PROPYL 2-(5-(1,3-DIOXO-4,5,6,7-TETRAHYDRO-1H-ISOINDOL-2(3H)-YL)-6-FLUOROBENZO[D]THIAZOL-2-YLTHIO)ACETATE


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	VTVBIIBOPGHXBN-UHFFFAOYSA-N
Smiles	CCCOC(=O)CSc1nc2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2s1
InChI	InChI=1S/C20H19FN2O4S2/c1-2-7-27-17(24)10-28-20-22-14-9-15(13(21)8-16(14)29-20)23-18(25)11-5-3-4-6-12(11)19(23)26/h8-9H,2-7,10H2,1H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C20H19FN2O4S2
Molecular Weight	434.5
AlogP	4.77
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	7.0
Polar Surface Area	130.1
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	29.0

Assay Description	Organism	Bioactivity
Herbicidal activity against Brassica juncea assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test	Brassica juncea	60.0 %
Herbicidal activity against Eclipta prostrata assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test	Eclipta prostrata	80.0 %
Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test	Amaranthus retroflexus	80.0 %
Herbicidal activity against Setaria faberi (Giant Foxtail) assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test	Setaria faberi	50.0 %
Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test	Digitaria sanguinalis	60.0 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test	Echinochloa crus-galli	60.0 %
Inhibition of Homo sapiens (human) recombinant protoporphyrinogen oxidase by UV-vis spectrophotometry	Homo sapiens	0.28 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2228326
PubChem	53342593

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).