2-(2-CHLORO-4-(4-CHLOROPHENOXY)PHENYL)-1,3-DI(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	KVKFSLYUIUDSOI-UHFFFAOYSA-N
Smiles	OC(Cn1cncn1)(Cn2cncn2)c3ccc(Oc4ccc(Cl)cc4)cc3Cl
InChI	InChI=1S/C19H16Cl2N6O2/c20-14-1-3-15(4-2-14)29-16-5-6-17(18(21)7-16)19(28,8-26-12-22-10-24-26)9-27-13-23-11-25-27/h1-7,10-13,28H,8-9H2

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C19H16Cl2N6O2
Molecular Weight	431.28
AlogP	3.23
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	7.0
Polar Surface Area	90.88
Molecular species	NEUTRAL
Aromatic Rings	4.0
Heavy Atoms	29.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Fusarium oxysporum assessed as growth inhibition at 1 ug/mL	Fusarium oxysporum	62.5 %
Fungicidal activity against Fusarium oxysporum assessed as growth inhibition at 5 ug/mL	Fusarium oxysporum	80.9 %
Fungicidal activity against Fusarium oxysporum assessed as growth inhibition at 50 ug/mL	Fusarium oxysporum	99.0 %
Fungicidal activity against Botryosphaeria berengeriana assessed as growth inhibition at 1 ug/mL	Botryosphaeria berengeriana	90.3 %
Fungicidal activity against Botryosphaeria berengeriana assessed as growth inhibition at 5 ug/mL	Botryosphaeria berengeriana	91.0 %
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	88.1 %
Fungicidal activity against Mycosphaerella arachidis assessed as growth inhibition at 50 ug/mL	Mycosphaerella arachidis	100.0 %
Fungicidal activity against Alternaria solani assessed as growth inhibition at 1 ug/mL	Alternaria solani	58.6 %
Fungicidal activity against Alternaria solani assessed as growth inhibition at 5 ug/mL	Alternaria solani	84.2 %
Fungicidal activity against Alternaria solani assessed as growth inhibition at 50 ug/mL	Alternaria solani	99.0 %
Fungicidal activity against Fusarium graminearum assessed as growth inhibition at 1 ug/mL	Fusarium graminearum	82.6 %
Fungicidal activity against Fusarium graminearum assessed as growth inhibition at 5 ug/mL	Fusarium graminearum	100.0 %
Fungicidal activity against Fusarium graminearum assessed as growth inhibition at 50 ug/mL	Fusarium graminearum	100.0 %
Fungicidal activity against Mycosphaerella arachidis assessed as growth inhibition at 5 ug/mL	Mycosphaerella arachidis	100.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2229578
PubChem	76307912
SureChEMBL	SCHEMBL15974147

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).