DIETHYL 2,2'-(ETHANE-1,2-DIYLBIS(AZAN-1-YL-1-YLIDENE))BIS(4-AMINO-3-PHENYL-2,3-DIHYDROTHIAZOLE-5-CARBOXYLATE)


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	HGMNQASBZXAGHC-ZUSIYWPSSA-N
Smiles	CCOC(=O)C1=C(N)N(\C(=N/CC\N=C\2/SC(=C(N)N2c3ccccc3)C(=O)OCC)\S1)c4ccccc4
InChI	InChI=1S/C26H28N6O4S2/c1-3-35-23(33)19-21(27)31(17-11-7-5-8-12-17)25(37-19)29-15-16-30-26-32(18-13-9-6-10-14-18)22(28)20(38-26)24(34)36-4-2/h5-14H,3-4,15-16,27-28H2,1-2H3/b29-25-,30-26+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C26H28N6O4S2
Molecular Weight	552.67
AlogP	3.93
Hydrogen Bond Acceptor	12.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	11.0
Polar Surface Area	186.44
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	38.0

Assay Description	Organism	Bioactivity
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of root growth at 100 mg/L relative to untreated control	Brassica napus	76.9 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of root growth at 10 mg/L relative to untreated control	Brassica napus	39.7 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of stalk growth at 100 mg/L relative to untreated control	Brassica napus	52.0 %
Herbicidal activity against Brassica napus (oilseed rape) assessed as inhibition of stalk growth at 10 mg/L relative to untreated control	Brassica napus	52.0 %
Herbicidal activity against barnyard grass Echinochloa crus-galli (barnyard grass) assessed as inhibition of root growth at 100 mg/L relative to untreated control	Echinochloa crus-galli	58.6 %
Herbicidal activity against barnyard grass Echinochloa crus-galli (barnyard grass) assessed as inhibition of root growth at 10 mg/L relative to untreated control	Echinochloa crus-galli	37.9 %
Herbicidal activity against barnyard grass Echinochloa crus-galli (barnyard grass) assessed as inhibition of stalk growth at 100 mg/L relative to untreated control	Echinochloa crus-galli	34.6 %
Herbicidal activity against barnyard grass Echinochloa crus-galli (barnyard grass) assessed as inhibition of stalk growth at 10 mg/L relative to untreated control	Echinochloa crus-galli	15.4 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2286518

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).