8-(4,6-DIMETHOXYPYRIMIDIN-2-YLOXY)-4-METHYLPHTHALAZIN-1(2H)-ONE

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Search structure


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	ZDKXJFILVZYXOD-UHFFFAOYSA-N
Smiles	COc1cc(OC)nc(Oc2cccc3C(=NNC(=O)c23)C)n1
InChI	InChI=1S/C15H14N4O4/c1-8-9-5-4-6-10(13(9)14(20)19-18-8)23-15-16-11(21-2)7-12(17-15)22-3/h4-7H,1-3H3,(H,19,20)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C15H14N4O4
Molecular Weight	314.3
AlogP	2.18
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	94.93
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	23.0

Assay Description	Organism	Bioactivity	Reference
Herbicidal activity against Chenopodium album assessed as growth inhibition at 150 g ai/ha applied as post-emergence treatment under green house conditions measured 15 days post compound treatment	Chenopodium album	50.0 %
Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 150 g ai/ha applied as post-emergence treatment under green house conditions measured 15 days post compound treatment	Amaranthus retroflexus	80.0 %
Herbicidal activity against Brassica juncea assessed as growth inhibition at 150 g ai/ha applied as post-emergence treatment under green house conditions measured 15 days post compound treatment	Brassica juncea	50.0 %
Herbicidal activity against Setaria viridis (green foxtail) assessed as growth inhibition at 150 g ai/ha applied as post-emergence treatment under green house conditions measured 15 days post compound treatment	Setaria viridis	80.0 %
Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 150 g ai/ha applied as post-emergence treatment under green house conditions measured 15 days post compound treatment	Digitaria sanguinalis	80.0 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 150 g ai/ha applied as post-emergence treatment under green house conditions measured 15 days post compound treatment	Echinochloa crus-galli	80.0 %
Herbicidal activity against Chenopodium album assessed as growth inhibition at 150 g ai/ha applied as pre-emergence treatment 24 hr after weeds seeds sowing under green house conditions measured 15 days post compound treatment	Chenopodium album	50.0 %
Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 150 g ai/ha applied as pre-emergence treatment 24 hr after weeds seeds sowing under green house conditions measured 15 days post compound treatment	Amaranthus retroflexus	50.0 %
Herbicidal activity against Brassica juncea assessed as growth inhibition at 150 g ai/ha applied as pre-emergence treatment 24 hr after weeds seeds sowing under green house conditions measured 15 days post compound treatment	Brassica juncea	50.0 %
Herbicidal activity against Setaria viridis (green foxtail) assessed as growth inhibition at 150 g ai/ha applied as pre-emergence treatment 24 hr after weeds seeds sowing under green house conditions measured 15 days post compound treatment	Setaria viridis	50.0 %
Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 150 g ai/ha applied as pre-emergence treatment 24 hr after weeds seeds sowing under green house conditions measured 15 days post compound treatment	Digitaria sanguinalis	50.0 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 150 g ai/ha applied as pre-emergence treatment 24 hr after weeds seeds sowing under green house conditions measured 15 days post compound treatment	Echinochloa crus-galli	50.0 %
Inhibition of wild type Arabidopsis thaliana acetohydroxyacid synthase	Arabidopsis thaliana	789000.0 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2253254

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).