perillic acid

C10H14O2 (166.0994)


C471 - Enzyme Inhibitor > C2020 - Farnesyl Transferase Inhibitor

   

4-[4-(3,4-Dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol

4-[4-(3,4-Dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol

C21H28O4 (344.1987)


   

(2s)-2-{[(9z,12z,15z,17r)-1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene]amino}-4-(c-hydroxycarbonimidoyl)butanoic acid

(2s)-2-{[(9z,12z,15z,17r)-1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene]amino}-4-(c-hydroxycarbonimidoyl)butanoic acid

C23H38N2O5 (422.2781)


   

4-[(2r,3s)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol

4-[(2r,3s)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol

C21H28O4 (344.1987)


   

(2r)-2-[(1r)-4-methylcyclohex-3-en-1-yl]propane-1,2-diol

(2r)-2-[(1r)-4-methylcyclohex-3-en-1-yl]propane-1,2-diol

C10H18O2 (170.1307)


   

2-{[(9z,12z,15z)-1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene]amino}-4-(c-hydroxycarbonimidoyl)butanoic acid

2-{[(9z,12z,15z)-1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene]amino}-4-(c-hydroxycarbonimidoyl)butanoic acid

C23H38N2O5 (422.2781)


   

1,4-dimethyl 2-[(3,4-dimethoxyphenyl)methylidene]-3-[(4-hydroxy-3-methoxyphenyl)methylidene]butanedioate

1,4-dimethyl 2-[(3,4-dimethoxyphenyl)methylidene]-3-[(4-hydroxy-3-methoxyphenyl)methylidene]butanedioate

C23H24O8 (428.1471)


   

(2r)-2-[(1s)-4-methylcyclohex-3-en-1-yl]propane-1,2-diol

(2r)-2-[(1s)-4-methylcyclohex-3-en-1-yl]propane-1,2-diol

C10H18O2 (170.1307)


   

2-[(1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene)amino]-4-(c-hydroxycarbonimidoyl)butanoic acid

2-[(1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene)amino]-4-(c-hydroxycarbonimidoyl)butanoic acid

C23H38N2O5 (422.2781)


   

(2s)-2-{[(9z,12z,15z,17s)-1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene]amino}-4-(c-hydroxycarbonimidoyl)butanoic acid

(2s)-2-{[(9z,12z,15z,17s)-1,17-dihydroxyoctadeca-9,12,15-trien-1-ylidene]amino}-4-(c-hydroxycarbonimidoyl)butanoic acid

C23H38N2O5 (422.2781)


   

(4r)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid

(4r)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid

C10H14O2 (166.0994)


   

2-(4-methylcyclohex-3-en-1-yl)propane-1,2-diol

2-(4-methylcyclohex-3-en-1-yl)propane-1,2-diol

C10H18O2 (170.1307)


   

(4s)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid

(4s)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid

C10H14O2 (166.0994)


   

1,4-dimethyl (2z,3z)-2-[(3,4-dimethoxyphenyl)methylidene]-3-[(4-hydroxy-3-methoxyphenyl)methylidene]butanedioate

1,4-dimethyl (2z,3z)-2-[(3,4-dimethoxyphenyl)methylidene]-3-[(4-hydroxy-3-methoxyphenyl)methylidene]butanedioate

C23H24O8 (428.1471)