ARGENTONE


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	FHNDXUYNRPSKDT-INIZCTEOSA-N
Smiles	COC1=C[C@]2(C)CCC(=CC2=C(C)C1=O)C(C)C
InChI	InChI=1S/C16H22O2/c1-10(2)12-6-7-16(4)9-14(18-5)15(17)11(3)13(16)8-12/h8-10H,6-7H2,1-5H3/t16-/m0/s1

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C16H22O2
Molecular Weight	246.34
AlogP	3.56
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	2.0
Polar Surface Area	26.3
Molecular species	None
Aromatic Rings	0.0
Heavy Atoms	18.0

Assay Description	Organism	Bioactivity
Ratio of mortality to compound consumption in Reticulitermes flavipes at 5.5 ug/disk after 10 days	Reticulitermes flavipes	2.0
Antitermitic activity against Reticulitermes flavipes assessed as mortality at 5.5 ug/disk after 10 days by no-choice paper disk assay	Reticulitermes flavipes	66.0 %
Antifeedant activity against Reticulitermes flavipes assessed as compound consumption at 5.5 ug/disk after 10 days by no-choice paper disk assay	Reticulitermes flavipes	33.0 %
Antifeedant activity against Reticulitermes flavipes assessed as feeding inhibition at 2.7 ug/disk after 3 days by choice paper disk assay	Reticulitermes flavipes	70.5 %
Antifeedant activity against Reticulitermes flavipes assessed as feeding inhibition after 3 days by choice paper disk assay	Reticulitermes flavipes	85.7 ppm

Cross References

Resources	Reference
ChEMBL	CHEMBL2269940
PubChem	10824338

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).