5-[[4-(4-PHENYLBENZOYLOXY)PHENYL]METHYL]-2-THIOXO-4-IMIDAZOLIDINONE


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	JDXUWYNBWXEGRR-UHFFFAOYSA-N
Smiles	O=C(Oc1ccc(CC2NC(=S)NC2=O)cc1)c3ccc(cc3)c4ccccc4
InChI	InChI=1S/C23H18N2O3S/c26-21-20(24-23(29)25-21)14-15-6-12-19(13-7-15)28-22(27)18-10-8-17(9-11-18)16-4-2-1-3-5-16/h1-13,20H,14H2,(H2,24,25,26,29)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C23H18N2O3S
Molecular Weight	402.47
AlogP	4.92
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	6.0
Polar Surface Area	99.52
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	29.0

Assay Description	Organism	Bioactivity
Herbicidal activity against Arabidopsis thaliana assessed as inhibition of seed germination at 200 ug/ml relative to control	Arabidopsis thaliana	5.0 %
Herbicidal activity against Triticum aestivum (wheat) assessed as inhibition of root growth at 200 ug/ml relative to control	Triticum aestivum	3.2 %
Herbicidal activity against Triticum aestivum (wheat) assessed as inhibition of height growth at 200 ug/ml relative to control	Triticum aestivum	20.9 %
Herbicidal activity against Zea mays (maize) assessed as inhibition of root growth at 200 ug/ml relative to control	Zea mays	48.7 %
Herbicidal activity against Zea mays (maize) assessed as inhibition of height growth at 200 ug/ml relative to control	Zea mays	42.4 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2272109
PubChem	76319788

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).