1-(2-((1-METHYL-1H-BENZO[D]IMIDAZOL-2-YL)METHOXY)PHENYL)ETHANONE


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	WLXCDFCGLOSESQ-UHFFFAOYSA-N
Smiles	CC(=O)c1ccccc1OCc2nc3ccccc3n2C
InChI	InChI=1S/C17H16N2O2/c1-12(20)13-7-3-6-10-16(13)21-11-17-18-14-8-4-5-9-15(14)19(17)2/h3-10H,11H2,1-2H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C17H16N2O2
Molecular Weight	280.32
AlogP	3.05
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	4.0
Polar Surface Area	44.12
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	21.0

Assay Description	Organism	Bioactivity
Antifungal activity against Fusarium solani assessed as inhibition of mycelium growth after 1 week	Fusarium solani	100.0 ug.mL-1
Antifungal activity against Alternaria solani assessed as inhibition of mycelium growth after 1 week	Alternaria solani	100.0 ug.mL-1
Antifungal activity against Botryotinia fuckeliana assessed as inhibition of mycelium growth after 1 week	Botryotinia fuckeliana	100.0 ug.mL-1
Antifungal activity against Colletotrichum gloeosporioides assessed as inhibition of mycelium growth after 1 week	Colletotrichum gloeosporioides	70.62 ug.mL-1
Antifungal activity against Cytospora sp. assessed as inhibition of mycelium growth after 1 week	Cytospora	100.0 ug.mL-1
Antifungal activity against Fusarium solani assessed as inhibition of mycelium growth at 100 ug/ml after 1 week	Fusarium solani	64.73 %
Antifungal activity against Botryotinia fuckeliana assessed as inhibition of mycelium growth at 100 ug/ml after 1 week	Botryotinia fuckeliana	64.91 %
Antifungal activity against Alternaria solani assessed as inhibition of mycelium growth at 100 ug/ml after 1 week	Alternaria solani	65.52 %
Antifungal activity against Cytospora sp. assessed as inhibition of mycelium growth at 100 ug/ml after 1 week	Cytospora	64.52 %
Antifungal activity against Colletotrichum gloeosporioides assessed as inhibition of mycelium growth at 100 ug/ml after 1 week	Colletotrichum gloeosporioides	71.43 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2287558
PubChem	71563192

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).