InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3 |
DSSYKIVIOFKYAU-UHFFFAOYSA-N |
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plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
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View more via ChEBI Ontology
1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
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bornan-2-one
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2-bornanone
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NIST Chemistry WebBook
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2-camphanone
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NIST Chemistry WebBook
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2-keto-1,7,7-trimethylnorcamphane
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ChemIDplus
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camphor
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UniProt
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Camphor
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KEGG COMPOUND
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camphor
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ChemIDplus
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Formosa camphor
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NIST Chemistry WebBook
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gum camphor
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ChemIDplus
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Japan camphor
|
NIST Chemistry WebBook
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Kampfer
|
NIST Chemistry WebBook
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laurel camphor
|
NIST Chemistry WebBook
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root bark oil
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ChemIDplus
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spirit of camphor
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ChemIDplus
|
470
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DrugCentral
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C00000135
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KNApSAcK
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C00809
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KEGG COMPOUND
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C18369
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KEGG COMPOUND
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Camphor
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Wikipedia
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Camphor
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MetaCyc
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D00098
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KEGG DRUG
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DB01744
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DrugBank
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LMPR0102120001
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LIPID MAPS
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View more database links |
1907611
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Beilstein Registry Number
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ChemIDplus
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3196099
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Reaxys Registry Number
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Reaxys
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464-48-2
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CAS Registry Number
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KEGG COMPOUND
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6475830
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Beilstein Registry Number
|
Beilstein
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76-22-2
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CAS Registry Number
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NIST Chemistry WebBook
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76-22-2
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CAS Registry Number
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ChemIDplus
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83275
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Gmelin Registry Number
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Gmelin
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17488023
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PubMed citation
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Europe PMC
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19384733
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PubMed citation
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Europe PMC
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20950270
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PubMed citation
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Europe PMC
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21562741
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PubMed citation
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Europe PMC
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21620923
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PubMed citation
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Europe PMC
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21777420
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PubMed citation
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Europe PMC
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21906366
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PubMed citation
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Europe PMC
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