1-T-BUTYL-3-(ALPHA-HYDROXY-4-NITROBENZYLIDENE)PYRROLIDINE-2,4-DIONE


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	FUWMPGOAHFYMJM-SEYXRHQNSA-N
Smiles	CC(C)(C)N1CC(=O)\C(=C(\O)/c2ccc(cc2)[N+](=O)[O-])\C1=O
InChI	InChI=1S/C15H16N2O5/c1-15(2,3)16-8-11(18)12(14(16)20)13(19)9-4-6-10(7-5-9)17(21)22/h4-7,19H,8H2,1-3H3/b13-12-

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C15H16N2O5
Molecular Weight	304.3
AlogP	1.38
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	3.0
Polar Surface Area	103.42
Molecular species	ACID
Aromatic Rings	1.0
Heavy Atoms	22.0

Assay Description	Organism	Bioactivity
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as plant bleaching effect at 100 ug/mL	Echinochloa crus-galli	None
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 100 ug/mL	Echinochloa crus-galli	9.8 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 10 ug/mL	Echinochloa crus-galli	0.0 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as growth inhibition at 100 ug/mL	Brassica napus	48.1 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as growth inhibition at 10 ug/mL	Brassica napus	1.8 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2252308
PubChem	76329990

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).