Phlorisovalerophenone (BioCAD00000016203)

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Metabolite Card

Formula: C11H14O4 (210.0892)
SMILES: CC(C)CC(=O)C1=C(O)C=C(O)C=C1O

Synonyms [en]

phlorisovalerophenone; 3-methyl-1-(2,4,6-trihydroxyphenyl)butan-1-one; PIVP; 6'-Trihydroxy-3-methylbutyrophenone; (2-methylpropyl) (2; AKOS022506150

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Phlorisovalerophenone. 数据之源，洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000016203). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

3-Methyl-1-(2,4,6-trihydroxyphenyl)-1-butanone is found in alcoholic beverages. 3-Methyl-1-(2,4,6-trihydroxyphenyl)-1-butanone is a constituent of Humulus lupulus (hops).

Cytoplasm Extracellular
Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 26103-97-9
  • PubChem: 441269
  • ChEBI: ChEBI:15951
  • HMDB: HMDB0033798
  • KEGG: C07350
  • BioCyc: 3-METHYL-1-246-TRIHYDROXYPHENYLBUTAN
  • Metlin: METLIN_66632
  • Coconut NaturalProduct: CNP0210081.0

Class / Ontology

Metabolic Network
ID EC Number Name
KEGG:R05331 2.3.1.156 isovaleryl-CoA:malonyl-CoA acyltransferase
Rhea:RHEA:23573 2.3.1.156 3-methylbutanoyl-CoA + 3 malonyl-CoA + 3 H+ => phlorisovalerophenone + 3 CO2 + 4 CoA
Rhea:RHEA:23574 2.3.1.156 phlorisovalerophenone + 3 CO2 + 4 CoA => 3-methylbutanoyl-CoA + 3 malonyl-CoA + 3 H+
Rhea:RHEA:23575 2.3.1.156 3-methylbutanoyl-CoA + 3 malonyl-CoA + 3 H+ <=> phlorisovalerophenone + 3 CO2 + 4 CoA
Rhea:RHEA:51765 2.5.1.136 phlorisovalerophenone + dimethylallyl diphosphate => 4-prenylphlorisovalerophenone + diphosphate
Rhea:RHEA:51766 2.5.1.136 4-prenylphlorisovalerophenone + diphosphate => phlorisovalerophenone + dimethylallyl diphosphate
Rhea:RHEA:51767 2.5.1.136 phlorisovalerophenone + dimethylallyl diphosphate <=> 4-prenylphlorisovalerophenone + diphosphate
BioCyc:2.3.1.156-RXN 2.3.1.156 ISOVALERYL-COA + 3 MALONYL-COA + 3 PROTON --> 3-METHYL-1-246-TRIHYDROXYPHENYLBUTAN + 3 CARBON-DIOXIDE + 4 CO-A
BioCyc:RXN-7811 2.5.1.136 CPD-4211 + 3-METHYL-1-246-TRIHYDROXYPHENYLBUTAN --> PPI + CPD-7109 + PROTON
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Organism Source

Taxonomy Source

  1. Alkanna cappadocica [ncbi taxid: 2650392]
  2. Artemisia dentata [ncbi taxid: ]
  3. Atalantia racemosa [ncbi taxid: 159026]
  4. Buddleja cordata [ncbi taxid: 168492]
  5. Buphane fischeri [ncbi taxid: ]
  6. Citrullus lanatus [ncbi taxid: 3654]
  7. Crambe tatarica [ncbi taxid: 71346]
  8. Diospyros eriantha [ncbi taxid: 1009467]
  9. Fritillaria ningguoensis [ncbi taxid: ]
  10. Hagenia abyssinica [ncbi taxid: 57921]
  11. Hoffmannia strigillosa [ncbi taxid: ]
  12. Humulus lupulus [ncbi taxid: 3486]
  13. Juniperus rigida var. conferta [ncbi taxid: 13102]
  14. Lemaireocereus griseus [ncbi taxid: ]
  15. Millettia erythrocalyx [ncbi taxid: 1679271]
  16. Mycobacterium leprae [ncbi taxid: 1769]
  17. Negombata magnifica [ncbi taxid: 344322]
  18. Ononis vaginalis [ncbi taxid: 798051]
  19. Prorocentrum micans [ncbi taxid: 2945]
  20. Pteris semipinnata [ncbi taxid: 265705]
  21. Rapanea lancifolia [ncbi taxid: ]
  22. Salvia hispanica [ncbi taxid: 49212]
  23. Scorzonera pseudodivaricata [ncbi taxid: ]
  24. Syncarpia hillii [ncbi taxid: 271921]
  25. Xenoacremonium recifei [ncbi taxid: 1036759]

Pathway Synthetic

pathway id name
BioCyc:META_PWY-5808 hyperforin and adhyperforin biosynthesis
BioCyc:META_PWY-5134 superpathway of bitter acids biosynthesis
BioCyc:META_PWY-5132 lupulone and humulone biosynthesis
PlantCyc:HOP_PWY-5134 superpathway of bitter acids biosynthesis
PlantCyc:PLANT_PWY-5132 lupulone and humulone biosynthesis
PlantCyc:HOP_PWY-5132 lupulone and humulone biosynthesis
PlantCyc:PLANT_PWY-5134 superpathway of bitter acids biosynthesis
PlantCyc:PLANT_PWY-5808 hyperforin and adhyperforin biosynthesis
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