[2-(2,4-DICHLOROPHENYL)-3-[1,2,4]TRIAZOL-1-YL-PROPYL]PROP-2-YNYLAMINE


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	DYSWLXHZWGAKMM-UHFFFAOYSA-N
Smiles	Clc1ccc(C(CNCC#C)Cn2cncn2)c(Cl)c1
InChI	InChI=1S/C14H14Cl2N4/c1-2-5-17-7-11(8-20-10-18-9-19-20)13-4-3-12(15)6-14(13)16/h1,3-4,6,9-11,17H,5,7-8H2

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C14H14Cl2N4
Molecular Weight	309.19
AlogP	3.46
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	6.0
Polar Surface Area	42.74
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	20.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Ustilago maydis ATCC 14826 assessed as inhibition of fungal cell count	Ustilago maydis	1.3 ug.mL-1
Fungicidal activity against Pyrenophora teres assessed as inhibition of radial growth	Pyrenophora teres	38.0 ug.mL-1
Fungicidal activity against Fusarium graminearum assessed as inhibition of radial growth	Fusarium graminearum	100.0 ug.mL-1
Fungicidal activity against Oculimacula yallundae assessed as inhibition of radial growth	Oculimacula yallundae	11.0 ug.mL-1
Fungicidal activity against Cercospora beticola assessed as inhibition of radial growth	Cercospora beticola	4.0 ug.mL-1
Fungicidal activity against Botryotinia fuckeliana assessed as inhibition of radial growth	Botryotinia fuckeliana	38.0 ug.mL-1

Cross References

Resources	Reference
ChEMBL	CHEMBL2251930
PubChem	23635098

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).