2-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)-1H-BENZO[D]IMIDAZOLE


UNII	1545W9H5TZ
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	RUGYNGIMTAFTLP-UHFFFAOYSA-N
Smiles	Cc1cc(C)n(n1)c2nc3ccccc3[nH]2
InChI	InChI=1S/C12H12N4/c1-8-7-9(2)16(15-8)12-13-10-5-3-4-6-11(10)14-12/h3-7H,1-2H3,(H,13,14)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C12H12N4
Molecular Weight	212.25
AlogP	2.54
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	1.0
Polar Surface Area	46.5
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	16.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Magnaporthe oryzae in rice seedlings assessed as control of rice blast at 500 ppm by preventive foliar treatment	Magnaporthe oryzae	None
Fungicidal activity against Magnaporthe oryzae in rice seedlings assessed as control of rice blast at 500 ppm by curative foliar treatment	Magnaporthe oryzae	0.0 %
Fungicidal activity against Magnaporthe oryzae by agar dilution method	Magnaporthe oryzae	100.0 ug.mL-1
Fungicidal activity against Magnaporthe salvinii by agar dilution method	Magnaporthe salvinii	25.0 ug.mL-1

Cross References

Resources	Reference
ChEMBL	CHEMBL2288250
FDA SRS	1545W9H5TZ
PubChem	38441
SureChEMBL	SCHEMBL21295
ZINC	ZINC01433017

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).