PYRENOCINE K

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Search structure


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	GUGDAUYYWAEZBO-QMMMGPOBSA-N
Smiles	COC1=CC(=O)OC2=C1CO[C@@H](CC(=O)C)C2
InChI	InChI=1S/C12H14O5/c1-7(13)3-8-4-11-9(6-16-8)10(15-2)5-12(14)17-11/h5,8H,3-4,6H2,1-2H3/t8-/m0/s1

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C12H14O5
Molecular Weight	238.24
AlogP	-0.32
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	3.0
Polar Surface Area	61.83
Molecular species	None
Aromatic Rings	0.0
Heavy Atoms	17.0

Assay Description	Organism	Bioactivity	Reference
Antifungal activity against Phytophthora infestans by agar diffusion test	Phytophthora infestans	0.0 mm
Antifungal activity against Zymoseptoria tritici by agar diffusion test	Zymoseptoria tritici	6.0 mm
Antifungal activity against Magnaporthe oryzae by agar diffusion test	Magnaporthe oryzae	0.0 mm
Antifungal activity against Botryotinia fuckeliana by agar diffusion test	Botryotinia fuckeliana	0.0 mm
Antifungal activity against Microbotryum violaceum by agar diffusion test	Microbotryum violaceum	5.0 mm
Antialgal activity against 'Chlorella' fusca by agar diffusion test	Chlorella fusca	6.0 mm
Antimicrobial activity against Escherichia coli by agar diffusion test	Escherichia coli	6.0 mm
Antimicrobial activity against Bacillus megaterium by agar diffusion test	Bacillus megaterium	8.0 mm

Cross References

Resources	Reference
ChEMBL	CHEMBL2288016
PubChem	76334677

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).