Amino-cyano-methyl-nitrophenyl-pyrazolo-pyridine-carbothioamide-Cpd7
Derivative 7 (LC50 = 0.16 microg/mL) exhibited the strongest insecticidal activity, outperforming chlorpyrifos (LC50 = 52.90 microg/mL)
General
Type : Pyridine, Pyrazol, Sulfur Compound, Cyanide, Carbothioamide
Chemical_Nomenclature : 6-amino-5-cyano-3-methyl-4-(4-nitrophenyl)-1 H-pyrazolo[3,4-b]pyridine-1-carbothioamide
Canonical SMILES : C1(=NC3=C(C(=C1C#N)C2=CC=C([N+](=O)[O-])C=C2)C(=N[N]3C(=S)N)C)N
InChI : InChI=1S\/C15H11N7O2S\/c1-7-11-12(8-2-4-9(5-3-8)22(23)24)10(6-16)13(17)19-14(11)21(20-7)15(18)25\/h2-5H,1H3,(H2,17,19)(H2,18,25)
InChIKey : AKGXJYOSTHHXPU-UHFFFAOYSA-N
Other name(s) : Compound 7
Target
References (1)
| Title : Design, synthesis, and insecticidal potency of novel 3-methyl-pyrazole derivatives against Culex pipiens larvae - Nofal_2026_Sci.Rep_16_14699 |
| Author(s) : Nofal HR , Ali AK , Ismail MF , Kamal M , Hosni EM , Abbass EM |
| Ref : Sci Rep , 16 : , 2026 |
| Abstract : |
| PubMedSearch : Nofal_2026_Sci.Rep_16_14699 |
| PubMedID: 42106391 |