2-[2-(1H-BENZOIMIDAZOL-2-YLSULFANYLMETHYL)-PHENYL]-3-METHOXYACRYLICACID METHYL ESTER


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	MCBJQZHKXGIAMY-RVDMUPIBSA-N
Smiles	CO\C=C(\C(=O)OC)/c1ccccc1CSc2nc3ccccc3[nH]2
InChI	InChI=1S/C19H18N2O3S/c1-23-11-15(18(22)24-2)14-8-4-3-7-13(14)12-25-19-20-16-9-5-6-10-17(16)21-19/h3-11H,12H2,1-2H3,(H,20,21)/b15-11+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C19H18N2O3S
Molecular Weight	354.42
AlogP	3.75
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	7.0
Polar Surface Area	89.51
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	25.0

Assay Description	Organism	Bioactivity
Antifungal activity against Colletotrichum gossypii assessed as inhibition rate at 50 ug/mL	Colletotrichum gossypii	52.0 %
Antifungal activity against Dothiorella gregaria assessed as inhibition rate at 50 ug/mL	Dothiorella gregaria	87.0 %
Antifungal activity against Fusarium graminearum assessed as inhibition rate at 50 ug/mL	Fusarium graminearum	53.0 %
Antifungal activity against Rhizoctonia solani assessed as inhibition rate at 50 ug/mL	Rhizoctonia solani	78.0 %
Antifungal activity against Botrytis cinereapers assessed as inhibition rate at 50 ug/mL	Botrytis	47.0 %
Antifungal activity against Fusarium oxysporum assessed as inhibition rate at 50 ug/mL	Fusarium oxysporum	45.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2251269
PubChem	16126937

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).