1-(4-TERT-BUTYLBENZYL)-2-PHENYL-4,5-DIHYDRO-1H-IMIDAZOLE


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	WSWNUODUGGIHOQ-UHFFFAOYSA-N
Smiles	CC(C)(C)c1ccc(CN2CCN=C2c3ccccc3)cc1
InChI	InChI=1S/C20H24N2/c1-20(2,3)18-11-9-16(10-12-18)15-22-14-13-21-19(22)17-7-5-4-6-8-17/h4-12H,13-15H2,1-3H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C20H24N2
Molecular Weight	292.42
AlogP	4.31
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	4.0
Polar Surface Area	15.6
Molecular species	BASE
Aromatic Rings	2.0
Heavy Atoms	22.0

Assay Description	Organism	Bioactivity
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) in second leaf stage of Phaseolus vulgaris var. Serena assessed as mortality at 100 ppm after 7 days	Tetranychus urticae	25.0 %
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) in second leaf stage of Phaseolus vulgaris var. Serena assessed as mortality at 500 ppm after 7 days	Tetranychus urticae	80.0 %
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) in second leaf stage of Phaseolus vulgaris var. Serena assessed as mortality at 200 ppm after 7 days	Tetranychus urticae	50.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2286384
PubChem	76316383

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).