2-(2-CHLORO-4-(4-CHLOROPHENOXY)PHENYL)-1-METHOXY-3-(1H-1,2,4-TRIAZOL-1-YL)PROPAN-2-OL


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	GDFDTFIZEZPZCB-UHFFFAOYSA-N
Smiles	COCC(O)(Cn1cncn1)c2ccc(Oc3ccc(Cl)cc3)cc2Cl
InChI	InChI=1S/C18H17Cl2N3O3/c1-25-10-18(24,9-23-12-21-11-22-23)16-7-6-15(8-17(16)20)26-14-4-2-13(19)3-5-14/h2-8,11-12,24H,9-10H2,1H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C18H17Cl2N3O3
Molecular Weight	394.25
AlogP	3.48
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	7.0
Polar Surface Area	69.4
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	26.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Fusarium oxysporum assessed as growth inhibition at 1 ug/mL	Fusarium oxysporum	89.9 %
Fungicidal activity against Fusarium oxysporum assessed as growth inhibition at 50 ug/mL	Fusarium oxysporum	100.0 %
Fungicidal activity against Botryosphaeria berengeriana assessed as growth inhibition at 1 ug/mL	Botryosphaeria berengeriana	99.2 %
Fungicidal activity against Botryosphaeria berengeriana assessed as growth inhibition at 50 ug/mL	Botryosphaeria berengeriana	100.0 %
Fungicidal activity against Mycosphaerella arachidis assessed as growth inhibition at 1 ug/mL	Mycosphaerella arachidis	78.6 %
Fungicidal activity against Mycosphaerella arachidis assessed as growth inhibition at 50 ug/mL	Mycosphaerella arachidis	99.1 %
Fungicidal activity against Alternaria solani assessed as growth inhibition at 1 ug/mL	Alternaria solani	98.7 %
Fungicidal activity against Alternaria solani assessed as growth inhibition at 50 ug/mL	Alternaria solani	100.0 %
Fungicidal activity against Fusarium graminearum assessed as growth inhibition at 1 ug/mL	Fusarium graminearum	63.2 %
Fungicidal activity against Fusarium graminearum assessed as growth inhibition at 50 ug/mL	Fusarium graminearum	98.7 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2229559
PubChem	44126741
SureChEMBL	SCHEMBL15823441

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).