(E)-3-(4-HYDROXY-3-METHOXYPHENYL)-1-(5-ISOBUTYLPYRAZIN-2-YL)PROP-2-EN-1-ONE


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	LWJHFQDVCFXRKC-GQCTYLIASA-N
Smiles	COc1cc(\C=C\C(=O)c2cnc(CC(C)C)cn2)ccc1O
InChI	InChI=1S/C18H20N2O3/c1-12(2)8-14-10-20-15(11-19-14)16(21)6-4-13-5-7-17(22)18(9-13)23-3/h4-7,9-12,22H,8H2,1-3H3/b6-4+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C18H20N2O3
Molecular Weight	312.36
AlogP	3.23
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	6.0
Polar Surface Area	72.31
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	23.0

Assay Description	Organism	Bioactivity
Antifungal activity against Trichophyton mentagrophytes 445 after 120 hr by microdilution broth method	Trichophyton mentagrophytes	None
Antimycobacterial activity against Mycobacterium tuberculosis H37Rv ATCC 27294 at 12.5 ug/ml by microplate alamar blue assay relative to control	Mycobacterium tuberculosis H37Rv	53.0 %
Antifungal activity against Trichophyton mentagrophytes 445 after 72 hr by microdilution broth method	Trichophyton mentagrophytes	250000.0 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2288837
PubChem	6474706

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).