((1R,7AR)-1-(FURAN-3-YL)-7A-METHYL-3-OXO-1,3,5,6,7,7A-HEXAHYDROISOBENZOFURAN-4-YL)METHYL 2-(NAPHTHALEN-1-YL)ACETATE


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	BUYIUHDBZGNBMU-AZGAKELHSA-N
Smiles	C[C@@]12CCCC(=C1C(=O)O[C@H]2c3cocc3)COC(=O)Cc4cccc5ccccc45
InChI	InChI=1S/C26H24O5/c1-26-12-5-9-19(23(26)25(28)31-24(26)20-11-13-29-15-20)16-30-22(27)14-18-8-4-7-17-6-2-3-10-21(17)18/h2-4,6-8,10-11,13,15,24H,5,9,12,14,16H2,1H3/t24-,26+/m0/s1

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C26H24O5
Molecular Weight	416.47
AlogP	4.89
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	6.0
Polar Surface Area	65.74
Molecular species	None
Aromatic Rings	3.0
Heavy Atoms	31.0

Assay Description	Organism	Bioactivity
Insecticidal activity against Mythimna separata (Oriental armyworm) in wheat leaves assessed as mortality rate at 1 mg/mL at 25 degC measured after 35 days by leaf-dipping method relative to control	Mythimna separata	48.1 %
Insecticidal activity against Mythimna separata (Oriental armyworm) in wheat leaves assessed as mortality rate at 1 mg/mL at 25 degC measured after 25 days by leaf-dipping method relative to control	Mythimna separata	33.3 %
Insecticidal activity against Mythimna separata (Oriental armyworm) in wheat leaves assessed as mortality rate at 1 mg/mL at 25 degC measured after 10 days by leaf-dipping method relative to control	Mythimna separata	20.7 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2229493
PubChem	60167060

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).