2-(PHENOXYMETHYL)-4H-3,1-BENZOXAZIN-4-ONE


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	RNHSRYWWLMTXNT-UHFFFAOYSA-N
Smiles	O=C1OC(=Nc2ccccc12)COc3ccccc3
InChI	InChI=1S/C15H11NO3/c17-15-12-8-4-5-9-13(12)16-14(19-15)10-18-11-6-2-1-3-7-11/h1-9H,10H2

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C15H11NO3
Molecular Weight	253.25
AlogP	2.98
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	3.0
Polar Surface Area	47.89
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	19.0

Assay Description	Organism	Bioactivity
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of stalk growth at 1 mg/L after 5 days by petri dish culture method relative to control	Brassica napus	27.0 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of stalk growth at 10 mg/L after 5 days by petri dish culture method relative to control	Brassica napus	79.4 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as inhibition of stalk growth at 1 mg/L after 5 days by petri dish culture method relative to control	Echinochloa crus-galli	-29.6 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as inhibition of stalk growth at 10 mg/L after 5 days by petri dish culture method relative to control	Echinochloa crus-galli	26.9 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of root growth at 1 mg/L after 5 days by petri dish culture method relative to control	Brassica napus	71.2 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of root growth at 10 mg/L after 5 days by petri dish culture method relative to control	Brassica napus	89.1 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as inhibition of root growth at 1 mg/L after 5 days by petri dish culture method relative to control	Echinochloa crus-galli	19.3 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as inhibition of root growth at 10 mg/L after 5 days by petri dish culture method relative to control	Echinochloa crus-galli	64.8 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2272458
PubChem	12626568

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).