N-(4-BROMOPHENYL)-5-METHOXY-[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE-2-SULFONAMIDE


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	BIIDPTRZWMXLTC-UHFFFAOYSA-N
Smiles	COc1ccn2nc(nc2n1)S(=O)(=O)Nc3ccc(Br)cc3
InChI	InChI=1S/C12H10BrN5O3S/c1-21-10-6-7-18-11(14-10)15-12(16-18)22(19,20)17-9-4-2-8(13)3-5-9/h2-7,17H,1H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C12H10BrN5O3S
Molecular Weight	384.21
AlogP	2.52
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	106.85
Molecular species	ACID
Aromatic Rings	3.0
Heavy Atoms	22.0

Assay Description	Organism	Bioactivity
Post-emergence herbicidal activity against Eclipta prostrata assessed as growth inhibition at 150 g ai/ha measured 15 days post compound treatment under green house conditions	Eclipta prostrata	50.0 %
Post-emergence herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 150 g ai/ha measured 15 days post compound treatment under green house conditions	Amaranthus retroflexus	50.0 %
Post-emergence herbicidal activity against Brassica juncea assessed as growth inhibition at 150 g ai/ha measured 15 days post compound treatment under green house conditions	Brassica juncea	50.0 %
Post-emergence herbicidal activity against Poa annua assessed as growth inhibition at 150 g ai/ha measured 15 days post compound treatment under green house conditions	Poa annua	50.0 %
Post-emergence herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 150 g ai/ha measured 15 days post compound treatment under green house conditions	Digitaria sanguinalis	50.0 %
Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 150 g ai/ha measured 15 days post compound treatment under green house conditions	Echinochloa crus-galli	50.0 %
Inhibition of wild type Arabidopsis thaliana acetolactate synthase by colorimetry	Arabidopsis thaliana	1000000.0 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2251937
PubChem	76329971

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).