5-(3-NITROBENZYLIDENE)-2-IMINO-3-(4-PHENYLTHIAZOL-2-YL)-THIAZOLIDIN-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	OTGYEYHJCWJWIR-UDIJICLVSA-N
Smiles	[O-][N+](=O)c1cccc(\C=C\2/SC(=N)N(C2=O)c3nc(cs3)c4ccccc4)c1
InChI	InChI=1S/C19H12N4O3S2/c20-18-22(19-21-15(11-27-19)13-6-2-1-3-7-13)17(24)16(28-18)10-12-5-4-8-14(9-12)23(25)26/h1-11,20H/b16-10-,20-18?

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C19H12N4O3S2
Molecular Weight	408.45
AlogP	4.62
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	156.41
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	28.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Botryotinia fuckeliana assessed as growth inhibition at 50 ppm after 48 hr relative to untreated control	Botryotinia fuckeliana	0.0 %
Fungicidal activity against Magnaporthe oryzae assessed as growth inhibition at 50 ppm after 48 hr relative to untreated control	Magnaporthe oryzae	3.2 %
Fungicidal activity against Fusarium graminearum assessed as growth inhibition at 50 ppm after 48 hr relative to untreated control	Fusarium graminearum	20.6 %
Fungicidal activity against Gaeumannomyces graminis assessed as growth inhibition at 50 ppm after 48 hr relative to untreated control	Gaeumannomyces graminis	0.0 %
Fungicidal activity against Pythium aphanidermatum assessed as growth inhibition at 50 ppm after 48 hr relative to untreated control	Pythium aphanidermatum	25.0 %
Fungicidal activity against Aspergillus niger assessed as growth inhibition at 50 ppm after 48 hr relative to untreated control	Aspergillus niger	49.7 %
Fungicidal activity against Pleurotus ostreatus assessed as growth inhibition at 50 ppm after 48 hr relative to untreated control	Pleurotus ostreatus	5.9 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2268735
PubChem	76326747

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).