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The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at The data is made available under the Creative Commons License (CC BY 3.0, For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

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Accession:CHEBI:39397 term browser browse the term
Definition:A phthalimide insecticide that has formula C19H25NO4.
Synonyms:exact_synonym: (1,3-dioxo-1,3,4,5,6,7-hexahydro-2H-isoindol-2-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
 related_synonym: Formula=C19H25NO4;   InChI=1S/C19H25NO4/c1-11(2)9-14-15(19(14,3)4)18(23)24-10-20-16(21)12-7-5-6-8-13(12)17(20)22/h9,14-15H,5-8,10H2,1-4H3;   InChIKey=CXBMCYHAMVGWJQ-UHFFFAOYSA-N;   Neo-pynamin;   Neopinamin;   Phthalthrin;   SMILES=CC(C)=CC1C(C(=O)OCN2C(=O)C3=C(CCCC3)C2=O)C1(C)C
 xref: Beilstein:1547171;   CAS:7696-12-0;   Drug_Central:4730;   KEGG:C18373;   KEGG:D07368
 xref_mesh: MESH:C009424
 xref: PPDB:628

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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        pesticide 0
          insecticide 0
            phthalimide insecticide 0
              tetramethrin 0
                (1R)-tetramethrin 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 0
    subatomic particle 0
      composite particle 0
        hadron 0
          baryon 0
            nucleon 0
              atomic nucleus 0
                atom 0
                  main group element atom 0
                    p-block element atom 0
                      carbon group element atom 0
                        carbon atom 0
                          organic molecular entity 0
                            organic group 0
                              organic divalent group 0
                                organodiyl group 0
                                  carbonyl group 0
                                    carbonyl compound 0
                                      dicarboxylic acids and O-substituted derivatives 0
                                        dicarboxylic acid 0
                                          C4-dicarboxylic acid 0
                                            butenedioic acid 0
                                              maleic acid 0
                                                maleimides 0
                                                  tetramethrin 0
                                                    (1R)-tetramethrin 0
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