N'-TERT-BUTYL-N'-(3,5-DIMETHYLBENZOYL)-2-METHYL-2,3-DIHYDROBENZOFURAN-6-CARBOHYDRAZIDE


Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	CALDISSJISJPMY-UHFFFAOYSA-N
Smiles	CC1Cc2ccc(cc2O1)C(=O)NN(C(=O)c3cc(C)cc(C)c3)C(C)(C)C
InChI	InChI=1S/C23H28N2O3/c1-14-9-15(2)11-19(10-14)22(27)25(23(4,5)6)24-21(26)18-8-7-17-12-16(3)28-20(17)13-18/h7-11,13,16H,12H2,1-6H3,(H,24,26)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C23H28N2O3
Molecular Weight	380.48
AlogP	4.42
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	58.64
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	28.0

Assay Description	Organism	Bioactivity
Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 200 mg/L measured after 4 days by leaf-dip method	Mythimna separata	100.0 %
Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 100 mg/L measured after 4 days by leaf-dip method	Mythimna separata	100.0 %
Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 50 mg/L measured after 4 days by leaf-dip method	Mythimna separata	100.0 %
Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 25 mg/L measured after 4 days by leaf-dip method	Mythimna separata	100.0 %
Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 10 mg/L measured after 4 days by leaf-dip method	Mythimna separata	70.0 %
Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 200 mg/L measured after 3 days by leaf-dip method	Spodoptera exigua	100.0 %
Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 100 mg/L measured after 3 days by leaf-dip method	Spodoptera exigua	100.0 %
Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 50 mg/L measured after 3 days by leaf-dip method	Spodoptera exigua	100.0 %
Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 10 mg/L measured after 3 days by leaf-dip method	Spodoptera exigua	90.0 %
Stomach toxicity against third-instar Plutella xylostella (diamondback moth) in compound treated fresh cabbage leaves assessed as insecticidal activity at 200 mg/L measured after 3 days by leaf-dip method	Plutella xylostella	80.0 %
Stomach toxicity against third-instar Ostrinia nubilalis (European corn borer) in compound treated fresh corn leaves assessed as insecticidal activity at 200 mg/L measured after 4 days by leaf-dip method	Ostrinia nubilalis	60.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2230231
PubChem	50940748

CONTENTS


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).