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ONTOLOGY REPORT - ANNOTATIONS


Term:fenpicoxamid
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Accession:CHEBI:136340 term browser browse the term
Definition:A carboxamide resulting from the formal condensation of the carboxy group of 3-[(isobutyryloxy)methoxy]-4-methoxypyridine-2-carboxylic acid with the amino group of (3S,6S,7R,8R)-3-amino-8-benzyl-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl 2-methylpropanoate. Introduced by Dow AgroSciences, it is an antibiotic fungicide with a new target site for disease control in Septoria species.
Synonyms:exact_synonym: (3S,6S,7R,8R)-8-benzyl-3-[({3-[(isobutyryloxy)methoxy]-4-methoxypyridin-2-yl}carbonyl)amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl 2-methylpropanoate
 related_synonym: Antibiotic UK 2A procide;   Formula=C31H38N2O11;   InChI=1S/C31H38N2O11/c1-17(2)28(35)42-16-41-26-23(39-6)12-13-32-24(26)27(34)33-22-15-40-30(37)21(14-20-10-8-7-9-11-20)25(19(5)43-31(22)38)44-29(36)18(3)4/h7-13,17-19,21-22,25H,14-16H2,1-6H3,(H,33,34)/t19-,21+,22-,25-/m0/s1;   InChIKey=QGTOTYJSCYHYFK-RBODFLQRSA-N;   Inatreq;   SMILES=O1C([C@H](CC=2C=CC=CC2)[C@H]([C@@H](OC([C@H](C1)NC(C=3N=CC=C(C3OCOC(C(C)C)=O)OC)=O)=O)C)OC(=O)C(C)C)=O;   UK 2A procide
 xref: CAS:517875-34-2 "Alan Wood's Pesticides";   Pesticides:fenpicoxamid "Alan Wood's Pesticides";   Reaxys:21250066 "Reaxys"


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  CHEBI ontology 0
    role 0
      application 0
        agrochemical 0
          fenpicoxamid 0
Path 2
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  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
                                      carboxylic acid 0
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            carbamoyl group 0
                                              carboxamide 0
                                                secondary carboxamide 0
                                                  fenpicoxamid 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.